Cellulose through the Lens of Microfluidics: A Review

Cellulose, a linear polysaccharide, is the most common and renewable biopolymer in nature. Because this natural polymer cannot be melted (heated) or dissolved (in typical organic solvents), making complicated structures from it necessitates specialized material processing design. In this review, we looked at the literature to see how cellulose in various shapes and forms has been utilized in conjunction with microfluidic chips, whether as a component of the chips, being processed by a chip, or providing characterization via chips. We utilized more than approximately 250 sources to compile this publication, and we sought to portray cellulose manufacturing utilizing a microfluidic system. The findings reveal that a variety of products, including elongated fibres, microcapsules, core–shell structures and particles, and 3D or 2D structured microfluidics-based devices, may be easily built utilizing the coupled topics of microfluidics and cellulose. This review is intended to provide a concise, visual, yet comprehensive depiction of current research on the topic of cellulose product design and understanding using microfluidics, including, but not limited to, paper-based microfluidics design and implications, and the emulsification/shape formation of cellulose inside


Introduction
The most prevalent and renewable biopolymer in nature is cellulose, which is a linear polysaccharide. Cellulose is an organic molecule with a formula comprising a polysaccharide composed of a linear polymer of hundreds or even thousands of connected D-glucose units. Cellulose is a structural component of the major cell wall of plants, many types of algae, and oomycetes [1][2][3]. This natural polymer cannot be melted (heated) or dissolved (in common organic solvents). By derivatized chemical modification or direct dissolving, cellulose can be converted into a processible liquid state [4]. As adsorbents, cellulose and cellulose derivatives have been utilized in the form of hydrogels [5,6], films [7,8], beads [9,10], microfibers [11], and microcrystals [12,13]. In all these applications, cellulose as a solid phase provides a large surface area that may separate chemicals from flowing liquids due to cellulose active functional groups. In chromatography [14], protein purification [15], and drug delivery [16][17][18][19], cellulose beads can be utilized as the stationary phase. Papermaking and the synthesis of micro fibrillated cellulose have both employed partially or considerably fibrillated cellulose. Micro fibrillated cellulose was created from wood using a high-pressure homogenization process [20] and has since been utilized as a filter aid as well as an excellent thickener [21]. In general, considerable energy consumption is unavoidable for the nanoscale fibrillation of wood or other cellulosed source items that need cleaves of interfibrillar hydrogen bonds [22].
Cellulose nanocrystals (CNCs) receive more research attention than their CNC counterparts (in this case micro fibrillated cellulose) [23,24]. The reason for this is because nanoparticles with their nanosized (higher surface area) have superior characteristics. The popularity of nanocellulose materials is continuously increasing. CNCs and nano fibrillated cellulose (CNF) (or alternatively cellulose nanofibrils) can be used in applications ranging from small-scale medical-grade items to larger-scale sorbent products. For instance, CNF in various shapes and forms has been utilized in conjunction with microfluidic chips, whether as a component of the chips, being processed by a chip, or providing characterization via chips. There are two primary categories that have been sought after in this review paper: cellulose or cellulose-based items being flown into a microfluidic device within the criteria we established previously, or cellulose itself being employed as a building block in the production of a microfluidic device. This research will help to open up another large chapter on cellulose, in which cellulose design and development will become more enhanced.

Design of Cellulose with Microfluidics
In the literature, microfluidic technology has been employed to enhance the fabrication of cellulose-based parts. Figure 1 shows how microfluidics may be used to generate distinct shapes in cellulose products.  [106][107][108][109]. (a) CNC-CNF joint orientation along channels of a microfluidic chip for particle production with optimized qualities. Adapted with permission from Ref. [109]. Copyright 2018 Wiley-VCH. (b) The assembly process of regenerated silk fibroin (RSF) fibrils suspended in RSF/CNF passing via a microfluidic channel is depicted. RSF and CNF are distributed; the majority of RSF molecules are in random-coil form. Adapted with permission from Ref. [106]. Copyright 2019 American Chemical Society. (c) The nanofibrils are focused in the channels, and a gelation agent (NaCl) is injected along the route to help the cellulose rods stay in place as they exit the channel. Adapted from Ref. [108]. (d) Microfluidics-based microparticle manufacturing with customizable final sizes. The setup for the experiment is shown at the bottom. Adapted from Ref. [107].
To create strong fibres from CNF and CNC, a continuous wet spinning technique based on microfluidic flow focusing has been devised. For the first time, fibres with an average breaking tenacity of 29.5 centi Newton per tex have been recorded. CNCs are an appealing building element for producing lightweight yet robust and flexible textiles due to their high strength and modulus. When CNCs are added to CNFs alone, the concentration of dope can be increased by 4 to 5 times [109] (See Figure 1a).
In Lu et al. [106], cellulose hydrogel was utilized to create a microfluidic device using a 3D printer. Indeed, silk fibroin and CNF hybrid fibres were dry-spun via a microfluidic chip that resembled the structure of a spider's main ampullate gland in this work [106].  [106][107][108][109]. (a) CNC-CNF joint orientation along channels of a microfluidic chip for particle production with optimized qualities. Adapted with permission from Ref. [109]. Copyright 2018 Wiley-VCH. (b) The assembly process of regenerated silk fibroin (RSF) fibrils suspended in RSF/CNF passing via a microfluidic channel is depicted. RSF and CNF are distributed; the majority of RSF molecules are in random-coil form. Adapted with permission from Ref. [106]. Copyright 2019 American Chemical Society. (c) The nanofibrils are focused in the channels, and a gelation agent (NaCl) is injected along the route to help the cellulose rods stay in place as they exit the channel. Adapted from Ref. [108]. (d) Microfluidicsbased microparticle manufacturing with customizable final sizes. The setup for the experiment is shown at the bottom. Adapted from Ref. [107].
To create strong fibres from CNF and CNC, a continuous wet spinning technique based on microfluidic flow focusing has been devised. For the first time, fibres with an average breaking tenacity of 29.5 centi Newton per tex have been recorded. CNCs are an appealing building element for producing lightweight yet robust and flexible textiles due to their high strength and modulus. When CNCs are added to CNFs alone, the concentration of dope can be increased by 4 to 5 times [109] (See Figure 1a).
In Lu et al. [106], cellulose hydrogel was utilized to create a microfluidic device using a 3D printer. Indeed, silk fibroin and CNF hybrid fibres were dry-spun via a microfluidic chip that resembled the structure of a spider's main ampullate gland in this work [106]. Many researchers have used nano-scale innovations, such as the use of titanium dioxide [110], graphene oxide [111], carbon nanotubes [112], and CNC, to improve the mechanical qualities of artificial silk. The authors' research in Lu et al. [106] revealed that CNF may easily be Appl. Biosci. 2022, 1 5 used to enhance the mechanical properties of silk fibres. Stress at break of RSF/CNF with 0.1 wt% CNF was determined to be about 485 ± 106 MPa, representing a 58 percent increase over RSF fibres spun from silkworm (maximum recorder was 686 MPa). The method of integration of the two ingredients is depicted in Figure 1b. Spider silks have amazing mechanical qualities; hence, one of the areas of research in the field of biomimetic fibres has been the construction of high-performance artificial silk fibres as waveguides [113]. Strong fibres such as the one introduced here might be useful in biological media, bio-photonics, and central nervous system interfaces [114]. Similarly, in other refs., the direction and alignment of silk-spinning through microfluidic chips have been optimized through flow analysis [115][116][117]. This finding sets the path for further research into the demystification of the enigma of the natural spinning process. It offers a complete and methodical look at the process of creating highly oriented artificial fibres for biological applications [118]. In the development, regeneration and characterization of a blended system combining Bombyx Mori silk fibroin protein and cellulose acetate, a cellulose derivative, silk may be mixed with cellulose derivatives [119]. Many studies on the combination of silk and cellulose acetate for filament/fibre manufacturing may be found in the literature [106,114,118,[120][121][122][123][124][125][126][127][128].
CNF, which has a lot of potential as a building component for biobased products, might need to have hydrodynamic alignment (alignment due to fluid-induced orientation) and a dispersion-gel transition involved in its process. Gelation can occur due to the introduction of NaCl, a coagulant that acts as a charge screener [2]. Knowing these two concepts, alignment and gradual gelation, led the author to design the microfluidic channel in Figure 1c. Based on mechanical examination, the filaments generated were shown to be more durable and stiffer than the precursor material, CNF, and equivalent CNF-based polymer nanocomposites in the literature [2]. The generated fibres are equally as tough and strong as cellulose pulp fibres when equal fibril orientation is used. Figure 1c depicts the assembly process for the design of this durable fiber. The cross section of the fibres is also represented as a diffractogram. The orientation of fibres as a function of residence time and shearing in the microfluidic channel was employed in all three studies listed above. It would have been ideal to assess the level of orientation using the plot introduced by Pignon et al. [129]; small-angle light scattering and small-angle X-ray scattering were used in this experiment. Cluster breakup may also be studied using a confocal setup because gelation is involved. Furthermore, utilizing rheology and theoretical models, the Folgar-Tucker orientation of fibres along the boundaries of the microfluidic setup and at the centre may be determined [29].
By merging microfluidic and flash-freezing methods [107], porous cellulose acetate microspheres with variable particle sizes and pore characteristics were effectively manufactured. These particles exhibited a large specific surface area and good adsorption properties. The diameter of the microspheres may be precisely adjusted by modifying the microfluidic settings. For oil, the developed porous structures were able to adsorb up to 30 times their weight, while for Congo red, they were able to adsorb up to 23.9 mg·g −1 . A pictograph of the procedure is shown in Figure 1d. The setup for the experiment is also shown at the bottom. Staying on the subject of using the microsphere as a way of extraction/separation, paclitaxel, one of the natural anticancer drugs that can be isolated from the bark of pacific yew tree, was recognized, and separated in Wu et al. [130] using a sophisticated design of microspheres [130]. These examples demonstrate how microfluidics may be used to design structures that are entirely adjustable and suited for specific applications such as separation.
The highlights of recent research utilizing microfluidics in the development of cellulosebased goods are shown in Table 1. Table 1. Presentation of research involving microfluidics in the creation of cellulose-based goods, as well as their highlights.

Study Application Highlight
Baek and Park [89] Creation of uniformly sized porous cellulose beads The creation of the cell/N-methyl morpholine N-oxide droplet in the ethylene glycol solution in the T-junction microfluidic chip could not be observed in situ using an optical microscope. As a model study, the form of a cellulose bead after coagulation was explored.
Gluconacetobacter xylinus may live and flourish in a variety of environments. Cellulose is a major constituent of these self-secreted protective coatings (made with Gluconacetobacter xylinus). The results achieved mark the first step toward the fabrication of self-assembled degradable cellulose capsule.
Duong et al. [132] Cellulose fiber membrane was sandwiched between two silicone elastomer poly(dimethylsiloxane) (PDMS) layers to mimic BBB In vitro, a microfluidic system was created to replicate the human blood-brain barrier (BBB). BBB formation was assessed using cell survival, actin filament (F-actin) formation, and transepithelial electrical resistance (TEER).
Overall, the model showed a simple to duplicate and low-cost framework for in vitro drug test.
Jayapiriya and Goel [133] Creation of paper-based energy harvesting device Using E. coli as the biocatalyst, a paper fuel cell can generate 11.8 W·cm −2 of electricity. Fuel cell construction that is both cost-effective and thrifty can be utilized to power a wide range of low-power point-of-care devices.
Sharratt et al. [134] Creation of hydrogel microparticles Hydrogel microparticles (HMPs) have a wide range of practical uses, from medication delivery to tissue development. The kinetics of gelation fronts are initially determined using 1D microfluidic studies. The effective diffusive coefficients rise with Fe 3+ content and drop with NaCMC concentration.
Chen et al. [135] Creation of core-shell microparticles Polysaccharides have been shown to be useful in medication encapsulation and delivery. Authors offered a multicompartment polysaccharide core-shell microparticle that may be used to build a long-lasting dual-release system of active molecules for wound healing. Microparticles reduced inflammation while also promoting granulation tissue development, collagen deposition, and angiogenesis.
Liu et al. [96] Creation of monodisperse ethyl cellulose (EC) hollow microcapsules A simple and new approach is used to effectively create monodisperse ethyl cellulose hollow microcapsules. Microfluidic double emulsification and solvent diffusion are used in this method. Microcapsules manufactured in an iso-osmotic environment have a flawless spherical form and no collapse.

Study Application Highlight
Li et al. [136] Using bacterial cellulose for wound healing Bacterial cellulose is a type of nano-biomaterial that may be used in tissue engineering. It is unknown how bacterial cellulose's nanoscale structure impacts skin wound healing. The lower portion of bacterial cellulose film can encourage cell migration to aid in wound healing.
Zhao et al. [137] Creation of cellulose-based flexible electronics Cellulose is a natural biopolymer with several benefits such as low cost, ease of processing, and degradability. It is extensively used in flexible electronics as a substrate, dielectric material, gel electrolyte, and derived carbon-made material.
Mahapatra et al. [138] Creation of cellulose-based sensing devices For its unique features, including biocompatibility, cellulose has the potential to be used in the creation of cytosensors, and organisms in a variety of materials.
Del Giudice et al. [139] Assessing morphological structure of hydroxyethyl cellulose with microfluidics Non-modified hydroxyethyl cellulose acts as a linear uncharged polymer when dissolved in water, with an entangled mass concentration of 0.3 wt%. For the first time, authors presented the concentrations scaling for hydroxy ethyl cellulose solutions with the longest relaxation period.
Zeng et al. [140] CNFs produced by microfluidic homogenization The purpose of this research was to investigate and compare the shape and rheology of cellulose nanofibrils derived from bleached softwood kraft pulp. CNFs had the greatest viscous, bulk modulus, and loss modulus, as well as the largest aspect ratio.
Wang et al. [141] Creation of uniform size CNCs via microfluidic technology CNC is a novel form of molecular substance derived from biomass. CNCs with a good dividend and consistency were achieved by hydrolysis process in a microfluidic system using a 60% sulfuric acid solution at 35 • C for 40 min.
Lari et al. [93] Creation of poly(ε-caprolactone) and cellulose acetate nanoparticles The purpose of this study was to compare two types of microfluidic-assisted nanoparticles (NPs) based on poly(-caprolactone) (PCL) and cellulose acetate (CA). It was discovered that CA NPs had a smaller average diameter (37 nm) and a lower polydispersity index (PDI) (0.035) than PCL NPs.
Carrick et al. [142] Creation of cellulose capsules For medication delivery or controlled release capsules, cellulose capsules with a limited size distribution might be advantageous. Capsules were carboxymethylated to make them pH responsive and to expand roughly 10% when the pH was changed from 3 to 10.

Study Application Highlight
Pei et al. [143] Cross-linked cellulose hydrogel was used for making a chip To create cellulose-collagen hybrid hydrogels, collagen, a critical extracellular component for cell culture, was cross-linked in the cellulose hydrogel. Researchers revealed that they have excellent structural reproduction ability, physical qualities, and cell culture cytocompatibility.
Zhang et al. [144] Creation of a technology for adsorption and isolation of nucleic acids on cellulose magnetic beads The use of a 3D-printed microfluidic chip enables the extraction of nucleic acids without the need of vortexes or centrifuges. Magnetic, interfacial, and viscous drag forces are described inside the chip's microgeometries. Across a variety of HPV plasmid levels, an overall extraction efficiency of 61% is reported.
Wenzlik et al. [145] In a microfluidic setting, cholesteric particles were made from cellulose derivatives Co-flowing injection of drops of liquid crystalline mixes of cellulose derivatives into microspheres on the micrometre scale is used in the process.
Miyashita et al. [146] The diamagnetic director for microfluidic systems is made up of microcrystal-like cellulose fibrils Cellulose is a potential material for the development of biogenic optical systems that imitate the unique optical capabilities of living creatures. In a microfluidic laboratory, magnetic orientation tests on microcrystalline cellulose were performed. During the dispersed light intensity process, light intensity altered depending on the direction of the magnetic field.
Chen et al. [147] A multilayer microfluidic device with a PDMS-cellulose composite film was developed This paper describes an integrated multilayer microfluidic system that can pre-treat raw samples and detect them using immunoassays.
Using the crossflow concept, a polydimethylsiloxane (PDMS)-cellulose composite film was employed to extract plasma from raw samples.

Włodarczyk and
Zarzycki [148] On silica and cellulose micro-TLC plates, the chromatographic behaviour of chosen colours was studied The chromatographic behaviour of 18 colourants, including amaranth, black PN, bromophenol blue, and bromocresol green, was investigated. Data were gathered using silica and cellulose-coated microplates under thermostatic settings (303 K). Dyes are frequently utilized as colourants in food and industry, as well as sensing compounds in analytical and medicinal purposes.
Ghorbani et al. [149] Creation of CNFstabilized perfluoro droplets In a variety of applications, hydrodynamic cavitation on microchips has been emphasised.
Cavitating flow patterns may be used to promote a wide range of industrial and technical applications. Inside microfluidic devices, a novel technique involving cellulose nanocomposites perfluoro droplets was tested.

Study Application Highlight
Park et al. [150] Wet-spun microcomposite filaments were made with cellulose To make microfilaments, cellulose nanocrystals were wet spun in a coagulation bath. The influence of sodium alginate on the characteristics of the micro composite filament was studied. The higher spinning rate of sodium alginate generated a rise in the alignment index of CNCs, leading to an improvement in the material's tensile characteristics.
Grate et al. [151] Creation of Alexa Fluor-labeled fluorescent CNCs A group of researchers discovered a mechanism to attach Alexa Fluor dyes to cellulose nanocrystals while preserving the nanocrystal's overall structure. Bioimaging tests revealed that the spatial positioning of solid cellulose deposits could be detected and their elimination over time under the action of Celluclast ® enzymes or microorganisms could be monitored.
Ke et al. [152] Microgels made from carboxymethyl cellulose for cell encapsulation Carboxy methyl cellulose was modified with 4-hydroxybenzylamine (CMC-Ph) to create carboxy methyl cellulose-based microgels for use in scaffolds. The ATDC5 chondrocytic cell line was grown for up to 40 days after being encased in carboxy methyl cellulose microgels.
Rao et al. [153] Creation of microfluidic paper fuel cell MMPFCs (Membraneless Microfluidic Paper Fuel Cells) are promising technologies for harvesting energy for a variety of portable applications. Because of the built-in co-laminar flow and integrated capillary, the devices remove the need for membranes and additional pumps.
Shen et al. [154] Creation of paper-based microfluidic fuel cells Microfluidic fuel cells made of paper are emerging as possible renewable energy sources for small-scale electronic systems. The textural qualities of the paper channels have a considerable impact on the performance of paper fuel cells. The use of paper with a bigger mean pore width may result in a greater peak power density and open circuit voltage.
Shefa et al. [155] A method of incorporation of curcumin (Cur) into a hydrogel system based on cellulose was developed A freeze-thaw technique was used to create a Cur including physically crosslinked TEMPO-oxidized CNC-polyvinyl-alcohol curcumin-hydrogel, that produced curcumin to speed wound healing. L929 fibroblast cells incorporated curcumin within 4 h of incubation, according to in vitro experiments.
Chen et al. [156] Separation of glycoproteins was achieved using bacterial cellulose microfluidic column A simple technique was used to produce a regenerated bacterial cellulose column containing concanavalin A (Con A) lectin immobilised in a microfluidic device to evaluate and separate glycoproteins. Schiff-base formation was used to covalently link lectin Con A to the RBC matrix surface. Table 1 displays a presentation of research involving microfluidics in the creation of cellulose-based goods, as well as their highlights. As a recap of Table 1, a study of silk-spinning through microfluidic chips has uncovered the secrets of the natural spinning process [114], a study easily extendable to cellulose. Paper as a substrate aids in reducing existing stiff wastes and inevitable pollution [90]. Polysaccharides have been shown to be useful in medication encapsulation and delivery. Using E. coli as a biocatalyst, a paper fuel cell can generate 11.8 W·cm −2 of electricity using paper cells [133]. Membrane-less Microfluidic Paper Fuel Cells are promising technologies for harvesting energy. H 2 O 2 is used as both fuel and oxidant in a paper-based microfluidic fuel cell for portable electronics. The fuel cell does not require precious-metal catalysts, and the fuel utilized is carbon free and environmentally friendly [157], with a peak energy capacity of 0.88 mW·cm −2 .
A 3D-printed microfluidic chip allows for nucleic acid extraction without the need of vortexes or centrifuges [158]. Inside the chip's microgeometries, magnetic, interfacial, and viscous drag forces are defined. Cavitating flow patterns have the potential to be utilized to promote a wide range of industrial and technological applications. In a coagulation bath, cellulose nanocrystals were wet spun [150]. The effect of sodium alginate on the properties of the micro composite filament was investigated. Bioimaging experiments demonstrated that solid cellulose deposits may be recognized in their spatial location [151].

Cellulose as a Microfluidic Building Block
We offered a generalization on the issue of microfluidics and cellulose in the preceding section. The use of cellulose as a microfluidics building component will be discussed here. Paper, elastomer, thermosets, silicon/glass, thermoplastics, and hydrogels are some of the materials that may be used to make microfluidics chips [159]. Here, we focus on paper-based microfluidics.
Paper-based microfluidics, often known as "lab on paper," is a revolutionary fluid management and analysis technology. The system is said to be low-cost, simple to use, disposable, and requires no equipment. Indeed, paper is an appealing substrate for these devices since it is omnipresent, ubiquitous, and incredibly inexpensive. As a result, the material is also compatible with a wide range of additional chemical, biomedical, biomedical, biochemical, and medicinal applications. It transfers liquid through capillary forces without the help of any external forces. Microfluidic paper-based analytical devices, for example, may be utilized to measure the concentration of various analytes in a solution while also serving as an excellent platform for point-of-care diagnostics (dubbed as POC). Furthermore, it has found use in water quality analysis, as water pollution is harmful to human health. In Chen et al. [160], a layered multilayer electrostatic printing approach for manufacturing nanofiber-based microfluidic chips for water quality analysis was created. Devices provide easy fabrication techniques, flexible prototyping, mass production possibilities, and multi-material integration.
As stated earlier, cellulose is a plentiful natural solid carbohydrate biopolymer that is vital to the biosphere and plays an important role in the global carbon budget [161]. The use of cellulose-derived nanoparticles for cell imaging, material science, sensors, and other medical applications is gaining popularity [161]. One application for cellulose is as a component in the manufacture of microfluidic chips. Overall, few procedures for developing microfluidic devices, photolithography [162][163][164], plotting using a plotter [165], etching [166][167][168], plasma [169], cutting [170,171] and wax printing [172][173][174], flexography printing [175], screen printing [176], and laser treatment [177] have been documented. These approaches can be utilized to make microfluidic devices; to classify them, photolithography, etching, spraying, screen printing, and dipping wax are examples of indirect patterning processes, whereas wax priming, plotting, flexography, writing, stamping, and inkjet printing are examples of direct patterning methods. Figure 2 shows the technology involved in patterning a PAD, including 3D printing, wax printing, flexography printing, cutting, photolithography, and plotting.
printing [175], screen printing [176], and laser treatment [177] have been documented. These approaches can be utilized to make microfluidic devices; to classify them, photolithography, etching, spraying, screen printing, and dipping wax are examples of indirect patterning processes, whereas wax priming, plotting, flexography, writing, stamping, and inkjet printing are examples of direct patterning methods. Figure 2 shows the technology involved in patterning a PAD, including 3D printing, wax printing, flexography printing, cutting, photolithography, and plotting. To explain some of the methods briefly: Wax printing uses a basic printer to design wax on paper, after which the wax is melted to produce channels. This process is quick but offers limited resolution due to the isotropy of melted wax [173]. A wax layer creates the hydrophobic boundaries that are needed to guide the flow of a hydrophilic liquid. Inkjet printing involves coating paper with a hydrophobic polymer and then applying an ink that selectively etches the polymer to allow the paper to emerge [180]. Photolithography is comparable to inkjet printing in that etching is accomplished using a photomask and a photoresist polymer [164]. Using a hydrophilizing agents such as fluorocarbon plasma polymerization, the paper first becomes hydrophobic, and then oxygen plasma etching is used to form hydrophilic patterns onto the paper [183]. In flexographic printing, the process involves the usage of conventional graphic printing, functional inks, and a substrate such as paper. Flexography, inkjet printing, wax printing, and 3D printing all have striking parallels in this regard. Filling the vacuum with a hydrophobic substance, such as a solid melted at a certain temperature or a hydrophobic polymer immersed in an organic solvent, is another approach for creating hydrophilic structures on paper. These materials may easily penetrate the porous network in their liquid state and form a barrier once solidified. For applications that demand portable yet small fluid handling, To explain some of the methods briefly: Wax printing uses a basic printer to design wax on paper, after which the wax is melted to produce channels. This process is quick but offers limited resolution due to the isotropy of melted wax [173]. A wax layer creates the hydrophobic boundaries that are needed to guide the flow of a hydrophilic liquid. Inkjet printing involves coating paper with a hydrophobic polymer and then applying an ink that selectively etches the polymer to allow the paper to emerge [180]. Photolithography is comparable to inkjet printing in that etching is accomplished using a photomask and a photoresist polymer [164]. Using a hydrophilizing agents such as fluorocarbon plasma polymerization, the paper first becomes hydrophobic, and then oxygen plasma etching is used to form hydrophilic patterns onto the paper [183]. In flexographic printing, the process involves the usage of conventional graphic printing, functional inks, and a substrate such as paper. Flexography, inkjet printing, wax printing, and 3D printing all have striking parallels in this regard. Filling the vacuum with a hydrophobic substance, such as a solid melted at a certain temperature or a hydrophobic polymer immersed in an organic solvent, is another approach for creating hydrophilic structures on paper. These materials may easily penetrate the porous network in their liquid state and form a barrier once solidified. For applications that demand portable yet small fluid handling, microfluidics parts made by 3D printing with paper as part of the operation is of great use. A 3D printer can also be used to produce hybrid channels. This technology is inexpensive and suited for household usage because it offers accurate fluid handling abilities, functionality (versatile), and user-friendliness [178]. A depiction of 3D-printed microfluidics is shown in Figure 2a. Some examples of other methods mentioned earlier are also depicted in Figure 2b-f.
Aside from selecting a good technique for microfluidic paper-based manufacturing, it is also critical to pick a material that can go through the process. Cellulose and cellulose derivatives are suitable materials for 3D printing; nevertheless, finding strong cellulose solvents is crucial for their efficient use because cellulose cannot be melted (processed). However, due to strong hydrogen bonding, cellulose is also insoluble in water and other organic solvents. Only a few effective solvent systems capable of dissolving cellulose have been discovered thus far. As a result, researchers discovered functionalization pro-cesses such as xanthation [184], esterification [185], and etherification [186] on the cellulose hydroxyl group as a method of disrupting hydrogen bonds and breaking cellulose's tenacity to dissolve. However, non-derivatizing solvents such as ionic liquid [187] can also dissolve cellulose without requiring chemical changes, which is advantageous in many instances [188].
The most significant cellulose derivatives are cellulose ethers and esters [186]. These are found in a variety of goods, including thickeners, binders [189], emulsifiers, coatings, and membranes. The esterification of cellulose allows for the transformation of cellulose into different forms [190]. Cellulose ethers are plentiful, low-cost, environmentally friendly compounds with exceptional characteristics. They have several uses in food, medicines, cosmetics, and other commercial items. They are also commonly employed in 3D printing, where they serve several purposes [191,192]. The properties of ink are vital in 3D printing; specifically, 3D printing ink requires a well-regulated viscoelastic response (such as high viscosity and shear thinning behaviour) [193]. The shear thinning properties of polymer solutions are frequently used to achieve this objective [194,195]. These expected rheological behaviours can be obtained using cellulose ethers. Cellulose ether has been used to change the viscosity of a variety of industrial products [196]. However, when an external force is applied, the mixing energy will break the hydrogen bonds between the cellulose chains, causing the chain to align in the low direction, as seen by the shear thinning of the pseudoplastic behaviour [197]. The qualities of cellulose ether solution are thus sought since they are low at greater shear rates and high when the flow is halted. Furthermore, these materials are thixotropic [191], which is advantageous for becoming an ink since it necessitates the rehabilitation of the structure following fracture via the nozzle. Table 2 contains a substantial amount of the literature devoted to the development of cellulose-based microfluidic devices that can showcase the objective behind developing such systems. Table 2. Presentation of research in which cellulose was employed as a chip-building material.

Study Highlights
Lin et al. [198] Three-dimensional microfluidic paper-based analytical devices (3D-µPADs) are a potential platform technology that enables for complicated fluid manipulation, parallel sample distribution, high throughput, and multiplex analysis assays. This technology can regulate the penetration depth of melted wax printed on both sides of a paper substrate, resulting in multilayer patterned channels in the substrate.
Martinez et al. [199] A novel family of point-of-care diagnostic devices is PADs. They are affordable, simple to operate, and particularly developed for usage in poor nations. When completely developed, they may deliver faster and less expensive bioanalyses.
Yamada et al. [200] On microfluidic PADs, "distance-based" detection patterns provide quantitative analysis without the need of signal output tools. Quantitative analysis is enabled by the distance-based quantified signal and the strong batch-to-batch production repeatability based on printing processes.
Li and Liu [201] A wax-printing process is used to create 3D microfluidic channels inside a single sheet of cellulose paper. It enabled the production of up to four layers of paper channels in a 315-micrometer-thick substrate surface without the need for process optimization.
Ardalan et al. [202] The smart wearable sweat patch (SWSP) is a non-invasive and in situ multi-sensing sweat biomarkers sensor that measures glucose, lactate, pH, chloride, and volume. A smartphone app was also created to use a detection algorithm to estimate the quantity of biomarkers.

Study Highlights
Arun et al. [203] The capillary-driven fluid flow of a combination of fuel and electrolyte drives the capillary-driven fluid flow of a microfluidic fuel cell. Various pencils are used to produce the graphite electrodes to study their influence on fuel cell performance. To improve performance, the paper fuel cell was also manufactured in different diameters and coupled as cell stacks.
Yan et al. [157] H 2 O 2 is used as both fuel and oxidant in a paper-based microfluidic fuel cell for portable electronics. It does have a peak energy capacity of 0.88 mW·cm −2 . The fuel cell does not require precious-metal catalysts, and the fuel utilized is carbon free and environmentally friendly.
del Torno-de Román et al. [204] The power and output current of a paper-based enzyme glucose/O 2 fuel cell can be enhanced by adopting a quasi-steady flow. The fuel cell's anode and cathode are composed of display carbon electrodes that have been correctly functionalized with protease inks.
Jia et al. [205] Because of its hydrophilic properties, cellulose paper has been widely employed in microfluidic devices. Cellulose is placed in paper at random, with no specific direction or pathways. White wood possesses natural microchannels as well as a quick and anisotropic liquid and big solid particle movement.
Cai et al. [90] By silanizing filter cellulose using a paper mask, authors created a new, low-cost, and straightforward approach for fabricating PADs. This procedure requires no expensive equipment and may be carried out by inexperienced persons.
Murase et al. [206] Cellulose nanofiber can be utilized as a component in PADs. The thixotropic characteristic of TEMPO-oxidized CNCs aqueous dispersion allowed for inkjet printability, which aided manufacturing.
Kumar et al. [207] Cancer diagnostics are not currently prioritised in resource-limited settings. However, budget-friendly and targeted screening test and diagnostic tools are in great need. Multi-layer cellulose nanofibril-based coverings on expendable microfluidics were tuned for targeted capture and efficient release of target cells.
Choi et al. [208] The microfluidic cellulose microfibre chip was prototyped by injecting 10 percent CM solutions onto CNC-milled substrates. It can identify exudative age-related macular degeneration in human aqueous sense organs.
Fu and Liu [209] PADs are typically mounted on a cellulose paper substrate. Covalent bonds with the target biomolecule can be achieved by modifying chemicals. The optimum performance for biosensing applications comes from potassium periodate (KIO 4 )-modified cellulose paper.
Lu et al. [114] Spider silks have amazing mechanical qualities; hence, one of the areas of research in biomimetic fibres was the construction of structures with high silk fibres as optical waveguides. The fibres might be useful in biological media, bio photonics, and central nervous system interfaces.
Bao et al. [210] Transistors built of van der Waals materials are allowed by an all-cellulose paper with CNF on the upper surface, which results in outstanding surface roughness and electrolyte absorption. These planar transistors can be employed as sensors in PADs, together with other components.

Study Highlights
Yadav et al. [211] Microfluidics has the potential to revolutionise point-of-care detection in smart healthcare. Paper as a substrate aids in reducing existing stiff wastes and inevitable pollution. Flexible microfluidic technology hardcopy provides a low-cost technical foundation for next-generation intelligent sensors.
Solin et al. [212] Point-of-care diagnosis can benefit from microfluidic technologies. Authors looked at the fluidic structure due to stencil painting on flexible surfaces. Combining minerals with cellulose fibrils resulted in optimal printability and flow profiles. The findings demonstrate the use of these pathways for drug and chemical analysis.
As a recap of Table 2, PADs have been developed for sub-microliter surface area/volume analysis. The wax-printing technology that was previously used to design paper substrates has been improved to make high-resolution designs patterned in filter paper. In recent years, paper-based microfluidics used for analytical purposes, also known as PADs, have attracted a lot of interest for carrying out a variety of traditional analytical activities. PADs' appealing characteristics are mostly due to them being made of paper (cellulose), which is inexpensive, readily disposable, and environmentally benign. Three-dimensional paper-based microfluidics with three layer channels made from a paper-made substrate demonstrates the enzymatic detection of biomarkers such as glucose, lactate and uric acid [201]. According to the ISI Web of Knowledge data collection, the market for these types of devices has been steadily growing, as seen by 942 publications published under the title microfluidic paper-based between the years 2018 and 2022. Clearly, the trend indicates the future growth of PADs. Figure 3 depicts a brief overview of the use of cellulose in the creation of microfluidic chips of varying scale, size, shape, and design. The technique of transport depends on hydrophilic cellulose or nitrocellulose fibres to transfer liquid from an input guided through a porous medium via capillary action. The benefit of paper-based microfluidics is their passively controlled activity, which distinguishes them from more sophisticated microfluidic designs. The following regions are found in paper-based devices: an inlet in a substrate that is commonly constructed of cellulose where liquid is manually dispersed, a channel in which a hydrophilic network controls liquid transport, and a flow amplifier in which flow velocity is impacted to impart a controlled velocity to flowing liquid. A flow resistor is a capillary element that imparts a lowered flow velocity to control residence time, a barrier is a wall that prevents liquid from penetrating out of the channels, and an outlet is a location where a chemical or biological reaction occurs. For instance, in Figure 3a,c, the µPAD is divided into three parts: sensing, substrate, and water addition. The distance between the regions of addition of water and substrate was designed to be 12 mm, while the area of sensing was estimated to be 11 mm.
Analytical application of µPAD are in, mass spectrometry [213,214] separation methods [215], flow control [216][217][218], electronic integration [219] physical integration [220], chemical integration [221], paper-based microfluidics for diagnostics [199], use of paper microfluidics in blood grouping [222], glucose detection [223], 3D devices for glucose detection [224] and environmental and food safety tests [225]. As a supporting material embedding for the microchannels, cellulose nanofibrils hydrogel, a 3D structuring ultrathin film, was employed. (c) The μPAD is divided into three parts: sensing (6.5 mm diameter), substrate (6.5 mm diameter), and water addition (11 mm diameter). The distance between the regions of addition of water and substrate was calculated to be 12 mm, while the area of sensing was estimated to be 11 mm. (d) Scanning electron microscopy (SEM) photos of white wood microchannels are shown, as well as high magnification SEM photographs of individual microchannels, to demonstrate the presence of pits with an average diameter of 2.5 μm in addition to obstructed mass transmission that these designs can offer. Reproduced with permissions from [199,205,206,226].
A novel family of point-of-care diagnostic devices is PADs. They are affordable, simple to operate, and particularly developed for usage in poor nations. When completely developed, they have the potential to produce bioanalyses that are faster, less costly, and highly multiplexed. PADs are a viable starting point for innovative solutions to the challenge of health-relevant tests in emerging nations. When completely built, we expect they will give a platform with a number of novel bioanalysis capabilities. They may also find use in farming, water, food, and other industries where they might help us comprehend how these compounds act [227]. An example of such inexpensive design is depicted in Figure 3a. As a test, authors employed a chemical process to create blue indigo by enzymatic hydrolysis.
Another method for creating a microfluidic chip using cellulose is 3D printing. Compared with ink, the matrix, a vital component responsible for maintaining the integrity of the material while being printed, has received less attention throughout the years. Ink refers to the substance that fills the matrix and is afterwards sucked out. The present primary challenge in 3D printing is the inability of the matrix after injection to retain its bulk structure. After ensuring that the design of the printed structure is sound, ink is sucked out to build the microchannels. Abbasi Moud et al. [31] employed a fluorescence after photo bleaching approach to monitor the healing of 3D-printed objects non-invasively. Cellulose is a plentiful resource on Earth, and cellulose nanofibrils, as a component of the cellulose domain, have been studied from a variety of perspectives in recent decades. Cellulose nanofibrils have been reported to be used to adjust the viscosity of inks (flow improver), as directional deformation structures, or as material padding for 3D printing; however, they have seldom been employed as a platform for the fabrication of a microfluidic device. CNF was employed as a hydrogel in the reference [226] and was 3D printed to create the microfluidic gadget. Figure 3b depicts the printed microfluidic chip, which is particularly adaptable in terms of pressure retention and can be readily printed. The cellulose nanofibrils matrix was injected which generated thin structures made of  [199]. Copyright 2010 American Chemical Society. (b) As a supporting material embedding for the microchannels, cellulose nanofibrils hydrogel, a 3D structuring ultrathin film, was employed. Adapted with permission from Ref. [266]. Copyright 2017 American Chemical Society. (c) The µPAD is divided into three parts: sensing (6.5 mm diameter), substrate (6.5 mm diameter), and water addition (11 mm diameter). The distance between the regions of addition of water and substrate was calculated to be 12 mm, while the area of sensing was estimated to be 11 mm. Adapted with permission from Ref. [206]. Copyright 2018 American Chemical Society. (d) Scanning electron microscopy (SEM) photos of white wood microchannels are shown, as well as high magnification SEM photographs of individual microchannels, to demonstrate the presence of pits with an average diameter of 2.5 µm in addition to obstructed mass transmission that these designs can offer. Adapted with permissions from Ref. [205]. Copyright 2018 American Chemical Society.
A novel family of point-of-care diagnostic devices is PADs. They are affordable, simple to operate, and particularly developed for usage in poor nations. When completely developed, they have the potential to produce bioanalyses that are faster, less costly, and highly multiplexed. PADs are a viable starting point for innovative solutions to the challenge of health-relevant tests in emerging nations. When completely built, we expect they will give a platform with a number of novel bioanalysis capabilities. They may also find use in farming, water, food, and other industries where they might help us comprehend how these compounds act [227]. An example of such inexpensive design is depicted in Figure 3a. As a test, authors employed a chemical process to create blue indigo by enzymatic hydrolysis.
Another method for creating a microfluidic chip using cellulose is 3D printing. Compared with ink, the matrix, a vital component responsible for maintaining the integrity of the material while being printed, has received less attention throughout the years. Ink refers to the substance that fills the matrix and is afterwards sucked out. The present primary challenge in 3D printing is the inability of the matrix after injection to retain its bulk structure. After ensuring that the design of the printed structure is sound, ink is sucked out to build the microchannels. Abbasi Moud et al. [31] employed a fluorescence after photo bleaching approach to monitor the healing of 3D-printed objects non-invasively. Cellulose is a plentiful resource on Earth, and cellulose nanofibrils, as a component of the cellulose domain, have been studied from a variety of perspectives in recent decades. Cellulose nanofibrils have been reported to be used to adjust the viscosity of inks (flow improver), as directional deformation structures, or as material padding for 3D printing; however, they have seldom been employed as a platform for the fabrication of a microfluidic device. CNF was employed as a hydrogel in the reference [226] and was 3D printed to create the microfluidic gadget. Figure 3b depicts the printed microfluidic chip, which is particularly adaptable in terms of pressure retention and can be readily printed. The cellulose nanofibrils matrix was injected which generated thin structures made of cellulose nanofibrils after the ideal selection of the rheological properties of cellulose nanofibrils and a petroleum ink. The inks were then readily removed to render the inside of the structure hollow. CNF-made microfluidic chips address fundamental challenges in PDMS-based microfluidic devices, such as flexibility and compactness.
CNF can be utilized as a component in the fabrication of PADs. The thixotropic characteristic of TEMPO-oxidized CNF aqueous dispersion allowed for inkjet printability, which aided manufacturing. It is proposed in Figure 3c that TEMPO-oxidized CNF can be used as a module of PADs due to features such as being an oxygen barrier in dry state (storage of unstable substance due to not allowing oxygen influx in), ability to exchange molecules while swollen with water (reaction site for biochemicals), and ability to immobilize enzymes (providing fixation to the sensing area); furthermore, because these materials may be inkjet printed, the manufacturing process is hygienic. Figure 3c depicts a schematic of the ultimate result of these devices [206].
Because of its hydrophilic properties, cellulose paper has been widely employed in microfluidic devices. Cellulose is placed in paper at random, with no specific direction or pathways. White wood possesses natural microchannels as well as a quick and anisotropic liquid and big solid particle movement. A simple one-step delignification method yielded an anisotropic highly porous microfluidic framework (white wood) from wood material. Without the help of an additional pump, white wood can easily convey huge solid particles. It has the potential to significantly broaden the variety of natural wood uses for biological purposes. Figure 3d illustrates a construction created as a wood framework for material delivery. For instance, carbon nanotubes ink in white wood exhibits anisotropic transport characteristics. Under capillary forces, carbon nanotubes ink carried by liquid can travel upwards on the channels. The greatest transfer distance of 17.5 mm was reached at 150 s and 4.8 mm in the first second. As the lignin in the wood is removed, it is referred to as white wood.

Advanced Integration of Cellulose in Microfluidcs
We went through the process of showing how cellulose may be used as a building block for microfluidics chips in the previous part; in this section, we will expand on that to include more complicated design. The layer-by-layer assembly comprises up to 5 layers of CNF that are placed inside a microfluidic channel and are synthesized and characterized with antibodies to trap probable cancer cells [207]. Cellulase enzymes were employed to dissolve the CNF and release the collected cells in 30 min with a negligible influence on cell viability. CNF is coated onto the channels of a microfluidic chip in Figure 4a. The impact of increasing the thickness of CNF layers on surface density, moieties immobilisation, enzymatic CNF release, and cell release is analyzed. As a side note, the dotted line denotes the boundaries of the microchannels and changing the fluorescence strength indicates the density of the layers. As you move from left to right, the intensity rises owing to denser CNF covered fluorescently marked layers (going from 1 to 5 layers). Microcapsules with regulated stability and porosity are in great demand for separating and encapsulating applications. At an oil-water emulsion interface, the authors established a bio-interfacial technique for producing robust yet elastic porous microcapsules from bacterial cellulose [92]. Because of the compressive properties of the cellulose structure, the capsules have a modest elastic modulus of roughly 100 Pa but remarkable robustness under distortion. They have a porous outer wall and a nanofiber inner cytoskeleton, which affords them the suppleness of red blood cells. Particle trajectories show dynamically diffusive behaviour both within and outside the microspheres (see fluorescently tagged molecules in Figure 4b floating around microsphere), but severely limited particle mobility inside the microcapsule, where fibre density is at its maximum. The movement of colloid tracer particles is measured by tracking their locations with picture frames [229].
Because G. xylinus metabolism is stimulated by oxygen, the creation of an air-medium contact is crucial. The authors of [228] describe the 3D manufacture of bacterial cellulose hydrogels using solid matrix-assisted 3D printing of an incubation medium. Because of its hydrophobic nature and bio inertness, a round polytetrafluoroethylene (PTFE) microparticle was considered as the most suitable for the solid matrix. PTFE microparticles and CNF hydrogels were used to create ink containing active microorganisms. Filling the needle path with contiguous matrix particles allowed for rapid matrix recovery, which was important to avoiding vertical misprinting. The exterior of the 3D-printed hydrogel facing the solid substrate had greater oxygen levels, whereas the interior of the printed structures had lower amounts. The variation in oxygen levels led to heterogeneity in the biosynthesis of bacterial cellulose, allowing the fabrication of a tubular structure of bacterial cellulose. Finally, a microfluidic vascular system of fibroblast cells was pushed In the picture at the bottom, yellow and blue liquids were injected independently. Adapted with permissions from Ref. [207]. Copyright 2020 Royal Society of Chemistry. (b) Under confocal lens for one week, oil cellulose-based microcapsules, marked with magenta with tracer with sizes of 0.5 µm that can freely find room to diffuse inside. Adapted with permissions from Ref. [92]. Copyright 2019 American Chemical Society. (c) The interaction of two sides of a bacterial cellulose film on cells and tissue can modify their behaviour. The findings of this study provide a new path for improving the wound healing efficiency of bacterial cellulose material. Adapted from Ref. [228]. (d) Relying on microfluidic chips for analysis, a stacked design (multilayered) electrostatic printing technology was perceived for producing CNF-based microfluidic chip for detecting water quality. This idea might be used to create a colorimetric platform that can quantitatively detect iron levels in water. Adapted from Ref. [160].
Microcapsules with regulated stability and porosity are in great demand for separating and encapsulating applications. At an oil-water emulsion interface, the authors established a bio-interfacial technique for producing robust yet elastic porous microcapsules from bacterial cellulose [92]. Because of the compressive properties of the cellulose structure, the capsules have a modest elastic modulus of roughly 100 Pa but remarkable robustness under distortion. They have a porous outer wall and a nanofiber inner cytoskeleton, which affords them the suppleness of red blood cells. Particle trajectories show dynamically diffusive behaviour both within and outside the microspheres (see fluorescently tagged molecules in Figure 4b floating around microsphere), but severely limited particle mobility inside the microcapsule, where fibre density is at its maximum. The movement of colloid tracer particles is measured by tracking their locations with picture frames [229].
Because G. xylinus metabolism is stimulated by oxygen, the creation of an air-medium contact is crucial. The authors of [228] describe the 3D manufacture of bacterial cellulose hydrogels using solid matrix-assisted 3D printing of an incubation medium. Because of its hydrophobic nature and bio inertness, a round polytetrafluoroethylene (PTFE) microparticle was considered as the most suitable for the solid matrix. PTFE microparticles and CNF hydrogels were used to create ink containing active microorganisms. Filling the needle path with contiguous matrix particles allowed for rapid matrix recovery, which was important to avoiding vertical misprinting. The exterior of the 3D-printed hydrogel facing the solid substrate had greater oxygen levels, whereas the interior of the printed structures had lower amounts. The variation in oxygen levels led to heterogeneity in the biosynthesis of bacterial cellulose, allowing the fabrication of a tubular structure of bacterial cellulose. Finally, a microfluidic vascular system of fibroblast cells was pushed through a CNF/bacterial cellulose hollow chamber (tube) and was allowed to incubate and perform cell attachment and proliferation (see Figure 4c). The cell grew at the inner wall and results were monitored by SEM. It is therefore conceivable to develop a generic tool for the flexible 3D printing of bio-organs and scaffolds [228].
Microfluidics devices have grown in prominence in recent years, with a wide range of applications spanning chemistry, biology, and energy generation [230]. When it comes to food, the application is limited to regulated emulsification methods that allow for the formation of highly structured droplets. The use of such emulsions can, for example, provide stability of small droplets in food beverages or products with a reduced caloric capacity, or it can be used to trigger the release of an active component of taste on demand (double emulsion) [231]. Aside from emulsification, phase change in liquid droplets may be exploited as a building component in meals. To recap, the most prevalent usage of microfluidics in food-related applications is in the creation of emulsions, where they enable precise control over droplet size and form. Cellulose is one food type that can benefit from the emulsification process of microfluidics [232][233][234][235][236][237]. The celluloses used for the emulsification of foods are carboxymethylcellulose [234,235,238], cellulose nanofibrils [237], microcrystalline cellulose [238] and bacterial cellulose [239]. Indeed, chemically modified cellulose derivatives play five key roles in foods: rheological property management [240], emulsification, foam stability, ice crystal formation and growth modulation, and waterbinding capacity.
Droplets develop in cross-roads of channels, such as those found in T-junctions or micro-channeled systems, in the design of chips to accomplish emulsification. Droplets can also be inserted in microchannels and then broken up further into tiny droplets when they escape the chip in the rest of the channel. Starting from the point where two liquids start to flow, the scattered phase flows into the continuous phase and forms a droplet at the channel openings. The droplet is pulled along the pore and distributed into the continuous phase in a shear-driven emulsification system. In a T-junction, the creation of non-Newtonian droplets can also be stimulated under the influence of an external electric field. Because of the direction of electric forces imparted to a droplet's surface, the stronger the electric field, the greater the droplet size. External electric or magnetic fields can be quite useful for controlling droplet sizes [241]. Microfluidics, which employs the same mechanism, can also result in foam generation [242]. The distributions of pore size and shape determine most of the physical properties of solid foams. The authors of ref. [242] show how CNF changes the structure of both the liquid foam template and the solid foam. The resulting nanocomposite foams have improved mechanical properties, but not proportionally to their size. Some of the studies in the literature that produce cellulose products using T-junction and Y-junctions are found in set of refs. [89,[241][242][243][244][245][246][247][248].
Many studies employed microfluidic devices to create nano or micro sized particles by establishing a hydrodynamic flow-focusing apparatus. For instance, because of its low toxicity, great stability, and outstanding biodegradability, cellulose acetate is one of the most significant cellulose products. In the reference [93], nanoparticles produced utilizing co-flow and flow-focusing glass capillary techniques were compared. They compared the effect of geometries such as the size of the inner capillary orifice and the device utilized in terms of co-flow or flow-focusing. Kwon and colleagues [249] employed microspheres and a flow-focusing microfluidic to create microspheres with a lower size than traditional approaches. They also looked at how the ratio of non-solvent to solvent flow rate affected the size of produced microspheres. In this case, raising the flow rate ratio of the phase resulted in an increase in the size of the particles. As a result, distinct emulsions or food items with diverse designs are produced. Microfluidics in terms of using co-flow design can also be manipulated to create cellulose products. Refs. [92,250,251] include studies that demonstrated the use of co-flow or flow-focusing technologies to create nano particles from cellulose alone or cellulose in conjunction with other substances.
The system that is monodispersed, whether oil-in-water or water-in-oil emulsions, may be easily manufactured utilizing a shear-driven system [252], and wettability is crucial in the type of emulsion being prepared. Aside from single and double emulsion, flow-focusing or co-flow devices may be used to create higher-order multiple emulsions [253,254]. In a nutshell, microfluidic devices have a lot of potential for making simple and higher-order multiple emulsions. The use of several systems leads to several operational issues that contribute to unreliable emulsification. This is especially difficult in food applications where droplet size must be less than 10 µm in most cases.
Similarly, relying on microfluidic chips for analysis, a stacked design (multilayered) electrostatic printing technology was perceived for producing CNF-based microfluidic chip for detecting water quality since water pollution has a substantial influence on human health. This idea might be used to create a colorimetric platform that can quantitatively detect iron levels in water [160]. The hydrophilic channels are printed with wax on the substrate by electrostatic interaction (see Figure 4d).

Using Microfluidics to Shape Cellulose-Based Products
As previously said, microfluidic design may be divided into three categories: flowfocusing, co-flow, and T-junction design. Figure 5 depicts these designs that can be applied for food-or non-food-related applications. For instance, case studies of microfluidics used to create food quality emulsions from cellulose may be found in refs. [96,131,234,255] and non-food applications in refs. [142,[256][257][258]. Creating a sophisticated design such as microcapsules with regulated stability and permeability are in great demand for separation and encapsulating applications. Sometimes, the design of complex structures is left to microorganisms such as bacteria. At an oil-water emulsion interface, the authors established a bio-interfacial technique for producing robust yet flexible porous microcapsules from bacterial cellulose (see Figure 5a). Bacteria were initially utilized to make the cellulose particles, as well as before and after shaping the microparticles [92]. Sometimes relying only on shear and flow field to create the optimized structure is not enough. To tackle this, using an innovative field-assisted flow-focusing approach, the authors in Wise et al. [94] discovered that an external electric field may be used to regulate/fine tune the structural ordering of anisotropic materials in a continuous flow process. The continuous fabrication of a macroscale filament with a diameter of 17 µm was carried out employing CNF (TEMPO-oxidized) using this flow-focusing microfluidic chip. Beyond a certain voltage, the influence of an AC external field on the material's structure became considerable, resulting in a CNF orientation of up to 16%. The set up for accomplishing this task is illustrated in Figure 5c as a flow-focused microfluidic design [94]. Figure 5b is an example of a T-junction design that here has been used as a mixing zone between gas and a non-Newtonian fluid. Microfluidics can also be used for the purpose of mixing, demixing [95,247] and internal orientation of particles [94,108]. The mixing of laminar non-Newtonian nanofluid flow in two-dimensional microchannels is quantitatively explored in this article [248]. Pseudoplastic behaviour is seen in an aqueous solution of 0.5 wt% carboxymethyl cellulose and 10 nm diameter TiO2 nanoparticles. In a similar study [246], gas-non Newtonian liquid two-phase flows in a horizontal rectangular microchannel were explored. Variable mass concentrations of polyacrylamide aqueous solutions were employed as non-Newtonian liquids at the same time as nitrogen gas being used as a test gas. The flow pattern, bubble length, liquid projectile length, and frictional pressure drop were all measured in a T-junction mixer by the authors. For the case of the orientation of particles, the authors designed a continuous and potentially industrially scalable and parallelizable method that prepared strong and stiff CNF-based filaments. This allowed the manufacturing of strong filaments from wood fibre raw material for the future production of high-performance bio-composites and textile production [108]. These experiments can assist in understanding how the final structure can be improved using just fluid and a different component addition approach. Figure 6 shows a complex cellulose-based pattern built using microfluidics technology. Microfluidics can also be used for the purpose of mixing, demixing [95,247] and internal orientation of particles [94,108]. The mixing of laminar non-Newtonian nanofluid flow in two-dimensional microchannels is quantitatively explored in this article [248]. Pseudoplastic behaviour is seen in an aqueous solution of 0.5 wt% carboxymethyl cellulose and 10 nm diameter TiO 2 nanoparticles. In a similar study [246], gas-non Newtonian liquid two-phase flows in a horizontal rectangular microchannel were explored. Variable mass concentrations of polyacrylamide aqueous solutions were employed as non-Newtonian liquids at the same time as nitrogen gas being used as a test gas. The flow pattern, bubble length, liquid projectile length, and frictional pressure drop were all measured in a T-junction mixer by the authors. For the case of the orientation of particles, the authors designed a continuous and potentially industrially scalable and parallelizable method that prepared strong and stiff CNF-based filaments. This allowed the manufacturing of strong filaments from wood fibre raw material for the future production of high-performance bio-composites and textile production [108]. These experiments can assist in understanding how the final structure can be improved using just fluid and a different component addition approach. Figure 6 shows a complex cellulose-based pattern built using microfluidics technology. CNCs in liquid crystalline form are materials that are both a hybrid of long-range organized structure belonging to crystal structure and mobility that can create an isotropic liquid. Among the several varieties of liquid crystals, cholesteric liquid crystals [262] are popular because they are one-dimensional photonic crystals with a photonic band gap (PBG) structure due to their helical structure. These materials have opalescent hues when the half value of the helical pitch length is the same size as the wavelength of visible light. Parker et al. [259] studied the self-assembly of cellulose nanocrystals synthesized in an oil phase, during which radial ordering occurred, and when the produced droplets were removed from the system, they buckled. The cholesteric character of particle orientation was maintained, as shown by SEM.
Wenzlik et al. [145] applied another droplet pattern for making microparticles, in combination with photopolymerization. Photocurable lyotropic mixtures of cellulose emulsified in oil/water droplets were made initially. Then, samples were flown in an area under irradiation of in situ ultraviolet (UV) light. The photopolymerization resulted in an interpenetrating network in which the cholesteric arrangement of particles remained locked in. Thus, the opalescent appearance was kept. Wang et al. [263], employed a nematic liquid crystalline phase in the form of droplets to create an environment (a droplet) that was ideal for polymerizing polymer microparticles. The process involved mixing polymer monomer and initiator inside the droplets, which were initially nonreacted Then, the droplets through photopolymerization solidified, which led to the liquid crystalline particle being locked inside a polymer that was now polymerized. In the next step, the non-reactive entities were removed through the addition of ethanol, and the polymerized liquid crystal droplets were shrunken anisotropically, which yielded solid particles with complex geometries. (a) Polarization of a micrograph depicting the production of cholesteric cellulose nanocrystals from oil in a water droplet. Swelling of microfluidic droplet-templated CNC microparticles (from 3 wt % CNC suspensions) when observed under polarized optical microscopy. Adapted with permission from Ref. [259]. Copyright 2016 American Chemical Society. (b) Pore network of a microfluidic device produced with PDMS using the micromolding process, with pillars and edges defining the flow channel and pore network clearly. Adapted with permission from Ref. [151]. Copyright 2015 American Chemical Society. (c) Dry sCNC microparticles display variable chiral nematic texturing due to the occurrence of kinetic arrest during drying, while chemically modified (and thus crosslinked) microparticles exhibited uniform radial ordering (the image at the right-bottom of (c). Adapted with permission from Ref. [260]. Copyright 2018 American Chemical Society. (d) Lipophilic molecule encapsulation inside oil small droplets or embedded emulsions might be used to encapsulate functional target chemicals. Adapted with permission from Ref. [261]. Copyright 2021 Elsevier. (e) Three-dimensional representation of a form-stable composite including CNF-shell-produced capsules. Adapted with permission from Ref. [107]. Copyright 2019 Elsevier.
CNCs in liquid crystalline form are materials that are both a hybrid of long-range organized structure belonging to crystal structure and mobility that can create an isotropic liquid. Among the several varieties of liquid crystals, cholesteric liquid crystals [262] are popular because they are one-dimensional photonic crystals with a photonic band gap (PBG) structure due to their helical structure. These materials have opalescent hues when the half value of the helical pitch length is the same size as the wavelength of visible light. Parker et al. [259] studied the self-assembly of cellulose nanocrystals synthesized in an oil phase, during which radial ordering occurred, and when the produced droplets were removed from the system, they buckled. The cholesteric character of particle orientation was maintained, as shown by SEM.
Wenzlik et al. [145] applied another droplet pattern for making microparticles, in combination with photopolymerization. Photocurable lyotropic mixtures of cellulose emulsified in oil/water droplets were made initially. Then, samples were flown in an area under irradiation of in situ ultraviolet (UV) light. The photopolymerization resulted in an interpenetrating network in which the cholesteric arrangement of particles remained locked in. Thus, the opalescent appearance was kept. Wang et al. [263], employed a nematic liquid crystalline phase in the form of droplets to create an environment (a droplet) that was ideal for polymerizing polymer microparticles. The process involved mixing polymer monomer and initiator inside the droplets, which were initially nonreacted Then, the droplets through photopolymerization solidified, which led to the liquid crystalline particle being locked inside a polymer that was now polymerized. In the next step, the non-reactive entities were removed through the addition of ethanol, and the polymerized liquid crystal droplets were shrunken anisotropically, which yielded solid particles with complex geometries.
Using sustainable and renewable biomaterials, a team of researchers [259] created a method for fabricating genuinely hierarchical solid-state designs from the nanoscale to the macroscopic scale. They were looking at how CNCs self-assemble within the micrometers of aqueous droplets. The author was able to establish a hierarchical structure over various length scales by directing the self-assembly process of CNCs in the microsphere. The droplets were created with a restricted distribution, allowing for a local evaluation of the CNC self-assembly process (See Figure 6a).
A group of scientists [151] discovered a mechanism to link Alexa Fluor dyes to CNCs. The authors suggest that developing a strategy to analyze local losses of solid cellulose is preferable to the traditional approach of batch sugar production. These observations are difficult to carry out in a natural context with muddy soil and sediments, but they are simple to carry out in a microfluidic chip. They became able to witness the elimination of solid cellulose layers over time as the number of single blinking dye molecules, rather than fluorescent signals, decreased. Two methods for conjugating contemporary dyes to solid cellulose material for bioimaging have been devised. Crystalline cellulose is more resistant to deterioration than amorphous areas, making it of special importance. These substances are known to monitor and track the elimination of spatially limited aggregates of solid cellulose materials because of hydrolysis. Figure 6b depicts a homogeneous pore network with deposited fluorescently labelled cellulose. The investigators flushed out the pore gaps with carbon-free media in multiple cycles, yet the bacterial population (injected originally) rebounded each time, validating the hypothesis that certain strains of bacteria can thrive via CNCs. The authors also shared the pore network with another comparable bacterial strain, cytophaga hutchisonii, which can degrade cellulose, and tracked the decrease in the fluorescence signal over time.
CNCs are cellulose-derived, stiff, rod-like nanoparticles. There are few methods for controlling the shape and size of constructed CNC structures. Water-in-oil droplet microfluidics can create consistent spherical CNC droplets in a nontoxic and environmentally friendly way. The authors of [260] demonstrated how to make stable spherical CNC microparticles by chemically cross-linking hydrazide-modified CNCs. The technique is based on droplet templating using microfluidics and uses only environmentally friendly and nontoxic ingredients. Microparticles generated via this study are shown in Figure 6c in which dry sCNC microparticles displayed variable chiral nematic texturing due to the occurrence of kinetic arrest during drying, while chemically modified (and thus crosslinked) microparticles exhibited uniform radial ordering.
Lipophilic chemical preservation inside alginate microgels is difficult, owing to the required oil-core matrix. The usage of glass microfluidic devices to manufacture emulsionfilled alginates was investigated in this work [261]. The size of the microgels was determined by the viscosity of the O/W emulsion and the flow rates. Alginate microspheres and emulsion-filled alginate hydrogel particles were uniformly shaped and spherical, with a very narrow size distribution. Lipophilic molecule encapsulation inside oil small droplets or embedded emulsions might be used to encapsulate functional target chemicals. Pictures of the microparticle produced in this study are shown in Figure 6d.
Microspheres of porous cellulose acetate with variable size of particles and pore characteristics have been successfully produced. The microfluidic settings were tweaked to obtain the appropriate microdroplet size. Controllable structures were created using a simple technique called microfluidics paired with the flash freezing approach. The pictograph of procedure is shown in Figure 6e. The diameter of the microspheres may be precisely adjusted by modifying the microfluidic settings. For oil, the developed porous structures were able to adsorb up to 30 times their weight, while for Congo red, they were able to adsorb up to 23.9 mg·g −1 [107].
Hydrogels are three-dimensional networks made up of cross-linked polymers that can contain a high amount of water in their particle interspace; most hydrogels are not soluble in water [29]. Hydrogels are frequently utilized for drug administration, scaffolds in tissue engineering, wound treatment, absorbent, thickeners, and packaging materials, and they may be used to make transparent contact lenses [264]. This kind of material's strong water retention capacity, paired with its porosity, is also useful for simulating the extracellular matrix microenvironment in vivo. Ca-alginate beads are among the most extensively used methods for immobilizing protein molecules, as well as for controlled medication release. The capacity to adjust particle size and size distribution is crucial, as particle diameter and distribution impact clearance rate from the body and, ultimately, dose. Alginate gels are enclosing gel spheres that may entrap cells in a three-dimensional region. They are created using a traditional gelation process in which the alginate is being pushed within a microfluidic chip. Because the structure of alginate is so similar to that of cellulose, most alginate research may be applied to cellulose with minor changes.
In T-junction, droplets of sodium alginate loaded with calcium carbonate can create an emulsion [265]. Similarly, in another study, the internal gelation system used to make alginate/pectin Janus beads was etched in a Y-junction with two co-flowing channels. Inside the bath containing calcium chloride, Janus droplets developed; later, in the bath, calcium chloride was added to fortify the beads [266].
Janus particles can be designed with the assistance of microfluidics, using a liquid crystal and a mineral oil component. Through lowering interfacial tension between cholesteric CNCs to mineral oil, the form of droplets transformed from dumbbell to spherical [267]. The produced nanoparticles are shown in Figure 7a. The creation of microgels with nontraditional forms was made possible by photopolymerizing the monomer introduced to the cholesteric CNC phase and then removing the mineral oil. This technique simply opens new doors to droplets produced from cholesteric CNC droplets by transferring these microgels into an aqueous medium where they swelled up to keep their cholesteric structures. The cholesteric phase's polarized optical microscope pictures revealed a multidomain mosaic pattern with distinct stripes. In a flow-focusing droplet-producing design, the cholesteric phase is isolated from the two-phase system. In conjunction with the cholesteric phase, a fluorinated oil containing 1.0 wt% surfactant was injected into the microfluidics. The shear force imposed by merging the two oil streams led to the production of uniformly sized droplets that were split up in the chip on a periodic basis. Later, polymer latex nanoparticles were injected into the cholesteric phase, and photos from this set of studies may be found at the bottom of Figure 7a. To examine the influence of confinement on the cholesteric phase, the additional latex particles that resulted in the formation of a core-shell structure were incorporated [268].
Magnetic stimulation might be a tempting supplement to other methods of remotely regulating and modifying light. A microfluidic emulsification method, in which waterbased droplets are created in a flow-focusing device, is used to make microparticles. An external magnetic field can be used to manipulate microparticles that are suspended in a fluid. It is possible to make magnetic sensitive birefringent microscopic particles with unique magneto-optical coupling capabilities. Using a distant external magnetic field, microparticles may be modified to sense the local rheological parameters of a fluid. Display technologies, microrheological studies, and camouflaging devices might all benefit from these capabilities. A sample of the results [269] of using a magnetic field to guide microparticle size production in depicted in Figure 7b. To make the microparticle (CNCladen) impressionable to magnetic fields, CNC building blocks were mixed with a small concentration of iron oxide nanoparticles. Figure 7c shows two microfluidic designs for creating Janus and simple microparticles, as well as a microfluidic design based on Figure 7a's results. The row at the bottom displays variation in droplet morphology and related polarized optical microscopy of photos. This method may also be used to synthesize core-shell particles with a liquid crystalline shell. (b) Spiraling tube to elongate the emulsion droplet before consolidation phase that makes the particle anisotropic. Particles with different aspect ratio synthesized using this approach. As the particles exited the tube, UV light was employed to rigidify them. (c) Two microfluidic device geometries to produce hydrogel particles and hydrogel Janus particles. The scheme on the left makes microbeads using a T-section design, whereas the diagram on the right is for flow focusing for production of Janus particles. Reproduced with permissions from [267][268][269][270].
Magnetic stimulation might be a tempting supplement to other methods of remotely regulating and modifying light. A microfluidic emulsification method, in which waterbased droplets are created in a flow-focusing device, is used to make microparticles. An external magnetic field can be used to manipulate microparticles that are suspended in a fluid. It is possible to make magnetic sensitive birefringent microscopic particles with unique magneto-optical coupling capabilities. Using a distant external magnetic field, microparticles may be modified to sense the local rheological parameters of a fluid. Display technologies, microrheological studies, and camouflaging devices might all benefit from these capabilities. A sample of the results [269] of using a magnetic field to guide microparticle size production in depicted in Figure 7b. To make the microparticle (CNC-laden) impressionable to magnetic fields, CNC building blocks were mixed with a small concentration of iron oxide nanoparticles. Figure 7c shows two microfluidic designs for creating Janus and simple microparticles, as well as a microfluidic design based on Figure 7a's results. Table 3 shows the different types of cellulose used and how they are used in the microfluidics framework. Table 3. Refs classified based on nanocellulose types involved and application in conjunction with microfluidics.

Study
Material Used Microfluidic Application Shin and Hyun [226] CNF Construction material for microfluidics Li and Liu [201] CNF Construction material for microfluidics Jia et al. [205] CNF Construction material for microfluidics Cai et al. [90] Filter paper Construction material for microfluidics, glucose assay The row at the bottom displays variation in droplet morphology and related polarized optical microscopy of photos. This method may also be used to synthesize core-shell particles with a liquid crystalline shell. Adapted from Ref. [268]. (b) Spiraling tube to elongate the emulsion droplet before consolidation phase that makes the particle anisotropic. Particles with different aspect ratio synthesized using this approach. As the particles exited the tube, UV light was employed to rigidify them. Adapted with permissions from Ref. [269]. Copyright 2019 WILEY-VCH. (c) Two microfluidic device geometries to produce hydrogel particles and hydrogel Janus particles. The scheme on the left makes microbeads using a T-section design, whereas the diagram on the right is for flow focusing for production of Janus particles. Adapted from Ref. [270]. Table 3 shows the different types of cellulose used and how they are used in the microfluidics framework.
A novel application of microfluidics to the production of cellulose microparticles is the encapsulation of cellulose-producing bacteria inside a core-shell design for long-term investigations on a static culture, which does not require the use of a chemical method to induce cellulose dissolution. In Yu et al. [271], for example, microfluidics was utilized to build a sacrificial template based on core-shell structured microparticles for bacterial encapsulation. After bacterial incubation inside the sphere and the manufacture of bacterial cellulose, the particle's template was dissolved, resulting in the formation of bacterial cellulose. Higashi et al. [257] employed microfluidics to produce a nanofibrous structure using bacterial cellulose in a similar investigation. Gelatin was used to enclose the bacteriainfested microsphere. The bacterial cellulose microspheres were recovered after the gelatin was removed. The authors also compared the microspheres generated by bacterial activity to those produced by the emulsification process, which clearly demonstrated the inefficiency of emulsification in contrast. Recently, in Pepicelli et al. [131], they customized the bacterial cellulose microcapsule with configurable size and being monodisperse, which was affected by bacterial concentration, droplet size, and surfactant type. As previously stated, cellulose microparticles are also being generated with cellulose derivates that are dissolved in solvent; for example, Zhang et al. [107] developed microspheres with configurable porosity and size using cellulose acetate. There is other research in the literature that might possibly expand Table 3; however, to keep this review brief and to the point, we will abstain from adding further resources here. Readers are urged to check numerous published publications in the literature that might provide further information on Table 3. Figure 8 depicts a variety of illustrative products of the microfluidics-aided cellulose-based design to summarize the information offered in this study in the form of a figure. It appears the range of products varies from fibers, buckled particles, and microfluidic devices to microcapsules. The inclusion of liquid crystalline feature is also possible.
Appl. Biosci. 2022, 1, FOR PEER REVIEW 25 products of the microfluidics-aided cellulose-based design to summarize the information offered in this study in the form of a figure. It appears the range of products varies from fibers, buckled particles, and microfluidic devices to microcapsules. The inclusion of liquid crystalline feature is also possible.

Conclusions and Projections in the Future
The incorporation of cellulose microfluidics into research projects via the literature has resulted in several benefits for the scientific community. Even while microfluidics as a design idea has several advantages, its value in investigating cellulose-based products and the use of cellulose as a building component is currently underutilized. Surprisingly, the sort of structure and process continuity for microfluidics is quite capable of developing novel designs that are impenetrable by conventional approaches. One example is the development of a platform for wound dressing screening, utilizing microfluidics to spin robust microfibers. Microfluidics can also produce microparticles for applications such as drug administration and sorption agents.
It should also be noted that research on microfluidic devices made of paper is still in its early stages, and significant efforts are required to make this field of research thrive further to provide a platform for technology in diagnostic and environmental monitoring. More research is needed to uncover new concepts and capabilities related to this technology. As a result, more exploratory investigations should be conducted in order to identify new concepts and possibilities of this critical technology. The feasibility of present and future approaches for making PADs must be studied and appraised by researchers for the purpose of the sdiagnostic market in terms of material and also the cost that comes with the production of these devices and their potential. For mass manufacturing, dependency on any other equipment must be assessed in order for them to be scaled to the industrial level. The dependability with which they interpret relatively easy-to-read test data and (b) Prepared cellulose capsules following isopropanol addition. Adapted with permission from Ref. [142]. Copyright 2014 The Royal Society of Chemistry. (c) The tissue of a microfluidic paperbased device is illustrated on the side under SEM. Adapted from Ref. [278]. (d) SEM pictures of CNF orientated within a microfluidics device (fibers are impregnated in an epoxy-based matrix). Adapted with permission from Ref. [109]. Copyright 2018 Wiley-VCH. (e) Images of buckled cellulose microcapsules under cross-polarizers and SEM images of particles. Adapted from Ref. [259]. (f) SEM pictograph of cellulose-based microcapsules, flow rates for the production of these microcapsules varied from 200 to 1200 µL/h. Adapted with permission from Ref. [96]. Copyright 2009 Elsevier.

Conclusions and Projections in the Future
The incorporation of cellulose microfluidics into research projects via the literature has resulted in several benefits for the scientific community. Even while microfluidics as a design idea has several advantages, its value in investigating cellulose-based products and the use of cellulose as a building component is currently underutilized. Surprisingly, the sort of structure and process continuity for microfluidics is quite capable of developing novel designs that are impenetrable by conventional approaches. One example is the development of a platform for wound dressing screening, utilizing microfluidics to spin robust microfibers. Microfluidics can also produce microparticles for applications such as drug administration and sorption agents.
It should also be noted that research on microfluidic devices made of paper is still in its early stages, and significant efforts are required to make this field of research thrive further to provide a platform for technology in diagnostic and environmental monitoring. More research is needed to uncover new concepts and capabilities related to this technology. As a result, more exploratory investigations should be conducted in order to identify new concepts and possibilities of this critical technology. The feasibility of present and future approaches for making PADs must be studied and appraised by researchers for the purpose of the sdiagnostic market in terms of material and also the cost that comes with the production of these devices and their potential. For mass manufacturing, dependency on any other equipment must be assessed in order for them to be scaled to the industrial level. The dependability with which they interpret relatively easy-to-read test data and their perfect interoperability with telemedicine are also other notable factors that must be tackled.
The 3D printing of these devices in the future may increasingly play a very different, very important role in tailoring novel applications such as disease screening application or even roles such as food quality testing. The expertise in controlling paper sheet structure, incorporating new materials such as nano fibres or other natural source fibres and functional materials into sheets using polymer electrolyte, and significantly improving printing technology, are also other factors for which the resources have remained untapped. Benefitting future development, of the paper-based microfluidic technology to date, most of the devices are being made with filter papers; however, in the future, endeavours must be made to develop better materials that offer properties that are unmatched by current filter papers. Future studies will also be required to work to comprehend capillary forces that in a paper sheet will be important for achieving more accurate control of lateral flow in the paper. The paper, surface energy, and structure are also additional aspects that must be addressed in further research. Vertical flow in paper, for example, liquid flowing through the paper thickness to a defined region, and control of it may necessitate more research. This specially becomes cumbersome with 3D-printed device; 3D-PADs need to regulate more than just liquid lateral flow. On paper, there is also a vertical flow approach with microfluidic biometric analytics and signal transfer.
It should be emphasized that there are additional sophisticated methods for structuring cellulose products that are currently underutilised, such as the merging of two microfluidic systems and electrospinning. Wet spinning and microfluidics designs were discussed in the previous section; however, more complicated designs exist, such as combining two streams and then employing jet extrusion from microfluidics to collect on a foil via electrospinning [279].
As a recap, the use of microfluidics in the design of cellulose-based products and the value of paper as a medium for manufacturing microfluidics were discussed in this review.

Funding:
The author received no financial support for the research.
Institutional Review Board Statement: Not applicable.

Informed Consent Statement: Not applicable.
Data Availability Statement: This study did not report any data.

Conflicts of Interest:
The author declares no conflict of interest.