We would like to thank Stacey Martina of the NanoLab TuE for help with HMDS vapour deposition. This research was funded by the Institute for Complex Molecular Systems (ICMS) at TU/e and by the Netherlands Organization for Scientific Research (NWO) Gravitation programme IMAGINE! (project number 24.005.009).

1. Soft lithography
NOTE: The microfluidic device is composed of two layers, flow layer and control layer (Figure 1A), and each layer is molded from individually patterned wafers using a positive and negative photoresist respectively (Refer to Table of Materials for details of photoresist and developers).
<ol>
	<li>Perform wafer fabrication for the flow layer as described below.
	<ol>
		<li>Dehydrate a silicon wafer (100 mm diameter, &#60;1-0-0&#62; oriented, 525) overnight (12-16 h) at 250 &#176;C.</li>
		<li>Allow the wafer to cool before proceeding to spin-coating. Apply 3-4 mL of the positive photoresist to the center of the wafer.</li>
		<li>Spin for 40 s at 1400 rpm (344 rpm/s) to obtain a feature height of 45 &#181;m.</li>
		<li>Soft bake on a hotplate using a temperature ramp, increasing at the rate of 450 &#176;C /h, from 35 &#176;C to 105 &#176;C. This step can also be carried out on microfiber tissues to prevent direct contact and minimize the bubbling of the photoresist. Remove the wafer from the hotplate and allow it to cool on microfiber tissues.</li>
		<li>Place the photomask (commercially produced) corresponding to the flow layer (emulsion side down) onto the resist-coated silicon wafer and expose it under a UV lamp, at 10&#160;mW/cm2, until a total exposure of 200 mJ/cm2 is reached.</li>
		<li>Use two hotplates - one at 65 &#176;C and the other at 95 &#176;C - to perform a post-exposure bake - for 1 min and 7 min respectively - on the plates.</li>
		<li>Develop the wafer by transferring it to a Petri dish filled with developer for positive photoresist. Agitate the Petri dish by shaking it on a benchtop shaker with the wafer completely submerged and refresh the developer solution periodically until the wafer is completely developed, and the features can be clearly seen.</li>
		<li>Use demineralized water to rinse off residual resist from the wafer and check under a stereo microscope for any residues inside the channels. Remove residues by returning the wafer to the developer solution or carefully adding the developer to the wafer with a micropipette. Once completed, dry the wafer using a nitrogen spray gun.</li>
		<li>Reflow the wafer by placing it on a hotplate set to 110 &#176;C for 25 min. This process results in rounded features.</li>
		<li>Proceed to silanization of the wafer as detailed in step 1.3. 
		&#8203;NOTE: Hexamethyldisilazane (HMDS) vapor deposition can also be carried out on the silicon wafers prior to application of the resist to improve adhesion between the resist and the wafer.</li>
	</ol>
	</li>
	<li>Perform Wafer fabrication for the control layer as described below.
	<ol>
		<li>Take another silicon wafer and dehydrate by placing it on a hotplate set at 110 &#176;C for 15 min.</li>
		<li>Remove the wafer and allow it to cool to room temperature before proceeding with spin coating.</li>
		<li>Apply 5 mL of the negative photoresist to the center of the wafer.</li>
		<li>Use the following spin protocol to obtain a feature height of 40 &#181;m: 5 s at 500 rpm (100 rpm/s acceleration), 33 s at 1400 rpm (300 rpm/s), and finally decelerate to 0 rpm for 5 s at 300 rpm/s.</li>
		<li>Soft bake using two separate hotplates set to 65 &#176;C and 95 &#176;C for 1 min and 15 min respectively. Remove the wafer from the hotplate and allow it to cool on microfiber tissues.</li>
		<li>Place the photomask (commercially produced) corresponding to the control layer (emulsion side down) onto the resist-coated wafer and expose the wafer under a UV lamp, set at 15&#160;mW/cm2, until a total exposure of 250 mJ/cm2 is reached.</li>
		<li>Use two hotplates - one at 65 &#176;C and the other at 95 &#176;C - and perform a post-exposure bake of the wafer for 2 min and then 5 min respectively. Remove the wafer from the hotplate and allow it to cool on microfiber tissues.</li>
		<li>Develop the wafer by transferring it to a Petri dish filled with developer for negative photoresist for 4 min. Refresh the developer and continue the process for 4 min more.</li>
		<li>Rinse the wafer with isopropanol to remove residual photoresist and use a stereo microscope to check the wafer for any residue inside the channels.</li>
		<li>Remove residues by returning the wafer to the developer solution or carefully adding the developer to the wafer with a micropipette. Once completed, dry the wafer using a nitrogen spray gun.</li>
		<li>Once fully developed, hard bake the photoresist by placing the wafer on a hotplate set at 95 &#176;C for 10 min.</li>
		<li>Proceed to silanization as detailed in step 1.3.</li>
	</ol>
	</li>
	<li>Carry out silanization as described below.
	<ol>
		<li>Place the wafer in a desiccator. Place a glass bottle in the desiccator and add 4-5 drops of 1,1,3,3 tetramethyldisiloxane. 
		CAUTION: 1,1,3,3 tetramethyldisiloxane is not toxic but is flammable. Other silanes can be used, but they might be toxic. It is recommended to carry out silanization in a fume hood while wearing necessary Personal Protective Equipment (PPE) such as lab coat, glasses, and nitrile gloves.</li>
		<li>Pull the vacuum for 15 min and seal the desiccator for 12-16 h to allow the silane to deposit on the wafer.</li>
		<li>Open the desiccator and dispose of the glass bottle. Place the wafer in a clean Petri dish.</li>
	</ol>
	</li>
	<li>Perform microfluidic device fabrication as described below. 
	NOTE: The following protocol has been adapted from previous works23.
	<ol>
		<li>Prepare two separate PDMS solutions - one for the flow layer and one for the control layer. For each solution, mix the base agent and curing agent of the PDMS kit in a beaker and stir using a mixing rod. The control layer requires 10 g of base agent and 0.5 g of curing agent (20:1 ratio) while the flow layer requires 40 g of the base agent and 8 g of the curing agent (5:1 ratio).</li>
		<li>Degas the PDMS solutions in a desiccator until the solutions are gas-free.</li>
		<li>Place the silanized flow layer wafer in a Petri dish covered with foil and pour the corresponding PDMS solution over the wafer. Place the Petri dish back in the desiccator and pull the vacuum to degas further (for approximately 20 min).</li>
		<li>Spin coat the silanized control layer wafer with its corresponding PDMS solution. Pour 3-4 mL of the solution onto the center of the wafer and spin for 20 s at 1500 rpm at 408 rpm/s. Place the wafer on a level surface in a closed Petri dish for 20 mins.</li>
		<li>Place both the flow and control layers in an oven at 80 &#176;C for 18-20 min. Periodically monitor the two layers to check if they are cured. The layers are ready when they are tough enough to be malleable yet slightly sticky, as this improves the bonding between the two layers.</li>
		<li>Cut out the PDMS around each of the devices on the flow layer wafer with a scalpel. Make sure to not cut too close to the features and leave approximately 2 cm of space between the feature and the edges of the PDMS. Once detached from the silicon wafer, cover the PDMS block with tape on the feature side to avoid any dust contamination.</li>
		<li>Once all PDMS blocks have been cut out, place them one by one on the corresponding control layer wafer performing a rough alignment by eye.</li>
		<li>After all the blocks have been placed on their corresponding areas on the control layer, adjust the position of each of the blocks such that the control valves overlap over the corresponding flow channels to complete the alignment. This can also be carried out with the help of a stereo microscope.</li>
		<li>Remove air pockets between the two layers by applying pressure. If the air pocket is on or near a feature, take care to not collapse the channels while applying pressure.</li>
		<li>Place the devices in the 80 &#176;C oven and leave them to bond for 12-16 h. Place 100 g weights on each of the devices to improve the bonding between the two layers.</li>
		<li>Take the wafer out and cut out each individual device. Peel the devices off the control layer wafer and cover the feature side with tape.</li>
		<li>Place each individual device on a cutting mat with the feature side facing upwards and punch a hole for each of the eight flow layer inlets, eight control layer channel inlets, the oil inlets, and the outlet using a 0.75 mm biopsy punch with the feature side facing upwards.</li>
		<li>Load the plasma asher with a microscope slide and a single device with the tape removed and the feature side facing upwards. Perform the oxygen plasma ashing with a power of 30 W for a duration of 20 s.</li>
		<li>Take the device and the glass slide out as soon as the ashing is complete and place the device with the feature side downwards onto the slide. The adhesion between PDMS and glass should be immediately visible to the naked eye. Apply pressure to any regions with air pockets to squeeze the air out.</li>
		<li>Place the devices on a hotplate set to 110 &#176;C for 60 min with a weight on top to improve the bonding of the PDMS to the glass.</li>
	</ol>
	</li>
</ol>
2. Hardware setup
NOTE: A schematic of the connections to the microfluidic device is shown in Figure 1B and a realization of such a scheme using the necessary hardware is shown in Figure 2.
<ol>
	<li>Set up the Pneumatic valves as described below. 
	NOTE: Each control channel, which regulates a PDMS valve on the chip is in turn controlled by a single solenoid valve. The prototype presented here consists of eight control channels (Figure 1A), and hence eight solenoid valves are required.
	<ol>
		<li>The solenoid valves are controlled using a custom LabVIEW software program (Main Interface Program; Figure 3 and Supplementary File 1, Supplementary File 2, Supplementary File 3, Supplementary File 4). This program sends MODBUS commands via a TCP connection (Supplementary File 5, Supplementary File 6), to a WAGO controller. Connect the WAGO device to the computer with the LabVIEW program using an ethernet cable. Proceed to connect the solenoid valves sequentially to the ports on the WAGO controller. For a more detailed description, please refer to previously described protocols23.</li>
		<li>Connect the solenoid valve array to a compressed air source using 1/4 in tubing and set the pressure of the valve array to 3.5 bar. In this system, the eight valves marked 9-16 were used.</li>
	</ol>
	</li>
	<li>Set up pressure regulators&#160;as described below. 
	NOTE: A commercially available pressure pump is used to control fluid flow (Figure 2). An eight-port and a four-port pump set were used to accommodate eight aqueous inlets and two oil inlets in the device. The pressure of each port is regulated via software that is provided by the manufacturers.
	<ol>
		<li>Connect the pressure pump to a compressed air source ensuring that the supplied pressure does not exceed the maximum pressure permitted by the pump (2.2 bar for both the eight-port and the four-port controllers).</li>
		<li>Connect the pressure pumps to a computer using a USB-connector.</li>
		<li>Once the pumps are switched on, they should be visible in the corresponding software. Set the pressures to zero while setting up the pumps.</li>
		<li>Connect a male luer to 3/32 in barb connector to each of the 12 female luer lock output ports on the controllers.</li>
		<li>Connect a piece of soft tubing (OD: 3 mm, ID: 1 mm, L: 15 cm) to the barb. Connect another male luer to 3/32 in barb connector to the other end of the soft tubing.</li>
		<li>Connect a luer stub (23 G, 0.5 in) to the barb connector. At this point, the pressure regulator is set up and ready to be used.</li>
	</ol>
	</li>
</ol>
3. Microfluidic device setup
<ol>
	<li>Connect the control channel tubing as described below (Figure 2).
	<ol>
		<li>For each control channel, cut a length of PolyTetraFluoroEthylene (PTFE) tubing (OD: 0.042 in, ID: 0.022 in). Insert the pin of a 23 G, 0.5&#160;in luer stub at one end.</li>
		<li>Connect the luer stub to a male luer to&#160;3/32 in barb nylon connector. Insert the barb of the connector into a length of polyurethane tubing (OD: 4 mm, ID: 2.5 mm). Connect the other end of the polyurethane tubing directly to a solenoid valve.</li>
		<li>Fill a syringe with water and connect a 23 G, 0.5 in luer stub at the end.</li>
		<li>Connect the free end of the PTFE tubing to this syringe and inject water until approximately halfway through the tubing.</li>
		<li>Disconnect the tubing from the syringe and insert the free end of the tubing into a punched hole of the corresponding control channel (Figure 1A-C1-8). Repeat until each control channel has been connected to its corresponding solenoid valve. 
		NOTE: In this paper, the solenoid valves 9-16 were connected to the control channels corresponding to C1 to C8, respectively. While these can be connected in any manner, it is important to remember the order and sequence of the connections, especially while operating the Main Interface program.</li>
		<li>Use the Main Interface program (Figure 3) to open all the solenoid valves (Pressurize all control channels). This will push the fluid from the tubing into the control channels of the microfluidic device and thereby filling it up. An example of pressurized and depressurized valves is shown in Figure 4.</li>
	</ol>
	</li>
	<li>Connect reagents and prime the device as described below.
	<ol>
		<li>Ensure that all control channels are pressurized by pressing the Pressurize all Control Channels button in the Main Interface program (Figure 3).</li>
		<li>For each of the aqueous reagents, cut a segment of PTFE tubing (OD: 0.042 in, ID: 0.022 in) long enough to connect the pumps to the inlets of the microfluidic device inlets. Connect one of the tubing to the luer stub from step 2.2.6.</li>
		<li>Fill a syringe with the required reagent and connect a 23 G, 0.5 in luer stub at the end.</li>
		<li>Inject the reagent into the corresponding PTFE tubing until the tubing is full. Take care that the reagent does not enter the output port on the pump set.</li>
		<li>Insert the free end of the tubing into a corresponding inlet in the microfluidic chip.</li>
		<li>Apply a pressure of 400 mbar to each of the inlet aqueous reagents using the software provided.</li>
		<li>Sequentially depressurize the control channels individually using the Main Interface program (Figure 3) to ensure that all the reagents have reached the T-junction of the device. Actuate individual valves , if needed, by pressing the corresponding buttons on the program in the box Control Channels Manual Pressurization.</li>
		<li>Repeat steps 3.2.3 to 3.2.5 for the oil reagents. Apply a pressure of 400 mbar to each of the inlet oil reagents.</li>
		<li>Simultaneously depressurize all the control channels by pressing Depressurize All Control Channels (Figure 3) until all the air has been removed from the device. This is observable by the naked eye or under a microscope.</li>
		<li>Pressurize all the control channels by pressing Pressurize All Control Channels button (Figure 3). At this stage, all reagents have been connected and the device is primed and ready to use.</li>
	</ol>
	</li>
	<li>Program and execute the experiment as described below.
	<ol>
		<li>Encode the composition, sequence, and replicates of each plug population to be produced in a .csv file as shown in Supplementary File 7 which serves as the input for the Automatic Experiment in the Main Interface program (Figure 3). Mark the necessary control channels with a 0 if its corresponding to an inlet needs to be open and a 1 if it needs to be closed. Each row in the .csv file corresponds to one distinct plug population.</li>
		<li>Load the .csv on to the Main Interface program by clicking on the Folder button in the Experiment File tab.</li>
		<li>Enter the relevant fields in the program such as Iterations of experiment (to determine how many times the given sequence of plugs are produced), Time of depressurization (to determine how long the inlet channels need to be open and the corresponding control channel needs to be depressurized in milliseconds), Time of pressurization (to determine how long the inlets need to be closed between sequences of plug population in milliseconds).</li>
		<li>Select the inlet channel(s) corresponding to barcode production in the Barcode Inlets (up to 3 channels) section along with the duration for which they need to be open (Time for Barcoding (ms)). Alternatively, these barcodes can also be hardcoded into the input .csv file as shown in Supplementary File 7.</li>
		<li>Reduce the pressure of the inlet oil reagents to 200 mbar.</li>
		<li>Connect a PTFE tubing (OD: 0.042 in, ID: 0.022 in) of the desired length at the outlet to collect the plugs. In order to ensure uniform plug production, use tubing of approximately 100 cm prefilled with plugs for collection. This is to neutralize the difference in pressure at the outlet which is exerted by the collection of plugs in the tubing.</li>
		<li>Press Run Experiment to start the program and plug production.</li>
	</ol>
	</li>
	<li>Perform data recording and analysis as described below (see Figure 5). 
	NOTE: This section specifically outlines a method for analyzing fluorescent plugs. Depending on the nature of the plugs generated, this section can be altered as required.
	<ol>
		<li>Fill a syringe with oil (either mineral oil or fluorinated oil) and connect a 23 G 0.5 in luer stub at the end. Fasten the syringe to a pump.</li>
		<li>Connect one of the ends of the filled collection tubing to the luer stub on the syringe. Affix the other end of the filled collection tubing above the objective lens of a microscope.</li>
		<li>Place a waste reservoir below the end of the tubing near the objective.</li>
		<li>Focus the microscope on a given region of the tubing and set it to record fluorescence in the desired channel(s).</li>
		<li>Set the pump to a flow rate of 50 &#181;L/min.</li>
		<li>Record the video of the fluorescent channel as an .avi file.</li>
		<li>Analyze the .avi file using the provided python script (Supplementary File 8) to extract the average fluorescence in a predefined region of interest (ROI) per frame of the .avi file (an example of which is given in Supplementary File 9).</li>
		<li>Use the provided customized R script (Supplementary File 10) to extract the conditions and plot the raw data and the peak heights. 
		NOTE: The R script in Supplementary File 10 was used for analysis in this paper. The custom-made R functions used in this script to cut data, detect conditions using barcodes, and analyze the peak heights for individual plugs and plotting are provided in Supplementary File 11.</li>
	</ol>
	</li>
</ol>

Setup of a Microfluidic Device for Combinatorial Plug  Production

F. E. is a freelancer for TheraMe! AG. The authors declare they have no competing financial interests.

In this paper, a set of protocols for the fabrication and operation of a PDMS-based microfluidic device for the automated generation of combinatorial libraries in water-in-oil compartments called plugs has been presented. The combination of microfluidics with droplet technology provides a powerful technique to encapsulate small quantity of reagents in a large number of compartments, therefore opening avenues for large-scale combinatorial screening.
Previously, several technologies have been described to generate chemically distinct compartments using microfluidics, each with its advantages and limitations. Kulesa et al.50, described a strategy to encapsulate cells with barcodes in droplets using microtiter plates and merging these droplets using an electric field to create a combinatorial library. While such an approach can generate a lot of combinations of droplets, it is limited by the need for manual handling steps in the workflow. Tomasi et al.51 developed a microfluidic platform to merge a spheroid (free floating cell aggregates)-containing droplet with a stimulus droplet, thereby allowing the manipulation of the spheroid microenvironment. This method allows for the study of important phenomena such as cell-cell interactions and the effect of drugs, but it is relatively low throughput. Eduati et al.46 and Utharala et al.47 developed a microfluidic valve-based platform that can generate high-throughput combinatorial libraries in an automated fashion. However, in these studies, the valves are operated using a Braille device, which necessitates cumbersome alignment steps between the microvalve and the microfluidic chip. A key feature of the system described in this paper is the implementation of pneumatic PDMS valves to regulate the flow of fluid in the input channels. Since these valves are PDMS-based, they can be incorporated rather smoothly into the fabrication steps of the microfluidic chip. Additionally, they are a relatively straightforward option to control the flow of liquids in the inlet channels, as they can be actuated by applying pressure through an external gas source. Finally, the duration and sequence of pressurization and depressurization of these valves can be programmed, thereby automating the production of distinct populations of plugs in a high-throughput manner. Another important feature is the use of constant pressure regimes for the injection of reagents through the inlet, which allows one to opt out of incorporating waste channels to relieve any pressure accumulation that arises in a constant flow rate regime. This simplifies the device design, reduces the need for additional valves and hardware to control the valves of the waste channel, and minimizes reagent wastage.
While the fabrication of devices with PDMS is relatively uncomplicated, the implementation of such devices does require the usage of extensive hardware paraphernalia such as the pneumatic solenoid valves (to control the actuation of the PDMS valves), pressure pumps (to control the flow of inlet and oil reagents) and software programs (to regulate the solenoid valves). While they represent a significant investment, such a setup provides consistency and reliability for the successful operation of the device. Additionally, the hardware components and architecture outlined in this protocol are set up in a modular way. Therefore, alternatives can be used for some modules to reduce costs or to adapt them to a specific need. For example, there exists a variety of pumps that can be used based on utility, budget, availability, and convenience52,53,54. Additional components such as fluid reservoirs and temperature regulators can be incorporated for sensitive inlet reagents23. Furthermore, this design can be scaled up or down to address specific scientific needs. For example, in this paper, an eight-inlet prototype is described which allows eight unique reagents to be combined to produce plugs. This can be upscaled to a 16-inlet device which allows for a higher number of inlets and larger combinations thereof. Consequently, it will need extra control channels and solenoid valves to address the inlets, but such a prototype allows larger and more diverse combinatorial libraries to be generated. Finally, in this paper, each plug population is produced by the opening of three out of the eight aqueous inlets of the microfluidic device. It was observed that for such a configuration, a pressure of approximately 200 mbar for the oil reagents and 400 mbar for the aqueous reagents corresponded to a regime of plug production, which is driven solely by valve actuation. When higher pressures were applied to the oil(s), a breakup of plugs was observed, and the application of lower pressures led to a fusion of plugs. The optimal pressure regime for plug production depends on a wide range of factors, such as the number of inlets contributing to the formation of a plug, the nature and viscosity of the fluids, and the dimensions of the channels, and should be optimized as and when necessary.
One of the drawbacks of operating in a constant-pressure regime is that fluids with different viscosities have different flow rates under constant pressure. Therefore, it needs to be ensured that the aqueous reagents flowing through the inlets are of comparable viscosities. The use of fluids of different viscosities will affect not only fluid flow in the inlet channels but also plug formation at the T-junction, thereby compromising the composition of the plug populations. Another drawback is the contamination of a plug population from residual reagents at the T-junction. When the device switches between the production of different plug populations, the first/last plug in the sequence of each population tends to be contaminated by the previous or the following population. This can be overcome by producing extra replicates of each population and discounting the contaminated plug during analysis. Finally, there is also the potential for variation between individual devices arising from inconsistencies in fabrication and/or external sources (pressure fluctuations). This issue can be mitigated by reusing a single microfluidic chip multiple times and ensuring that a complete run of a combinatorial library is performed on a single chip to minimize the effect of these inconsistencies.
The microfluidic device and the accompanying set of operational protocols presented in this paper have been used to demonstrate the production of a quantitative combinatorial library of plugs. This platform can, therefore, rapidly generate combinatorial libraries of distinct plug populations in a high-throughput manner. As a result, such technologies can be used for a variety of screening purposes including, but not limited to, combinatorial drug screening on patient biopsy samples - whereby a small number of cells retrieved from a biopsy can be distributed in a large number of droplets and treated with a large combination of the anti-cancer drug to optimize individual therapy for a given patient sample - and therefore accelerate personalized cancer therapy46,48,55.

Microfluidics allows for the manipulation of small amounts of fluids in microchannels1. The scale of operation of typical microfluidic devices is tens to hundreds of micrometers which allows the miniaturization of chemical and biological reactions, thereby enabling such reactions to be carried out with relatively small quantities of reagents. Initially, microfluidic devices were fabricated with materials such as silicon2 and glass3. Although they are still in use4, they pose certain issues, such as solvent compatibility, high cost of manufacture, and difficulties in integrating controls for fluid flow5,6. PDMS-based fabrication methodologies, termed soft-lithography, offer an inexpensive alternative for the rapid prototyping of devices7 and an avenue to fabricate complex multilayered devices8. The addition of valves and pumps to PDMS devices allows for the ability to control the routing and speed of fluids in devices9,10. Several methods to design and actuate microvalves in a reversible or irreversible manner have been developed - for example, bimetallic valves made from silicon and aluminum, which are thermally actuated11 or using gas generated from an electrochemical reaction to deflect a silicon nitride membrane12. Gu et al.&#160;demonstrate the use of the mechanical pins of a Braille display to apply pressure on microchannels to regulate flow13. One set of microvalves that has gained popularity is the pneumatic PDMS-based valves pioneered by the group of Stephen Quake14. Typically, such valves are composed of two orthogonal microchannels - a flow channel and a control channel. Upon pressurization of the control channel, a thin PDMS membrane deflects upon the flow channel, closing it off and thereby interrupting fluid flow. Once depressurized, the membrane relaxes, thereby opening the flow channel and allowing the resumption of fluid flow. PDMS valves thereby allow flow regulation in a robust and reversible manner since the control channel can be pressurized and depressurized multiple times15. Additionally, since such valves can be actuated by the application of pressure, they open up avenues for digital control and automation16. Furthermore, as they are of the same material, they can be integrated seamlessly into the fabrication of PDMS-based devices using soft-lithography techniques8,17,18. These features make PDMS valves an attractive choice for flow regulation in microfluidic devices. Thorsen et al. used the principle of such valves to design a fluidic multiplexer - a combinatory array of pneumatic valves - to address nearly a thousand input flow channels with twenty control channels19. This principle has been extended to selectively route fluids to in-chip microfluidic chemostats such that unique reactions can be carried out simultaneously in each reactor20,21,22,23. However, such microreactors, while useful in optimizing the usage of limited reagents, cannot parallelize multiple reactions and are not sufficient for high-throughput studies.
Droplet microfluidics is a subcategory of microfluidics that involves the production of droplets through the manipulation of immiscible, multiphasic liquid flow in microfluidic devices24. Droplet formation involves the breakup of a continuous fluid by the introduction of an immiscible fluid, resulting in a pinch-off due to instability in the interfacial energy and in the formation of an emulsion25. Surfactants aid in the formation of rounded droplets when emulsions leave the microchannel by stabilizing the interfacial energies26. Larger droplets, called plugs, are less stable and can be collected in a holding compartment (such as a length of tubing) as an array of aqueous compartments spaced on either side by one or more immiscible liquids27. In addition to miniaturization and compartmentalization, droplet microfluidics also offers increased throughput of biological reactions, as a large number of monodisperse droplets can be produced - each serving as a nanoreactor28. Droplets, once generated, can also be subjected to further manipulations, such as splitting29,30, fusion31,32, sorting33,34, and assemblage into higher order structures35,36. Droplet microfluidics has revolutionized several scientific fields and technologies - from PCR37 to single-cell transcriptomics38, from drug-discovery39,40 to virology41, from next-generation sequencing42 to chemical synthesis43.
Integration of PDMS-based soft-lithography and microvalves with droplet technology is a potent combination that allows for the regulation of fluid flow in microchannels and subsequent control over droplet contents. Depending on the opening and closing of channels, it is possible to produce distinct populations of droplets, each with a specific composition. Such a platform could miniaturize, compartmentalize, and parallelize biochemical reactions and therefore be a useful technique for combinatorial screening44. Combinatorial screening is a high-throughput method to generate tens of thousands of combinations of selected reagents to produce libraries which consist of individual populations of known composition. Combinatorial screening has been used to discover synergistic effects between drugs and antibiotics for bacterial growth inhibition45. In the field of cancer therapy, combinatorial screening has been used to test combinations of anti-cancer drugs for a given patient thereby advancing personalized therapy46,47. Mathur et al. have built on this technology by integrating a combinatorial DNA barcoding approach to assess transcriptome changes in high-throughput drug screening48. Thus, combinatorial screening is a powerful yet nascent technology, and there is a need for developing diverse microfluidic technologies to execute and facilitate such screening procedures.
The goal of this manuscript is to present a complete set of protocols for the fabrication of a bilayer microfluidic device capable of generating a combinatorial library of water-in-oil plugs and describe the hardware and software needed for the operation of such a device. The fluid flow is regulated using pressure-controlled PDMS-based pneumatic valves, which are in turn controlled by a custom LabVIEW program. Flow of reagents in the device is achieved using commercially available pressure pumps. An eight-inlet prototype is presented wherein a plug is formed by the contents of three inlets, each containing an aqueous reagent. The aqueous phase meets a continuous oil phase, and plugs are produced at a T-junction with a frequency of 0.33 Hz. The functioning of the system is demonstrated by producing a quantitative library containing three distinct populations of fluorescent plugs. This technology and set of protocols will help to expedite the production of combinatorial libraries for high-throughput screening purposes.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>1,1,3,3 tetramethyldisiloxane</td>
			<td>Merck Life Science NV</td>
			<td>MFCD00008256</td>
			<td></td>
		</tr>
		<tr>
			<td>4 channel digital input/output module</td>
			<td>WAGO Kontakttechnik GmbH</td>
			<td>750-504</td>
			<td></td>
		</tr>
		<tr>
			<td>Acetone</td>
			<td>Boom Labs</td>
			<td>BOOMSKEUZW3</td>
			<td></td>
		</tr>
		<tr>
			<td>Analysis Software</td>
			<td>Eindhoven University of Technology</td>
			<td>https://github.com/SysBioOncology/BilayerMicrofluidicsAnalysis_JoVE</td>
			<td></td>
		</tr>
		<tr>
			<td>AZ 40XT 11D</td>
			<td>Merck Life Science NV&#160;</td>
			<td>212299</td>
			<td>&#160;Positive photoresist&#160;</td>
		</tr>
		<tr>
			<td>AZ 726 MIF developer</td>
			<td>Merck Life Science NV</td>
			<td>10055824960</td>
			<td>Developer for positive photoresist</td>
		</tr>
		<tr>
			<td>Biopsy Punch, Rapid Core</td>
			<td>World Precision Instruments Germany, GMBH</td>
			<td>504529</td>
			<td>0.75 mm ID, W/Plunge</td>
		</tr>
		<tr>
			<td>Blue food dye</td>
			<td>PME</td>
			<td>FC1036</td>
			<td></td>
		</tr>
		<tr>
			<td>Controller end module&#160;</td>
			<td>WAGO Kontakttechnik GmbH&#160;</td>
			<td>750-600</td>
			<td></td>
		</tr>
		<tr>
			<td>Ethernet Controller&#160;</td>
			<td>WAGO Kontakttechnik GmbH&#160;</td>
			<td>750-881</td>
			<td></td>
		</tr>
		<tr>
			<td>FC-40</td>
			<td>Merck Millipore</td>
			<td>F9755-100ML</td>
			<td></td>
		</tr>
		<tr>
			<td>Fluigent flow unit</td>
			<td>Fluigent</td>
			<td>FLU-S-D</td>
			<td></td>
		</tr>
		<tr>
			<td>Fluigent pressure system&#160;</td>
			<td>Fluigent&#160;</td>
			<td>MFCS-EZ&#160;</td>
			<td>0 - 2 bar</td>
		</tr>
		<tr>
			<td>Fluorescein</td>
			<td>Merck Life Science NV</td>
			<td>MFCD00005050</td>
			<td></td>
		</tr>
		<tr>
			<td>Hot plate&#160;</td>
			<td>Torrey Pines Scientific&#160;</td>
			<td>HP61</td>
			<td></td>
		</tr>
		<tr>
			<td>Inverted microscope&#160;</td>
			<td>Nikon Instruments&#160;</td>
			<td>Eclipse Ti-E</td>
			<td></td>
		</tr>
		<tr>
			<td>Isopropanol</td>
			<td>Boom Labs</td>
			<td>BOOMSKEUZE3</td>
			<td></td>
		</tr>
		<tr>
			<td>LabVIEW (Software Version 20)</td>
			<td>Eindhoven University of Technology</td>
			<td>https://github.com/SysBioOncology/BilayerMicrofluidicsAnalysis_JoVE/tree/main/LabVIEW_8_inlet_device_ 
			VERSION_1</td>
			<td>All files have been saved for LabVIEW version 20. It is advised to use this version or higher to open the files.</td>
		</tr>
		<tr>
			<td>Luer stubs&#160;</td>
			<td>Instech Laboratories, Inc.&#160;</td>
			<td>LS23</td>
			<td>23 ga, 0.5&#34;</td>
		</tr>
		<tr>
			<td>Male Luer to barb connectors&#160;</td>
			<td>Cole Parmer&#160;</td>
			<td>45505-32&#160;</td>
			<td>3/32&#34; ID</td>
		</tr>
		<tr>
			<td>MasterFlex PTFE tubing</td>
			<td>Avator/VWR</td>
			<td>48634</td>
			<td></td>
		</tr>
		<tr>
			<td>Microscope Slides</td>
			<td>VWR</td>
			<td>470150-480</td>
			<td></td>
		</tr>
		<tr>
			<td>Microscope slides,&#160; Plain</td>
			<td>Corning</td>
			<td>2947-75X50</td>
			<td></td>
		</tr>
		<tr>
			<td>Mineral Oil</td>
			<td>Merck Millipore</td>
			<td>330760-1L</td>
			<td></td>
		</tr>
		<tr>
			<td>mr DEV 600</td>
			<td>Micro resist Technology</td>
			<td>R815100</td>
			<td>Developer for negative photoresist</td>
		</tr>
		<tr>
			<td>Oven</td>
			<td>Thermo Scientific</td>
			<td>&#160;Heraeus T6P 50045757</td>
			<td></td>
		</tr>
		<tr>
			<td>Oxygen plasma asher</td>
			<td>Quorum Technologies</td>
			<td>K1050X</td>
			<td></td>
		</tr>
		<tr>
			<td>Photomask</td>
			<td>CAD/Art Services, Inc.</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Photomask Design</td>
			<td>Eindhoven University of Technology (Adapted from Merten Lab, EPFL)</td>
			<td>https://github.com/SysBioOncology/BilayerMicrofluidicsAnalysis_JoVE/blob/main/8_inlet_JoVE_device_design.dwg</td>
			<td></td>
		</tr>
		<tr>
			<td>Pneumatic valve array</td>
			<td>FESTO</td>
			<td></td>
			<td>1x 8 valve array, Normally closed valves</td>
		</tr>
		<tr>
			<td>Silicon Wafers</td>
			<td>Silicon Materials</td>
			<td></td>
			<td>&#60;1-0-0&#62;, 100 mm diameter, 525 &#956;m thickness</td>
		</tr>
		<tr>
			<td>Single edge blades&#160;</td>
			<td>GEM Scientific</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Soft tubing</td>
			<td>Fluigent</td>
			<td></td>
			<td>1 mm ID, 3 mm OD</td>
		</tr>
		<tr>
			<td>Spin coater&#160;</td>
			<td>Laurell Technologies Corporation&#160;</td>
			<td>WS-650MZ-23NPPB</td>
			<td></td>
		</tr>
		<tr>
			<td>Stereo microscope&#160;</td>
			<td>Olympus Corporation&#160;</td>
			<td>SZ61</td>
			<td></td>
		</tr>
		<tr>
			<td>SU-8 3050</td>
			<td>Kayakli Advanced Materials</td>
			<td>Y311075 1000L1GL</td>
			<td>Negative photoresist</td>
		</tr>
		<tr>
			<td>Sylgard 184 Silicone Elastomer Kit (PDMS)</td>
			<td>Dow</td>
			<td>1317318</td>
			<td></td>
		</tr>
		<tr>
			<td>Syringe</td>
			<td>B Braun Injekt - F Fine Dosage Syringe</td>
			<td>10303002</td>
			<td></td>
		</tr>
		<tr>
			<td>UV-LED exposure system</td>
			<td>Idonus</td>
			<td>UV-EXP150S-SYS</td>
			<td></td>
		</tr>
		<tr>
			<td>Vacuum pump</td>
			<td>&#160;Vacuumbrand GmbH&#160;</td>
			<td>MD1C</td>
			<td></td>
		</tr>
		<tr>
			<td>Weighing scales&#160;</td>
			<td>Sartorius&#160;</td>
			<td>M-prove</td>
			<td></td>
		</tr>
	</tbody>
</table>

bilayer microfluidic device for combinatorial plug production

Droplet microfluidics is a versatile tool that allows the execution of a large number of reactions in chemically distinct nanoliter compartments. Such systems have been used to encapsulate a variety of biochemical reactions - from incubation of single cells to implementation of PCR reactions, from genomics to chemical synthesis. Coupling the microfluidic channels with regulatory valves allows control over their opening and closing, thereby enabling the rapid production of large-scale combinatorial libraries consisting of a population of droplets with unique compositions. In this paper, protocols for the fabrication and operation of a pressure-driven, PDMS-based bilayer microfluidic device that can be utilized to generate combinatorial libraries of water-in-oil emulsions called plugs are presented. By incorporating software programs and microfluidic hardware, the flow of desired fluids in the device can be controlled and manipulated to generate combinatorial plug libraries and to control the composition and quantity of constituent plug populations. These protocols will expedite the process of generating combinatorial screens, particularly to study drug response in cells from cancer patient biopsies.

Watch this Scientific Journal Video about Author Spotlight: Integrating Computational and Experimental Approaches in Precision Oncology at JoVE.com

Author Spotlight: Integrating Computational and Experimental Approaches in Precision Oncology

The fabrication of a polydimethylsiloxane (PDMS)-based bilayer device for the production of combinatorial libraries in water-in-oil emulsions (plugs) is presented here. The necessary hardware and software required to automate plug production are detailed in the protocol, and the production of a quantitative library of fluorescent plugs is also demonstrated.

Bilayer Microfluidic Device for Combinatorial Plug Production

Droplet microfluidics is a versatile tool that allows the execution of a large number of reactions in chemically distinct nanoliter compartments. Such ...

bilayer-microfluidic-device-for-combinatorial-plug-production

Universidad de Cartagena UDEC

Research

JoVE Journal

Bioengineering

750 Views.  Eindhoven University of Technology. The fabrication of a polydimethylsiloxane (PDMS)-based bilayer device for the production of combinatorial libraries in water-in-oil emulsions (plugs) is presented here. The necessary hardware and software required to automate plug production are detailed in the protocol, and the production of a quantitative library of fluorescent plugs is also demonstrated. 

Video: Author Spotlight: Integrating Computational and Experimental Approaches in Precision Oncology

Microfluidic Device for Recreating a Tumor Microenvironment in Vitro

We have developed a microfluidic device that mimics the delivery and systemic clearance of drugs to heterogeneous three-dimensional tumor tissues in vitro. Nutrients delivered by vasculature fail to reach all parts of tumors, giving rise to heterogeneous microenvironments consisting of viable, quiescent and necrotic cell types. Many cancer drugs fail to effectively penetrate and treat all types of cells because of this heterogeneity. Monolayers of cancer cells do not mimic this heterogeneity, making it difficult to test cancer drugs with a suitable in vitro model. Our microfluidic devices were fabricated out of PDMS using soft lithography. Multicellular tumor spheroids, formed by the hanging drop method, were inserted and constrained into rectangular chambers on the device and maintained with continuous medium perfusion on one side. The rectangular shape of chambers on the device created linear gradients within tissue. Fluorescent stains were used to quantify the variability in apoptosis within tissue. Tumors on the device were treated with the fluorescent chemotherapeutic drug doxorubicin, time-lapse microscopy was used to monitor its diffusion into tissue, and the effective diffusion coefficient was estimated. The hanging drop method allowed quick formation of uniform spheroids from several cancer cell lines. The device enabled growth of spheroids for up to 3 days. Cells in proximity of flowing medium were minimally apoptotic and those far from the channel were more apoptotic, thereby accurately mimicking regions in tumors adjacent to blood vessels. The estimated value of the doxorubicin diffusion coefficient agreed with a previously reported value in human breast cancer. Because the penetration and retention of drugs in solid tumors affects their efficacy, we believe that this device is an important tool in understanding the behavior of drugs, and developing new cancer therapeutics.

Microfluidic Device for Recreating a Tumor Microenvironment in Vitro

We present the procedure for fabrication and operation of a microfluidic device that recreates heterogeneous tumor microenvironments in vitro. The variability in apoptosis within tumor tissue was quantified using fluorescent stains and the effective diffusion coefficient of the chemotherapeutic drug doxorubicin into tumor tissue was evaluated.

We have developed a microfluidic device that mimics the delivery and systemic clearance of drugs to heterogeneous three-dimensional tumor tissues in ...

A Microfluidic Device for Studying Multiple Distinct Strains

The study of cell responses to environmental changes poses many experimental challenges: cells need to be imaged under changing conditions, often in a comparative manner. Multiwell plates are routinely used to compare many different strains or cell lines, but allow limited control over the environment dynamics. Microfluidic devices, on the other hand, allow exquisite dynamic control over the surrounding conditions, but it is challenging to image and distinguish more than a few strains in them. Here we describe a method to easily and rapidly manufacture a microfluidic device capable of applying dynamically changing conditions to multiple distinct yeast strains in one channel. The device is designed and manufactured by simple means without the need for soft lithography. It is composed of a Y-shaped flow channel attached to a second layer harboring microwells. The strains are placed in separate microwells, and imaged under the exact same dynamic conditions. We demonstrate the use of the device for measuring protein localization responses to pulses of nutrient changes in different yeast strains.

We present a simple method to produce microfluidic devices capable of applying similar dynamic conditions to multiple distinct strains, without the need for a clean room or soft lithography.

The study of cell responses to environmental changes poses many experimental challenges: cells need to be imaged under changing conditions, often in a ...

Lipid Bilayer Vesicle Generation Using Microfluidic Jetting

Bottom-up synthetic biology presents a novel approach for investigating and reconstituting biochemical systems and, potentially, minimal organisms. This emerging field engages engineers, chemists, biologists, and physicists to design and assemble basic biological components into complex, functioning systems from the bottom up. Such bottom-up systems could lead to the development of artificial cells for fundamental biological inquiries and innovative therapies1,2. Giant unilamellar vesicles (GUVs) can serve as a model platform for synthetic biology due to their cell-like membrane structure and size. Microfluidic jetting, or microjetting, is a technique that allows for the generation of GUVs with controlled size, membrane composition, transmembrane protein incorporation, and encapsulation3. The basic principle of this method is the use of multiple, high-frequency fluid pulses generated by a piezo-actuated inkjet device to deform a suspended lipid bilayer into a GUV. The process is akin to blowing soap bubbles from a soap film. By varying the composition of the jetted solution, the composition of the encompassing solution, and/or the components included in the bilayer, researchers can apply this technique to create customized vesicles. This paper describes the procedure to generate simple vesicles from a droplet interface bilayer by microjetting.

Microfluidic jetting against a droplet interface lipid bilayer provides a reliable way to generate vesicles with control over membrane asymmetry, incorporation of transmembrane proteins, and encapsulation of material. This technique can be applied to study a variety of biological systems where compartmentalized biomolecules are desired.

Bottom-up synthetic biology presents a novel approach for investigating and reconstituting biochemical systems and, potentially, minimal organisms. This ...

Protocol for Biofilm Streamer Formation in a Microfluidic Device with Micro-pillars

Several bacterial species possess the ability to attach to surfaces and colonize them in the form of thin films called biofilms. Biofilms that grow in porous media are relevant to several industrial and environmental processes such as wastewater treatment and CO2 sequestration. We used Pseudomonas fluorescens, a Gram-negative aerobic bacterium, to investigate biofilm formation in a microfluidic device that mimics porous media. The microfluidic device consists of an array of micro-posts, which were fabricated using soft-lithography. Subsequently, biofilm formation in these devices with flow was investigated and we demonstrate the formation of filamentous biofilms known as streamers in our device. The detailed protocols for fabrication and assembly of microfluidic device are provided here along with the bacterial culture protocols. Detailed procedures for experimentation with the microfluidic device are also presented along with representative results.

Protocols for the study of biofilm formation in a microfluidic device that mimics porous media are discussed. The microfluidic device consists of an array of micro-pillars and biofilm formation by Pseudomonas fluorescens in this device is investigated.

Several bacterial species possess the ability to attach to surfaces and colonize them in the form of thin films called biofilms. Biofilms that grow in ...

Analyzing Mixing Inhomogeneity in a Microfluidic Device by Microscale Schlieren Technique

In this paper, we introduce the use of microscale schlieren technique to measure mixing inhomogeneity in a microfluidic device. The microscale schlieren system is constructed from a Hoffman modulation contrast microscope, which provides easy access to the rear focal plane of the objective lens, by removing the slit plate and replacing the modulator with a knife-edge. The working principle of microscale schlieren technique relies on detecting light deflection caused by variation of refractive index1-3. The deflected light either escapes or is obstructed by the knife-edge to produce a bright or a dark band, respectively. If the refractive index of the mixture varies linearly with its composition, the local change in light intensity in the image plane is proportional to the concentration gradient normal to the optical axis. The micro-schlieren image gives a two-dimensional projection of the disturbed light produced by three-dimensional inhomogeneity.
To accomplish quantitative analysis, we describe a calibration procedure that mixes two fluids in a T-microchannel. We carry out a numerical simulation to obtain the concentration gradient in the T-microchannel that correlates closely with the corresponding micro-schlieren image. By comparison, a relationship between the grayscale readouts of the micro-schlieren image and the concentration gradients presented in a microfluidic device is established. Using this relationship, we are able to analyze the mixing inhomogeneity from associate micro-schlieren image and demonstrate the capability of microscale schlieren technique with measurements in a microfluidic oscillator4. For optically transparent fluids, microscale schlieren technique is an attractive diagnostic tool to provide instantaneous full-field information that retains the three-dimensional features of the mixing process.

Herein, we describe a procedure that employs microscale schlieren technique to measure mixing inhomogeneity in a microfluidic device. Through calibration, distribution of concentration gradient can be derived from the micro-schlieren image.

In this paper, we introduce the use of microscale schlieren technique to measure mixing inhomogeneity in a microfluidic device. The microscale schlieren ...

Biomembrane Fabrication by the Solvent-assisted Lipid Bilayer (SALB) Method

In order to mimic cell membranes, the supported lipid bilayer (SLB) is an attractive platform which enables in vitro investigation of membrane-related processes while conferring biocompatibility and biofunctionality to solid substrates. The spontaneous adsorption and rupture of phospholipid vesicles is the most commonly used method to form SLBs. However, under physiological conditions, vesicle fusion (VF) is limited to only a subset of lipid compositions and solid supports. Here, we describe a one-step general procedure called the solvent-assisted lipid bilayer (SALB) formation method in order to form SLBs which does not require vesicles. The SALB method involves the deposition of lipid molecules onto a solid surface in the presence of water-miscible organic solvents (e.g., isopropanol) and subsequent solvent-exchange with aqueous buffer solution in order to trigger SLB formation. The continuous solvent exchange step enables application of the method in a flow-through configuration suitable for monitoring bilayer formation and subsequent alterations using a wide range of surface-sensitive biosensors. The SALB method can be used to fabricate SLBs on a wide range of hydrophilic solid surfaces, including those which are intractable to vesicle fusion. In addition, it enables fabrication of SLBs composed of lipid compositions which cannot be prepared using the vesicle fusion method. Herein, we compare results obtained with the SALB and conventional vesicle fusion methods on two illustrative hydrophilic surfaces, silicon dioxide and gold. To optimize the experimental conditions for preparation of high quality bilayers prepared via the SALB method, the effect of various parameters, including the type of organic solvent in the deposition step, the rate of solvent exchange, and the lipid concentration is discussed along with troubleshooting tips. Formation of supported membranes containing high fractions of cholesterol is also demonstrated with the SALB method, highlighting the technical capabilities of the SALB technique for a wide range of membrane configurations.

Biomembrane Fabrication by the Solvent-assisted Lipid Bilayer SALB Method

We present an experimental protocol to form a supported lipid bilayer on solid substrates without using lipid vesicles. We demonstrate a one-step method to form a lipid bilayer on silicon dioxide and gold as well as supported membranes with cholesterol-enriched domain for various biological applications.

In order to mimic cell membranes, the supported lipid bilayer (SLB) is an attractive platform which enables in vitro investigation of membrane-related ...

Fully Automated Centrifugal Microfluidic Device for Ultrasensitive Protein Detection from Whole Blood

Enzyme-linked immunosorbent assay (ELISA) is a promising method to detect small amount of proteins in biological samples. The devices providing a platform for reduced sample volume and assay time as well as full automation are required for potential use in point-of-care-diagnostics. Recently, we have demonstrated ultrasensitive detection of serum proteins, C-reactive protein (CRP) and cardiac troponin I (cTnI), utilizing a lab-on-a-disc composed of TiO2 nanofibrous (NF) mats. It showed a large dynamic range with femto molar (fM) detection sensitivity, from a small volume of whole blood in 30 min. The device consists of several components for blood separation, metering, mixing, and washing that are automated for improved sensitivity from low sample volumes. Here, in the video demonstration, we show the experimental protocols and know-how for the fabrication of NFs as well as the disc, their integration and the operation in the following order: processes for preparing TiO2 NF mat; transfer-printing of TiO2 NF mat onto the disc; surface modification for immune-reactions, disc assembly and operation; on-disc detection and representative results for immunoassay. Use of this device enables multiplexed analysis with minimal consumption of samples and reagents. Given the advantages, the device should find use in a wide variety of applications, and prove beneficial in facilitating the analysis of low abundant proteins.

This protocol demonstrates how to achieve femto molar detection sensitivity of proteins in 10 &#181;L of whole blood within 30 min. This can be achieved by using electrospun nanofibrous mats integrated in a lab-on-a-disc, which offers high surface area as well as effective mixing and washing for enhanced signal-to-noise ratio.

Enzyme-linked immunosorbent assay (ELISA) is a promising method to detect small amount of proteins in biological samples. The devices providing a platform ...

Automated Lipid Bilayer Membrane Formation Using a Polydimethylsiloxane Thin Film

An artificial lipid bilayer, or black lipid membrane (BLM), is a powerful tool for studying ion channels and protein interactions, as well as for biosensor applications. However, conventional BLM formation techniques have several drawbacks and they often require specific expertise and laborious processes. In particular, conventional BLMs suffer from low formation success rates and inconsistent membrane formation time. Here, we demonstrate a storable and transportable BLM formation system with controlled thinning-out time and enhanced BLM formation rate by replacing conventionally used films (polytetrafluoroethylene, polyoxymethylene, polystyrene) to polydimethylsiloxane (PDMS). In this experiment, a porous-structured polymer such as PDMS thin film is used. In addition, as opposed to conventionally used solvents with low viscosity, the use of squalene permitted a controlled thinning-out time via slow solvent absorption by PDMS, prolonging membrane lifetime. In addition, by using a mixture of squalene and hexadecane, the freezing point of the lipid solution was increased (~16 &#176;C), in addition, membrane precursors were produced that can be indefinitely stored and readily transported. These membrane precursors have reduced BLM formation time of &#60; 1 hr and achieved a BLM formation rate of ~80%. Moreover, ion channel experiments with gramicidin A demonstrated the feasibility of the membrane system.

We demonstrate a storable, transportable lipid bilayer formation system. A lipid bilayer membrane can be formed within 1 hr with over 80% success rate when a frozen membrane precursor is brought to ambient temperature. This system will reduce laborious processes and expertise associated with ion channels.

An artificial lipid bilayer, or black lipid membrane (BLM), is a powerful tool for studying ion channels and protein interactions, as well as for ...

Co-culture of Living Microbiome with Microengineered Human Intestinal Villi in a Gut-on-a-Chip Microfluidic Device

Here, we describe a protocol to perform long-term co-culture of multi-species human gut microbiome with microengineered intestinal villi in a human gut-on-a-chip microphysiological device. We recapitulate the intestinal lumen-capillary tissue interface in a microfluidic device, where physiological mechanical deformations and fluid shear flow are constantly applied to mimic peristalsis. In the lumen microchannel, human intestinal epithelial Caco-2 cells are cultured to form a &#39;germ-free&#39; villus epithelium and regenerate small intestinal villi. Pre-cultured microbial cells are inoculated into the lumen side to establish a host-microbe ecosystem. After microbial cells adhere to the apical surface of the villi, fluid flow and mechanical deformations are resumed to produce a steady-state microenvironment in which fresh culture medium is constantly supplied and unbound bacteria (as well as bacterial wastes) are continuously removed. After extended co-culture from days to weeks, multiple microcolonies are found to be randomly located between the villi, and both microbial and epithelial cells remain viable and functional for at least one week in culture. Our co-culture protocol can be adapted to provide a versatile platform for other host-microbiome ecosystems that can be found in various human organs, which may facilitate in vitro study of the role of human microbiome in orchestrating health and disease.

We describe an in vitro protocol to co-culture gut microbiome and intestinal villi for an extended period using a human gut-on-a-chip microphysiological system.

Here, we describe a protocol to perform long-term co-culture of multi-species human gut microbiome with microengineered intestinal villi in a human ...

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 ...

Bilayer Microfluidic Device for Combinatorial Plug Production

Summary

Explore More Videos

Chapters in this video

Microfluidic Device for Recreating a Tumor Microenvironment in Vitro

A Microfluidic Device for Studying Multiple Distinct Strains

Lipid Bilayer Vesicle Generation Using Microfluidic Jetting

Protocol for Biofilm Streamer Formation in a Microfluidic Device with Micro-pillars

Analyzing Mixing Inhomogeneity in a Microfluidic Device by Microscale Schlieren Technique

Biomembrane Fabrication by the Solvent-assisted Lipid Bilayer (SALB) Method

Fully Automated Centrifugal Microfluidic Device for Ultrasensitive Protein Detection from Whole Blood

Automated Lipid Bilayer Membrane Formation Using a Polydimethylsiloxane Thin Film

Co-culture of Living Microbiome with Microengineered Human Intestinal Villi in a Gut-on-a-Chip Microfluidic Device

Multi-step Variable Height Photolithography for Valved Multilayer Microfluidic Devices