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Search Results (4)

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Keywords = on-chip and on-demand

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25 pages, 9895 KB  
Review
Harnessing Microfluidics for the Effective and Precise Synthesis of Advanced Materials
by Xinlei Qi and Guoqing Hu
Micromachines 2025, 16(10), 1106; https://doi.org/10.3390/mi16101106 - 28 Sep 2025
Viewed by 1879
Abstract
Microfluidic methods are powerful platforms for synthesizing advanced functional materials because they allow for precise control of microscale reaction environments. Microfluidics manipulates reactants in lab-on-a-chip systems to enable the fabrication of highly uniform materials with tunable properties, which are crucial for drug delivery, [...] Read more.
Microfluidic methods are powerful platforms for synthesizing advanced functional materials because they allow for precise control of microscale reaction environments. Microfluidics manipulates reactants in lab-on-a-chip systems to enable the fabrication of highly uniform materials with tunable properties, which are crucial for drug delivery, diagnostics, catalysis, and nanomaterial design. This review emphasizes recent progress in microfluidic technologies for synthesizing functional materials, with a focus on polymeric, hydrogel, lipid-based, and inorganic particles. Microfluidics provides exceptional control over the size, morphology, composition, and surface chemistry of materials, thereby enhancing their performance through uniformity, tunability, hierarchical structuring, and on-chip functionalization. Our review provides novel insights by linking material design strategies with fabrication methods tailored to biomedical applications. We also discuss emerging trends, such as AI-driven optimization, automation, and sustainable microfluidic practices, offering a practical and forward-looking perspective. As the field advances toward robust, standardized, and user-friendly platforms, microfluidics has the potential to increase industrial adoption and enable on-demand solutions in nanotechnology and personalized medicine. Full article
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17 pages, 7694 KB  
Article
Analysis of Sequential Micromixing Driven by Sinusoidally Shaped Induced-Charge Electroosmotic Flow
by Haizhen Sun, Ziyi Li, Yongji Wu, Xinjian Fan, Minglu Zhu, Tao Chen and Lining Sun
Micromachines 2022, 13(11), 1985; https://doi.org/10.3390/mi13111985 - 16 Nov 2022
Cited by 6 | Viewed by 2314
Abstract
Multi-fluid micromixing, which has rarely been explored, typically represents a highly sought-after technique in on-chip biochemical and biomedical assays. Herein, we propose a novel micromixing approach utilizing induced-charge electroosmosis (ICEO) to implement multicomplex mixing between parallel streams. The variations of ICEO microvortices above [...] Read more.
Multi-fluid micromixing, which has rarely been explored, typically represents a highly sought-after technique in on-chip biochemical and biomedical assays. Herein, we propose a novel micromixing approach utilizing induced-charge electroosmosis (ICEO) to implement multicomplex mixing between parallel streams. The variations of ICEO microvortices above a sinusoidally shaped floating electrode (SSFE) are first investigated to better understand the microvortex development and the resultant mixing process within a confined channel. On this basis, a mathematical model of the vortex index is newly developed to predict the mixing degree along the microchannel. The negative exponential distribution obtained between the vortex index and mixing index demonstrates an efficient model to describe the mixing performance without solving the coupled diffusion and momentum equations. Specifically, sufficient mixing with a mixing index higher than 0.9 can be achieved when the vortex index exceeds 51, and the mixing efficiency reaches a plateau at an AC frequency close to 100 Hz. Further, a rectangle floating electrode (RFE) is deposited before SSFE to enhance the controlled sequence for three-fluid mixing. One side fluid can fully mix with the middle fluid with a mixing index of 0.623 above RFE in the first mixing stage and achieve entire-channel mixing with a mixing index of 0.983 above SSFE in the second mixing stage, thereby enabling on-demand sequential mixing. As a proof of concept, this work can provide a robust alternative technique for multi-objective issues and structural design related to mixers. Full article
(This article belongs to the Special Issue X-fluidics at the Micro/Nanoscale)
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12 pages, 1641 KB  
Article
Parity-Time Symmetry Enabled Band-Pass Filter Featuring High Bandwidth-Tunable Contrast Ratio
by Xinda Lu, Nuo Chen, Boqing Zhang, Haofan Yang, Yuntian Chen, Xinliang Zhang and Jing Xu
Photonics 2022, 9(6), 380; https://doi.org/10.3390/photonics9060380 - 26 May 2022
Cited by 6 | Viewed by 2872
Abstract
Integrated optical filters based on microring resonators play a critical role in many applications, ranging from wavelength division multiplexing and switching to channel routing. Bandwidth tunable filters are capable of meeting the on-demand flexible operations in complex situations, due to their advantages of [...] Read more.
Integrated optical filters based on microring resonators play a critical role in many applications, ranging from wavelength division multiplexing and switching to channel routing. Bandwidth tunable filters are capable of meeting the on-demand flexible operations in complex situations, due to their advantages of scalability, multi-functionality, and being energy-saving. Recent studies have investigated how parity-time (PT) symmetry coupled-resonant systems can be applied to the bandwidth-tunable filters. However, due to the trade-off between the bandwidth-tunable contrast ratio and insertion loss of the system, the bandwidth-tunable contrast ratio of this method is severely limited. Here, the bandwidth-tunable contrast ratio is defined as the maximum bandwidth divided by the minimum bandwidth. In this work, we show that a high bandwidth-tunable contrast ratio and low insertion loss of the system can be achieved simultaneously by increasing the coupling strength between the input port and the resonant. Theoretical analysis under different coupling states reveals that the low insertion loss can be obtained when the system initially operates at the over-coupling condition. A high bandwidth-tunable contrast ratio PT-symmetry band-pass filter with moderate insertion loss is shown on the Silicon platform. Our scheme provides an effective method to reduce the insertion loss of on-chip tunable filters, which is also applicable to the high-order cascaded microring systems. Full article
(This article belongs to the Special Issue Advances in Photonic Integrated Devices and Circuits)
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13 pages, 2269 KB  
Article
A Simple and Efficient Microfluidic System for Reverse Chemical Synthesis (5′-3′) of a Short-Chain Oligonucleotide Without Inert Atmosphere
by Rahul Bhardwaj, Phan T. Tue, Manish Biyani and Yuzuru Takamura
Appl. Sci. 2019, 9(7), 1357; https://doi.org/10.3390/app9071357 - 31 Mar 2019
Cited by 7 | Viewed by 5980
Abstract
Reverse DNA synthesis (5′-3′) plays diverse functional roles in cellular biology, biotechnology, and nanotechnology. However, current microfluidic systems for synthesizing single-stranded DNAs at a laboratory scale are limited. In this work, we develop a simple and efficient polydimethylsiloxane- (PDMS-) based microfluidic system for [...] Read more.
Reverse DNA synthesis (5′-3′) plays diverse functional roles in cellular biology, biotechnology, and nanotechnology. However, current microfluidic systems for synthesizing single-stranded DNAs at a laboratory scale are limited. In this work, we develop a simple and efficient polydimethylsiloxane- (PDMS-) based microfluidic system for the reverse chemical synthesis of short-chain oligonucleotides (in the 5′-3′ direction) under ambient conditions. The use of a microfluidics device and anhydrous conditions effectively surpass the problem of moisture sensitivity during oligonucleotide synthesis. With optimized microfluidic synthesis conditions, the system is able to synthesize up to 21 bases-long oligonucleotides in air atmosphere. The as-synthesized oligonucleotides, without further purification, are characterized using matrix-assisted laser desorption ionization–time of flight (MALDI-TOF/TOF) mass spectroscopy (MS) supported by the denatured polyacrylamide gel electrophoresis (PAGE) analysis. This developed system is highly promising for producing the desired sequence at the nanomolar scale on-chip and on-demand in the near future. Full article
(This article belongs to the Section Applied Biosciences and Bioengineering)
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