High-Throughput Bioprinting Method for Modeling Vascular Permeability in Standard Six-well Plates with Size and Pattern Flexibility

Summary

We present a protocol for high-throughput production of vascular channels with flexible sizes and desired patterns on a standard six-well plate using 3D bioprinting technology, referred to as vessels-on-a-plate (VOP). This platform has the potential to advance the development of therapeutics for the disorders associated with compromised endothelium.

Abstract

Vascular permeability is a key factor in developing therapies for disorders associated with compromised endothelium, such as endothelial dysfunction in coronary arteries and impaired function of the blood-brain barrier. Existing fabrication techniques do not adequately replicate the geometrical variation in vascular networks in the human body, which substantially influences disease progression; moreover, these techniques often involve multi-step fabrication procedures that hinder the high-throughput production necessary for pharmacological testing. This paper presents a bioprinting protocol for creating multiple vascular tissues with desired patterns and sizes directly on standard six-well plates, overcoming existing resolution and productivity challenges in bioprinting technology. A simplified fabrication approach was established to construct six hollow, perfusable channels within a hydrogel, which were subsequently lined with human umbilical vein endothelial cells to form a functional and mature endothelium. The computer-controlled nature of 3D bioprinting ensures high reproducibility and requires fewer manual fabrication steps than traditional methods. This highlights VOP's potential as an efficient high-throughput platform for modeling vascular permeability and advancing drug discovery.

Introduction

The vascular network throughout the human body functions as a crucial transport barrier by dynamically regulating the exchange of molecules and cells between the blood and surrounding tissues. This regulation is essential for preventing tissue edema and enabling selective nutrient and cell exchange, thus supporting tissue metabolism and homeostasis¹. Altered endothelial permeability, a factor in many health conditions, affects both disease severity and treatment efficacy². Vascular endothelium acts as a selective barrier, facilitating the transfer between vessels, tissues, and organs. This regulation involves several mechanisms, such as the basic filtering of solutes and small molecules, intentional disruption of the vascular barrier, and the influence of molecules such as prostaglandins and growth factors on permeability levels³.

Key factors in this regulation include endothelial cell junctions, the migration of leukocytes, and the functionality of the blood-brain barrier⁴. Given its complexity, the process varies across different environments, involving various blood vessel types and utilizing distinct anatomical pathways. Comprehending the biological underpinnings of vascular permeability is crucial for devising therapeutic approaches to treat conditions associated with abnormal vascular permeability. Maintaining vascular permeability is crucial for the health of the vascular system and surrounding tissues; consequently, impairment of this function leads to endothelial dysfunction, a state in which the endothelium loses its normal functionality.

Endothelial dysfunction is a precursor to several prevalent human diseases, including hypertension, coronary artery disease, diabetes, and cancer^5,6,7. This condition can present in several ways, including decreased vasodilation, increased vessel permeability, and a tendency toward a pro-inflammatory state. This pathological state is the earliest stage of several critical cardiovascular issues, such as coronary artery disease, stroke, and peripheral artery disease⁸, which continue to be the leading causes of mortality in the United States¹. Endothelial dysfunction affects cardiovascular health as well as the blood-brain barrier (BBB) and plays a major role in the progression of various neurological disorders. Dysfunction can increase BBB permeability, thus allowing toxins, pathogens, and immune cells to infiltrate into the central nervous system and contributing to neurological disorders such as stroke, Alzheimer's disease, multiple sclerosis, and brain infections⁹.

Endothelial dysfunction in diabetes is marked by the compromised ability of the endothelium to regulate vascular tone and produce vasodilator mediators, such as nitric oxide, leading to impaired vasodilation¹⁰. This condition is exacerbated by hyperglycemia-induced pathways such as protein kinase C activation and oxidative stress, contributing significantly to the progression of diabetic vascular disease¹¹. Moreover, an inflammatory environment has been found to enhance tumor cell adhesion to brain microvascular endothelial cells while a leaky endothelium has been reported to be a major factor in cancer metastasis^12,13. The geometry of blood vessels has been found to directly influence brain cancer metastasis. Tumor cells preferentially attach to areas of greater blood vessel curvature⁷. This finding underscores the importance of vascular geometry in cancer metastasis. More importantly, in conditions such as fibrosis and cancer, disrupted endothelial barrier function not only plays a role in disease development but also hinders treatment effectiveness by hindering adequate drug delivery¹⁴. Research on vascular permeability is crucial for advancing cardiovascular disease treatment and offering insights into managing other diseases involving compromised vascular function.

Given the crucial role of vascular permeability in health and disease, considerable research has focused on examining the selective nature of the endothelial barrier for therapeutic development by using animal models, alongside traditional 2D and 3D in vitro testing platforms. However, animal models have limitations because of species-specific differences and ethical issues, as well as high costs^15,16. For instance, Pfizer, in 2004, stated that over the previous 10 years, it had spent over $2 billion on drug developments that showed promising effects in animal models but eventually failed in advanced human testing stages¹⁷. Moreover, traditional 2D models do not accurately mimic the three-dimensional (3D) architecture and the complex geometric structure of vascular channels.

With advancements in biofabrication technologies, extensive efforts have been aimed at fabricating vascular channels while recapitulating 3D architecture. Microscale vascular channels can be effectively fabricated within microfluidic chips by using soft lithography, thus offering an advantage of real-time analysis^18,19. Alternative methods, such as hydrogel casting or wrapping cell sheets around a mold or mandrel, can be used to create freestanding tubular structures with the desired diameter^20,21. However, these methods have limitations; for example, microfluidic chips are restricted to microchannel configurations, and hydrogel casting around a mold does not effectively replicate multiple geometries.

With the emergence of 3D bioprinting technology²², replicating complex geometries by precisely depositing various extracellular matrix (ECM)-based hydrogel materials has become possible^23,24. Some bioprinting methods, such as those using concentrically arranged nozzles, e.g., coaxial and triaxial^25,26, cannot create bifurcated tubes; however, complex structures can be achieved with sacrificial patterning methods²⁷. None of these bioprinting methods have been demonstrated to enable high-throughput in vitro modeling-a crucial requirement for pharmacological research in drug discovery. Herein, we present a method for efficiently fabricating endothelialized vascular channels with efficient control over dimensions.

We established a straightforward approach using commercially available six-well plates, combined with a sacrificial patterning method in which a bioprinter fabricates vascular channels of desired sizes and patterns within an ECM hydrogel. Human umbilical vein endothelial cells (HUVECs) were seeded to endothelialize these channels and evaluate the functionality of endothelium through a permeability assay. This design enables pumpless perfusion by creating media reservoirs on both sides of the channel and uses gravity-driven flow with the help of a commonly used 2D rocker to mimic the dynamic culture. This approach eliminates the need for peristaltic pumps and facilitates the scalability of this platform for high-throughput applications. The computer-controlled nature of 3D bioprinting technology also streamlines the fabrication process, thus decreasing the likelihood of errors during manufacturing. The VOP model shows promise as a valuable tool for pharmacological testing in drug discovery.

Protocol

1. Generation of G-code for the bioprinter

1. To generate and visualize the printing path, visit an online G-code simulation tool (e.g., NCviewer).
2. Click the New File icon on the interface to create a new G-code file.
3. Generate a printing path by manually writing the G-code commands for the sacrificial channel and the silicon chamber. Use the dimensions of a standard six-well plate as a reference for creating the geometry.
   NOTE: G-code used here is based on Computer Numerical Control (CNC) code. The functions of each command are provided in Supplemental Table S1. The six-well plate format was selected because of its compatibility with commercial microplate readers and microscopy setups and its ability to accommodate adequate volumes of media to support endothelium maturation, thereby minimizing the need for frequent media changes. This fabrication protocol can also be adapted for use with other standard well plates.
4. Once the G-code is completed, click the Save File icon on the interface to download the file with a .nc extension.
   NOTE: Any other available G-code generation algorithm can be used to generate the printing paths. The geometry of the vascular channel can be manipulated in this G-code.

2. Preparation of sacrificial and silicon chamber inks

NOTE: Sources for all materials used in this protocol are listed in the Table of Materials.

1. Combine two types of silicone polymers, SE1700 and polydimethylsiloxane (PDMS), in a 10:2 ratio. Add curing agent of each polymer in a ratio of 10:1, polymer to curing agent.
2. Use a planetary mixer to thoroughly mix and degas the polymer mixture at 2,000 rpm.
3. With a spatula, transfer the mixed silicone polymer into a 10 mL disposable syringe. Centrifuge the loaded syringe at 400 × g for 3 min at 5 °C to ensure uniform consistency and avoid bubbles during printing.
   NOTE: The chamber ink should be used within 2 h after the addition of the curing agents to ensure optimal printing quality. Store the syringe at 5 °C while preparing for printing. This process helps slow ink curing, which can otherwise alter the printing parameters.
4. Weigh Pluronic F-127 (PF127) to prepare a 40% (w/v) stock solution of PF127 in distilled water.
5. Mix the PF127 solution in a planetary mixer for 3 min at 400 × g to achieve homogeneity. Keep the homogenized mixture at 4 °C for complete dissolution of PF127.
6. Prepare a thrombin stock solution of 1,000 units/mL in Dulbecco's phosphate-buffered saline (DPBS).
   NOTE: Store thrombin stock solution in 100 µL aliquots to avoid repeated freeze-thaw cycles. The aliquots should be stored at -20 °C for no longer than 6 months.
7. Before printing, prepare sacrificial ink by mixing thrombin at a 1:10 dilution with PF127 to a final working concentration of 36% (w/v) for PF127 and 100 units/mL for thrombin. To prepare 1 mL of sacrificial ink, mix 100 µL of thrombin stock solution with 900 µL of PF127 stock solution.
   NOTE: When preparing the sacrificial ink for printing a single plate, a total volume of 1 mL is more than sufficient.

3. Fabrication process

1. Before starting the fabrication process, treat a six-well plate with oxygen (O₂) plasma at a strength of 100 watts for 1 min.
2. Follow the procedure outlined in section 2 to prepare both the sacrificial and silicon inks, ensuring that the inks are free of bubbles and homogeneously mixed for consistent printing. Carefully load the inks in the printhead of the bioprinter. Set the temperature of the bioprinter's head to 37 °C for the sacrificial ink and 5 °C for the silicon ink.
3. Attach a 22 G double-screw thread tapered nozzle to the silicon syringe. For the sacrificial ink, choose the nozzle size according to the desired channel diameter.
   NOTE: Here, we demonstrated three sizes of nozzles: 18 G, 20 G, and 22 G. Optimal printing parameters including printing pressure and printhead speed, are outlined in Table 1.
4. Load the desired G-code and press the servo ready function on the bioprinter's software interface for 3 s. Position the plate on the stage at the starting point of the G-code and click start to initiate the printing process.
   NOTE: Typically, fabrication of one plate containing six chambers requires approximately 1 h and 10 min. Step 3.4, involving the loading and execution of the G-code, is subject to variation depending on the specific bioprinter used. Ensure that sterile conditions are maintained while using the bioprinter to avoid contamination.
5. Place a lid over the plate and transfer the plate to a humidified CO₂ incubator at 37 °C for 72 h to cure the silicon chambers.
   NOTE: Although the silicon curing may occur at a slower rate inside the incubator, the plate must not be placed inside a dry oven.

4. Hydrogel preparation and channel embedding

1. Prepare a 50 mL conical tube containing 20 mL of 1x PBS. Place 0.01 g of lithium phenyl-2,4,6-trimethylbenzoylphosphinate (LAP) into the conical tube to make a 0.05% (w/v) LAP solution. Vortex it until the powder is completely dissolved.
   NOTE: Wrap the conical tube in foil to prevent exposure to light. Store the LAP stock solution at 4 °C.
2. Add 3 g of gelatin methacrylate (GelMA) and 0.2 g of fibrinogen to 20 mL of LAP solution to achieve a final concentration of 15% GelMA and 1% fibrinogen (referred to as GelFib). Place the mixture in a 37 °C water bath, and periodically vortex mix until the solution is fully dissolved.
3. After fabrication as outlined in Section 3, add 300 µL of prewarmed GelFib into each hydrogel chamber to embed the sacrificial pattern. Rapidly crosslink the GelMA with ultraviolet (UV) light at a wavelength of 405 nm with an intensity of 85 mW/cm² for 120 s. Repeat this procedure for all other wells.
   NOTE: Fibrinogen crosslinks rapidly upon contact with the sacrificial pattern containing thrombin. We recommend adding hydrogel and performing UV crosslinking individually for each well to avoid unwanted gelation of GelMA at room temperature. Additionally, sterile conditions should be maintained to prevent contamination during the UV curing process.
4. Add 1 mL of DPBS to each side of the vascular channel in each well, and keep the plate at 4 °C for 15 min to liquefy the PF127.
5. After 15 min, suction off the DPBS, and repeat step 4.5 3x for complete washing of PF127.
6. Before introducing cells into the channels, perfuse DMEM F12 containing 1% Matrigel for 30 min through the channels to enhance cell attachment.

5. HUVEC culture

1. Prewarm endothelial cell growth medium (ECGM) in a 37 °C water bath for 30 min.
2. Meanwhile, retrieve a vial of cryopreserved HUVECs from the nitrogen tank, gently loosen the vial's cap, and then retighten it to release nitrogen from the threads. Immediately thaw the cells by submerging the vial in a 37 °C water bath for 2 min, ensuring that a small amount of ice remains inside the vial. Rinse the vial with 70% ethanol to prevent contamination.
   NOTE: Wear safety goggles when retrieving cells from the nitrogen tank. The vial's cap must be kept above the water level during this process.
3. Prepare a 15 mL conical tube containing 5 mL of prewarmed ECGM. With a micropipette, carefully transfer the thawed cells from the vial into the conical tube. To ensure that no cells are left behind, add 1 mL of fresh prewarmed medium to the cryovial, rinse the inside, and transfer any remaining cells into the conical tube.
4. Centrifuge the conical tube at 200 × g for 3 min to obtain a cell pellet. Discard the supernatant, resuspend the cells in 10 mL of fresh medium, transfer the cells to a T75 flask, and place the flask inside a 37 °C humidified CO₂ incubator.
   NOTE: This step is important to remove dimethyl sulfoxide present in the freezing medium in the cryovial through centrifugation.
5. Refresh the medium every other day until cells reach 80-90% confluency.

6. Endothelialization of channels

1. Prewarm ECGM, DPBS, trypsin-neutralizing solution, and trypsin ethylenediaminetetraacetic acid (TE) in a 37 °C water bath for 30 min.
2. At 90% confluency, rinse the cells in a T75 flask with 10 mL of DPBS, add 1 mL of 0.25% TE to the flask, and incubate it for 3 min.
3. Gently tap the sides of the flask and add 5 mL of trypsin-neutralizing solution to neutralize the TE. Transfer the cells to a 15 mL conical tube. Use 5 mL of fresh ECGM to collect the remaining cells and add them to the conical tube.
4. Centrifuge the conical tube at 250 × g for 3 min to collect the cell pellet.
5. Discard the supernatant and resuspend the cell pellet in 1 mL of fresh ECGM. Count the cells with a hemocytometer and repeat Step 6.4 to obtain a cell pellet. Resuspend 3 million cells in 90 µL of fresh ECGM.
6. Before introducing the cell suspension into the channel, briefly vacuum suction the channel to clear the lumen.
   NOTE: Avoid prolonged suction of the channel to avoid damaging its integrity.
7. Gently load the channel with a cell suspension at a seeding density of 0.5 million cells per well. Use a micropipette to add ~15 µL of this suspension to fill the channel.
   NOTE: The seeding density may vary depending on the size of the channel. This density is optimized for a channel printed with a 20 G nozzle and an internal diameter of approximately 900 µm.
8. Place the plate flat inside the incubator for 2 h. Subsequently, invert the plate to 180°, maintaining it in a flat position for the following 2 h.
9. After 4 h, wash the channel with DPBS to remove non-adherent and dead cells. Add 2 mL of fresh ECGM to each well (1 mL to each side of the channel). Start the dynamic culture on a rocker at a 10° tilt angle and 5 rpm by positioning the plate on the rocker with the channels parallel to the direction of rocking. Refresh the growth medium every other day.
   NOTE: Dynamic culture enhances medium exchange between the reservoirs and channels and helps the cells proliferate overnight.

7. Endothelium maturation assessment

1. Prewarm ECGM and DPBS in a 37 °C water bath for 30 min and Cell Counting Kit-8 (CCK8) reagent at room temperature.
2. Make a working solution of CCK8 by mixing 100 µL of CCK8 reagent with 1 mL of fresh ECGM for each well. While working for a plate/6 channel, prepare 600 µL of CCK8 reagent by combining it with 6 mL of fresh ECGM.
3. Remove the growth medium by suction and rinse the channels with DPBS. Add 1 mL of CCK8 working solution to each well and allow the plate to remain flat inside the incubator for 30 min. Afterward, start the dynamic culture on a rocker as described in step 6.9, and continue this process for the next 3 h.
4. After 3 h, remove the contents from each well by tilting the plate to one side, and transfer them to a new six-well plate. Rinse the channels with DPBS and add fresh medium.
   NOTE: Cover the plate with aluminum foil until absorbance measurement. Maintain a consistent reagent volume across all wells to ensure uniform readings. While pipetting, carefully avoid introducing air bubbles, which can disrupt the accuracy of optical density readings.
5. After gently shaking the plate for 15 s to ensure an even mixing of the colors, use a microplate reader to measure the absorbance at 450 nm.
6. Repeat this procedure at predefined time intervals. Calculate the mean optical density for each time point and plot a growth curve in graphing software. This curve indicates the relative maturation of the endothelium over time.

8. Permeability assay

1. Remove the medium from one well of interest.
   NOTE: For the permeability assay, processing each well separately is recommended to prevent other channels from drying out, which might alter their vascular permeability.
2. Prepare 6 mL of 0.1 mg/mL solution of FITC-conjugated dextran by dissolving 70 kDa FITC dextran in DPBS.
   NOTE: Prepare a 20 mg/mL stock solution of FITC dextran by dissolving 100 mg of FITC dextran in 5 mL of DPBS. After gently vortexing the solution, aliquot 500 µL into 1.5 mL tubes to avoid repeated freeze-thaw cycles. These aliquots can be stored at -20 °C for a maximum of 6 months. Before conducting the assay, dilute the stock solution to a working concentration of 0.1 mg/mL.
3. Position the plate firmly on the microscope stage and adjust the objective's magnification in phase contrast mode to ensure clear visibility of the channel wall at the region of interest, along with the gel located nearby, within the field of view.
   NOTE: For effective permeability assessment, try to maximize the area of the gel surrounding the region of interest in the field of view; this aspect is key to accurate monitoring of dextran transport.
4. After focusing on the desired area, change from phase contrast to fluorescence mode. Under the image acquisition tab, add FITC into the widefield channel, and acquire an image before adding dextran solution, to calculate the background fluorescence intensity. Then, add 1 mL of FITC dextran working solution to one side of the channel and let the solution flow toward the other side of the well, driven by the hydrostatic pressure difference.
5. Acquire images at predetermined time intervals-more frequently for channels with high permeability and less frequently for those with lower permeability.

9. Fluorescence intensity measurement in ImageJ

1. In ImageJ image analysis software, measure the intensity at the initial time point (I_t1)_, the average intensity observed at the later time point (I_t2), and the intensity due to background noise (I_b), as outlined below. Use equation (1) to calculate the permeability coefficient (P_d). t₁ and t₂ refer to the initial and later time points of image acquisition.
           (1)
   1. Start ImageJ, and open the image acquired at the initial time point.
   2. Set the scale in ImageJ. Navigate to Analyze | Set Scale. Input the known scale and unit of measurement.
   3. Select the rectangle tool and draw a rectangle over the area of the gel where the fluorescence intensity measurement is required.
   4. Navigate to Analyze | Set Measurements and ensure that the Mean gray value is checked.
      NOTE: This option measures the average intensity within the selected area. Other parameters can be selected as needed for the given analysis.
   5. With the area still selected, navigate to Analyze | Measure or simply press M. Wait for a results window to open, showing the mean fluorescence intensity and any other parameters selected.
   6. Take three measurements and calculate the average fluorescence intensity value in a spreadsheet.
   7. Repeat this procedure for the images captured at the subsequent time point t₂, as well as those taken before the addition of the dextran solution for calculation of fluorescence intensity at the later time point, to determine the background fluorescence.

Results

The VOP platform, featuring flexibility in size and pattern, was fabricated with a multi-head bioprinting system. Channels, both hollow and capable of perfusion, were seeded with HUVECs to facilitate endothelialization and were subsequently assessed with a permeability assay (Figure 1A). To demonstrate the multiscale manufacturing capability of this method, we printed three distinct configurations: straight, bifurcated, and convoluted (Figure 1B). Through a stra...

Discussion

Taking advantage of the precision, automation, and computer-controlled nature of 3D bioprinting technology, we established a streamlined method for fabricating vascular channels in standard six-well plates, which were chosen for their compatibility with commercial microplate readers and microscope imaging setups. The plate's design can accommodate multi-size channels and a sufficient volume of media for the growth of larger channels while decreasing the necessary frequency of media changes. Future adaptations of this...

Materials

Name	Company	Catalog Number	Comments
10 mL Serological Pipette	SPL	SPL 91010
10 mL syringe	Shinchang Medical
15 mL conical tube	SPL	50015
3D Bioprinter	T&R Biofab	3DX-Printer
6-well plate	SPL	37206
Biological Safety Cabinets	CHC LAB	PCHC-777A2-04,
Brightfield Inverted Microscopes	Leica	DMi1
Cell Counting Kit (CCK8)	GlpBio	GK10001
Cell Counting Kit (CCK8)	GlpBio	GK10001
Cell Culture Flask 75T	SPL	70075
Corning Matrigel Growth Factor Reduced (GFR) Basement Membrane Matrix, LDEV-free, 10 mL	Corning	354230
Distilled water
DMEM/F12	Gibco	11320033
DMSO, Cell Culture Grade	Sigma aldrich	D2438
Dow-Corning, PDMS-Sylgard 184a Kit	DOW	DC-184
DOWSIL SE 1700 Clear W/C 1.1 KG Kit	DOW	2924404
D-PBS - 1x	Welgene	LB001-01
Endothelial Cell Growth Medium MV 2 (Ready to use)	Promocell	C-22022
Eppendorf Micro pipette(1000,200,100,20,10)	eppendorf
Ethyl Alcohol 99.9%	Duksan	D5
Excel	Microsoft
Fibrinogen from bovine plasma	Sigma Aldrich	F8630-1G
FITC Dextran 70 kDa	Sigma Aldrich	46945-100MG-F
Fluorescent beads (1.0 μm, green)	Sigma Aldrich	L1030-1ML
GelMA-powder (Gelatin methacrylate) 50 g	3D Materials	20JT29
Gibco, Recovery Cell Culture Freezing Medium, 50 mL	Gibco
HUVECs (Human Umbillical Vein Endothelial Cells)	Promocell
ImageJ software	NIH
Incubator	Thermo SCIENTIFIC	Forma STERI-CYCLE i160 CO2 Incubator
Invitrogen, Live/dead viability/cytotoxicity Kit (for mammalian cells)	Thermo Fisher	L3224
Lithium Phenyl (2,4,6-trimethylbenzoyl) phosphate powder	Tokoyo Chemical Industry CO.	85073-19-4
Marienfeld Superior, Counting chamber cover	Marienfeld Superior
Marienfeld Superior, Hemocytometer, cell counting chamber	Marienfeld Superior	HSU-0650030
Microcentrifuge	eppendorf	Centrifuge 5920 R
NCViewer.com
Nitrogen tank	WORTHINGTON INDUSTRIES	LS750
Omnicure UV Laser	EXCELITAS	SERIES 1500
Parafilm M	amcor	PM-996
Penicillin-Streptomycin Solution (100x)	GenDEPOT	CA005-010
Planetary Mixer	THINKY CORPORATION, japan	ARE-310
Plasma treatment machine	FEMTO SCIENCE	CUTE-1MPR
Pluronic F-127	Sigma aldrich	P2443-250G
Pre-made buffer, (P2007-1) 10x PBS	Biosesang	PR4007-100-00
Reagent storage cabinet	ZIO FILTER TECH	SC2-30F-1306D1-BC
Real time Live cell Imaging Microscope	Carl ZEISS
Refrigerator	SAMSUNG	RT50K6035SL
ROCKER 2D digital	IKA	4003000
Scoop-Spatula	CacheBy	SL-SCO7001-EA
sigma,Trypsin-EDTA solition, 0.25%	Sigma aldrich	T4049-100ML
Sodium Dodecyl Sulfate (SDS)	Thermo Fisher scientific	151-21-3
Syringe Barrel Tip Cap	FISNAR	3051806
Tally counter	Control Company	C23-147-050
Tapered Nozzle (18 G)	Mushashi	TPND-18G-U
Tapered Nozzle (22 G)	Mushashi	TPND-22G-U
Tapered nozzle 20 G	Musashi	TPND-20G-U
Thrombin from bovine plasma	Sigma Aldrich	T7326-1KU
Timer, 4-channel	ETL	SL.Tim3005
Trypan Blue Solution 0.4%	Gibco	15250061
Trypsin Neutralizing Solution	Promocell	C-41120
UG 24 mL UG ointment jar	Yamayu	No. 3-53
UG 58 mL UG ointment jar	Yamayu	No. 3-55
Water Bath	DAIHAN Scientific	WB-11
Weight machine	Sartorius	bce2241-1skr