Name: fabricating highly open porous microspheres (hopms) via microfluidic technology
Uploaded: 2022-05-16T15:00:00
Description: Watch this Scientific Journal Video about Fabricating Highly Open Porous Microspheres HOPMs via Microfluidic Technology at JoVE.com

SCL, YW, RKK, and AZC acknowledge financial support from the National Natural Science Foundation of China (NSFC, 32071323, 81971734, and U1605225) and Program for Innovative Research Team in Science and Technology in Fujian Province University. YSZ was neither supported by any of these programs nor received payment of any type; instead, support from the Brigham Research Institute is acknowledged.

1. Preparation of solutions
<ol>
	<li>Prepare the PVA stock solution in advance by heating the PVA solution in a 80 &#176;C water bath and subsequently placing it in the refrigerator at 4 &#176;C. Cool to room temperature (RT) for experimental usage.</li>
	<li>Prepare the emulsion-precursor by adding the aqueous gelatin solution (1 mL, 7.5%, w/v) to the organic phase of PLGA (2 mL, 2%, w/v in dichloromethane, DCM) (see Table of Materials). 
	&#8203;NOTE: Generally, microfluidic te...

<ol>
	<li>Kankala, R. K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Highly+porous+microcarriers+for+minimally+invasive+in+situ+skeletal+muscle+cell+delivery.">Highly porous microcarriers for minimally invasive in situ skeletal muscle cell delivery.</a> Small. 15 (25), 1901397 (2019).</li><li>Wang, Y., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Modeling+endothelialized+hepatic+tumor+microtissues+for+drug+screening.">Modeling endothelialized hepatic tumor microtissues for drug screening.</a> Advanced Science. 7 (21), 2002002 (2020).</li><li>Li, Q., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Tripeptide-based+macroporous+hydrogel+improves+the+osteogenic+microenvironment+of+stem+cells.">Tripeptide-based macroporous hydrogel improves the osteogenic microenvironment of stem cells.</a> Journal of Materials Chemistry B. 9 (30), 6056-6067 (2021).</li><li>Liu, Y., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=PLGA+hybrid+porous+microspheres+as+human+periodontal+ligament+stem+cell+delivery+carriers+for+periodontal+regeneration.">PLGA hybrid porous microspheres as human periodontal ligament stem cell delivery carriers for periodontal regeneration.</a> Chemical Engineering Journal. 420, 129703 (2021).</li><li>Wei, P., Xu, Y., Zhang, H., Wang, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Continued+sustained+insulin-releasing+PLGA+nanoparticles+modified+3D-printed+PCL+composite+scaffolds+for+osteochondral+repair.">Continued sustained insulin-releasing PLGA nanoparticles modified 3D-printed PCL composite scaffolds for osteochondral repair.</a> Chemical Engineering Journal. 422, 130051 (2021).</li><li>Sang, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Biocompatible+chitosan/polyethylene+glycol/multi-walled+carbon+nanotube+composite+scaffolds+for+neural+tissue+engineering.">Biocompatible chitosan/polyethylene glycol/multi-walled carbon nanotube composite scaffolds for neural tissue engineering.</a> Journal of Zhejiang University-Science B. 23 (1), 58-73 (2022).</li><li>Ghasemian, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hydrodynamic+characterization+within+a+spinner+flask+and+a+rotary+wall+vessel+for+stem+cell+culture.">Hydrodynamic characterization within a spinner flask and a rotary wall vessel for stem cell culture.</a> Biochemical Engineering Journal. 157, 107533 (2020).</li><li>Wang, Y., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Minimally+invasive+co-injection+of+modular+micro-muscular+and+micro-vascular+tissues+improves+in+situ+skeletal+muscle+regeneration.">Minimally invasive co-injection of modular micro-muscular and micro-vascular tissues improves in situ skeletal muscle regeneration.</a> Biomaterials. 277, 121072 (2021).</li><li>Kang, S. 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This article describes an efficient strategy to fabricate PLGA-based architectures, namely the PLGA-HOPMs. It is to be noted that several critical steps must be taken carefully, including avoiding solvent volatilization of PLGA and gentle adjustment of the ultrasonic power to the target position during the preparation of the emulsion. In addition, the liquid outlet of the 20 mL syringe can be adjusted to a certain extent to solve the phase separation of emulsified precursors. However, a limitation is that, since the stat...

Cell-laden microspheres offer favorable advantages, such as enhanced cell retention capacity in situ, efficient delivery of cells, and subsequent ability of cell proliferation in vivo1. To date, numerous investigations have been put forward for developing a successful scaffolding structure to support a conducive environment for cells for tissue regeneration or drug screening applications2. However, the hypoxia environment is oftentimes inevitable in the interiors due to insufficient supplies of nutrients/oxygen and metabolic waste accumulation3. To overcome these problems, highly porous microspheres (PMs) have been developed using various biomaterials4,5,6. Additionally, in dynamic culture, the scaffolds suffer from excessive shear stress7, and the unstable state of the culture medium might break the fidelity of PMs. Alternatively, poly(lactic-co-glycolic acid) (PLGA) could be used to process PMs with good mechanical strength for dynamic culture1. For example, we demonstrated co-injection of mouse myoblast (C2C12)-laden PLGA highly open PMs (HOPMs) and human umbilical vein endothelial cell (HUVEC)-laden poly(ethylene glycol) hollow microrods to heal volumetric muscle loss, achieving remarkable improvement of in situ skeletal muscle regeneration8.
Notably, PMs are characterized by large surface areas and high porosities, which is of specific interest for cell adhesion and growth towards minimally invasive cell delivery9. In view of these aspects, various biocompatible materials have been employed to fabricate the PMs10,11. These designable PMs cocultured with cells offer excellent adhesion, considerable mechanical strength, and highly interconnected windows, which could improve cell proliferation for repairing damaged tissues12. In this regard, various technologies have also been developed to fabricate porous spheres13,14. On the one hand, PMs were produced using gas-forming agents, such as NH4HCO3, which were restrained due to insufficient interconnectivity15,16,17. On the other hand, PMs were directly sheared after emulsification, which led to polydisperse PMs18. In the end, the droplet microfluidic technology based on the emulsion-templating approach is perhaps an efficient method for constructing PMs, as it often results in uniform-sized particles19. Notably, the morphological attributes of the microspheres often depend on the quality of the generated emulsion droplets (i.e., water-in-oil, W/O, or oil-in-water, O/W), which may significantly affect the attributes of the biomaterials20. It is worth noting that the predesigned microfluidic platform can be applied to generate the microfibers or microspheres. In an instance, Yu et al. demonstrated the production of cell-laden microfibrous structures based on capillary-based microfluidic platforms, which could be used to assemble cellular networks for mimicking natural tissues21. In another instance, Ye et al. fabricated photonic crystal microcapsules by the template replication of silica colloidal crystal beads through microfluidic technologies, which could overcome many limitations of current techniques that require complex labeling and specific apparatus22.
Indeed, the rationale behind the utilization of this technique is due to various advantages, such as being facile in nature, requiring no sophisticated equipment, and its convenience in synthesizing uniform-sized PMs for cell delivery and regenerative medicine applications. In this context, with predesigned components of emulsion-templating, PMs with high porosities and interconnectivity can be conveniently obtained from a microfluidic device assembled from poly(vinyl chloride) (PVC) tubing, a glass capillary, and a needle. A W/O emulsion-precursor is prepared by homogenizing an aqueous solution of gelatin and an organic solution of PLGA. By selectively injecting the applicable portion of the emulsion into the microfluidic platform, the PMs with uniform particle sizes and interconnected pores throughout the surface to the interior are fabricated. The present protocol aims to fabricate the PLGA-HOPMs by emulsion-templating in the microfluidic platform. It is believed that this protocol allows reproducible production of PLGA-HOPMs and will potentially be applicable in their related fields of tissue engineering and drug screening.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Centrifuge tube</td>
			<td>Solarbio, Beijing, China</td>
			<td></td>
			<td>5 mL &#38; 50 mL (sterility)</td>
		</tr>
		<tr>
			<td>Confocal laser scanning microscopy</td>
			<td>Leica, Wetzlar, Germany</td>
			<td></td>
			<td>TCS SP8</td>
		</tr>
		<tr>
			<td>Dichloromethane</td>
			<td>Sinopharm Chemical Reagent Co., Ltd, Shanghai, China</td>
			<td>20161110</td>
			<td>Research Grade</td>
		</tr>
		<tr>
			<td>Dispensing needle</td>
			<td>Kindly, Shanghai, China</td>
			<td></td>
			<td>26 G, ID: 250 &#956;m, OD: 460 &#956;m</td>
		</tr>
		<tr>
			<td>DMEM/F-12</td>
			<td>Gibco; Life Technologies Corporation, Calsbad, USA</td>
			<td>15400054</td>
			<td>DMEM/F-12 50/50, 1x (Dulbecco&#39;s 
			Mod. Of Eagle&#39;s Medium/Ham&#39;s F12 
			50/50 Mix) with L-glutamine</td>
		</tr>
		<tr>
			<td>Ethyl alcohol</td>
			<td>Sinopharm Chemical Reagent Co., Ltd, Shanghai, China</td>
			<td>20210918</td>
			<td>Research Grade</td>
		</tr>
		<tr>
			<td>Ethyl-enediaminetetraacetic acid (EDTA)-trypsin</td>
			<td>Biological Industries, Kibbutz Beit-Haemek, Isra</td>
			<td></td>
			<td>Trypsin (0.25%), EDTA (0.02%)</td>
		</tr>
		<tr>
			<td>Fetal bovine serum (FBS)</td>
			<td>Biological Industries, Kibbutz Beit-Haemek, Isra</td>
			<td></td>
			<td>Research Grade</td>
		</tr>
		<tr>
			<td>Freeze drier</td>
			<td>Bilon, Shanghai, China</td>
			<td></td>
			<td>FD-1B-50</td>
		</tr>
		<tr>
			<td>Gelatin</td>
			<td>Sigma-Aldrich Co. Ltd, St. Louis, USA</td>
			<td>lot# SZBF2870V</td>
			<td>From porcine skin, Type A</td>
		</tr>
		<tr>
			<td>Glass bottom plate</td>
			<td>Biosharp, Hefei, China</td>
			<td></td>
			<td>BS-15-GJM, 35 mm</td>
		</tr>
		<tr>
			<td>Glass capillary</td>
			<td>Huaou, Jiangsu, China</td>
			<td></td>
			<td>0.9-1.1 &#215; 120 mm</td>
		</tr>
		<tr>
			<td>Incubator shaker</td>
			<td>Zhicheng, Shanghai, China</td>
			<td>ZWYR-200D</td>
			<td></td>
		</tr>
		<tr>
			<td>Live dead kit cell imaging kit</td>
			<td>Solarbio, Beijing, China</td>
			<td>60421211112</td>
			<td>Green fluorescence in live cells (ex/em 488 nm/515 nm). Red fluorescence in dead cells (ex/em 570 nm/602 nm)</td>
		</tr>
		<tr>
			<td>Low-speed centrifuge</td>
			<td>Xiangyi, Hunan, China</td>
			<td></td>
			<td>TD5A</td>
		</tr>
		<tr>
			<td>Magnetron sputter</td>
			<td>Riye electric Co. Ltd, Suzhou, China</td>
			<td>MSP-2S</td>
			<td></td>
		</tr>
		<tr>
			<td>Microflow injection pump</td>
			<td>Harvard Apparatus, Holliston, USA</td>
			<td></td>
			<td>Harvard Pump 11 Plus</td>
		</tr>
		<tr>
			<td>Penicillin-streptomycin</td>
			<td>Biological Industries, Kibbutz Beit-Haemek, Isra</td>
			<td>2135250</td>
			<td>Research Grade</td>
		</tr>
		<tr>
			<td>Phosphate buffered saline (PBS)</td>
			<td>Servicebio Technology Co.,Ltd. Wuhan, China</td>
			<td>GP21090181556</td>
			<td>PBS 1x, culture grade, no Calcium, no Magnesium</td>
		</tr>
		<tr>
			<td>Poly(lactic-co-glycolic acid)</td>
			<td>Sigma-Aldrich Co. Ltd, St. Louis, USA</td>
			<td>lot# MKCF9651</td>
			<td>66&#8211;107 kDa, lactide:glycolide 75:25</td>
		</tr>
		<tr>
			<td>Poly(vinyl alcohol)</td>
			<td>Sigma-Aldrich Co. Ltd, St. Louis, USA</td>
			<td>lot# MKCK4266</td>
			<td>13-13 kDa, 98% Hydrolyzed</td>
		</tr>
		<tr>
			<td>PVC tube</td>
			<td>Shenchen, Shanghai, China</td>
			<td></td>
			<td>Inner diameter, ID: 1 mm</td>
		</tr>
		<tr>
			<td>Rat bone marrow mesenchyml stem cells</td>
			<td>Procell, Wuhan, China</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Scanning electron microscope</td>
			<td>Phenom pure, Eindhoven, Netherlands</td>
			<td></td>
			<td>Set acceleration voltage at 5 kV</td>
		</tr>
		<tr>
			<td>Syrine for medical purpose</td>
			<td>Kindly, Shanghai, China</td>
			<td></td>
			<td>5 mL &#38; 50 mL (with the needle)</td>
		</tr>
		<tr>
			<td>Temperature water bath</td>
			<td>Mingxiang, Shenzhen, China</td>
			<td></td>
			<td>36 W</td>
		</tr>
		<tr>
			<td>Transformer</td>
			<td>Riye electric Co. Ltd, Suzhou, China</td>
			<td>SZ-2KVA</td>
			<td></td>
		</tr>
		<tr>
			<td>Ultrasonic cell breaker</td>
			<td>JY 92-IID, Scientz, Ningbo, China</td>
			<td></td>
			<td>JY 92-IID</td>
		</tr>
		<tr>
			<td>UV curing glue</td>
			<td>Zhuolide, Foshan, China</td>
			<td></td>
			<td>D-3100</td>
		</tr>
	</tbody>
</table>

fabricating highly open porous microspheres (hopms) via microfluidic technology

Compared to bulk scaffolds and direct injection of cells alone, the injectable modular units have garnered enormous interest in repairing malfunctioned tissues due to convenience in the packaging of cells, improved cell retention, and minimal invasiveness. Moreover, the porous conformation of these microscale carriers could enhance the medium exchange and improve the level of nutrients and oxygen supplies. The present study illustrates the convenient fabrication of poly(lactic-co-glycolic acid)-based highly open porous microspheres (PLGA-HOPMs) by the facile microfluidic technology for cell delivery applications. The resultant monodispersed PLGA-HOPMs possessed particle sizes of ~400 &#181;m and open pores of ~50 &#181;m with interconnecting windows. Briefly, the emulsified oil droplets (PLGA solution in dichloromethane, DCM), wrapped with the 7.5% (w/v) gelatin aqueous phase, were introduced into the 1% (w/v) continuous flowing poly(vinyl alcohol) (PVA) aqueous solution through the coaxial nozzle in the customized microfluidic setup. Subsequently, the microspheres were subjected to solvent extraction and lyophilization procedures, resulting in the production of HOPMs. Notably, various formulations (concentrations of PLGA and porogen) and processing parameters (emulsifying power, needle gauge, and flow rate of dispersed phase) play crucial roles in the qualities and characteristics of the resulting PLGA HOPMs. Moreover, these architectures might potentially encapsulate various other biochemical cues, such as growth factors, for extended drug discovery and tissue regeneration applications.

Based on previous work that optimized the major parameters1, PLGA was dissolved in the evaporable DCM solvent. The primary W/O emulsion was prepared by homogenizing with gelatin under ultrasonic probe treatment. The customized co-flow fluidic structure was simplistically assembled, in which a syringe was employed to introduce the flows constantly. Furthermore, sufficient rinsing procedures were carried out to eliminate PVA and gelatin of PLGA microspheres (Figure 1A, ...

Watch this Scientific Journal Video about Fabricating Highly Open Porous Microspheres HOPMs via Microfluidic Technology at JoVE.com

Fabricating Highly Open Porous Microspheres HOPMs via Microfluidic Technology

The present protocol describes the fabrication of poly(lactic-co-glycolic acid)-based highly open porous microspheres (HOPMs) via the single-emulsion formulation based facile microfluidic technology. These microspheres have potential applications in tissue engineering and drug screening.

Fabricating Highly Open Porous Microspheres (HOPMs) via Microfluidic Technology

Compared to bulk scaffolds and direct injection of cells alone, the injectable modular units have garnered enormous interest in repairing malfunctioned ...

In this protocol, we demonstrate an effective procedure for fabricating PLGA-based highly-open porous microspheres, which offer several advantages like convenience of packaging cells, improved cell retention, and minimal invasiveness. The resultant monodispersed PLGA-based highly-open porous microspheres possessed particle sizes of approximately 400 micrometers and open pores of approximately 50 micrometers with interconnecting windows for improved cell retention efficacy. These minimally invasive microcarriers may support a platform of an intricate 3D tumor model for drug screening and facile tools to construct cell laden micro tissues for tissue regeneration.This approach is quite facile, as the microfluidic device can be assembled from polyvinyl chloride tubing, a glass capillary, and a needle. Demonstrating the procedure will be Sheng-Chang Luo, a doctoral student in the laboratory. Begin by constructing a co-flow microfluidic generator using a glass capillary, polyvinyl chloride tubes, and a 26 gauge dispensing needle.Then connect the glass capillary to the end of the polyvinyl chloride tube, and pierce the connection between the two with a needle. For the droplet generation, place the other end of the polyvinyl chloride tube in the continuous phase, and cure with the ultraviolet glue to seal the gaps at the joint. Now take a 50 milliliter syringe to load the continuous phase, and a five milliliter syringe for emulsion formation.Then set the flow rates of the continuous phase at two milliliters per minute, and the dispersion phases at 0.08 milliliters per minute. Place a 500 milliliter beaker in an ice bath, and fill it with a pre-cooled polyvinyl alcohol aqueous solution. To prepare the emulsion, immediately decant the aqueous gelatin solution into the DCM solution of PLGA, and emulsify using the ultrasonic device.Then adjust the ultrasonic power to 400 watts, and the total processing time to 90 seconds, and constantly change the probe's position manually. Stabilize the resulted emulsion for syringe suction and droplet generation in approximately 20 minutes. After ultrasonic treatment, rapidly load the prepared emulsion in the five milliliter syringe in the microfluidic platform and introduce the unstable water oil emulsion into the microfluidic device as the discontinuous phase.Simultaneously, use the aqueous solution of polyvinyl alcohol as the continuous phase. After injecting proper portions of the emulsion into the microfluidic device, collect the microsphere containing the emulsion at the bottom of the collecting beaker and place the sample at four degrees Celsius overnight for further stabilization. Normalize the stored microspheres to room temperature and eliminate the residual DCM by stirring with a glass rod for one hour at 60 RPM.Then, carefully decant the collecting phase in a 500 milliliter beaker and wash off the residual polyvinyl alcohol from the surface of porous microspheres with deionized water thrice. Dissolve the gelatin wrapped in the PLGA backbone by placing the PLGA microspheres in the water bath at 37 degrees Celsius for 30 minutes. Then remove the residual gelatin by rinsing the resultant microspheres with the deionized water twice, and pre-cool for lyophilization at minus 80 degrees Celsius for 24 hours.The PLGA-based highly-open porous microspheres displayed sizes of 350 to 500 micrometer with an arbitrary sized pore of 10 to 100 micrometers, and interconnected windows, which could facilitate high efficiency in oxygen metabolic waste transport. The bone marrow mesenchymal stem cells cultured within the PLGA-based highly-open porous microspheres adhered to the scaffolds in one day, representing extensive adhesion and migration capabilities of cells. The calcium-AM and propidium iodide staining showed that the cells are live and distributed uniformly.It is essential to set the ultrasonic power and the probe's position. The reproducible production of PLGA-based highly-open porous micro spheres will pave the way to construct off the shelf graphs to induce regeneration or drug screening.

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Research

JoVE Journal

Bioengineering

Electrospinning Growth Factor Releasing Microspheres into Fibrous Scaffolds

This procedure describes a method to fabricate a multifaceted substrate to direct nerve cell growth. This system incorporates mechanical, topographical, adhesive and chemical signals. Mechanical properties are controlled by the type of material used to fabricate the electrospun fibers. In this protocol we use 30% methacrylated Hyaluronic Acid (HA), which has a tensile modulus of ~500 Pa, to produce a soft fibrous scaffold. Electrospinning on to a rotating mandrel produces aligned fibers to create a topographical cue. Adhesion is achieved by coating the scaffold with fibronectin. The primary challenge addressed herein is providing a chemical signal throughout the depth of the scaffold for extended periods. This procedure describes fabricating&#160;poly(lactic-co-glycolic acid) (PLGA) microspheres that contain Nerve Growth Factor (NGF) and directly impregnating the scaffold with these microspheres during the electrospinning process. Due to the harsh production environment, including high sheer forces and electrical charges, protein viability is measured after production. The system provides protein release for over 60 days and has been shown to promote primary nerve cell growth.

This protocol combines electrospinning and microspheres to develop tissue engineered scaffolds to direct neurons. Nerve growth factor was encapsulated within PLGA microspheres and electrospun into Hyaluronic Acid (HA) fibrous scaffolds. The protein bioactivity was tested by seeding the scaffolds with primary chick Dorsal Root Ganglia and culturing for 4-6 days.

This procedure describes a method to fabricate a multifaceted substrate to direct nerve cell growth.  This system incorporates mechanical, topographical, ...

Porous Silicon Microparticles for Delivery of siRNA Therapeutics

Small interfering RNA (siRNA) can be used to suppress gene expression, thereby providing a new avenue for the treatment of various diseases. However, the successful implementation of siRNA therapy requires the use of delivery platforms that can overcome the major challenges of siRNA delivery, such as enzymatic degradation, low intracellular uptake and lysosomal entrapment. Here, a protocol for the preparation and use of a biocompatible and effective siRNA delivery system is presented. This platform consists of polyethylenimine (PEI) and arginine (Arg)-grafted porous silicon microparticles, which can be loaded with siRNA by performing a simple mixing step. The silicon particles are gradually degraded over time, thereby triggering the formation of Arg-PEI/siRNA nanoparticles. This delivery vehicle provides a means for protecting and internalizing siRNA, without causing cytotoxicity. The major steps of polycation functionalization, particle characterization, and siRNA loading are outlined in detail. In addition, the procedures for determining particle uptake, cytotoxicity, and transfection efficacy are also described.

Delivery remains the main challenge for the therapeutic implementation of small interfering RNA (siRNA). This protocol involves the use of a multifunctional and biocompatible siRNA delivery platform, consisting of arginine and polyethylenimine grafted porous silicon microparticles.

Small interfering RNA (siRNA) can be used to suppress gene expression, thereby providing a new avenue for the treatment of various diseases. However, the ...

Fabricating Cotton Analytical Devices

A robust, low-cost analytical device should be user-friendly, rapid, and affordable. Such devices should also be able to operate with scarce samples and provide information for follow-up treatment. Here, we demonstrate the development of a cotton-based urinalysis (i.e., nitrite, total protein, and urobilinogen assays) analytical device that employs a lateral flow-based format, and is inexpensive, easily fabricated, rapid, and can be used to conduct multiple tests without cross-contamination worries. Cotton is composed of cellulose fibers with natural absorptive properties that can be leveraged for flow-based analysis. The simple but elegant fabrication process of our cotton-based analytical device is described in this study. The arrangement of the cotton structure and test pad takes advantage of the hydrophobicity and absorptive strength of each material. Because of these physical characteristics, colorimetric results can persistently adhere to the test pad. This device enables physicians to receive clinical information in a timely manner and shows great potential as a tool for early intervention.

To investigate simple fabrication approaches for multiple assay needs, we created a fluid-absorbing channel system made of cotton material. This device was used to establish a multiple detection platform, and solve contamination issues that commonly affect lateral flow-based biomedical devices, for clinical urinalysis of nitrite, total protein, and urobilinogen.

A robust, low-cost analytical device should be user-friendly, rapid, and affordable. Such devices should also be able to operate with scarce samples and ...

Fabricating Degradable Thermoresponsive Hydrogels on Multiple Length Scales via Reactive Extrusion, Microfluidics, Self-assembly, and Electrospinning

While various smart materials have been explored for a variety of biomedical applications (e.g., drug delivery, tissue engineering, bioimaging, etc.), their ultimate clinical use has been hampered by the lack of biologically-relevant degradation observed for most smart materials. This is particularly true for temperature-responsive hydrogels, which are almost uniformly based on polymers that are functionally non-degradable (e.g., poly(N-isopropylacrylamide) (PNIPAM) or poly(oligoethylene glycol methacrylate) (POEGMA)). As such, to effectively translate the potential of thermoresponsive hydrogels to the challenges of remote-controlled or metabolism-regulated drug delivery, cell scaffolds with tunable cell-material interactions, theranostic materials with the potential for both imaging and drug delivery, and other such applications, a method is required to render the hydrogels (if not fully degradable) at least capable of renal clearance following the required lifetime of the material. To that end, this protocol describes the preparation of hydrolytically-degradable hydrazone-crosslinked hydrogels on multiple length scales based on the reaction between hydrazide and aldehyde-functionalized PNIPAM or POEGMA oligomers with molecular weights below the renal filtration limit. Specifically, methods to fabricate degradable thermoresponsive bulk hydrogels (using a double barrel syringe technique), hydrogel particles (on both the microscale through the use of a microfluidics platform facilitating simultaneous mixing and emulsification of the precursor polymers and the nanoscale through the use of a thermally-driven self-assembly and cross-linking method), and hydrogel nanofibers (using a reactive electrospinning strategy) are described. In each case, hydrogels with temperature-responsive properties similar to those achieved via conventional free radical cross-linking processes can be achieved, but the hydrazone cross-linked network can be degraded over time to re-form the oligomeric precursor polymers and enable clearance. As such, we anticipate these methods (which may be generically applied to any synthetic water-soluble polymer, not just smart materials) will enable easier translation of synthetic smart materials to clinical applications.

Protocols are described for the fabrication of degradable thermoresponsive hydrogels based on hydrazone cross-linking of polymeric oligomers on the bulk scale, microscale, and nanoscale, the latter for preparation of both gel nanoparticles and nanofibers.

While various smart materials have been explored for a variety of biomedical applications (e.g., drug delivery, tissue engineering, bioimaging, etc.), ...

Multi-step Variable Height Photolithography for Valved Multilayer Microfluidic Devices

Microfluidic systems have enabled powerful new approaches to high-throughput biochemical and biological analysis. However, there remains a barrier to entry for non-specialists who would benefit greatly from the ability to develop their own microfluidic devices to address research questions. Particularly lacking has been the open dissemination of protocols related to photolithography, a key step in the development of a replica mold for the manufacture of polydimethylsiloxane (PDMS) devices. While the fabrication of single height silicon masters has been explored extensively in literature, fabrication steps for more complicated photolithography features necessary for many interesting device functionalities (such as feature rounding to make valve structures, multi-height single-mold patterning, or high aspect ratio definition) are often not explicitly outlined. 
Here, we provide a complete protocol for making multilayer microfluidic devices with valves and complex multi-height geometries, tunable for any application. These fabrication procedures are presented in the context of a microfluidic hydrogel bead synthesizer and demonstrate the production of droplets containing polyethylene glycol (PEG diacrylate) and a photoinitiator that can be polymerized into solid beads. This protocol and accompanying discussion provide a foundation of design principles and fabrication methods that enables development of a wide variety of microfluidic devices. The details included here should allow non-specialists to design and fabricate novel devices, thereby bringing a host of recently developed technologies to their most exciting applications in biological laboratories.

Multilayer microfluidic devices often involve the fabrication of master molds with complex geometries for functionality. This article presents a complete protocol for multi-step photolithography with valves and variable height features tunable to any application. As a demonstration, we fabricate a microfluidic droplet generator capable of producing hydrogel beads.

Microfluidic systems have enabled powerful new approaches to high-throughput biochemical and biological analysis. However, there remains a barrier to ...

Microfluidic Platform with Multiplexed Electronic Detection for Spatial Tracking of Particles

Microfluidic processing of biological samples typically involves differential manipulations of suspended particles under various force fields in order to spatially fractionate the sample based on a biological property of interest. For the resultant spatial distribution to be used as the assay readout, microfluidic devices are often subjected to microscopic analysis requiring complex instrumentation with higher cost and reduced portability. To address this limitation, we have developed an integrated electronic sensing technology for multiplexed detection of particles at different locations on a microfluidic chip. Our technology, called Microfluidic CODES, combines Resistive Pulse Sensing with Code Division Multiple Access to compress 2D spatial information into a 1D electrical signal. In this paper, we present a practical demonstration of the Microfluidic CODES technology to detect and size cultured cancer cells distributed over multiple microfluidic channels. As validated by the high-speed microscopy, our technology can accurately analyze dense cell populations all electronically without the need for an external instrument. As such, the Microfluidic CODES can potentially enable low-cost integrated lab-on-a-chip devices that are well suited for the point-of-care testing of biological samples.

We demonstrate a microfluidic platform with an integrated surface electrode network that combines resistive pulse sensing (RPS) with code division multiple access (CDMA), to multiplex detection and sizing of particles in multiple microfluidic channels.

Microfluidic processing of biological samples typically involves differential manipulations of suspended particles under various force fields in order to ...

Reconfigurable Microfluidic Channel with Pin-discretized Sidewalls

Microfluidic components need to have various shapes to realize different key microfluidic functions such as mixing, separation, particle trapping, or reactions. A microfluidic channel that deforms even after fabrication while retaining the channel shape enables high spatiotemporal reconfigurability. This reconfigurability is required in such key microfluidic functions that are difficult to achieve in existing "reconfigurable" or "integrated" microfluidic systems. We describe a method for the fabrication of a microfluidic channel with a deformable sidewall consisting of a laterally aligned array of the ends of rectangular pins. Actuating the pins in their longitudinal directions changes the pins' end positions, and thus, the shape of discretized channel sidewalls.Pin gaps can cause unwanted leakage or adhesion to adjacent pins caused by meniscus forces. To close the pin gaps, we have introduced hydrocarbon-fluoropolymer suspension-based gap filler accompanied by an elastomeric barrier. This reconfigurable microfluidic device can generate strong temporal in-channel displacement flow, or can stop the flow in any region of the channel. This feature will facilitate, on demand, the handling of cells, viscous liquids, gas bubbles, and non-fluids, even if their existence or behavior is unknown at the time of fabrication.

A microfluidic channel with deformable sidewalls offers flow control, particle handling, channel dimension customization and other reconfigurations while in use. We describe a method for fabricating a microfluidic channel with sidewalls made of an array of pins that allows their shape to change.

Microfluidic components need to have various shapes to realize different key microfluidic functions such as mixing, separation, particle trapping, or ...

Designing Porous Silicon Films as Carriers of Nerve Growth Factor

Despite the great potential of NGF for treating neurodegenerative diseases, its therapeutic administration represents a significant challenge as the protein does not cross the blood-brain barrier, owing to its chemical properties, and thus requires long-term delivery to the brain to have a biological effect. This work describes fabrication of nanostructured PSi films as degradable carriers of NGF for sustained delivery of this sensitive protein. The PSi carriers are specifically tailored to obtain high loading efficacy and continuous release of NGF for a period of four weeks, while preserving its biological activity. The behavior of the NGF-PSi carriers as a NGF delivery system is investigated in vitro by examining their capability to induce neuronal differentiation and outgrowth of PC12 cells and dissociated DRG neurons. Cell viability in the presence of neat and NGF-loaded PSi carriers is evaluated. The bioactivity of NGF released from the PSi carriers is compared to the conventional treatment of repetitive free NGF administrations. PC12 cell differentiation is analyzed and characterized by the measurement of three different morphological parameters of differentiated cells; (i) the number of neurites extracting from the soma (ii) the total neurites' length and (iii) the number of branching points. PC12 cells treated with the NGF-PSi carriers demonstrate a profound differentiation throughout the release period. Furthermore, DRG neuronal cells cultured with the NGF-PSi carriers show an extensive neurite initiation, similar to neurons treated with repetitive free NGF administrations. The studied tunable carriers demonstrate the long-term implants for NGF release with a therapeutic potential for neurodegenerative diseases.

Here, we present a protocol to design and fabricate nanostructured porous silicon (PSi) films as degradable carriers for the nerve growth factor (NGF). Neuronal differentiation and outgrowth of PC12 cells and mice dorsal root ganglion (DRG) neurons are characterized upon treatment with the NGF-loaded PSi carriers.

Despite the great potential of NGF for treating neurodegenerative diseases, its therapeutic administration represents a significant challenge as the ...

An Open Source Technology Platform to Manufacture Hydrogel-Based 3D Culture Models in an Automated and Standardized Fashion

Current mixing steps of viscous materials rely on repetitive and time-consuming tasks which are performed mainly manually in a low throughput mode. These issues represent drawbacks in workflows that can ultimately result in irreproducibility of research findings. Manual-based workflows are further limiting the advancement and widespread adoption of viscous materials, such as hydrogels used for biomedical applications. These challenges can be overcome by using automated workflows with standardized mixing processes to increase reproducibility. In this study, we present step-by-step instructions to use an open source protocol designer, to operate an open source workstation, and to identify reproducible mixtures. Specifically, the open source protocol designer guides the user through the experimental parameter selection and generates a ready-to-use protocol code to operate the workstation. This workstation is optimized for pipetting of viscous materials to enable automated and highly reliable handling by the integration of temperature docks for thermoresponsive materials, positive displacement pipettes for viscous materials, and an optional tip touch dock to remove excess material from the pipette tip. The validation and verification of mixtures are performed by a fast and inexpensive absorbance measurement of Orange G. This protocol presents results to obtain 80% (v/v) glycerol mixtures, a dilution series for gelatin methacryloyl (GelMA), and double network hydrogels of 5% (w/v) GelMA and 2% (w/v) alginate. A troubleshooting guide is included to support users with protocol adoption. The described workflow can be broadly applied to a number of viscous materials to generate user-defined concentrations in an automated fashion.

This protocol serves as a comprehensive tutorial for standardized and reproducible mixing of viscous materials with a novel open source automation technology. Detailed instructions are provided on the operation of a newly developed open source workstation, the usage of an open source protocol designer, and the validation and verification to identify reproducible mixtures.

Current mixing steps of viscous materials rely on repetitive and time-consuming tasks which are performed mainly manually in a low throughput mode. These ...

Generation of Dynamical Environmental Conditions using a High-Throughput Microfluidic Device

Mimicking in vivo environmental conditions is crucial for in vitro studies on complex life machinery. However, current techniques targeting live cells and organs are either highly expensive, like robotics, or lack nanoliter volume and millisecond time accuracy in liquid manipulation. We herein present the design and fabrication of a microfluidic system, which consists of 1,500 culture units, an array of enhanced peristaltic pumps and an on-site mixing modulus. To demonstrate the capacities of the microfluidic device, neural stem cell (NSC) spheres are maintained in the proposed system. We observed that when the NSC sphere is exposed to CXCL in day 1 and EGF in day 2, the round-shaped conformation is well maintained. Variation in the input order of 6 drugs causes morphological changes to the NSC sphere and the expression level representative marker for NSC stemness (i.e., Hes5 and Dcx). These results indicate that dynamic and complex environmental conditions have great effects on NSC differentiation and self-renewal, and the proposed microfluidic device is a suitable platform for high throughput studies on the complex life machinery.

We present a microfluidic system for high throughput studies on complex life machinery, which consists of 1500 culture units, an array of enhanced peristaltic pumps and an on-site mixing modulus. The microfluidic chip allows for the analysis of the highly complex and dynamic micro-environmental conditions in vivo.

Mimicking in vivo environmental conditions is crucial for in vitro studies on complex life machinery. However, current techniques targeting live cells and ...