- freely available
Int. J. Mol. Sci. 2011, 12(6), 3648-3704; doi:10.3390/ijms12063648
Abstract: Micro Electromechanical Systems (MEMS) based microfluidic devices have gained popularity in biomedicine field over the last few years. In this paper, a comprehensive overview of microfluidic devices such as micropumps and microneedles has been presented for biomedical applications. The aim of this paper is to present the major features and issues related to micropumps and microneedles, e.g., working principles, actuation methods, fabrication techniques, construction, performance parameters, failure analysis, testing, safety issues, applications, commercialization issues and future prospects. Based on the actuation mechanisms, the micropumps are classified into two main types, i.e., mechanical and non-mechanical micropumps. Microneedles can be categorized according to their structure, fabrication process, material, overall shape, tip shape, size, array density and application. The presented literature review on micropumps and microneedles will provide comprehensive information for researchers working on design and development of microfluidic devices for biomedical applications.
Microfluidics is a relatively new branch of science and technology which has made extensive progress in the last few years. Microfluidic systems deal with the fluid flow in diminutive amounts, typically a few microlitres (μL) in a miniaturized system. The main functions performed by these systems are sample preparation, purification, separation, reaction, transport, immobilization, labeling, biosensing and detection. Fluid behavior at macro scale is quite different from micro and nano scale. Factors such as surface tension may become dominant in microfluidic devices. When the size of biological samples is close to the flow channels or needles through which the samples are transported, then the sample flow may not be envisaged on the basis of conventional fluidic systems. Considerable research has been made in recent years in the field of microfluidic components, devices, systems and fabrication methods. The use of micro and nano electromechanical systems (MEMS and NEMS) technology has been increasing rapidly to fabricate microfluidic devices for biomedical applications. Due to MEMS and NEMS technology, the fabrication of miniature size and high performance medical devices has become practicable to congregate the critical medical requirements like controlled delivery with negligible side effects, improved bioavailability and therapeutic effectiveness [1,2]. In recent years, the most important advancement of MEMS and NEMS in biomedicine is microfluidic transdermal drug delivery (TDD) systems . TDD systems deal with the movement of pharmaceutical compound through the skin to reach the systemic circulation for subsequent distribution in the human body . TDD system consists of micropumps, microneedles, reservoir, micro-flow sensor, blood pressure sensor, and required electronic circuit for necessary operations. Among them, micropumps and microneedles are the most important components of microfluidic system particularly for drug delivery applications. Micropumps are used for delivery and treatment purposes. Microneedles can be used as stand-alone devices and part of complicated microfluidic system in which microneedles are integrated with other devices in the system. The schematic illustration of transdermal drug delivery system is shown in Figure 1.
In recent years, a few TDD products have been reported and approved by the US FDA. IONSYS (Fentanyl ionophoretic), a product by Alza Corporation was approved in 2006 for patient controlled pain management. Emsam, a product by Bristol-Myers Squibb (Princeton, NJ, USA) was approved in 2006 for major depressive disorder. Fentanyl generic by Watson Pharmaceuticals was approved in 2007 as an analgesic. Neupro, by Schwarz Pharma (Mequon, WI, USA) was approved in 2007 for Parkinson’s disease. Exelon, by Novartis (East Hannover, NJ, USA) was approved in 2007 for dementia . Similarly various researchers have presented microfluidic devices for different medical applications. Particularly micropumps and microneedles have been extensively studied in this decade for biomedicine. But there is still a need to present the latest updates on the development of micropumps and microneedles for biomedicine because these devices are still at the research level and have limited availability for commercial use. Some earlier reviews on various applications of MEMS in the biomedical field have been reported, such as the therapeutic microsystem, surgical microsystem and drug therapy. These reviews provide basic information on various devices such as microneedles, micropumps, micro-reservoirs, etc. [6–9]. Various researchers have reported reviews on design and development of micropumps only [10–14]. Laser and Santiago  presented a comprehensive review on micropumps. But the review did not cover some actuation methods, e.g., ion conductive polymer film (ICPF), development of evaporation micropump and advance applications of micropumps in biomedicine. Woias  presented a concise overview of different types of micropumps and their applications. However, the electrowetting micropump, evaporation micropump and ICPF have not been described in the review. Tsai and Sue  reported introductory overview on the importance of micropumps for medical applications, but significant details about the applications of various kinds of micropumps for drug delivery have not been presented. Nisar et al.  presented a comprehensive and good review on various types of micropumps and their applications in biomedical applications. Some key features of micropumps like actuation techniques, performance parameters, working principles, structure, fabrication and applications have been reported, but this review has not covered latest developments in micropumps for biomedical applications. The review does not provide up-to-date information about bio-MEMS devices as there is an exponential increase in design and development in the bio-medicine field. Amirouche et al.  presented a review on current developments in micropumps. The focus of this review was on mechanical micropumps and their applications in the biomedical field. However this review has not covered non-mechanical type of micropumps. Grayson et al.  reported a brief review on various integrated MEMS devices such as biosensors, stents, immunoisolation devices, reservoirs, microneedles, etc. This review has not described all parameters of MEMS devices like design, development, actuation methods, fabrication techniques, etc. Karman et al.  reported a very basic and introductory review on drug delivery devices like micropumps, microneedles, microvalves, microactuators, microreservoirs, etc. This review has not covered important parameters such as actuation techniques, working principles, performance constraints, design, fabrication and applications of MEMS devices. Bao-jian et al.  presented information on the development and applications of MEMS based microneedles. This review has not covered some important aspects of design and development, forces experienced by microneedles, testing, structural/fluidic analyses, etc. Khanna et al.  reported a review on the particular design requirements of microneedles for diabetic therapy. This review has not covered the key parameters like development, fabrication, failure analysis, etc. Sachdeva and Banga  reported good comprehensive review on microneedles design, development, safety and regulatory issue, therapeutic applications and limitations of microneedles for commercialization. However, this review has not described the fabrication techniques of microneedles, failure of microneedles due to various applied forces, structural and fluidic analysis and integration issues of microneedles with micropumps. All reviews that have been discussed above present the information about micropumps or microneedles only. Here the authors have presented a review on micropumps and microneedles that covers most recent advancement of MEMS technology in biomedicine. This is the first comprehensive and updated review that covers latest information of microfluidic devices regarding the design, development, actuation methods, performance parameters, working principles, structure, fabrication techniques, material used for fabrication, safety issue, challenges, limitations of commercialization and applications. This comprehensive review will be helpful for researchers who would like to work in the fast growing field of bio-MEMS and bio-NEMS.
Pioneering work on micropumps started in the 1970s and developments based on microfabrication technology was initiated in the 1980s. The MEMS based micropump was developed in 1990s. The micropump is the main component of drug delivery system that provides the actuation mechanism to deliver specific volumes of therapeutic agents/drugs from the reservoir. The requirements for drug delivery include a minimum flow rate in order of 10 μL per minute or more, small size and high reliability . Normally a micropump consists of the following components: diaphragm membrane, chamber, actuator, microchannels, microvalves, inlet, outlet, etc. Micropumps can be categorized into two classes: One type has a mechanical moving part and is known as a mechanical micropump; the other has no moving part and is known as a non-mechanical micropump.
2.1. Design Specifications and Parameters of Micropumps
Design of micropumps plays an important role for practical applications of devices. To develop a suitable design of micropumps for real time applications, it is very important to understand terms like actuator, valves, chamber or reservoir, nozzle diffuser mechanism and pumping parameters properly.
The actuator is the necessary and driving part of a micropump that converts energy into motion. It is used to provide force for fluid flow in micropumps. The actuator takes energy from electricity, heat, liquid pressure, air pressure and converts it into some kind of motion. In most micropumps reported in literature, the actuation disk is attached with membrane which is used to push the fluid. Some types of time diaphragm are fabricated in such a way that it produces energy itself which pushes the fluid. In peristaltic micropumps more than one actuator is fabricated sequentially.
In micropumps, valves are used to control the fluid flow by opening, closing and partially hindering passageways. In microfluidic systems, active and passive valves have been reported. In passive valves there is no actuation mechanism. The control of fluid flow is dependent on the pressure difference in liquid chamber and the fluid flow is normally in one direction. In active valves, active elements are present for opening and closing that are operated by an external actuation source. Mostly, separate components have been reported for active micro-valves for regulating the fluid flow in microfluidic systems. It is very easy to control the active valves but they are more complicated in integrated microfluidic system.
2.1.3. Chamber or Reservoir
Chamber design is very critical in microfluidic systems and it can significantly influence the volume stroke, pressure characteristics and nozzle-diffuser loss coefficients. Most of the micropumps reported in literature have a single chamber configuration. But in order to improve the performance, two or three chamber micropumps have also been reported. Micropumps in which pumping chambers are arranged sequentially or fabricated in such a way that the multiple chambers are in series or in parallel arrangements, are known as peristaltic micropumps.
2.1.4. Nozzle/Diffuser Element
Nozzle/diffuser element is mostly used in valveless micropumps as a flow rectifier. A schematic illustration of the nozzle/diffuser action in micropumps is shown in Figure 2. Nozzle/diffuser element works in such a way that during supply mode more fluid enters in the chamber through an inlet than fluid that exiting the outlet. While in pump mode the reverse action occurs. Stemme and Stemme  were the first to report valveless miniature micropumps in which they used a nozzle/diffuser element as flow rectifying element.
2.1.5. Pumping Parameters
Various design parameters are important to optimize the performance of micropumps such as maximum flow rate (Qmax), pump power (Ppump), maximum back pressure (hmax) and pump efficiency (η). Qmax is highest at zero hmax and Qmax is zero when highest value of hmax. For incompressible flow, the pump head (h) can be calculated from the steady flow energy equation .
Where, P is pressure, γ is pressure head, is velocity head and Z is elevation.
The pump efficiency (η) in the form of power can be expressed as:
Ideally, losses are zero and both quantities Ppump and Pactuator are identical. Efficiency is governed by frictional losses, fluid leakage losses and losses due to imperfect pump construction. The total efficiency can be expressed as .
Where ηm, is mechanical efficiency, ηv is volumetric efficiency and ηh is hydraulic efficiency.
2.2. Mechanical Micropumps
The mechanical micropumps have moving parts so require a physical actuator for the pumping process. The most common mechanical micropumps are displacement type micropumps that involve a pumping chamber which is closed with a flexible diaphragm. The fluid flow is achieved by the oscillation of a diaphragm. Due to these oscillations, the pressure (ΔP) is created. This pressure is a function of stroke volume (ΔV) inside the chamber produced by the actuator. The actuator has to run itself with the dead (V0) volume in chamber. Compression ratio is the important parameter for mechanical diaphragm type micropumps. The compression ratio is defined by the equation (4):
The performance of mechanical micropump is normally limited by its mechanical components. The piezoelectric, electrostatic, thermopneumatic, electromagnetic, bimetallic, ion conductive polymer films (ICPF), phase change and shape memory alloy (SMA) are examples of mechanical micropumps. A detailed description of mechanical micropumps is given below.
2.2.1. Piezoelectric Micropumps
The conversion of mechanical energy to electronic signal (voltage) and vice versa is known as the piezoelectric effect. The materials which exhibit piezoelectric effect normally have no center of symmetry in their structure. A stress applied to such materials will alter the separation between the positive and negative charges that leads to the net polarization at the surface. An electrical field with voltage potential is created in those materials due to the polarization. This property can be used to form the actuator, micropump, inkjet printer head, etc. The effectiveness of energy and vice versa can be expressed by factor K:
Piezoelectric actuator shows large actuation and fast response time, but the fabrication of such materials is complicated on a single chip. Piezoelectric micropumps exhibit small stroke volume at high voltages. A schematic of a piezoelectric micropump is shown in Figure 3.
The first piezoelectric micropump was fabricated using micromachining technology by Van Lintel et al. . The micropump consisted of a pumping chamber, passive silicon (Si) check valve, and a thin glass membrane actuated by piezo disk. The maximum flow rate of 8 μL/min and back pressure of 9.8 kPa were observed at applied 125 V with 1 Hz frequency. Esashi et al.  reported a three layers piezoelectric pump with flow rate of 15 μL/min and back pressure of 6.4 kPa at applied 90 V with 30 Hz frequency. Olsson et al.  reported a two chamber piezoelectric micropump to improve the performance. Koch et al.  presented piezoelectric micropump based on screen printing of PZT (Lead Zirconate Titanate) on Si membrane. The flow rate of 120 μL/min and back pressure 2 kPa were observed at applied 600 V with 200 Hz frequency. Schabmueller et al.  fabricated piezoelectric micropump with passive valves. The flow rate of 1500 μL/min and back pressure of 1 kPa were achieved using ethanol. Feng and Kim  reported piezoelectric micropump that consisted of one way parylene valves. The flow rate of 3.2 μL/min and back pressure of 0.2 kPa were observed at applied 80 V with lower power consumption of 3mW. Geipel et al.  reported a novel design of micropump with back flow pressure independent flow rate. The back pressure independency was reported up to 20 kPa at low frequency. Trenkle et al.  reported a piezostack actuated peristaltic micropump. The flow rate of 40 μL/min was obtained at the frequency of 28.6 Hz using water. The flow rates were observed to be independent of backpressure up to 7 kPa, with a maximum backpressure of 45 kPa at 140 V. Johari et al.  reported the fabrication of a piezoelectric micropump for drug delivery system using two optical masks. Fluidic characteristics analysis was performed using CoventorWare simulator. Wang et al.  studied the effect of longitudinal flow asymmetry on pumping capability by using a simple pumping system comprised of a piezoelectric buzzer imbedded in a channel. Ali et al.  studied the dynamic piezoelectric micropump process. The quantitative measurement of the pressure generated, applied electrical field, frequency and length of the actuator, were observed. Liu et al.  proposed a disposable high performance piezoelectric micropump with four chambers in serial connection for closed loop insulin therapy system. Outflow resolution of 6.23 × 10−5 mL/pulse was observed. The maximum backpressure of 22 kPa was reported at applied voltage of 36 Vpp and 200 Hz frequency.
2.2.2. Electrostatic Micropumps
Electrostatic micropumps involve electrostatic forces for actuation mechanism. Electrostatic force F is defined as “the electrical force of attraction and repulsion induced by an electric field (E)”. The like charges repel each other and unlike charges attract each others. The electrostatic force applied on the electrostatic plates can be expressed by the equation (6):
Where, F is electrostatic attraction force, W is energy stored, ɛ is dielectric constant, A is area of electrodes, X is electrode spacing and V is applied voltage.
Electrostatic actuation is widely used in microfluidic devices. The fabrication of such mechanisms on electronic chip is very easy, but electrostatic actuator has only a small stroke, typically 10 μm. The main advantages of electrostatic micropump are low power consumption and fast time response. The schematic of an electrostatic micropump is shown by Figure 4.
The first electrostatic micropump was fabricated by Judy et al.  using surface micromachining technology. It consisted of active check valve, chamber and active outlet valve. Pumping results were not reported. The first experimental results of electrostatic micropump were reported by Zengerle et al. . The flow rate of 70 μL/min and back pressure of 2.5 kPa were observed at applied 170 V with frequency 25 Hz. Cabuz et al.  presented dual diaphragm electrostatic micropump using injection molding technique. Micropump was capable of bidirectional operation but only used for gases. The flow rate of 30 μL/min was observed at applied 160 V with frequency of 30 Hz and power of 8 mW. Machauf et al.  presented membrane based electrostatically actuated micropump across the working fluid. The concept was based on high and low electric permittivity of working fluid. This pump was limited only for conducting fluid. The flow rate of 1 μL/min was achieved at 50 V. Astle et al.  proposed a pumping mechanism using electrostatic actuation for gas chromatograph applications. The flow rate of 3 mL/min and backpressure of 7 kPa were observed at frequency of 14 kHz. Lee et al.  fabricated and tested a peristaltic electrostatic gas micropump that employed fluidic resonance for high flow rate and multi stage peristaltic configuration. The micropump presented the pressure ranges from 7.3 to 3.3 kPa and flow rates from 0.29 to 0.07 sccm at the duration time ranges from 0.05 and 0.35 cycles for opening of valves. Liu  reported the “pull in phenomena” in electrostatic micropump using reduced order model of membrane. Various parameters like radius, thickness, initial gap, residual stress on pull in voltage and pull in position were investigated. Lil et al.  presented the modeling of micropump membrane with electrostatic actuator. MATLAB platform was used for modeling. The resonant frequency of 635 Hz for silicon electrostatic actuating membrane was calculated. Using FEM, 680 Hz frequency was reported.
2.2.3. Thermopneuamtic Micropumps
In thermopneumatic micropumps, the actuator is based on thermal expansion. The chamber is full of air and thermopneumatic micropump is expanded and compressed periodically by the heater and cooler. The periodic change in volume of chamber provides the membrane with a regular momentum that results in fluid out flow. The pressure increase is expressed by the equation (7).
Where, ΔP is pressure change, ΔT is temperature change, β is thermal expansion, is a percentage of volume change.
The thermopneumatic type of micropump generates relatively strong pressure and displacement of membrane. However, the driving power has to be constantly maintained above a certain level. The schematic diagram of thermopneumatic micropump is shown by the Figure 5.
The first thermopneumatic micropump based on microfabrication was proposed by Van De Pol et al. . The flow rate of 34 μL/min was observed at applied voltage of 6 V with temperature around 30 ˚C. Jeong and Yang  reported a thermopneumatic micropump with corrugated diaphragm. The flow rate of 14 μL/min was observed at applied voltage of 8 V with frequency of 4 Hz. A thermopneumatic micropump consisting of a thin film heater, flow strictor and two reservoirs has been proposed by Cooney and Towe . The maximum flow rate of 1.4 μL/min for 4.5 h was observed with an average power of 200 mW. Kim et al.  proposed a thermopneumatic micropump with a glass layer, indium tin oxide heater, polydimethylsiloxane (PDMS) chamber, PDMS membrane and PDMS cavity. The flow rate of 0.078 μL/min was achieved at applied voltage of 55 V with frequency of 6 Hz. Jeong and Konishi  fabricated a peristaltic micropump consisting of three cascaded thermopneumatic actuators and microfluidic channel connecting two fluidic inlet/outlet ports. The flow rate of 73.9 μL/min was achieved for the de-ionized (DI) water at zero backpressure. Chia et al.  proposed a novel thermopneumatic peristaltic micropump comprised of two separate zones for air heating and fluid squeezing. The temperature elevation of 2.0 K was reported on the fluid pumping area. Tan et al.  fabricated a peristaltic micropump by bonding a PDMS part with microchannels to the PDMS/PMMA (polymethylmethacrylate) part where PDMS/adhesive membrane worked like a pneumatic actuator. The maximum flow rate of 96l μL/min was achieved.
2.2.4. Electromagnetic Micropumps
Electromagnet is a kind of magnet that is based on the combination of electric and magnetic fields. When the current passes through the coils the magnetic field is produced. The strength of electromagnet can be easily varied by changing the electric current flowing through the coils. The force experienced by the point charge due to the electromagnetic field is known as the Lorentz force. The Lorentz force can be expressed by equation (8).
Where, F is force and B is magnetic field.
Electromagnetic actuation is large and covers a longer distance as compared to electrostatic actuation. It needs low voltage but an external source is required for actuation such as a permanent magnet. On small scale, this type of actuation has no benefit because it is reduced by the cube of scaling factor. The driving coils or permanent magnets bond directly with the membrane and provide a magnetic field. However, at the same time, the size is compromised. Usually electromagnetic micropumps have high power consumption and heat dissipation. A schematic of an electromagnetic micropump is shown in Figure 6.
The first electromagnetic micropump with 7 μm thick Ni80Fe20 film electroplated on 17 μm thick Si membrane was proposed by Zheng and Ahn . The maximum flow rate of 20 μL/min was observed at applied voltage of 3 V with 5 Hz frequency and 300 mA induced current. A plastic micropump with electromagnetic actuation has been reported by Bohm et al.  that consisted of two folded valves with a thin membrane in center, inlet/outlet at bottom and pump membrane at top. The maximum flow rates of 40,000 μL/min for air and 2100 μL/min for water were observed with power consumption of 0.5 W. A four layer electromagnetic micropump was designed and its static/dynamic properties were investigated by Gong et al. . The membrane deflection by different magnetic driving forces was analyzed by ANSYS FEM. The maximum flow rate of 70 μL/min was observed at frequency of 125 Hz. Yamahata et al.  reported a PMMA micropump with electromagnetic actuation. The maximum flow rate of 400 μL/min and back pressure of 1.2 kPa were observed at resonant frequencies of 12 Hz and 200 Hz. Su et al.  reported the analysis and fabrication of a valveless electromagnetic micropump with two parallel flexible diaphragms. The maximum flow rate of 6 μL/s and the displacement of 0.30 mm were observed at 100 Hz frequency with 0.3 A induced current. Balaji et al.  reported the design, fabrication and testing of a flat pump with millimeter thickness. The maximum flow rate of 15 μL/min was observed at applied voltage of 2.5 V with 68 Hz frequency and 19 mA current. Yu-feng et al.  reported a parallel dynamic micropump with valve, diaphragm and electromagnetic coil. The maximum flow rate of 6 μL/s and the diaphragm displacement of 30 μm were observed at 100 Hz frequency with 0.3 A of current. Shen et al.  fabricated and characterized a reciprocating PMMA ball valve micropump with electromagnetic actuation. The micropump showed a backpressure of 35 kPa and flow rate of 6 mL/min at 2 W electromagnetic actuation power with 20 Hz resonant frequency. Halhouli et al.  worked on the design of a novel electromagnetic pump that based on the rotation of two hard magnets kept in channel, with opposing polarity. The maximum flow rate of 13.7 mL/min at 200 rpm and a pressure of 785 Pa at 136 rpm were observed.
2.2.5. Bimetallic Micropumps
Bimetal refers to an object that is composed of two different metals jointed together. The thermal expansion coefficients of these metals are different. The deflection of a diaphragm made of bimetallic materials is induced against thermal alternation as long as the two chosen materials possess adequately discriminative thermal expansion factors. A block diagram of bimetallic micropump is shown in Figure 7.
Zhan et al.  reported Si based bimetallic micropump with 10 μm thick layer of aluminum (Al) on Si substrate. The flow rate of 45 μL/min and back pressure of 12 kPa were observed at applied voltage of 5.5 V with 0.5 Hz frequency. Zou et al.  designed a micropump that operated on both bimetallic thermal actuation and thermal pneumatic actuation mechanisms. When the bimetallic actuator made of Al/Si membrane was heated, the membrane deformed in downward direction. At the same time, the gas in the air chamber expended due to the heat to support bimetallic actuation. The flow rate of 336 μL/min was achieved when the open pressure was 0.5 kPa. A novel micropump operated on bimetallic and electrostatic actuation mechanisms was reported by Pang et al. . Experimental results showed that the on/off flow ratio of the micropump was 180. Yang et al.  presented a bimetallic thermally actuated membrane micropump that consisted of two chips, pump chamber, two bimetallic actuators and two check valves. The maximum flow rate of 43 μL/min was achieved at applied voltage of 16 V and 0.9 Hz frequency. The forces generated through bimetallic actuation are large and the implementation is simple. Usually the thermal expansion coefficients of materials that are involved in bimetallic micropumps are small. That is why the diminutive deflections are achieved in bimetallic actuation mechanism. The bimetallic micropumps require low voltage values as compared to other micropump types. But the drawback of bimetallic micropumps is that they are not suitable to work at high frequencies.
2.2.6. Ion Conductive Polymer Film (ICPF) Micropumps
ICPF actuator shows high speed response. However, the positioning control is difficult. The core layer of ICPF is made of a sort of perfluorosulfonic acid polymer. Physically it looks like a “sandwich” diaphragm between two thin films that are placed on both sides of the polymer. These two films have high electrical conductivity. One end of the diaphragm is fixed and the ICPF diaphragm can be controlled by bending in the direction of either upside or downside as long as an appropriate pair of voltages is applied at the electrodes. The ICPF actuator is commonly called an artificial muscle because of the large bending displacement, low actuation voltage and biocompatibility. A schematic of ICPF and the bending principle is shown in Figure 8.
ICPF actuators have been developed for various applications. Guo et al.  reported a new model of micro catheter with active guide wire that had two bending degrees of freedom using ICPF actuator. Tadokoro et al.  developed multi-degree-of-freedom (DOF) micro motion devices using ICPF soft gel actuator. Guo and Asaka  proposed an underwater fish like microrobot using ICPF actuator as the servo actuator swimming motion with three degrees of freedom. Nguyen et al.  reported the design and fabrication of a flap valve ionic polymer/metal composite micropump with the diaphragm supported by a flexible material. A maximum flow rate of 760 μL/min and backpressure of 1.5 kPa were observed at the applied voltage of 3 V with 3 Hz frequency. Chen et al.  proposed the design of an integrated sensory actuator. The polyvinylidene fluoride (PVDF) films were used for simultaneous feedback of bending and force outputs of the actuator. Fang and Tan  proposed a control oriented model to envisage the deformation of diaphragm and the flow rate. Experimental results of the polypyrrole (PPy) actuated micropump showed that the maximum flow rate of 1260 μL/min was observed at the voltage of 4 V.
2.2.7. Phase Change Micropumps
The basic principle used in phase change type actuators and micropumps is the vaporization and condensation phenomenon. In vaporization, the phase transition occurs from liquid phase to vapor phase. While in condensation, the change of the physical state occurs from gaseous phase to liquid phase. The phase change type micropump consists of a heater, diaphragm and working fluid chamber. A schematic of phase change micropump is shown in Figure 9.
Sim et al.  proposed a phase change type micropump consisting of a pair of Al flap valves and a phase-change type actuator. The actuator comprised of a heater, working fluid chamber and silicone rubber diaphragm. The diaphragm was actuated by the vaporization and the condensation of the working fluid in the chamber of the pump. The maximum flow rate of 6.1 μL/min was achieved at applied voltage of 10 V with 0.5 Hz frequency and 60% duty ratio for zero pressure difference. Boden et al.  reported a high pressure micropump with polymeric paraffin actuation. The flow rate of 74 μL/min was achieved at a low voltage waveform with water as a pumping fluid. When the pressures up to 1MPa were applied on the valves, the micropump showed no leakage. Sim et al.  reported the fabrication and testing of a micropump comprised of a pair of Al flap valves and a phase change type actuator. The actuator was composed of a heater, diaphragm and fluid chamber. The maximum flow rate of 97 μL/min was observed at applied voltage of 8 V with 70% duty ratio and 2 Hz frequency for zero pressure difference.
2.2.8. Shape Memory Alloy (SMA) Micropumps
SMA are the metals which exhibit two very unique properties such as pseudo elasticity and the shape memory (SM) effect. They have the capability of changing their shapes upon application of an external stimulus. The SM effect involves a phase transformation between two solid phases. At high temperature the phase is called austenite and at low temperature the phase is called martensite. SMA starts in martensite phase and transforms into austenite phase after being heated. This property of materials is useful to make SMA micropumps. A schematic of an SMA micropump is shown in Figure 10.
The first thin film SMA micropump with two different actuation configurations was reported by Benard et al. . The pump was driven by an electrical drive signal provided directly through the Titanium/Nickel (Ti/Ni) thin films, resulting in Joule heating induced phase transformation that initiated the SM effect. The maximum flow rate of 50 μL/min was observed at 0.9 Hz frequency. Makino et al.  reported the development of SMA actuated micropump to use in micro analysis and micro dosage systems. The maximum flow rate of 0.4 μL/cycle was observed at a bias pressure of 100 kPa. Xu et al.  developed a micro SMA pump composed of a NiTi/Si composite membrane, pump chamber and two inlet/outlet check valves. The flow rate of 340 μL/min and back pressure of 100 kPa were achieved. Shuxiang and Fukuda  developed SMA micropump composed of SMA coil actuator, two diffusers, pump chamber and a casing. The maximum flow rate of 500–700 μL/min was achieved by changing the frequency. Zhang and Qiu  reported a Ti/Ni/Copper (Cu) shape memory thin film micropump comprised of a TiNiCu/Si driving membrane, pump chamber and two inlet and outlet check valves. The hysteresis width ΔT of 9 °C was observed. Setiawan  reported the performance assessment of SMA spring as actuator for gripping manipulation. The SMA actuator was a TiNi tensile spring with diameter of 50 mm wire and 350 gram hanging mass. SMA have many attractive properties like high force to volume ratio, ability to recover large transformation stress and strain upon heating and cooling processes, high damping capacity, chemical resistance and biocompatibility. Usually the deformation of SMA cannot be precisely controlled and investigated due to temperature sensitivity. Additionally, the designs based on TiNi film devices with more practical, effective and complex characteristics, are required through multiple DOF and compact structures. Recently reported mechanical micropumps are listed in Table 1.
2.3. Non-Mechanical Micropumps
The non-mechanical micropumps have no moving mechanical part so that generally they need a type of mechanism that can convert non-mechanical energy into kinetic momentum. In general, non-mechanical pumps do not need physical actuation components so the geometry, design and fabrication of these micropumps are relatively simple and easy. These micropumps have certain limitations, such as the use of only low conductivity fluids and the actuation mechanisms interfere with the pumping liquids. A detailed description of non-mechanical micropumps is given below.
2.3.1. Electroosmotic (EO) Micropumps
EO flow is the motion of the liquid that is induced by an applied potential across a capillary tube or microchannels. The fluid with electric conductivity feature is driven by appropriately exerting an external electrical field upon the channel walls that are naturally charged. A schematic diagram of an electroosmotic micropump is shown in Figure 11.
Zeng et al.  fabricated an EO micropump that used DI water as working fluid. The maximum flow rate of 3.6 μL/min and pressure of 2026.5 kPa were obtained at applied voltage of 2 kV. Takemori et al.  reported an EO micropump with high pressure. The flow rate of 0.47 μL/min and pressure of 72 kPa were observed at applied 3 kV. Hu and Chao  investigated the EO flow in EO micropump with an overlapped electrical double layer (EDL). The results showed that the flow was relatively different from the channel with a dimension greater than the EDL, which demonstrated plug like flow properties. Good et al.  performed the mathematical modeling and experimental testing of water activated micropump that was actuated using the osmotic effect. The maximum flow rate of 17 μL/min/mg of dry polymer particles, with a 355–425 μm diameter, was achieved. Ryu et al.  proposed a biodegradable osmotic micropump for long use and controlled discharge of basic fibroblast growth factor (bFGF). The release of bFGF was regulated at a rate of 40 ng/day for duration of four weeks. Yairi and Richter  developed an EO micropump based on voltage control. The flow rate of 0.054 mL/min and pressure of 5.5 kPa were achieved. Borowsky et al.  fabricated a high pressure EO micropump and tested the performance of fluid dynamic. The maximum flow rate of 85 μL/min and pressure of 25 atm were achieved. Wang et al.  reported the general characteristics, fabrication technologies and applications of EO micropumps. The transport of various solutions compositions into capillaries can cause problems in the flow constancy of an EO pumped system in some applications. Sometimes flow rates are modified due to adsorption of compounds from the samples or sample matrix on the surfaces of the pumping elements. This problem can be solved by separating the pump fluid from the sample and reagent solutions in the analytical system.
2.3.2. Electrowetting (EW) Micropumps
EW is a microfluidic phenomenon that is currently used as a driving mechanism for fluidic devices. EW involves modifying the natural surface tension or capillary forces intrinsic to an oil and water interface at small length scales. At less than 1 mm distance, the electrical and surface tension forces are much stronger than gravity. The digital EW is applied to control the surface tension between solid phase electrode and liquid phase droplet. A schematic of an EW micropump is shown in Figure 12.
Yun et al.  reported a continuous EW micropump. For the actuation energy of micropump, the surface tension induced motion of mercury drop in a microchannel filled with electrolyte was used. The micropump consisted of a stack of three wafers bonded together. The flow rate of 70 μL/min and pressure of 0.8 kPa were achieved at 2.3 V with frequency of 25 Hz and power consumption of 170 μW. Hoshino et al.  reported the pico liter liquid actuation in a microinjector by using a pulled glass tube as the device structure. The tube caused pumping and ejection by EW on dielectrics. 500 picoliter water was pumped up at the maximum applied voltage of 1400 V. In pumping pressure, an increase value of 0.6 Pa was calculated. Colgate and Matosumoto  reported a detailed model of a test device showing liquid flow in a small channel for the study of EW. EW gives direct fluid pumping without any moving mechanical parts that can be valuable in many application areas of microelectronic devices. The initial results showed that EW might be used to get pressures on the order of 0.01 MPa in a 10 μm radius channel. Chang et al.  reported the driving characteristics of the EW-on-dielectric device with aluminum oxide (Al2O3) deposited by using the method of atomic layer deposition. When the voltage was applied between control electrode and reference electrode then the flow of 2 μL for water droplet in an air environment was achieved.
2.3.3. Electrochemical Micropumps
The most common feature of electrochemical micropumps is the generation of bubbles by electrolysis in which the decomposition of water occurs into its constituents, such as hydrogen gas (H2) and oxygen gas (O2), when the current is passed through water. During this mechanism, the key component is a bubble reservoir filled with a redox electrolyte solution. The reaction of electrolysis can be described by the equations (9) and (10).
A schematic of electrochemical micropump is shown in Figure 13.
Suzuki and Yoneyama [93,94] fabricated an electrochemical syringe pump by using micromachining for low operating voltage and power consumption. A microfluidic system was developed by integrating an on-chip micropump and check valves that worked through a H2 bubble generated electrochemically. Thin film electrodes were used with a platinum black working electrode. PDMS substrate was used to make flow channels and containers for electrolyte solutions. Two dye solutions were transported and merged in a flow channel and sheath flows were observed. Yoshimi et al.  developed an artificial synapse using the electrochemical micropump. The micropump consisted of a glass nozzle and two blackened platinum electrodes filled with a neurotransmitter solution for the electrolysis process. To drive the solution towards the neuron, a potential difference of 3.0 V was applied to the electrodes. Kim et al.  reported a PPy-membrane microfluidic pump. The pumping action was stimulated by an electrochemical actuated PPy-PDMS membrane. The check valves were used to control the direction of flow. The maximum flow rate of 52 μL/min was obtained at ±1.5 V with input power of 55 mW.
2.3.4. Evaporation Micropumps
In evaporation micropumps, a controlled evaporation of liquid is used. Evaporation is a process in which liquid is converted from its liquid form to vapor form. The reverse of this process is known as condensation. The pumping principle of the evaporation type micropump is the same as the xylem transport system in plants. A schematic of an evaporation micropump is shown in Figure 14.
Effenhauser et al.  reported the evaporation based disposable micropump for continuous monitoring systems. The controlled evaporation of liquid was done through a membrane into gas space that contained a sorption agent. In the gas chamber, the vapor pressure was kept lower than saturation. During this process, the fluid evaporation from membrane was substituted by capillary forces that resulted in a flow from the reservoir. The average flow rate of 0.35 μL/min was achieved. Namasivayam et al.  reported the micropump based on the generally observed phenomenon of transpiration in plant leaves for continuous very low flow rates. As the vapor diffused out due to heating, a new transport of liquid was supplied into the channel from a reservoir for steady state operation. Guan et al.  reported a micropump based on capillary-evaporation effects for a microfluidic flow injection chemiluminescence system. The average flow rate of 3.02 μL/min was achieved with an ambient temperature of 20–21 °C and relative humidity of 30–32% for fluctuation within 2 h. Heuck et al.  reported the evaporation-based micropump integrated into a scanning force microscope probe for the flow of liquid through its hollow cantilever and tip areas. A flow rate of 11 pL/s was obtained at room temperature.
2.3.5. Bubble Micropumps
The bubbles micropump is based on periodic expansion and collapse in the volume controlled by voltage input. The volume change in chamber is incorporated with the diffuser/nozzle mechanism that is used to determine the direction of fluidic flow. The bubbles are generated by heating process. A schematic of the bubble micropump is shown in Figure 15.
Tsai and Lin [101,102] reported a valveless thermal-bubble micropump. Later they developed a microfluidic mixer system with a gas bubble filter using the bubble micropump. The maximum flow rate of 5 μL/min was achieved at 250 Hz with applied periodic voltage, 10% duty cycle and power consumption of 1 W. Lew et al.  developed a collapsing bubble micropump. The bubbles with a radius of about 3–5 mm were investigated through the experimental set up that employed a low voltage electrical spark of 55 V created with a capacitor for bubble generation. It was reported that the proposed theory could also work with even smaller bubbles. Jung and Kwak  reported the fabrication and testing of bubble type micropumps using an embedded microheater. The micropump comprised of a pair of nozzle/diffuser, flow controller, microchannels and a pumping chamber. The maximum flow rates of 6 μL/min at duty ratio of 60% for circular chamber and 8 μL/min at duty ratio of 40% for the square chamber were achieved. Cheng and Liu  reported an electrolysis-bubble micropump based on the roughness-gradient design in the microchannel. The electrolysis actuation and the surface tension effect were used for the micropump. The maximum flow rate of 114 μL/min was obtained at applied voltage of 15 V with a frequency of 4.5 Hz. Chan et al.  developed a bubble type micropump with high frequency flow reversal using embedded electrodes in a closed microfluidic microchannel. The micropump consisted of a microfluidic chamber and microelectrodes on a glass substrate that was assembled by PDMS-sheet. The maximum flow rate of 37.8 μL/min was achieved at voltage of 5 V.
2.3.6. Magnetohydrodynamic (MHD) Micropumps
MHD is a field in which the dynamics of electrically conducting fluids is studied. The Lorentz force is the driving source perpendicular to the electric and magnetic fields for MHD type of micropumps. The working fluid is selected to achieve conductivity of 1 s/m or higher, in addition to externally providing electric and magnetic fields. The Lorentz force can be expressed by the equation (11).
Where, F is force, E is electric field, V is instantaneous velocity of particles, B is magnetic field and Q is electric charge of the particle.
A schematic of the MHD micropump is shown in Figure 16.
Jang and Lee  reported the MHD micropump. The pressure head difference of 18 mm at 38 mA and a flow rate of 63 μL/min at 1.8 mA were achieved with an inside diameter of 2 mm for inlet/outlet tube and a magnetic flux density of 0.44 T. Zhong et al.  reported the fabrication of MHD micropump using ceramic tapes. Experiments were performed using mercury slugs, saline solutions and DI water. Eijkel et al.  developed a circular ac MHD micropump for chromatographic applications. The device comprised of a glass-gold-laminate-glass sandwich structure with the channel defined in the electroformed gold layer. Reversible flow rate of 40 μm/s was achieved. Patel and Kassegne  reported a MHD micropump with EO-thermal effects using 3D-MHD equations. The use of a developed numerical framework, flow channel geometries, Joule heating, effects of non-uniform magnetic/electric fields and EO in MHD micropumps were investigated. Duwairi and Abdullah  developed a model to envisage the fluid flow in the MHD micropump. By applying the finite difference method and the SIMPLE algorithm, the transient, incompressible, laminar and flow equations were numerically solved. Kang and Choi  reported the design and fabrication of MHD micropump with a mixing function in which the fluids were mixed and pumped at the same time by coupling between Lorentz force and the moving force of an electric charge in the electric field.
2.3.7. Flexural Planer Wave (FPW) Micropumps
The FPW micropumps are driven ultrasonically. The fluidic motion induced by traveling FPW can be used for the transport of liquids. The liquid motion is in the direction of wave propagation and the speed is proportional to the square of acoustic amplitude. Low operating voltage is required for acoustic streaming. A schematic of the FPW micropump is shown in Figure 17.
Moroney et al.  reported the process of water pumping induced by 4.7 MHz ultrasonic Lamb waves. The waves were moving in a composite membrane of silicon nitride and piezoelectric zinc oxide with a thickness of 4 μm. The observed speed was 100 μm/s at the applied rf voltage of 8 V with 6.5 nm wave amplitude. Nguyen and White  reported the design and numerical model of an ultrasonic FPW micropump and microfluidic system. The effects of channel height, wave amplitude, and backpressure on the velocity and flow rate were studied. The influence of thermal transport of the acoustic streaming was also investigated. Results showed that the micropumps with channel heights of a few micrometers exhibited high-quality performance because the flow rate and hydraulic impedance against backpressure were high. Nguyen et al.  reported a FPW micropump integrated with flow sensor for in situ measurement. The FPW micropump and the flow sensor made a complex microfluidic system capable of controlling the fluid flow in the device. Meng et al.  reported the ultrasonic FPW micropump. The waves travelled along a thin membrane to stimulate an acoustic field in the fluid that was in contact with the membrane. The micropump with a combination of radial transducers and unidirectional fluid flow resulted in a flow speed of 1.15 mm/s. Jang et al.  investigated the actuating frequency control of acoustic-streaming flow patterns in a diaphragm driven microfluidic chamber. Microfluidic circulatory flow was achieved using the resonant vibration of diaphragms. Experiments were performed to study in-plane velocity profiles near the interface of circulations where the acoustic intensity was measured to be large. The proposed flow process was reported to be useful for pumping, active mixing and particle focusing applications. Singh and Bhethanabotla  studied the enhancement in the efficiency of acoustic-streaming. Microfluidic and biosensing applications of surface-acoustic wave devices depend on the acoustic-streaming process resulting from high intensity sound waves that interact with the fluid medium.
2.3.8. Electrohydrodynamic (EHD) Micropumps
In an EHD micropump, the force is generated by the interaction of electric field and mobile charges in the fluid. These pumps have emitter and collector electrodes that are regularly spaced along a microchannel and require no moving parts such as impellers, bellows or valves. The electrical charges generated from the electrodes mobilize according to the direction of the electric field that is built up by the electrodes and tract in the surrounding liquid molecules to move together by the ion dragging force. The force acting on the fluid is given by the equation (12).
Where, F is force on fluid, I is current, d is distance between electrodes, k is ion mobility coefficient of the dielectric fluid. A schematic of an EHD micropump is shown in Figure 18.
Ritcher and Sandmaier  fabricated the first dc charged injection EHD micropump comprised of two electrically isolated grids. The flow rate of 15,000 μL/min and the pressure head of 1.72 kPa were achieved at applied voltage of 800 V. Fuhr et al.  developed the first EHD micropump based on travelling wave-induced electroconvection. The flow rates of 0.05–5 μL/min were achieved. Darabi et al. [121,122] reported the EHD polarization micropump for electronic cooling and EHD ion drag pump. The model devices exhibited a maximum cooling capacity of 65 W/cm2 with pumping head of 250 Pa. Yang et al.  reported an ejection type EHD micropump using indium-tin-oxide (ITO) planar electrodes to deal with the aging problem. The planar electrodes could drive the ethyl alcohol with a flow rate of 356 μL/min at applied dc voltage of 61 V. Lin and Jang  reported the numerical microcooling analysis for EHD micropump. The micropump offered the pumping power using the dipole moment force generated from polarizing fluid molecules. The pressure head of 13 kPa and wall heat flux of 10 W/cm2 were observed at applied voltage of 500 V with pitch of 500 μm for parallel electrodes. Darabi and Rhodes  reported the computational fluid model of ion drag EHD micropump. The micropump consisted of an array of interdigitated electrodes with the top and bottom parts of the channel. Singhal and Garimella  reported induction based EHD micropump for high heat flux cooling process. The numerical model was developed by solving the three dimensional transient fluid flow and charge transport problem due to simultaneous actuation of EHD and the vibrating diaphragm. Recently reported non-mechanical micropumps are listed in Table 2.
Microneedles are very useful delivery devices. These devices provide an interface between the drug reservoir and the patient’s body for releasing or extracting the fluid. The length of microneedles should be long enough that it penetrates the epidermis and short enough not to reach the dermis, in order to avoid pain. The concept of microneedles was proposed in the 1970s but it was not realized experimentally until the 1990s when the industry of microelectronics provided the microfabrication tools essential to make such small structures. The first microneedle arrays reported in the literature were developed by etching the Si wafer for intracellular delivery . These needles were inserted into cells and nematodes to increase molecular uptake and gene transfection. After that a number of attempts have been made by various researchers to develop the fabrication processes and different designs of microneedles. MEMS technology is the most promising to fabricate the optimal design of microneedles for particular applications. The typical diameter and length of MEMS-based microneedles are in the range of micrometers. These microneedles are different from standard hypodermic needles used in biomedicine. Generally, the length of the MEMS-based microneedles is less than 1 mm. Thus microneedles are significantly smaller in length than ordinary needles [4,133]. Microneedles or microneedle arrays can be used as a stand-alone microfluidic device as well as part of biological detection, fluid extraction or delivery system. Microneedles can be integrated with micropumps, biosensors, microelectronic devices and microfluidic chips.
3.1. Categories of Microneedles
Different designs of microneedles have been reported in literature for various applications. Microneedles can be classified in various ways such as according to structure, overall shape, tip shape, length, array density, material used for fabrication and applications [3,4]. Details of microneedle categories are shown in Table 3.
3.1.1. Structure of Microneedles
Structure is the most important consideration for microneedles design and fabrication. Based on the fabrication process, the microneedles are classified in two types.
In in-plane microneedles, the microneedle shafts or lumens are parallel to the substrate surface. The major advantage of in-plane microneedles is that the length of the microneedles can be easily and accurately controlled during fabrication process. The limitation of in-plane microneedles is that it is very difficult to fabricate microneedle arrays with 2D geometry. In out-of-plane microneedles, the lengths of the microneedles protrude out of the substrate surface and it is easier to fabricate out-of-plane microneedles in 1D or 2D arrays. However, fabrication of out-of-plane microneedles with length and high aspect ratio structure is challenging [4,134]. A schematic illustration of in-plane and out-of-plane microneedles is shown in Figure 19.
In-plane microneedles were developed in the 1980s  and not intended for drug delivery or fluid transport. An implantable ten-channel microelectrode recording array with an on-chip signal processing probe was fabricated for long term recording of neural bio-potentials. The length of probe and thickness were 4.7 mm and 15 μm respectively. A 1D array of micro neural probes  and more sophisticated 2D array have been developed . After that various attempts have been made to develop in-plane microneedles for different applications. The major drawback associated with in-plane microneedles is the limited density. To overcome this limitation, out-of-plane microneedles have been developed. One of the earliest out-of-plane microneedle array consisted of 100 microneedles with a length of 1.5 mm was reported in 1991 .
Microneedles can also be categorized as solid or hollow according to the structure. Hollow needles were invented in 1844  and gained increasing importance in the biomedical field. There are no other effective ways to transport the fluid into the human body . Hollow needles have become more important after the invention of microneedles. Hollow microneedles have an internal bore or lumen which allows flow of fluid/drug through the microneedles. A combination of surface and bulk micromachining techniques was used to fabricate hollow in-plane microneedles with 1-6 mm length and fully enclosed channels of silicon nitride . The channels were 9 μm in height. The solid microneedles have solid lumens and exhibit more strength than hollow microneedles. Solid microneedles can be further categorized into coated and dissolving microneedles. In coated microneedles, the drug particles are coated on lumen surface and injected into patient body. The microneedles are withdrawn from the body after dissolution of the coated drug. In dissolving microneedles, the base is non-dissolving and withdrawn from the skin after dissolution of the microneedles. Various types of solid coated and dissolving microneedles have been reported . Coated Ti microneedles arrays with a length of 190 μm have been reported for the delivery of parathyroid hormone (I—34) in human body for the treatment of osteoporosis by Zosano Pharma, Inc. (formerly Macroflux®, ALZA Corp.) . The successful delivery of drug depends on the methods used for coating of microneedles [141,142]. References [143,144] fabricated the first out-of-plane sharp solid microneedles for drug and gene delivery. A schematic of hollow and solid microneedles is shown in Figure 20.
Hollow silicon dioxide (SiO2) microneedles have been fabricated using deep reactive ion etching technique . Reference  fabricated SiO2 microneedles which mimic a jagged mosquito’s needle. In-plane hollow metallic hypodermic microneedles and microneedle array were reported using electroplated palladium (Pd) alloys and Ni [147–149]. Using a combination of isotropic and an isotropic etching process, sharp tip hollow out-of-plane single crystal Si microneedles were fabricated . One of the earliest solid microneedles design was in the form of pyramidal Si microprobes . Sharp Si solid microstructures with a height of 150 μm were fabricated with anisotropic dry etching technique using SF6 and O2. Such type of solid microneedles was used to increase permeability of human skin up to fourth order of magnitude in vitro. Solid microneedles for TDD were reported for the first time in 1998 .
3.1.2. Shape of Microneedles
The shape of the microneedle is very critical and important during design and fabrication. Microneedles can be classified on the basis of overall shape and tip shape. Different designs of microneedles have been proposed and fabricated such as cylindrical, canonical, pyramid, candle, spike, spear, square, pentagonal, hexagonal, octagonal and rocket shape [3,4]. Microneedles have also been reported with various tip shapes like volcano, snake fang, cylindrical, canonical, micro-hypodermis and tapered. Schematic illustrations of various designs of microneedles with respect to shape and tips are shown in Figure 21.
Rocket shape microneedles have been fabricated using two photon polymerization method . Octagonal solid out-of-plane Si microneedle array has been fabricated for drug delivery . Solid Si-tip microneedles have been fabricated using wet etching technology . Pyramidal out-of-plane Si microneedle array has been fabricated by wet etching for transcutaneous drug delivery . Side opened sharp tip out-of-plane solid microneedle has been fabricated by hot embossing to improve skin permeability for hydrophilic molecules . Cylindrical hollow out-of-plane microneedles with tapered tip using combination of ICP etching have been fabricated for TDD .
3.1.3. Materials Used for Microneedles
Microneedles can be classified on the basis of materials. Material selection is very important to design and fabricate microneedles for any particular application. Many researchers used Si for microneedles fabrication [4,157–162], which is a brittle material  and can be harmful to health. Different researchers have understood this critical issue and used polymeric material instead. Most polymers have a strong history of biocompatibility. They exhibit excellent mechanical and chemical properties  that are suitable for microneedle fabrication. Fabrication of microneedles has been reported using various polymers such as (Polyglycolic acid) PGA, (Poly-L-Lactide acid) PLLA, PC, PDMS, PMMA, etc. Fabrication of polymeric microneedles has been reported by various researchers [165,166]. Some other materials have also been reported such as glass, metal, alloy, etc. . Glass hollow elliptical tip microneedles have been fabricated using micropipette pulling technique for intrascleral delivery . In-plane Ti microneedles have been fabricated using bulk micromachining for drug delivery . Tungsten microneedles have been reported for nerve penetration .
3.1.4. Microneedles Applications
On the basis of applications, microneedles can be categorized into various types because different types of microneedles are suitable for specific applications. The suitable length of microneedles for drug delivery is 100 μm to 300 μm, but for blood extraction the appropriate length of microneedles is 1100 μm to 1600 μm . Solid microneedles are suitable for cell surgery. Microneedles have been reported for drug delivery, blood extraction, fluid sampling, cancer therapy, microdialysis, ink-jet printing and sensing electrodes. Hollow Ti microneedles have been fabricated for blood extraction using sputtering and deposition methods . SiO2 hollow square microneedles have been reported for flow delivery systems using electrochemical etching technique. Hollow out-of-plane SiO2 microneedles have been fabricated using lithography for cell surgery . Stainless-steel hollow and solid microneedles have been reported using surface micromachining and etching techniques for dermal diphtheria and influenza vaccination . Hollow out-of-plane Si microneedles have been fabricated for TDD . The extensive detail of materials used for microneedle’s designs, structure, array size, fabrication techniques, analysis and application has been presented in Table 4, Table 5 and Table 6.
3.2. Forces Experienced by Microneedles during Penetration
Fluid is transported through hollow microneedles while solid microneedles are coated with pharmaceutical materials to transfer the drugs into patient body. Microneedles are under the influence of various forces during penetration such as bending, buckling, lateral, axial and resistive. To bear all these forces, the design of microneedles is very important. Microneedles can break during penetration into the skin because of these forces. An axial force is more dominant on the tip of microneedle during insertion. This axial force is compressive and leads to buckling of the microneedle. The microneedles also experience resistive force exerted by skin. Hence, in order to pierce the microneedle into skin, the applied axial force must be greater than skin resistance. Due to uneven skin surface or human error during needle penetration, bending may occur. So, it is very important to study the relation between microneedle geometry and mechanical properties of the material for accurate microneedle design and prediction of microneedles failure. The buckling force acting on the hollow microneedle during skin insertion is given by [4,133,196,197].
Where, E is Young’s modulus of material, I(m4) is moment of inertia of cylindrical section and L(m) is length of the microneedle.
Moment of inertia (I) for hollow cylindrical section of microneedle is calculated by equation (14).
Where, D is outer diameter and d is inner diameter of hollow cylindrical section.
The bending force, which the microneedle can withstand without breaking is given by:
The axial force (compressive force), which a microneedle can withstand without breaking is given by:
Where, σy is the yield strength of the material and A is cross-sectional area of the microneedle tip.
Microneedle experiences 3.18 MPa resistive forces exerted by the skin against penetration of microneedle. To penetrate the microneedles into skin, the external applied force or pressure should be greater than the resistive skin force. The resistive force offered by the skin before puncturing is given by the following equation:
Where, Ppierce is the required pressure to pierce the microneedle into skin.
As the microneedle penetrates the skin, the resistive force falls drastically . After the skin is pierced by the microneedle, the only force that acts on the microneedles is the frictional force due to contact of tissue with the microneedle.
3.3. Fabrication of Microneedles
Various fabrication techniques have been developed and used for microneedles fabrication such as hot embossing , photolithography , micropipette pulling technique , surface micromachining , bi-mask technique , laser micromachining , micro-molding , deep x-ray lithography , DRIE , lithography, electroplating, molding (LIGA) , UV excimer laser , coherent porous Si etching (CPS) , injection molding  and ICP etching [3,4]. In these processes, Si and polymer can be used as substrate materials for microfabrication. Each fabrication technique has its own advantages and limitations. A detailed discussion on microneedles fabrication techniques will be presented in a subsequent paper.
Lithography and DRIE techniques are mostly used for fabrication of silicon microneedles. Deposition and etching are the most important phenomenon during the development of microneedles. Deep holes or free standing structures can be fabricated in silicon wafer with the help of anisotropic etching process. These high aspect ratio structures are of considerable interest in developing micro devices for various applications. The general steps of silicon microneedles fabrication are wafer cleaning, photoresist coating, soft back, masking, exposure, development, hard back, and lift off. These steps can be repeated according to requirements with desired parameters. For polymeric microneedles molding, hot embossing, and laser drilling are promising fabrication techniques. The general steps for polymeric microneedles fabrication are sheet preparation, mold preparation, heating and pressing mold, de-molding and laser drilling for different lumens/reservoir.
3.4. Microneedles Testing
The concept of microneedles was introduced three decade ago but the first microneedle array for TDD was fabricated in 1998. After that, various researchers have been involved in developing the most suitable fabrication method and optimal design of microneedles for biomedical applications. After 2005, the interests of researchers changed and they shifted their attention towards the testing of microneedles along with design and fabrication. Most of the research groups have been involved in the structural analysis and skin penetration tests of microneedles in 2010. The testing of microneedles has been reported on potato skin, chicken skin , mouse skin [156,172,180,187,193], cadaver skin [167,182], pig skin [173,177], chicken leg, beef liver , and human skin [156,174,178,183]. Microneedle patches coated with solid state influenza vaccine have been reported to improve the effectiveness of the vaccine when tested on mouse skin . Dry coated microinjection arrays have been developed to deliver HSV-2-gD2 DNA vaccine to sensitive regions of mouse skin . The pretreatment of skin by microneedles was combined with the use of highly water soluble pegylated naltrexone for its transdermal delivery at different concentrations . A new design of probe integrated with hollow microneedles for atomic force microscope (AFM) has been developed to realize cellular function analysis in a single living cell . The geometry of microneedles affects its strength. The shear strength of hollow silicon microneedles can be increased by variation in microneedles geometry . Using novel microneedle technology, hydrophobic dye called Nile red has been delivered into porcine skin . The effect of microneedle geometry has been studied on the transport of a fluorescent dye into human skin . To envisage the effect of microneedle geometry and force of application, optical coherence tomography has been used by penetrating microneedles arrays into neonatal porcine skin . Short densely packed microinjection array has been developed to see the effect of strain rate on the precision of penetration into human skin . Reference  has investigated that influenza virus like particles coated on microneedles can cause stimulatory effect on langerhans cells in human skin. The super short microneedles have been fabricated using Si wet etching technology and tested for TDD into human skin . The separable arrowhead microneedles have been introduced and tested for painless delivery of drugs and vaccines into human cadaver skin . A minimally invasive system has been developed using microneedle electrode array to deliver macromolecular drugs to the deep skin tissues and tested on hairless rat skin . Solid silicon microneedles arrays have been used with different lengths and geometry to penetrate epidermal membrane of human cadaver skin . The microneedles coated with influenza virus like particles have been used to test the immunogenicity and protective efficacy after vaccination of mice skin . Microneedles rollers have been developed and tested on human and porcine skin to increase skin permeability and to treat skin for cosmetic purposes . Microneedles have been used to deliver PLGA (poly-lactic-co-glycolic-acid) nanoparticles in the human skin . Solid polymeric microneedles have been developed to investigate the transepidermal water loss measurements of dermatomed human skin . The efficacy of transdermal delivery of insulin has been investigated by using microneedles rollers on diabetic rats . The administration of virus like particles influenza vaccine has been studied using microneedles patch on lungs and bone marrow cells of mouse . Hollow microneedles array with sonophoretic emitter has been used on pig skin to improve the efficiency of drug delivery .
MEMS and NEMS based microfluidic devices have many important characteristics that make them attractive for biomedical applications. Microfluidic devices have the ability to control their physical and chemical characteristics from a very small scale up to the nanometer range. These devices have made it possible to meet critical medical needs such as nearly constant drug level at the site of action, prevention of peak-valley fluctuations, site specific drug delivery, reduced side effects and increased therapeutic effectiveness . However, there are certain medical conditions for which constant drug release pattern is not suitable. These conditions demand delayed release of drug. Such a release pattern is known as pulsatile release. Recent research has shown that some diseases have a predictable cyclic rhythm and the timing of drug release can significantly improve the outcome of a desired effect . This condition requires release of drug as a pulse after a time delay. Some of the diseases where pulsatile drug delivery devices are promising include duodenal ulcer, cardiovascular diseases, arthritis, asthma, diabetes, neurological disorder, cancer, hypertension and hypercholesterolemia . That is why study of pulsatile flow is extremely important at small scales in microfluidic devices. Using MEMS and NEMS technology, complex drug release patterns (such as simultaneous constant and pulsatile release) can be achieved using integrated microfluidic systems. Microfluidic devices have ability to control both release time and release rate. Micropumps and microneedles are essential components for such biomedical systems. Micropumps are used for fluid transport and microneedles provide interface between drug reservoir and patient body [4,13,6]. Material selection is a critical issue in biomedical devices. Si has been widely used as material for such microfluidic devices, but polymeric materials like PGA, PDMS, PMMA, PLLA, PLA, PC, etc. are replacing Si due to biocompatibility, low cost, ease of fabrication and excellent structural properties. Various factors are important during the selection of micropumps for particular biomedicine applications. Operating voltage, pressure and flow rate of micropumps are critical issues to analyze the performance and suitability of micropumps for certain medical applications. A schematic illustration of operating voltages and flow rates of mechanical micropumps is shown in Figure 22.
Piezoelectric and electromagnetic mechanical micropumps have been reported extensively for microfluidic systems among the mechanical micropumps. The major limitation related to these types of micropumps is very high operating voltage . Electrostatic micropump is easy to fabricate on integrated microfluidic systems but it also requires high operating voltage. The ICPF micropump has an adequate flow rate at a relatively low operating voltage but with complex geometry. The schematic illustration of operating voltages and flow rates of non-mechanical micropumps is shown in Figure 23.
In non-mechanical micropumps, MHD micropump has gained more attention in recent years and has been presented by many researchers for microfluidic systems. However, the electrochemical type of micropump is more suitable for low voltage and high flow rate applications. Most micropumps and microneedles have been reported in literature as an individual device for medical applications. Only a few researchers have presented integrated devices . Integration of micropumps and hollow microneedles is a great challenge, but research on solid microneedles coated with nano-particles and drugs has recently commenced in the biomedical field. However, hollow microneedles are more attractive for fluid/drug transport. Microneedles can be integrated with micropumps or used as stand-alone biomedical device. Various types of microneedles have been presented by different researchers. In hollow microneedles, the side opened double lumen reservoir based microneedles are more suitable for fluid transport. The pressure difference in the lumen regions is useful to avoid the clogging effect. In solid microneedles, the sharper tip microneedles are more practical for drug transport. Effectiveness of drug transport has also been presented in recent years by various researchers using microneedles on mouse, pig, chicken and human. Various researchers have reported the structure and fracture analyses of microneedles by applying force and pressure to predict the bending and failure of microneedles. The schematic illustration of comparison of force and stress for microneedles has been shown in Figure 24.
5. Challenges and Future Aspects
In biomedical field, there are many challenges relating to the microfluidic devices (micropumps, microneedles) such as design level issue, fabrication level issue, packaging level issues, use in practical application, etc. At design and fabrication level, the most important issues and specifications that must be fulfilled by the micropumps for particular applications are appropriate design for maintaining a specific flow rate, control of back pressure, dosing accuracy, drugs resistive material selection for fabrication, ease of fabrication, energy utilization, power supply at such small level, bubble tolerance, durability and reliability. The most important issues relating to microneedles at design and fabrication level are avoidance of clogging effect, suitable length, robustness, strength, sharp tip to avoid pain, drugs resistance, less fabrication cost, reliability, biocompatibility, etc. Suitable batch fabrication techniques need to be adopted to reduce cost of devices. Packaging of these devices is very important consideration . Packaging should be robust and strong enough to prevent infection or damage of microfluidic devices. Simultaneously, the unintentional discharge of drug/fluid during storage from the reservoir should be prevented. A protecting wrap may be possibly required to secure such small size devices like micropumps and sharp tip microneedles. Mostly the micropumps and microneedles reported in literature have been proposed as stand-alone devices. Integration of micropump and microneedles is a great challenge that limits the use of these devices commercially for biomedical applications. The final cost of these delivery devices should be affordable for the end users/patients. The trend is now shifting towards the use of polymeric materials like PGA, PDMS, PMMA, etc. for the fabrication of micropumps and microneeldes to overcome most of the above described issues as these materials are cheap, biocompatible, exhibit excellent mechanical/chemical properties, etc. [4,13,19,202]. Zosano Pharma  has developed the user friendly and simple TDD patch system that can deliver vaccines, proteins, peptides and small molecules. 3 M has developed the microneedles based transdermal system demonstrating good results on research level studies for peptides, vaccines and protein . Birchall et al.  conducted a survey to learn more about the opinion of end users with regard to the convenience, efficacy and worth of microneedle technology. Research on MEMS-based delivery devices shows that these devices are suitable for commercial applications. However, the development of these devices is limited to research level due to some factors such as investment, expertise for device development, marketing, awareness of public, motivation, lack of collaboration between companies and research institutes, medical staff training/recommendations, etc. Surveys, seminars, workshops, etc., need to be organized to promote the benefits and convenience of using these delivery devices to end users. The availability of reliable and manufacturable microfluidic devices will have a strong impact on the biomedicine field to meet critical health care needs.
Fluid transport using microfluidic devices such as micropumps and microneedles is a relatively new and attractive method that has many advantages. Microfluidic devices have received much more attention in recent years due to their potential applications in the biomedicine field. Various types of micropumps and microneedles structures using different materials like glass, silicon, metals, polymers, etc., have been reported for biomedical applications, but Si has been mostly used as substrate material for fabrication of microfluidic devices among other materials. Si is brittle and always some risk involves for health care. Biocompatibility is very important for health and because of this reason the trend is transferring towards polymeric materials. Most polymers, e.g., PGA, PDMS, PLA and PMMA, are very suitable for biomedical devices due to their good biocompatibility, low cost, ease of fabrication and excellent chemical and mechanical properties. Solid microneedles are easy to fabricate and have more strength than hollow microneedles. However, the disadvantage of solid microneeldes is the risk of fracture/breaking within the skin after being inserted. Drug particles can be coated in restricted amounts. Hollow microneeldes are considered more suitable for TDD systems due to the precise delivery of the desired amount of drug at a specific site with rapid action. ICPF and electrostatic micropumps are considered suitable for drug/fluid delivery systems due to low operating voltage and direct integration with electronic circuit respectively. The disadvantages of hollow microneeldes and micropumps are complicated/costly fabrication, clogging effect, back pressure, requirement of flow rate regulation, etc. Based on the presented literature review, the authors conclude that MEMS based microfluidic devices for biomedical applications remain at the research level. Only a few devices have been converted into commercial products due to some important issues like complicated structure of microfluidic devices, difficulties in integration with other devices, investment, expertise for device fabrication, marketing, public awareness, lack of collaboration between companies and research institutes, medical staff training/recommendation and finally packaging. To present microfluidic devices for practical applications in medical field, motivated researchers still need to continue their work on the development of microfluidic devices.
- Hsu, T. MEMS & Microsystem Design and Manufacturing, 1st ed; McGraw-Hill: New York, NY, USA, 2002. [Google Scholar]
- Hardt, S; Schonfeild, F. Microfluidic Technologies for Maniaturized Analysis System, 1st ed; Springer: Berlin, Germany, 2010. [Google Scholar]
- Ashraf, MW; Tayyaba, S; Afzulpurkar, N; Nisar, A. Fabrication and analysis of tapered tip silicon microneedles for mems based drug delivery system. Sens. Transducer 2010, 122, 158–173. [Google Scholar]
- Ashraf, MW; Tayyaba, S; Nisar, A; Afzulpurkar, N; Bodhale, DW; Lomas, T; Poyai, A; Tuantranont, A. Design, fabrication and analysis of silicon hollow microneedles for transdermal drug delivery system for Treatment of Hemodynamic Dysfunctions. Cardiovasc. Eng. J 2010, 3, 91–108. [Google Scholar]
- Prausnitz, MR; Langer, R. Transdermal drug delivery. Nat. Biotechnol 2008, 26, 1261–1268. [Google Scholar]
- Polla, DL. BioMEMS Applications in Medicine. Proceedings of International Symposium on Micromechatronics and Human Science, Nagoya, Japan, 9–12 September 2001; pp. 13–15.
- Shawgo, SR; Amy, C; Grayson, R; Yawen, L; Cima, JM. BioMEMS for drug delivery. Curr. Opin. Solid-State Mater. Sci 2002, 6, 329–334. [Google Scholar]
- Amy, C; Grayson, R; Shawgo, RS; Li, Y; Cima, MJ. Electronic MEMS for triggered delivery. Adv. Drug Deliv. Rev 2004, 56, 173–184. [Google Scholar]
- Staples, M; Daniel, K; Cima, MJ; Langer, R. Application of micro and nano electromechanical devices to drug delivery. Pharm. Res 2006, 23, 847–863. [Google Scholar]
- Laser, DJ; Santiago, JG. Areview of micropumps. J. Micromech. Microeng 2004, 14, 35–64. [Google Scholar]
- Woias, P. Micropumps-past, progress and future prospects. Sens. Actuators B 2005, 105, 28–38. [Google Scholar]
- Tsai, NC; Sue, CY. Review of MEMS based drug delivery and dosing systems. Sens. Actuators A 2007, 134, 555–564. [Google Scholar]
- Nisar, A; Afzulpurkar, N; Mahaisavariya, B; Tuantranont, A. MEMS-based micropumps in drug delivery and biomedical applications. Sens. Actuators B 2008, 130, 917–942. [Google Scholar]
- Amirouche, F; Zhou, Y; Johnson, T. Current micropump technologies their biomedical applications. Microsyst. Technol 2009, 15, 647–666. [Google Scholar]
- Grayson, AR; Shawgo, RS; Johnson, AM; Flynn, NT; Yawen, L; Cima, MJ; Langer, R. A BioMEMS review: MEMS technology for physiologically integrated devices. Proc. IEEE 2004, 92, 6–21. [Google Scholar]
- Karman, S; Ibrahim, F; Soin, N. A review of MEMS drug delivery in medical application, Biomed 06. Proc. IFMBE 2007, 15, 312–315. [Google Scholar]
- Bao-jian, X; Qing-hui, J; Jian-long, Z. An review of MEMS-Based microneedles technology developments. Micronanoelectron Technol 2005, 4. 1671-4776.0.2005-04-002.. [Google Scholar]
- Khanna, P; Storm, JA; Malone, JI; Bhansali, S. Microneedle-Based Automated Therapy for Diabetes Mellitus. J. Diabetes Sci. Technol 2008, 2, 1122–1129. [Google Scholar]
- Sachdeva, V; Banga, AK. Microneedles and their applications. Recent Pat. Drug Deliv. Formul 2011, 5, 95–132. [Google Scholar]
- Stemme, E; Stemme, G. A valveless diffuser/nozzle based fluid pump. Sens. Actuators A 1993, 39, 159–167. [Google Scholar]
- White, FM. Fluid Mechanics, International Student Edition; McGraw Hill Inc: Columbus, OH, USA, 1979; pp. 161–162. [Google Scholar]
- Van Lintel, HTG; Van de Pol, FCM; Bouwstra, S. A piezoelectric micropump based on micromachining of silicon. Sens. Actuators A 1988, 15, 153–168. [Google Scholar]
- Esashi, M; Shoji, S; Nakano, A. Normally close microvalve and micropump fabricated on a silicon wafer. Proceedings of IEEE Micro Electro Mechanical Systems, An Investigation of Micro Structures, Sensors, Actuators Machines and Robots, Salt Lake City, UT, USA, 20–22 February 1989; pp. 29–34.
- Olsson, A; Stemme, G; Stemme, E. A valve-less planar fluid pump with two pump chambers, Sens. Actuators A 1995, 47, 549–556. [Google Scholar]
- Koch, M; Harris, N; Evans, AGR; White, NM; Brunnschweiler, A. A novel micromachined pump based on thick film piezoelectric actuation. Sens. Actuators A 1998, 70, 98–103. [Google Scholar]
- Schabmueller, CGJ; Koch, M; Mokhtari, ME; Evans, AGR; Brunnschweiler, A; Sehr, H. Self-aligning gas/liquid micropump. J. Micromech. Microeng 2002, 12, 420–424. [Google Scholar]
- Feng, GH; Kim, ES. Piezoelectrically actuated dome-shaped diaphragm micropump. J. Microelectromech. Syst 2005, 14, 92–199. [Google Scholar]
- Geipel, A; Doll, A; Goldschmidtboing, F; Jantscheff, P; Esser, N; Massing, U; Woias, P. Istanbul, Turkey, 22–26 January 2006; 2006; pp. 786–789.
- Trenkle, F; Haeberle, S; Zengerle, R. Normally-closed peristaltic micropump with re-usable actuator and disposable fluidic chip. Procedia Chem 2009, 1, 1515–1518. [Google Scholar]
- Johari, J; Yunas, J; Yeopmajlis, B. Piezoeletric Micropump for Drug Delivery System Fabricated Using Two Optical Masks. Adv. Mat. Res 2009, 74, 279–282. [Google Scholar]
- Wang, C; Leu, T; Sun, J. Asymmetrical flow effect applied to pumping performance of simple duct channel. Sens. Actuators A 2009, 155, 203–209. [Google Scholar]
- Ali, MY; Kuang, C; Khan, J; Wang, G. A dynamic piezoelectric micropumping phenomenon. Microfluid. Nanofluid 2010, 9, 385–396. [Google Scholar]
- Liu, G; Shen, C; Yang, Z; Cai, X; Zhang, H. A disposable piezoelectric micropump with high performance for closed-loop insulin therapy system. Sens. Actuators A 2010, 163, 291–296. [Google Scholar]
- Judy, JW; Tamagawa, T; Polla, DL. Surface-machined Micromechanical Membrane Pump. Proceedings of the IEEE Micro Electro Mechanical systems, Nara, Japan, 30 January–2 February 1991; pp. 182–186.
- Zengerle, R; Richter, A; Sandmaier, H. A Micro Membrane Pump with Electrostatic Actuation. Proceedings of Micro Electro Mechanical Systems 1992, An Investigation of Micro Structures, Sensors, Actuators, Machines and Robot IEEE, Travemunde, Germany, 4–7 February 1992; pp. 19–24.
- Cabuz, C; Herb, WR; Cabuz, EI; Lu, ST. The dual diaphragm pump. Proceedings of the 14th IEEE International Conference on Micro Electro Mechanical Systems, Interlaken, Switzerland, 21–25 January 2001; pp. 519–522.
- Machauf, A; Nemirovsky, Y; Dinnar, U. A membrane micropump electrostatically actuated across the working fluid. J. Micromech. Microeng 2005, 15, 2309–2316. [Google Scholar]
- Astle, AA; Kim, HS; Bernal, LP; Najafi, K; Washabaugh, PD. Theoretical and experimental performance of a high frequency gas micropump. Sens. Actuators A 2006, 134, 245–256. [Google Scholar]
- Lee, S; Yee, SY; Besharatian, A; Kim, H; Bernal, LP; Najafi, K. Adaptive gas pumping by colntrolled timing of active microvalves in peristaltic micropumps. Proceedings of Transducers, Denver, CO, USA, 21–25 June 2009.
- Liu, W. Changsha, China, 11–12 May 2010.
- Lil, L; Zhu, R; Zhou, Z; Ren, J. Modeling of a Micropump Membrane with Electrostatic Actuator. Proceedings of 2nd International Conference on Advanced Computer Control (ICACC), Shenyang, China, 27–29 March 2010.
- Van de Pol, FCM; van Lintel, HTG; Elwenspoek, M; Fluitman, JHJ. A thermopneumatic micropump based on microengineering techniques. Sens. Actuators A 1990, 21, 198–202. [Google Scholar]
- Jeong, OC; Yang, SS. Fabrication and test of a thermopneumatic micropump with a corrugated p diaphragm, Sens. Actuators 2000, 83, 249–255. [Google Scholar]
- Cooney, CG; Towe, BC. A thermopneumatic dispensing micropump. Sens. Actuators A 2004, 116, 519–524. [Google Scholar]
- Kim, JH; Na, KH; Kang, CJ; Kim, YS. A disposable thermopneumatic actuated micropump stacked with PDMS layers and ITO coated glass, Sens. Actuators A 2005, 120, 365–369. [Google Scholar]
- Jeong, OC; Konishi, S. Fabrication of a peristaltic micro pump with novel cascaded actuators. J. Micromech. Microeng 2008, 18, 025022. [Google Scholar]
- Chia, BT; Liao, H; Yang, Y. A novel thermo-pneumatic peristaltic micropump with low temperature elevation on working fluid. Sens. Actuators A 2010, 165, 86–93. [Google Scholar]
- Tan, HY; Loke, WK; Nguyen, N. A reliable method for bonding polydimethylsiloxane (PDMS) to polymethylmethacrylate (PMMA) and its application in micropumps. Sens. Actuators B 2010, 151, 133–139. [Google Scholar]
- Zheng, W; Ahn, CH. A Bi-directional Magnetic Micropump on a Silicon Wafer. Proceedings of Technical Digest Solid-State Sensor and Actuator Workshop 1996, Hilton Head Island, SC, USA, 3–6 June 1996.
- Bohm, S; Olthuis, W; Bergveld, P. A plastic micropump constructed with conventional techniques and materials. Sens. Actuators A 1999, 77, 223–228. [Google Scholar]
- Gong, Q; Zhou, Z; Yang, Y; Wang, X. Design, optimization and simulation on microelectromagnetic pump. Sens. Actuators A 2000, 83, 200–207. [Google Scholar]
- Yamahata, C; Lotto, C; Al Assaf, E; Gijs, MAM. A PMMA valveless micropump using electromagnetic actuation. Microfluid. Nanofluid 2005, 1, 197–207. [Google Scholar]
- Su, Y; Chen, W; Cui, F; Zhang, W. Analysis and fabrication process of an electromagnetically actuated valveless micropump with two parallel flexible diaphragms. Proc. IMechE 2005, 219, 1007–1014. [Google Scholar]
- Balaji, G; Singh, S; Ananthasuresh, GK. Electro-magnetically Actuated Minute Polymer Pump Fabricated using Packaging Technology. J. Phys 2006, 34, 258–263. [Google Scholar]
- Yu-feng, SU; Wen-yuan, C; Feng, C; Wei-ping, Z. Design and fabrication process of electromagnetically actuated valveless micropump with two parallel flexible diaphragms. J. Shanghai Univ 2007, 11, 79–83. [Google Scholar]
- Shen, M; Yamahata, C; Gijs, MAM. Miniaturized PMMA ball-valve micropump with cylindrical electromagnetic actuator. Microelectr. Eng 2008, 85, 1104–1107. [Google Scholar]
- Al-Halhouli, AT; Kilani, MI; Büttgenbacha, S. Development of a novel electromagnetic pump for biomedical applications. Sens. Actuators A 2010, 162, 172–176. [Google Scholar]
- Zhan, C; Lo, T; Liu, LP. A silicon membrane micropump with integrated bimetallic actuator. Chin. J. Electron 1996, 5, 29–35. [Google Scholar]
- Zou, JX; Ye, YZ; Zhou, Y; Yang, Y. A Novel Thermally Actuated Silicon Micropump. Proceedings of International Symposium on Micromechatronics and Human Science, Nagoya, Japan, 5–8 October 1997.
- Pang, J; Zou, Q; Tan, Z; Qian, X; Liu, L; Li, Z. The Study of Single Chip Integrated Microfluidic System. Proceedings of 5th International Conference on Solid State and Integrated Circuit Technology, Beijing, China, 21–23 October 1998; pp. 895–898.
- Yang, Y; Zhaoying, Z; Xiongying, Y; Xiaoning, J. Bimetallic Thermally Actuated Micropump. Proceedings of International Mechnical Engineering Congross and Exposition (ASME 1996), Atlanta, GA, USA, 17–22 November 1996.
- Guo, S; Nakamura, T; Fukuda, T; Oguro, K. Design and Experiments of Micropump Using ICPF Actuator. Proceedings of 7th International IEEE Symposium on Micro Machine and Human Science, Nagoya, Japan, 2–4 October 1996; pp. 235–240.
- Tadokoro, S; Yamagami, S; Ozawa, M. Soft Micromanipulation Device with Multiple Degrees of Freedom Consisting of High Polymer Gel Actuators. Proceedings of IEEE International Conference on Microelectromechanical Systems, Orlando, FL, USA, 17–21 January 1999; pp. 37–42.
- Guo, S; Asaka, K. Polymer Based New Type of Micropump for Biomedical Applications. Proceedings of IEEE Conference on Robotics & Automation, Taipei, Taiwan, 14–19 September 2003; pp. 1830–1835.
- Nguyen, TT; Goo, NS; Nguyen, VK; Yoo, Y; Park, S. Design, fabrication, and experimental characterization of a flap valve IPMC micropump with a flexibly supported diaphragm. Sens. Actuators A 2008, 141, 640–648. [Google Scholar]
- Chen, Z; Kwon, K; Tan, X. Integrated IMPC/PVDF sensory actuator and its validation in feedback control. Sens. Actuators A 2008, 144, 231–241. [Google Scholar]
- Fang, T; Tan, X. A novel diaphragm micropump actuated by conjugated polymer petals: Fabrication, modeling, and experimental results. Sens. Actuators A 2010, 158, 121–131. [Google Scholar]
- Sim, WY; Yoon, HJ; Jeong, OC; Yang, SS. A phase change type of micropump with aluminum flap valves. J. Micromech. Microeng 2003, 13, 286–294. [Google Scholar]
- Boden, R; Lehto, M; Simu, U; Thornell, G; Hjort, K; Schweitz, JA. A Polymeric Paraffin Micropump with Active Valves for High Pressure Microfluidics. Proceedings of 13th International Conference on Solid State Sensors, Actuators and Microsystems, Seoul, Korea, 5–9 June 2005; pp. 201–204.
- Sim, WY; Lee, SW; Yang, SS. The Fabrication and Test of a Phase-change Type Micropump, 2008. Available online: http://click.ndsl.kr/servlet/LinkingFullTextView?service_code=04&dbt=JAKO&cn=JAKO200011919587765 accessed on 20 February 2011.
- Benard, WL; Kahn, H; Heuer, AH; Huff, MA. Thin-film shapememory alloy actuated micropumps. J. Microelectromech. Syst 1998, 7, 245–251. [Google Scholar]
- Makino, E; Mitsuya, T; Shibata, T. Fabrication of TiNi shape memory micropump. Sens. Actuators A 2001, 88, 256–262. [Google Scholar]
- Xu, D; Wang, L; Ding, G; Zhou, Y; Yu, A; Cai, B. Characteristics and fabrication of NiTi/Si diaphragm micropump. Sens. Actuators A 2001, 93, 87–92. [Google Scholar]
- Shuxiang, G; Fukuda, T. SMA Actuator Based Novel Type of Micropump for Biomedical Application. Proceedings of IEEE International Conference Robotics and Automation, Takamatsu, Japan, 26 April–1 May 2004; 2, pp. 1616–1621.
- Zhang, HJ; Qiu, CJ. A TiNiCu thin film micropump made by magnetron Co-sputtered method. Mat. Trans 2006, 47, 532–535. [Google Scholar]
- Setiawan, MA. The performance evaluation of SMA Spring as actuator for gripping manipulation. J. Teknik Elektro 2007, 7, 110–120. [Google Scholar]
- Zhu, M; Kirby, P; Wacklerle, M; Herz, M; Richter, M. Optimization design of multi-material micropump using finite element method. Sens. Actuators A 2009, 149, 130–135. [Google Scholar]
- Kang, J; Auner, GW. Simulation and verification of a piezoelectrically actuated diaphragm for check valve micropump design. Sens Actuators A 2011. in press. [Google Scholar]
- Shen, M; Dovat, L; Gijs, MAM. Magnetic active-valve micropump actuated by a rotating magnetic assembly. Sens. Actuators B 2009, 154, 52–58. [Google Scholar]
- Teymoori, MM; Abbaspour-Sani, E. Design and simulation of a novel electrostatic peristaltic micromachined pump for drug delivery applications. Sens. Actuators A 2005, 117, 222–229. [Google Scholar]
- Zeng, S; Chen, CH; Mikkelsen, JC; Santiago, JG. Fabrication and characterization of electroosmotic micropumps. Sens. Actuators B 2001, 79, 107–114. [Google Scholar]
- Takemori, Y; Horiike, S; Nishimoto, T; Nakanishi, H; Yoshida, T. High Pressure Electroosmotic Pump Packed with Uniform Silica Nanosphers. Proceedings of 13th International Conference on Solid State Sensors, Actuators and Microsystems, Seoul, Korea, 5–9 June 2005.
- Hu, JS; Chao, CYH. Numerical study of electroosmotic (EO) flow in microfabricated EO pump with overlapped electrical double layer (EDL). Int. J. Refrig 2007, 30, 290–298. [Google Scholar]
- Good, BT; Bowman, CN; Davis, RT. A water-activated pump for portable microfluidic applications. J. Colloid Interface Sci 2007, 305, 239–249. [Google Scholar]
- Ryu, WH; Huang, Z; Prinz, FB; Goodman, SB; Fasching, R. Biodegradable microosmotic pump for long term and controlled release of basic fibroblast growth factor. J. Control. Release 2007, 124, 98–105. [Google Scholar]
- Yairi, M; Richter, C. Massively parallel microfluidic pump. Sens. Actuators A 2007, 137, 350–356. [Google Scholar]
- Borowsky, J; Lu, Q; Collins, GE. High pressure electroosmotic pump based on a packed bed planar microchip. Sens. Actuators B 2008, 131, 333–339. [Google Scholar]
- Wang, X; Wang, S; Gendhar, B; Cheng, C; Byun, CK; Li, G; Zhao, M; Liu, S. Electroosmotic pumps for microflow analysis. Trends Anal. Chem 2009, 28, 64–74. [Google Scholar]
- Yun, KS; Cho, IJ; Bu, JU; Kim, CJ; Yoon, E. A surface tension driven micropump for low voltage and low power operations. J. MEMS 2002, 11, 454–461. [Google Scholar]
- Hoshino, K; Triteyaprasert, S; Matsumoto, K; Shimoyama, I. Electrowetting-based pico-liter liquid actuation in a glass-tube microinjector. Sens. Actuators A 2004, 114, 473–477. [Google Scholar]
- Colgate, ED; Matsumoto, H. An investigation of electrowetting based microactuation. J. Vac. Sci. Technol. A 1990, 4, 3625–3633. [Google Scholar]
- Chang, J; Choi, DY; Han, S; Pak, JJ. Driving characteristics of the electrowetting-on-dielectric device using atomic-layer-deposited aluminum oxide as the dielectric. Microfluid. Nanofluid 2010, 8, 269–273. [Google Scholar]
- Suzuki, H; Yoneyama, R. Areversible electrochemical nanosyringe pump and some considerations to realize low power consumption. Sens. Actuators B 2002, 86, 242–250. [Google Scholar]
- Suzuki, H; Yoneyama, R. Integrated microfluidic system with electrochemically actuated on-chip pumps and valves. Sens. Actuators B 2003, 96, 38–45. [Google Scholar]
- Yoshimi, Y; Shinoda, K; Mishima, M; Nakao, K; Munekane, K. Development of an artificial synapse using an electrochemical micropump. J. Artif. Organs 2004, 7, 210–215. [Google Scholar]
- Kim, JH; Laua, KT; Shepherd, R; Wu, Y; Wallace, G; Diamond, D. Performance characteristics of a polypyrrole modified polydimethylsiloxane (PDMS) membrane based microfluidic pump. Sens. Actuators A 2008, 148, 239–244. [Google Scholar]
- Effenhauser, CS; Harttig, H; Kramer, P. An evaporation-based disposable micropump concept for continuous monitoring applications. Biomed. Microdev 2002, 4, 27–33. [Google Scholar]
- Namasivayam, V; Larson, RG; Burke, DT; Burns, MA. Transpirationbased micropump for delivering continuous ultra low flow rates. J. Micromech. Microeng 2003, 13, 261–271. [Google Scholar]
- Guan, Y; Xua, Z; Dai, J; Fang, Z. The use of a micropump based on capillary and evaporation effects in a microfluidic flow injection chemiluminescence system. Talanta 2006, 68, 1384–1389. [Google Scholar]
- Heuck, F; Hug, T; Akiyama, T; Frederix, PLTM; Engel, A; Meister, A; Heinzelmann, H; de Rooij, NF; Staufer, U. Evaporation based micro pump integrated into a scanning force microscope probe. Microelectr. Eng 2008, 85, 1302–1305. [Google Scholar]
- Tsai, JH; Lin, L. A Thermal Bubble Actuated Micro Nozzle-diffuser Pump. Proceedings of 14th IEEE International Conference Microelectromechanical Systems, Interlaken, Switzerland, 21–25 January 2001; pp. 409–412.
- Tsai, JH; Lin, L. Active microfluidic mixture and gas bubble filter driven by thermal bubble micropump. Sens Actuators A 2002, 97-98, 665–671. [Google Scholar]
- Lew, KSF; Klaseboer, E; Khoo, BC. A collapsing bubble-induced micropump: An experimental study. Sens. Actuators A 2007, 133, 161–172. [Google Scholar]
- Jung, JY; Kwak, HY. Fabrication and testing of bubble powered micropumps using embedded microheater. Microfluid. Nanofluid 2007, 3, 161–169. [Google Scholar]
- Cheng, CM; Liu, CH. An Electrolysis-Bubble-Actuated micropump based on the roughness gradient design of hydrophobic surface. J. Microelectromech. Syst 2007, 16, 1095–1105. [Google Scholar]
- Chan, SC; Chen, CR; Liu, CH. A bubble-activated micropump with high-frequency flow reversal. Sens. Actuators A 2010, 163, 501–509. [Google Scholar]
- Jang, J; Lee, SS. Theoretical and experimental study of MHD (magnetohydrodynamic) micropump. Sens. Actuators A 2000, 80, 84–89. [Google Scholar]
- Zhong, J; Yi, M; Bau, HH. Magneto Hydrodynamic (MHD) pump fabricated with ceramic tapes. Sens. Actuators A 2002, 96, 59–66. [Google Scholar]
- Eijkel, JCT; Dalton, C; Hayden, CJ; Burt, JPH; Manz, A. A circular ac magnetohydrodynamic micropump for chromatographic applications. Sens. Actuators B 2003, 92, 215–221. [Google Scholar]
- Patel, V; Kassegne, SK. Electroosmosis and thermal effects in Magnetohydrodynamic (MHD) micropumps using 3D MHD equations. Sens. Actuators B 2007, 122, 42–52. [Google Scholar]
- Duwairi, HM; Abdullah, M. Numerical Computation of Fluid Flow in a Magnetohydrodynamic Micropump. Turkish J. Eng. Env. Sci 2008, 32, 1–5. [Google Scholar]
- Kang, H; Choi, B. Development of the MHD micropump with mixing function. Sens. Actuators A 2010, 165, 439–445. [Google Scholar]
- Moroney, RM; White, RM; Howe, RT. Microtransport induced by ultrasonic lamb waves. Appl. Phys. Lett 1991, 59, 774–776. [Google Scholar]
- Nguyen, NT; White, RM. Design and optimization of an ultrasonic flexural plate wave micropump using numerical simulation. Sens. Actuators A 1999, 77, 229–236. [Google Scholar]
- Nguyen, NT; Meng, AH; Black, J; White, RM. Integrated flow sensor for insitu measurement and control of acoustic streaming in flexural plate wave micropumps. Sens. Actuators A 2000, 79, 115–121. [Google Scholar]
- Meng, AH; Nguyen, NT; White, RM. Focused flow micropump using ultrasonic flexural plate waves. Biomed Microdevices 2000, 2–3, 169–174. [Google Scholar]
- Jang, LS; Chao, SH; Holl, MR; Meldrum, DR. Microfluidic circulatory flows induced by resonant vibration of diaphragms. Sens. Actuators A 2005, 122, 141–148. [Google Scholar]
- Singh, R; Bhethanabotla, VR. Enhancement in Ultrasonic Micro-Transport Using Focused Inter-Digital Transducers in a Surface Acoustic Wave Device: Fluid-Structure Interaction Study. Proceedings of IEEE Sensors, Christchurch, New Zealand, 25–28 October 2009.
- Richter, A; Sandmaier, H. An Electrohydrodynamic Micropump. Proceedings of IEEE Microelectromechanical Systems, Napa Valley, CA, USA, 11–14 February 1990; pp. 99–104.
- Fuhr, G; Hagedorn, R; Muller, T; Benecke, W; Wagner, B. Pumping of Water Solutions in Microfabricated Electrohydrodynamic Systems. Proceedings of IEEE Micro Electro Mechanical Systems. An Investigation of Micro Structures, Sensors, Actuators, Machines and Robots MEMS, Travemunde, Germany, 4–7 February 1992; pp. 25–30.
- Darabi, J; Ohadi, MM; DeVoe, D. An Electrohydrodynamic polarization micropump for electronic cooling. J. Microelectromech. Syst 2001, 10, 98–106. [Google Scholar]
- Darabi, J; Rada, M; Ohadi, M; Lawler, J. Design, fabrication and testing of an electrohydrodynamic ion drag micropump. J. Microelectromech. Syst 2002, 11, 684–690. [Google Scholar]
- Yang, LJ; Wang, JM; Huang, YL. The micro ion drag pump using indium-tin-oxide (ITO) electrodes to resist aging. Sens. Actuators A 2004, 111, 118–122. [Google Scholar]
- Lin, CW; Jang, JY. 3D numerical micro-cooling analysis for an electrohydrodynamic micro-pump. Sens. Actuators A 2005, 122, 167–176. [Google Scholar]
- Darabi, J; Rhodes, C. CFD modeling of an ion-drag micropump. Sens. Actuators A 2006, 127, 94–103. [Google Scholar]
- Singhal, V; Garimella, SV. Induction electrohydrodynamics micropump for high heat flux cooling. Sens. Actuators A 2007, 134, 650–659. [Google Scholar]
- Wakui, D; Imai, N; Nagaura, Y; Sato, H; Sekiguchi, T; Konishi, S; Shoji, S; Homma, T. EHD Micropump using Pyrolyzed Polymer 3-D Carbon Mesh Electrodes. Proceedings of 22nd IEEE International Conference on Micro Electro Mechanical Systems, Sorrento, Italy, 25–29 January 2009; pp. 499–502.
- Litster, S; Suss, ME; Santiago, JG. A two-liquid electroosmotic pump using low applied voltage and power. Sens. Actuators A 2010, 163, 311–314. [Google Scholar]
- Xu, Z; Yang, C; Liua, C; Zhou, Z; Fang, J; Wang, J. An osmotic micro-pump integrated on a microfluidic chip for perfusion cell culture. Talanta 2010, 80, 1088–1093. [Google Scholar]
- Lim, S; Choi, B. A study on the MHD (magnetohydrodynamic) micropump with side-walled electrodes. J. Mech. Sci. Technol 2009, 23, 739–749. [Google Scholar]
- Luginbuhl, P. Microfabricated lamb wave device based on PZT sol-gel thin film for mechanical transport of solid particles and liquids. J. Microelectromech. Syst 1997, 6, 337–345. [Google Scholar]
- Campbell, PK; Jones, KE; Huber, RJ; Horch, KW; Normann, RA. A silicon-based three dimensional neural interface: Manufacturing processes for an intracortical electrode array. IEEE Trans. Biomed. Eng 1991, 38, 758–768. [Google Scholar]
- Bodhale, DW; Nisar, A; Afzulpurkar, N. Structural and microfluidic analysis of hollow side-open polymeric microneedles for transdermal drug delivery applications. Microfluid. Nanofluid 2010, 8, 373–392. [Google Scholar]
- Najafi, K; Wise, K. An implantable multielectrode array with on-chip signal processing. IEEE J. Solid-State Circ 1986, 21, 1035–1044. [Google Scholar]
- Chen, J; Wise, K; Hetke, J; Bledsoe, S. A multichannel neural probe for selective chemical delivery at the cellular level. IEEE Trans. Biomed. Eng 1997, 44, 760–769. [Google Scholar]
- Bai, Q; Wise, K; Anderson, D. A high-yield microassembly structure for three dimensional microelectrode arrays. IEEE Trans. Biomed. Eng 2000, 47, 281–289. [Google Scholar]
- The World Book Encyclopedia, Hypodermic injection. In The world book encyclopedia; World Book Chic, 1999; Volume 9, pp. 480–481.
- McAllister, DV; Allen, MG; Prausnitz, MR. Microfabricated microneedles for gene drug delivery. Annu. Rev. Biomed. Eng 2000, 2, 289–313. [Google Scholar]
- Lin, L; Pisano, A. Silicon processed microneedles. J. Microelectromech. Syst 1999, 8, 78–84. [Google Scholar]
- Zosano Pharma. Available online: http://www.zosanopharma.com accessed on 27 April 2011.
- Ameri, M; Daddona, P; Maa, Y. Demonstrated solid-state stability of parathyroid hormone PTH(1-34) coated on a novel transdermal microprojection delivery system. Pharm. Res 2009, 26, 2454–2463. [Google Scholar]
- Ameri, M; Daddona, P; Maa, Y. Parathyroid hormone PTH(1–34) formulation that enables uniform coating on a novel transdermal microprojection delivery system. Pharm. Res 2009, 27, 303–313. [Google Scholar]
- Dizon, R; Han, H; Russell, A; Reed, M. An ion milling pattern transfer technique for fabrication of three-dimensional micromechanical structures. J. Microelectromech. Syst 1993, 2, 151–159. [Google Scholar]
- Henry, S; McAllister, D; Allen, M; Prausnitz, M. Microfabricated microneedles: A novel approach to transdermal drug delivery. J. Pharm. Sci 1998, 87, 922–925. [Google Scholar]
- Chun, K; Hashiguchi, G; Toshioyoshi, H; Pioufle, B; Ishikawa, J; Murakami, Y; Tamiya, E; Kikuchi, Y; Fujita, H. DNA injection into cell conglomerates by micromachined hollow microcapillary arrays. Proceedings of Digital Transducers, 10th International Conference Solid-State Sensors and Actuators, Sendai, Japan, 7–10 June 1999; pp. 41–47.
- Oka, K; Aoyagi, S; Arai, Y; Isono, Y; Hashiguchi, G; Fujita, H. Fabrication of a microneedle for a trace blood test. Sens Actuators A 2002, 97-98, 478–485. [Google Scholar]
- Brazzle, J; Papautsky, I; Frazier, B. Hollow metallic micromachined needle arrays. J. Biomed. Devices 2000, 2, 197–205. [Google Scholar]
- Chandrasekaran, S; Brazzle, JD; Frazier, AB. Surface micromachined metallic microneedles. J. Microelectromech. Syst 2003, 12, 289–295. [Google Scholar]
- Chandrasekaran, S; Frazier, AB. Characterization of surface micromachined metallic microneedles. J. Microelectromech. Syst 2003, 12, 281–288. [Google Scholar]
- Stoeber, B; Liepmann, D. Design, Fabrication and Testing of a MEMS Syringe. Proceedings of Solid-State Sensors, Actuator and Microsystems Workshop, Hilton Head Island, SC, USA, 2–6 June 2002; pp. 77–80.
- Hashmi, S; Ling, P; Hashmi, G; Reed, M; Gaugler, R; Trimmer, W. Genetic transformation of nematodes using arrays of micromechanical piercing structures. Biotechniques 1995, 19, 766–770. [Google Scholar]
- Narayan, JR; Doraiswamy, A; Chrisey, DB; Chichkov, BN. Medical prototyping using two photon polymerization. Materialstoday 2010, 12, 43–48. [Google Scholar]
- Wu, Y; Qiu, Y; Zhang, S; Qin, G; Gao, Y. Microneedle-based drug delivery: Studies on delivery parameters and biocompatibility. Biomed. Microdevices 2008, 10, 601–610. [Google Scholar]
- Coulman, SA; Ansteyb, A; Gateleyb, C; Morrisseyc, A; McLoughlind, P; Allendera, C; Birchalla, JC. Microneedle mediated delivery of nanoparticles into human skin. Int. J. Pharm 2009, 366, 190–200. [Google Scholar]
- Haq, MI; Smith, E; John, DN; Kalavala, M; Edwards, C; Anstey, A; Morrissey, A; Birchall, JC. Clinical administration of microneedles: skin puncture, pain and sensation. Biomed. Microdevices 2009, 11, 35–47. [Google Scholar]
- Oh, JH; Park, HH; Do, KY; Han, M; Hyun, DH; Kim, CG; Kim, CH; Lee, SS; Hwang, SJ; Shin, SC; Cho, CW. Influence of the delivery systems using a microneedle array on the permeation of a hydrophilic molecule, calcein. Eur. J. Pharm. Biopharm 2008, 69, 1040–1045. [Google Scholar]
- Stoeber, B; Liepmann, D. Fluid Injection Through Out-of-plane Microneedles. Proceedings of 1st Annual International Conference on Microtechnologies in Medicine and Biology, Berkeley, CA, USA, 12–14 October 2000.
- Griss, P; Stemme, G. Side-opened out-of-plane microneedles for microfluidics transdermal liquid transfer. J Microelectromech. Syst 2003, 12, 296–301. [Google Scholar]
- Paik, SJ; Byuna, S; Lima, JM; Park, Y; Leea, A; Chungb, S; Changa, J; Chuna, K; Cho, D. In-plane single-crystal-silicon microneedles for minimally invasive microfluidic systems. Sens. Actuators A 2004, 114, 276–284. [Google Scholar]
- Wilke, N; Hibert, C; O’Brien, J; Morrissey, A. Silicon microneedle electrode array with temperature monitoring for electroporation. Sens Actuators A 2005, 123–124, 319–325. [Google Scholar]
- Choi, JW; Park, IB; Ha, YM; Jung, MG; Lee, SD; Lee, SH. Insertion Force Estimation of Various Microneedle Array-type Structures Fabricated by a Microstereolithography Apparatus. Proceedings of International Joint Conference SICE-ICASE, Busan, Korea, 18–21 October 2006; pp. 3678–3681.
- Shibata, T; Nakanishi, A; Sakai, T; Kato, N; Kawashima, T; Mineta, T; Makino, E. Fabrication and mechanical characterization of microneedle array for cell surgery. Proceedings of Solid-State Sensors, Actuators and Microsystems Conference, Transducers, Lyon, France, 10–14 June 2007; pp. 719–722.
- Runyam, WR; Bean, KE. Semiconductor Integrated Circuit Processing Technology; Addison-Wisley: New York, NY, USA, 1990. [Google Scholar]
- Ambrose, CG; Clanto, TO. Bioabsorbable implants, review of clinical experience in orthopedic surgery. Ann. Biomed. Eng 2004, 32, 171–177. [Google Scholar]
- Park, JH; Allen, MG; Prausnitz, MR. Biodegradable polymer microneedles: fabrication, mechanics and transdermal drug delivery. J. Control. Release 2005, 104, 51–66. [Google Scholar]
- Aoyagi, S; Izumi, H; Fukuda, M. Biodegradable polymer needle with various tip angles and consideration on insertion mechanism of mosquito’s proboscis. Sens. Actuators A 2008, 143, 20–28. [Google Scholar]
- Jiang, J; Moore, JS; Edelhauser, HF; Prausnitz, MR. Intrascleral drug delivery to the eye using hollow microneedles. Pharm. Res 2009, 26, 395–403. [Google Scholar]
- Parker, ER; Rao, MP; Turner, KL; Meinhart, CD; MacDonald, NC. Bulk micromachined Titanium microneedles. J Microelectromech Syst 2007, 16(2), 289–295. [Google Scholar]
- Yoshida, K; Lewinsky, I; Nielsen, M; Hylleberg, M. Implantation mechanics of tungsten microneedles into peripheral nerve truks. Med. Bio. Eng. Comput 2007, 45, 413–420. [Google Scholar]
- Ashraf, MW; Tayyaba, S; Afzulpurkar, N; Nisar, A; Punyasai, C; Saejok, K; Supadech, J; Atthi, N; Hruanun, C; Poyai, A. Optimization of Fabrication Process for MEMS based Microneedles Using ICP Etching Technology. Proceedings of 6th international Conference on MEMS, Nano and Smart System (ICMENS), Changsha, China, 14–15 December 2010; pp. 356–359.
- Tsuchiya, K; Nakanishi, N; Uetsuji, Y; Nakamachi, E. Development of Blood Extraction System for Health Monitoring System. Biomed. Devices 2005, 7, 347–353. [Google Scholar]
- Ding, Z; Verbaan, FJ; Bivas-Benita, M; Bungener, L; Huckriede, A; van den Berg, DG; Kersten, G; Bouwstra, JA. Microneedles arrays for the transcutaneous immunization of diphtheria and influenza in BALB/c mice. J. Control. Release 2009, 136, 71–78. [Google Scholar]
- Chen, B; Wei, J; Iliescu, C. Sonophoretic enhanced microneedles array (SEMA)-improving the efficiency of transdermal drug delivery. Sens. Actuators B 2010, 145, 54–60. [Google Scholar]
- Zhang, W; Gao, J; Zhu, Q; Zhang, M; Ding, X; Wang, X; Hou, X; Fan, W; Ding, B; Wu, X; Wang, X; Gao, S. Penetration and distribution of PLGA nanoparticles in the human skin treated with microneedles. Int. J. Pharm 2010, 402, 205–212. [Google Scholar]
- Zhang, P; Dalton, C; Jullien, GA. Design and fabrication of MEMS based microneedle arrays for medical applications. Microsyst. Technol 2009, 15, 1073–1082. [Google Scholar]
- Yu, LM; Tay, FEH; Guo, DG; Xu, L; Yap, KL. A microfabricated electrode with Hollow microneedles for ECG measurement. Sens. Actuators A 2009, 151, 17–22. [Google Scholar]
- Chen, B; Wei, J; Tay, FEH. Silicon microneedle array with biodegradable tip for transdermal drug delivery. Microsyst. Technol 2008, 14, 1015–1019. [Google Scholar]
- Roxhed, N; Griss, P; Stemme, G. Membrane-seald hollow microneedles and related administration schemes for transdermal drug delivery. Biomed. Microdevices 2008, 10, 271–279. [Google Scholar]
- Bhandari, R; Negi, S; Solzbacher, F. A novel mask-less method of fabricating high aspect ratio microneedles for blood sampling. Proceedings of IEEE 58th Electronic Components and Technology Conference, Lake Buena Vista, FL, USA, 27–30 May 2008; pp. 1306–1309.
- Donnelly, RF; Morrow, DIJ; McCarron, PA; Woolfson, AD; Morrissey, A; Juzenas, P; Juzeniene, A; Lani, V; McCarthy, HO; Moan, J. Microneedle-mediated Intradermal delivery of 5-aminolevulinic acid: Potential for enhanced topical photodynamic therapy. J. Control. Release 2008, 129, 154–162. [Google Scholar]
- Lee, JW; Park, JH; Prausnitz, MR. Dissolving microneedles for transdermal drug delivery. Biomaterials 2008, 29, 2113–2124. [Google Scholar]
- Park, JH; Choi, S; Seo, S; Choy, YB; Prausnitz, MR. A microneedle roller for transdermal drug delivery. Eur. J. Pharm. Biopharm 2010, 76, 282–289. [Google Scholar]
- Gomaa, YA; Morrow, DIJ; Garland, MJ; Donnelly, RF; El-Khordagui, LK. Effects of microneedle length, densty, insertion time and multiple applications on human skin barrier function: Assessments by transdermal water loss. Toxicol. in Vitro 2010, 24, 1971–1978. [Google Scholar]
- Donnelly, RF; Morrow, DIJ; Fay, F; Scott, CJ; Abdelghany, S; Sing, RRT; Garland, MJ; Woolfson, AD. Microneedle-mediated Intradermal nanopartile delivery: Potential for ehnaced local administration of hydrophobic pre-formed photosensitisers. Photodiagn. Photodynam 2010, 7, 222–231. [Google Scholar]
- Matteucci, M; Fanetti, M; Casella, M; Gramatica, F; Gavioli, L; Tormen, M; Grenci, G; Angelis, FD; Fabrizio, ED. Poly vinyl alcohol re-usable masters for microneedles replication. Microelectron. Eng 2009, 86, 752–756. [Google Scholar]
- Han, MH; Kim, DK; Kang, SH; Yoon, HR; Kim, BY; Lee, SS; Kim, KD; Lee, HG. Improvement in antigen-delivery using fabrication of a grooves-embedded microneedle array. Sens. Actuators B 2009, 137, 274–280. [Google Scholar]
- Jin, CY; Han, MH; Lee, SS. Mass producible and biocompatible microneedle patch and functional verification of its usefulness for transdermal drug delivery. Biomed. Microdevices 2009, 11, 1195–1203. [Google Scholar]
- Emam, M; Abashiya, Y; Chareunsack, B; Skordos, J; Oh, JH; Choi, Y; Kralick, F; Noh, H. A novel microdevice for the treatment of hydrocephalus: design and fabrication of an array of microvales and microneedles. Microsyst. Technol 2008, 14, 371–378. [Google Scholar]
- Hsu, CC; Chen, YT; Tsai, CH; Kangl, SW. Fabrication of Microneedles. Proceedings of 2nd IEEE International Conference on Nano/Micro Engineered and Molicular System, Bangkok, Thailand, 16–19 January 2007; pp. 639–642.
- Kim, YC; Quan, FS; Compans, RW; Kang, SM; Prausnitz, MR. Formulation and coating of microneedles with inactivated influenza virus to improve vaccine stability and immunogenicity. J. Control. Release 2010, 142, 187–195. [Google Scholar]
- Kato, N; Kawashima, T; Shibata, T; Mineta, T; Makino, E. Micromachning of a newly designed AFM probe integrated with hollow microneedle for cellular function analysis. Microelectr. Eng 2010, 87, 1185–1189. [Google Scholar]
- Hou, W; Das, B; Jiang, Y; Qian, S; Zheng, X; Yang, J; Pi, X; Liu, H; Zheng, J; Zhang, Y. On A Microfabricated Ti-alloy-based Microneedle Array for Transdermal Drug Delivery. Proceedings of 3rd IEEE International Conference on Nano/Micro Engineered and Molecular System, Sanya, China, 6–9 January 2008; pp. 453–456.
- Kolli, CS; Banga, AK. Characterization of Solid Maltose Microneedles and their Use for Transdermal Delivery. Pharm. Res 2008, 25, 104–113. [Google Scholar]
- Verbaan, FJ; Bal, SM; van den Berg, dj; Dijksman, JA; van Hecke, M; Verpoorten, H; van den Berg, A; Luttge, R; Bouwstra, JA. Improved piercing of microneedle arrays in dermatomed human skin by an impact insertion method. In J Control Release; 2008; Volume 128, pp. 80–88. [Google Scholar]
- Kim, K; Lee, J. High aspect ratio tapered hollow metallic microneedle arrays with microfluidic interconnector. Microsyst. Technol 2007, 13, 231–235. [Google Scholar]
- Gere, J; Timoshenko, S. Mechanics of Materials, 4th ed; Prentice Hall: Upper Saddle River, NJ, USA, 1999. [Google Scholar]
- Zahn, JD; Talbot, NH; Liepmann, D; Pisano, AP. Micro fabricated polysilicon microneedles for minimally invasive biomedical devices. Biomed. Microdevices 2000, 2, 295–303. [Google Scholar]
- Aggarwal, P; Johnston, CR. Geomertrical effects in mechanical characterizing of microneedle for biomedical applications. Sens. Actuators B 2004, 102, 226–234. [Google Scholar]
- Frick, TB; Maruccia, DD; Cartmill, JA; Martin, CJ; Walsh, WR. Resistance forces acting on suture needles. J. Biomech 2001, 34, 1335–1340. [Google Scholar]
- Khumpuang, S; Horade, M; Fujioka, K; Sugiyama, S. Geometrical Strengthening and tip-sharping of a microneedle array fabricated by X-ray lithography. Microsyst. Technol 2007, 13, 209–214. [Google Scholar]
- Davis, SP; Martanto, W; Allen, MG; Prausnitz, MR. Hollow metal microneedles for insulin delivery to diabetic rats. IEEE Trans. Biomed. Eng 2005, 52, 909–915. [Google Scholar]
- Ashraf, MW; Tayyaba, S; Afzulpurkar, N. MEMS based Polymeric Drug Delivery System. Proceedings of 6th IEEE Conference on Automation Science and Engineering (CASE), Toronto, Canada, 21–24 August 2010; pp. 192–197.
- Rajaraman, S; Henderson, HT. A unique fabrication approach for microneedles using coherent porous silicon technology. Sens. Actuators B 2005, 105, 443–448. [Google Scholar]
- Sammoura, F; Kang, J; Heo, Y; Jung, T; Lin, L. Polymeric microneedle fabrication using a microinjection molding technique. Microsyst. Technol 2007, 13, 517–522. [Google Scholar]
- Chen, X; Kask, AS; Crichton, ML; McNeilly, C; Yukiko, S; Dong, L; Marshak, JO; Jarrahian, C; Fernando, GJP; Chen, D; Koelle, DM; Kendall, MAF. Improved DNA vaccination by skin-targeted delivery using dry-coated densely-packed microprojection arrays. J. Control. Release 2010, 148, 327–333. [Google Scholar]
- Milewski, M; Yerramreddy, TR; Ghosh, P; Crooks, PA; Stinchcomb, AL. In vitro permeation of a pegylated naltrexone prodrug across microneedle-treated skin. J. Control. Release 2010, 146, 37–44. [Google Scholar]
- Khann, P; Silv, H; Bhansali, S. Variation in microneedle geometry to increase the shear strength. Proc. Eng 2010, 5, 977–980. [Google Scholar]
- Bal, SM; Kruithof, AC; Zwier, R; Dietz, E; Bouwstra, JA; Lademann, J; Meinke, MC. Influence of microneedle shape on the transport of a fluorescent dye into human skin in vivo. J. Control. Release 2010, 147, 218–224. [Google Scholar]
- Donnelly, RF; Garland, MJ; Morrow, DIJ; Migalska, K; Singh, TRR; Majithiya, R; Woolfson, AD. Optical coherence tomography is a valuable tool in the study of the effects of microneedle geometry on skin penetration characteristics and in-skin dissolution. J. Control. Release 2010, 147, 333–341. [Google Scholar]
- Crichton, ML; Ansaldo, A; Chen, X; Prowa, TW; Fernando, GJP; Kendall, MAF. The effect of strain rate on the precision of penetration of short densely-packed microprojection array patches coated with vaccine. Biomaterials 2010, 31, 4562–4572. [Google Scholar]
- Pearton, M; Kang, SM; Song, JM; Kim, YC; Quan, FS; Anstey, A; Ivory, M; Prausnitz, MR; Compans, RW; Birchall, JC. Influenza virus-like particles coated onto microneedles can elicit stimulatory effects on Langerhans cells in human skin. Vaccine 2010, 28, 6104–6113. [Google Scholar]
- Li, W-Z; Hou, M-R; Zhou, J-P; Zhou, Y-Q; Hao, B-H; Liu, T; Zhang, Y. Super-short solid silicon microneedles for transdermal drug delivery applications international. J. Pharm 2010, 389, 122–129. [Google Scholar]
- Chu, LY; Prausnitz, MR. Separable arrowhead microneedles. J. Control. Release 2010, 149, 242–249. [Google Scholar]
- Yan, K; Todo, H; Sugibayashi, K. Transdermal drug delivery by in-skin electroporation using a microneedle array. Int. J. Pharm 2010, 397, 77–83. [Google Scholar]
- Yan, G; Warner, KS; Zhang, J; Sharma, S; Gale, BK. Evaluation needle length and density of microneedle arrays in the pretreatment of skin for transdermal drug delivery. Int. J. Pharm 2010, 391, 7–12. [Google Scholar]
- Song, JM; Kim, YC; Barlow, PG; Hossain, MJ; Park, KM; Donis, RO; Prausnitz, MR; Compans, RW; Kang, SM. Improve protection against avian influenza H5N1 virus by a single vaccination with virus-like particles in skin using microneedles. Antivir. Res 2010, 88, 244–247. [Google Scholar]
- Zhou, CP; Liu, YL; Wang, HL; Zhang, PX; Zhang, JL. Transdermal delivery of insulin using microneedle rollers in vivo. Int. J. Pharm 2010, 392, 127–133. [Google Scholar]
- Quan, FS; Kim, YC; Compans, RW; Prausnitz, MR; Kang, SM. Dose sparing enabled by skin immunization with influenza virus-like particle vaccine using microneedles. J. Control. Release 2010, 147, 326–332. [Google Scholar]
- Bussemer, T; Otto, I; Bodmeier, R. Pulsatile drug delivery systems. Crit. Rev. Ther. Drug Carrier Syst 2001, 18, 433–458. [Google Scholar]
- Ma, HK; Chen, BR; Gao, JJ; Lin, CY. Development of an OAPCP-micropump liquid cooling system in a laptop. Int. Commun. Heat Mass Transf 2009, 36, 225–232. [Google Scholar]
- Xia, F; Tadigadapa, S; Zhang, QM. Electroactive polymer based microfluidic pump. Sens. Actuators A 2006, 125, 346–352. [Google Scholar]
- Jeong, OC; Konishi, S. Fabrication and drive test of pneumatic PDMS micro pump Sens. Actuators A 2007, 135, 849–856. [Google Scholar]
- Makino, E; Shibata, T. Micropump with TiNi shape memory diaphragm actuator. J. Surface Finish. Soc. Jpn 2005, 56, 213–218. [Google Scholar]
- Ashraf, MW; Tayyaba, S; Nisar, A; Afzulpurkar, N. MEMS based System for Drug Delivery. Proceedings of 6th International Conference on Emerging Technologies (ICET), Islamabad, Pakistan, 18–19 October, 2010; pp. 82–87.
- Kabata, A; Suzuki, H. Microsystem for Injection of Insulin and Monitoring of Glucose Concentration. Proceedings of 5th International Conference on Sensors, Irvine, CA, USA, 30 October–3 November 2005; pp. 171–174.
- Yang, SC; Liu, CH. An Electrolysis-bubble-actuated micropump using electrowetting on dielectric (EWOD) for 1XN micro-sample switches. Proceedings of Transducers, Denver, CO, USA, 21–25 June 2009; pp. 2018–2021.
- Ma, B; Liu, S; Gan, Z; Liu, G; Cai, X; Zhang, H; Yang, Z. A PZT Insulin Pump Integrated with a Silicon Micro Needle Array for Transdermal Drug Delivery. Proceedings of 56th Electronic Components and Technology Conference, San Diego, CA, USA, 30 May–2 June 2006; pp. 667–681.
- Tayyaba, S; Ashraf, MW; Afzulpurkar, N. Design and Simulation of Double Lumen Polymeric Microneedles for Blood Transport. Proceedings of International Conference on Mechanical and Electrical Technology (ICMET), Singapore, 10–12 September 2010; pp. 615–618.
- Najafi, K. Micropackaging technologies for integrated microsystems: Applications to MEMS and MOEMS. Proc SPIE 2003, 4979. [Google Scholar] [CrossRef]
- 3M. Available online: http://solutions.3m.com/wps/portal/3M/en_WW/DrugDeliverySystems/DDSD accessed on 27 April 2011.
- Birchall, JC; Clemo, R; Anstey, A; John, DN. Microneedles in clinical practice-an exploratory study into the opinions of healthcare professionals and the public. Pharm. Res 2011, 28, 95–106. [Google Scholar]
|Reference||Actuation Method||Materials used for fabrication||Size||Pumping Chamber||Pumping Medium||Valve||Voltage (V)||Frequency||Back Pressure/Applied Pressure||Flow Rate (μL/min)||Applications|
|Liu et al. 2010 ||Piezoelectric||Polycarbonate (PC), PMMA, PDMS, PZT, (Titanium) Ti||15 × 8 mm||4||Insulin||2||36||200 Hz||22 kPa||6.23 × 10−5 mL/min||Insulin therapy system|
|Zhu et al. 2009 ||Piezoelectric||Polyetheretherketone/PDMS/Metal/Ceramics||Not reported||1||Air/Water||2||100||225 Hz for air, 17 Hz for water||Not reported||39 mL/min for air, 1.8 mL/min for water||Drug delivery applications|
|Kang and Auner 2011 ||Piezoelectric||Si/Epoxy H31/PZT-5A||14.5 × 9 × 1.1 mm||1||Not reported||2||240||20–100 Hz||0–10 psi||0.52 mL/min||Microfluidic applications|
|Halhouli et al. 2010 ||Electromagnetic||PC, Plexiglass||16 × 18 mm||1||Water||Not report ed||Not reported||Not reported||785 Pa||13.7 mL/min||Biomedical applications|
|Shen et al. 2009 ||Electromagnetic||PDMS, Glass||24 × 40 × 0.4 mm||3||Water||2||0.7||12 Hz||70 mbar||2.4 mL/min||Portable LOC applications|
|Lee et al. 2009 ||Electrostatic||Si||Not reported||2||Gas||19||Not reported||2.2–2.8 KHz||7.3–3.3 kPa||0.29–0.07 SCCM||Not reported|
|Teymoori and Sani 2005 ||Electrostatic||Si, Glass||7 × 4 × 1 mm||3||Not reported||3||18.5||50 Hz||Not reported||9.1 μL/min||Drug delivery applications|
|Chia et al. 2010 ||Thermopneumatic||PDMS, Glass||16 × 18 × 5 mm||3||Not reported||Not reported||9||1.2 Hz||490 Pa||20.01 μL/min||Biomedical applications|
|Tan et al. 2010 ||Thermopneumatic||PDMS, PMMA||Not reported||3||Compressed air||3||Not reported||10 Hz||138 kPa||96 μL/min||Microfluidic devics|
|Zou et al. 1997 ||Bimetallic||Al, Si, Glass||13 × 7 × 2 mm||2||Gas/Water||2||15||Not reported||0.5 kPa||5.6 μL/s||Not reported|
|Fang and Tan 2010 ||ICPF||PDMS, Polypyrrole, Stainless steel, Polyvinylidene fluoride||25 × 25 × 10 mm||1||Water||4||4||0.5 Hz||1.3 kPa||1260 μL/min||Biomedical devices|
|Sim et al. 2008 ||Phase Change||Al, Silicon, Silicone rubber, Glass||Not reported||1||Water||2||8||2 Hz||0 mm H2O||97 μL/min||Not reported|
|Zhang and Qiu 2006 ||SMA||Ti, Nickel (Ni), Copper (Cu)||8 × 8 × 1.8 mm||1||DI water||2||Not reported||80 Hz||Not reported||235 μL/min||Not reported|
|Reference||Actuation Method||Material used for Fabrication||Size||Pumping Chamber||Pumping Medium||Valve||Voltage (V)||Frequency||Back Pressure/Applied Pressure||Flow Rate (μL/min)||Applications|
|Chan et al. 2010||Bubble type||PDMS, Glass, Si||Not reported||2||DI water, Phosphate- buffered solution||Not reported||5||300 Hz||Not reported||37.8 μL/min||Miniature electronic devices|
|Jung and Kwak 2007 ||Bubble type||Si, Pyrex glass||Not reported||1||DI water||Not reported||30||0.5–2.0 Hz||Not reported||6–8 μL/min||Microfluidic applications|
|Wakui et al. 2009 ||EHD||Polymer, Carbon, Glass||Not reported||Not reported||Fluorinert||Not reported||500||Not reported||23 Pa||400 μL/min||Microfluidic devices|
|Singhal and Garimella 2007 ||EHD||Al||1500 × 200 × 50 μm||1||Water||Not reported||3.3||373 kHz||Not reported||10.5 μL/min||Microchannel cooling system|
|Lister et al. 2010 ||EO||Glass, Platinum||Not reported||Not reported||Borate buffer, DI water||Not reported||2.9||Not reported||1.6 kPa||13 μL/min||Drug delivery|
|Xu et al. 2010 ||EO||Glass, PDMS||Not reported||2||Water||1||Not reported||Not reported||Not reported||0.33 μL/min||Perfusion cell culture|
|Kang and Choi 2010 ||MHD||Au (gold), PDMS||Not reported||Not reported||PBS solution||Not reported||3.6||Not reported||Not reported||2.83 μL/min||LOC applications|
|Lim and Choi 2009 ||MHD||Si, Pyrex glass, Al||40 × 25 × 1 mm||Not reported||PBS solution||Not reported||Not reported||Not reported||100000N/m2||0.3 μL/min||Drug delivery|
|Yun et al. 2002 ||EW||Glass, Si, Platinum||Not reported||2||Mercury||2||2.3||25 Hz||800 Pa||70 μL/min||Biomedical Devices|
|Kim et al. 2008 ||Electrochemical||Ppy, PDMS, PMMA||5.6 × 16 × 26 mm||1||Water||2||±1.5||Not reported||11 mbar||52 μL/min||Microfluidic applications|
|Heuck et al. 2008 ||Evaporation||Si||Not reported||Not reported||DI water||Not reported||Not reported||Not reported||Not reported||11 pL/s||Biological sampling|
|Guan et al. 2006 ||Evaporation||Pdms, PMMA, Stainless steel||25 × 15 × 3 mm||Not reported||Water||Not reported||Not reported||Not reported||23.5 kPa||3.02 μL/min||Microfluidics system|
|Luginbuhl 1997 ||FPW||Si, Platinum, Ceramic||Not reported||Not reported||Water||Not reported||6||2–3 MHz||Not reported||0.255 μL/min||Fluid delivery system|
|Structure||Overall Shape||Tip Shape||Material Used||Application|
|Solid||Cylindrical||Volcano||Single crystal silicon||Drug delivery|
|Hollow||Canonical||Snake fang||Polysilicon||Gene delivery|
|In-plane||Pyramid||Cylindrical||Silicon dioxide||Blood extraction|
|Out-of-plane||Candle||Canonical||Silicon nitride||Fluid sampling|
|Rocket||Ti- alloy||Allergies diagnosis|
|Stainless steel||Sensing electrodes|
|Reference||Material||Structure of microneedles||Shapes of microneedles||Dimensions||Array size/Needles||Analysis type||Testing||Fabrication techniques||Application|
|Waseem et al. 2010 ||Silicon||Hollow/Out-of plane||Cylindrical||L = 200 μm|
Di = 60 μm
Do = 150 μm
|5 × 5||Structural/CFD (Static/Transient)||Not reported||ICP etching||Transdermal drug delivery|
|Chen et al. 2010 ||Silicon||Hollow/Out-of plane||Cylindrical base||L = 100 μm|
D = 80 μm
|30 × 30||Fluidic analysis||Pig Skin||Deep reactive ion etching (DRIE)||Transdermal drug delivery|
|Zhang et al. 2010 ||Silicon||Solid/Out-of plane||Star shape||L = 200 μm||10 × 10||PLGA nano Particles distribution||Human skin||RIE/Thin film deposition Photolithography||Transdermal drug delivery|
|Waseem et al. 2010 ||Silicon||Hollow/Out-of plane||Cylindrical base tapered tip||L = 200 μm|
Di = 40 μm
Do = 425 μm
|6 × 6||Structural/Fluidic (Static/Transient)||Not reported||ICP etching||Transdermal drug delivery|
|Zhang et al. 2009 ||Silicon||Hollow/Out-of plane||Cylindrical/Side opened at tip||L = 200 μm|
Di = 40 μm
Dt = 450 nm
|10 × 11||Fluidic analysis||Potato skin/Chicken skin||Bi-mask technique||Drug delivery/fluid sampling|
|Ding et al. 2009 ||Silicon||Solid/Hollow||Tangentially cut tip||L1 = 300 μm to 900 μm|
L2 = 300 μm
D2 = 200 μm
L3 = 245 μm
|4 × 4|
9 × 9
|Fluidic analysis/Statistical||Mouse skin||Surface micromachining/Etching||Dermal diphtheria/influenza vaccination|
|Haq et al. 2009 ||Silicon||Hollow/Out-of- plane||Pyramidal||L1 = 180 μm|
L2 = 280 μm
Db = 180 μm
|6 × 6||Fluidic analysis||Human skin||Wet etching||Transcutaneous drug delivery|
|Yu et al. 2009 ||Silicon||Hollow/Out-of plane||Cylindrical||DP = 200 μm|
D = 100 μm
|Not reported||Structural analysis||One-lead ECG recording system||DRIE||ECG measurement|
|Coulman et al. 2009 ||Silicon||Solid||Pyramidal shape/Pointed/Frustum tip||L = 280 μm, Db = 200 μm||16 needles||Diffusion of nano particles||Human epidermal membrane||Wet etching||Transdermal/Intradermal drug delivery|
|Chen et al. 2008 ||Silicon||Out-of plane||Macro porous tip||Not reported||Not reported||Fluidic analysis||Pig skin||DRIE||Transdermal drug delivery|
|Roxhed et al. 2008 ||Silicon||Out-of- plane/Hollow||Cross/Circler||L1 = 310 μm, L2 = 400 μm||25 needles||Fluidic analysis||Human skin||DRIE||Transdermal drug delivery|
|Bhandari et al. 2008 ||Silicon||Hollow/Out- of-plane||Square base canonical||Not reported||10 × 10||Not reported||Not reported||Laser micromachining/Dicing/Etching||Blood sampling|
|Donnelly et al. 2008 ||Silicon||Not reported||Sharp 3D Tip/Grooves- embedded shaft||L = 270 μm, Db = 240 μm||Not reported||Fluidic analysis/Statistical||Mouse skin/Porcine skin of piglets||Wet etching||Photodynamic therapy|
|Lee et al. 2008 ||Silicon||Solid/Out- of plane||Conical/Pyramidal||L1 = 800 μm, Db = 200 μm, Dt = 20 μm, L2 = 600 μm, Wb = 300 μm||3 × 3||Structural analysis||Not reported||Micromolding||Drug delivery|
Notations: L = Length of needle, Wb = Base width, Do = Outer diameter, Di = Inner diameter, Db = Base diameter, Dt = Tip diameter, DP = Depth.
|Reference||Materials||Structure of microneedles||Shapes of microneedles||Dimensions||Array size/Needles||Analysis type||Testing||Fabrication techniques||Application|
|Park et al. 2010 ||PLA||Solid/Out-of- plane||Canonical/Square base||L = 600 μm|
Wb = 250 μm
|10 × 10||Diffusion of trypan blue||Human/Porcine cadaver skin||UV lithography||Transdermal drug delivery|
|Gomaa et al. 2010 ||PMVE/MA||Solid/Out-of- plane||Canonical||L1 = 400 μm|
L2 = 600 μm
L3 = 100 μm
|11 × 11|
14 × 14
19 × 19
|Effect of Skin Permeability with microneedle density||Human skin||Laser micromachining||Drug delivery|
|Donnelly et al. 2010 ||Polymeric (Gantrez)||Solid/Out-of- plane||Canonical||Not reported||Not reported||Statistical||Porcine skin||Molding process||Intradermal delivery|
|Bodhale et al. 2010 ||PGA||Hollow/Out-of plane||Side opened/Sharp tip||L = 200 μm|
Di = 30 μm
Do = 150 μm
Db = 300 μm
|25 × 25||Structural/Fluidic||Not reported||Hot embossing/UV excimer laser(Proposed)||Drug delivery|
|Matteucci et al. 2009 ||PMMA||Hollow/Out-of plane||Rounded tip/Sharp tip||L = 500 to 1100 μm|
Bevel angle = 30° to 40°
|10 arrays||Not reported||Not reported||DXRL||Not reported|
|Han et al. 2009 ||PLLA||Solid/Out-of plane||Sharp 3D Tip/Grooves-embedded shaft||L = 880 ± 20 μm, Wb = 710 ± 15 μm|
T = 145 ± 15 μm
|Not reported||Protein transportation analysis||Mouse skin/Serum||Lithography/Ni electroplating/PDMS replication/Hot embossing||Intradermal immunization|
|Jin et al. 2009 ||PMMA/PC||Solid/In-plane||Quadrangular/Pyramidal||L = 200–1500 mm||Not reported||Drug transportation||Mouse skin and serum||DXRL/Hot embossing||Transdermal drug delivery|
|Oh et al. 2008 ||PC||Solid/Out-of plane||Sharp tip/Spear||L = 200–500 μm||Not reported||Hydrophilic molecules transportation||Mouse skin||Molding/Hot embossing||To improve skin permeability for hydrophilic molecules|
|Emam et al. 2008 ||SU-8||Out-of-plane/Hollow||Sharp tip||L = 500 μm, Wb = 100 μm||Not reported||Fluid analysis||Not reported||Deposition/Lithography/Etching||Treatment of hydrocephalus|
|Aoyagi et al. 2007||PLA||Solid/Out-of plane||Straight/Harpoon shape/Sharp tip||L = 400 μm|
Wb = 90, 120, 150, 230 μm
T = 115 μm
Tip angle = 10°, 20°, 30°, 40°
|Not reported||Structural||Artificial skin of silicone rubber||Etching/Injection molding||Drug delivery|
|Hsu et al. 2007 ||SU-8 2050||Out-of-plane||V-groove||L1 = 236 μm|
L2 = 350 μm
|Not reported||Not reported||Not reported||Molding/KOH etching||Biomedicine technology|
Notations: L = Length of needle, T = Thickness, Wb = Base width, Do = Outer diameter, Di = Inner diameter, Db = Base diameter.
|Reference||Materials||Structure of Microneedles||Shapes of microneedles||Dimensions||Array size/Needles||Analysis Type||Testing||Fabrication Techniques||Applications|
|Kim et al. 2010 ||Stainless steel||Solid/In-plane||Spear/Sharp tip||L = 700 μm|
Wb = 160 μm
T = 50 μm
|5 microneedles||Drug transportation/Statistical analysis||Mouse skin||Infrared Laser||Vaccine delivery|
|Kato et al. 2010 ||SiO2||Hollow/Out- of-Plane||Circular Tip||L = 77 μm|
Do = 5.5 μm
Di = 3.5 μm
|Not reported||Structural (Panitration)||Gelatin||DRIE/Micromachining||Cellular function analysis|
|Ding et al. 2009 ||Stainless steel||Solid/Hollow/Out-of-Plane||Tangentially cut tip||L = 245, 300–900 μm|
D2 = 200 μm
|4 × 4|
9 × 9
|Drug transportation/Statistical||Mouse skin||Surface micromachining/Etching||Dermal diphtheria/Influenza vaccination|
|Jiang et al. 2009 ||Glass||Hollow||Elliptical tip opening||L = 3–4 cm||Not reported||Histological/Microscopic image analysis||Human cadaver eyes||Micropipette pulling technique||Intrascleral delivery|
|Jin et al. 2009 ||Ni||Solid/In-plane||Triangular/Pyramidal||L= 200–1500 mm||Not reported||Drug transportation||Mouse skin and serum||DXRL/Hot embossing||Transdermal drug delivery|
|Hou et al. 2008 ||Ti-alloy||Hollow/Out- of-Plane||Not reported||L = 120 μm||10 × 10||Fluidic analysis||Not reported||Not reported||Transdermal drug delivery|
|Kolli and Banga 2008 ||Maltose||Solid/In-plane||Tetrahedron/Sharp tip||L = 500 μm|
Dt = 6 μm
|27 needle per array||Drug transportation||Mouse skin/Jacketed Franz diffusion cells||Micro-molding||Transdermal drug delivery|
|Verbaan et al. 2008 ||Metal||Solid/Hollow||Triangular tip/Tapered shaft||L = 245, 300 μm|
D = 200, 300 μm
Beveled angle = 45°
Db = 250 μm
|4 × 4|
6 × 6
9 × 9
|Waters HPLC System||Human skin||Surface micromachining/Etching||Transdermal drug delivery|
|Parker et al. 2007 ||Ti||Hollow/In- plane||Spare/Sharp tip||L = 500, 750, 1000 μm|
Wb = 100 μm
Tip taper angle = 60°
|10 needles||Fluidic/Structural analysis||Pressure Testing apparatus||Bulk micromachining/Multilayer lamination||Drug delivery|
|Shibata et al. 2007 ||SiO2||Hollow/Out-of- plane||Circler tip/Cylindrical||L = 77 μm, Do = 5.5 μm|
Di = 3.5 μm
|Not reported||Structural analysis||Gelatin||Photolithography/DRIE||Cell surgery|
|Kim and Lee 2007 ||Metallic||Hollow/Out-of- plane||Tapered tip||L1 = 200 μm|
T = 10 μm
L2 = 400 μm
T = 20 μm
Tapering angle < 5°
|10 × 10||Fluidic analysis||Not reported||SU-8 based UV LIGA||Drug delivery/Body fluid sampling|
|Tsuchiya et al. 2005 ||Ti||Hollow/Out-of- plane||Cylindrical||L = 1 mm|
Di = 25 μm
Do = 60 μm
|Not reported||Fluidic analysis||Not reported||Sputter deposition||Blood extraction|
Notations: L = Length of needle, T = Thickness, Wb = Base width, Do = Outer diameter, Di = Inner diameter, Db = Base diameter, Dt = Tip diameter.
© 2011 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).