Synthesis of Biocompatible Liquid Crystal Elastomer Foams as Cell Scaffolds for 3D Spatial Cell Cultures

Summary

This study presents a methodology to prepare 3D, biodegradable, foam-like cell scaffolds based on biocompatible side-chain liquid crystal elastomers (LCEs). Confocal microscopy experiments show that foam-like LCEs allow for cell attachment, proliferation, and the spontaneous alignment of C2C12s myoblasts.

Abstract

Here, we present a step-by-step preparation of a 3D, biodegradable, foam-like cell scaffold. These scaffolds were prepared by cross-linking star block co-polymers featuring cholesterol units as side-chain pendant groups, resulting in smectic-A (SmA) liquid crystal elastomers (LCEs). Foam-like scaffolds, prepared using metal templates, feature interconnected microchannels, making them suitable as 3D cell culture scaffolds. The combined properties of the regular structure of the metal foam and of the elastomer result in a 3D cell scaffold that promotes not only higher cell proliferation compared to conventional porous templated films, but also better management of mass transport (i.e., nutrients, gases, waste, etc.). The nature of the metal template allows for the easy manipulation of foam shapes (i.e., rolls or films) and for the preparation of scaffolds of different pore sizes for different cell studies while preserving the interconnected porous nature of the template. The etching process does not affect the chemistry of the elastomers, preserving their biocompatible and biodegradable nature. We show that these smectic LCEs, when grown for extensive time periods, enable the study of clinically relevant and complex tissue constructs while promoting the growth and proliferation of cells.

Introduction

There are several examples of biological and biocompatible synthetic materials designed for application in cell studies and for tissue regeneration aiming at cell attachment and proliferation^1,2,3,4,5. There have been a few examples of biocompatible materials, known as liquid crystal elastomers (LCEs), that could respond to external stimuli with anisotropic molecular ordering^6,7. LCEs are stimuli-responsive materials that combine the mechanical and elastic properties of elastomers with the optical functionality and molecular ordering of liquid crystals^8,9. LCEs can experience changes in shape, mechanical deformation, elastic behavior, and optical properties in response to external stimuli (i.e., heat, stress, light, etc.)^{10,11,12,13,14,15,16}. Earlier studies have shown that liquid crystals (LCs) can sense the growth and orientation of cells^4,17. It is possible then to assume that LCEs may be suitable for biologically and medically relevant applications, including cell scaffolding and alignment. We have previously reported the preparation of smectic biocompatible, biodegradable, cast-molded, and thin LCEs films featuring a "Swiss-cheese type" porous morphology^6,18. We also prepared nematic biocompatible LCEs with globular morphology as scaffolds for cell growth^19,20. Our work was aimed at tuning the mechanical properties of the materials to match those of the tissue of interest²¹. Also, these studies focus on understanding elastomer-cell interactions, as well as cellular response when the elastomers are subject to external stimuli.

The main challenges were in part to tailor the porosity of the LCEs to allow for cell attachment and permeation through the elastomer matrix and for better mass transport. The porosity of these thin films⁶ allowed for cell permeation through the bulk of the matrix, but not all pores were fully interconnected or had a more regular (homogeneous) pore size. We then reported on biocompatible nematic LCE elastomers with globular morphologies. These nematic elastomers allowed for the attachment and proliferation of cells, but the pore size ranged only from 10-30 µm, which prevented or limited the use of these elastomers with a wider variety of cell lines^19,20.

Previous work by Kung et al. relating to the formation of graphene foams using a "sacrificial" metal template showed that the obtained graphene foam had a very regular porous morphology dictated by the chosen metal template²². This methodology offers full control of porosity and pore size. At the same time, the malleability and flexibility of the metal template allow for the formation of different template shapes prior to foam preparation. Other techniques, such as material leaching²³, gas templating²⁴, or electro-spun fibers^25,26 also offer the potential for the preparation of porous materials, but they are more time consuming and, in some cases, the pore size is limited to only a few micrometers. Foam-like 3D LCEs prepared using metal templates allow for a higher cell load; an improved proliferation rate; co-culturing; and, last but not least, better mass transport management (i.e., nutrients, gases, and waste) to ensure full tissue development²⁷. Foam-like 3D LCEs also appear to improve cell alignment; this is most likely in relation to the LC pendants sensing cell growth and cell orientation. The presence of LC moieties within the LCE appears to enhance cell alignment with respect to cell location within the LCE scaffold. Cells align within the struts of the LCE, while no clear orientation is observed where the struts join together (junctions)²⁷.

Overall, our LCE cell scaffold platform as a cell support medium offers opportunities to tune the elastomer morphology and elastic properties and to specifically direct the alignment of (individual) cell types to create an ordered, spatial arrangements of cells similar to living systems. Apart from providing a scaffold capable of sustaining and directing long-term cellular growth and proliferation, LCEs also allow for dynamic experiments, where cell orientation and interactions may be modified on the fly.

Protocol

NOTE: The following steps for the 3D LCE foam-like preparation using the 3-arm star block copolymer are shown in Figure 1. For nuclear magnetic resonance (NMR) characterization, the spectra are recorded in deuterated chloroform (CDCl₃) at room temperature on a Bruker DMX 400-MHz instrument and internally referenced residual peaks at 7.26. Fourier transform infrared (FT-IR) spectra are recorded using a Bruker Vector 33 FT-IR spectrometer using attenuated total reflectance mode. For each step of the following protocol, it is important to wear appropriate personal protective clothing (PPE).

1. Synthesis of α-Chloro-ε-caprolactone (Monomer) (According to the Procedure in Jérôme et al.²⁸)

1. Before beginning the synthesis, purify 27 g of 3-chloroperbenzoic acid as follows:
   1. In 800 mL of distilled water, add 1.28 g of sodium phosphate monobasic monohydrate and 8.24 g of sodium phosphate dibasic heptahydrate. Adjust the pH to 7.4 (using sodium hydroxide or hydrochloric acid) and reserve 30 mL of this solution; this is the buffer solution.
   2. Using a separatory funnel, dissolve 3-chloroperbenzoic acid in 35 mL of diethyl ether. Wash the organic solution with 10 mL of buffer solution (prepared in step 1.1.1.). Repeat the wash three times.
   3. Add 3 g of sodium sulfate directly to the organic solution; this drying agent absorbs water from the organic solution.
   4. Filter the solution to remove the drying agent. Concentrate the filtrate under reduced pressure by using a rotary evaporator at 850 mbar and 40 °C.
2. Solubilize 18.5 g of purified 3-chloroperbenzoic acid in 150 mL of dry dichloromethane by stirring in an ultrasonic bath; this process typically takes 20 min. Place the solution inside a separatory funnel.
3. Inside a two-neck, round-bottom flask, dissolve 13.1 g of 2-chlorocyclohexanone in 15 mL of dry dichloromethane using a magnetic stirrer under nitrogen gas. Keep stirring.
4. Fit the separatory funnel containing 3-chloroperbenzoic acid solution (from step 1.2) to the two-neck flask in step 1.3. Flush the system with nitrogen gas. Adjust the opening of the separatory funnel so that the chloroperbenzoic acid solution falls dropwise into the 2-chlorocyclohexanone solution (1 drop every other second) and continue stirring the mixture under nitrogen gas for 96 h.
5. Cool the reaction mixture to -20 °C for 1 h to precipitate the m-chlorobenzoic acid (m-CBA) byproduct.
6. Filter the m-chlorobenzoic acid (m-CBA) and wash the remaining solution with saturated solutions of sodium thiosulfate, sodium bicarbonate, and sodium chloride.
7. Remove the solvent under reduced pressure using a rotary evaporator at 850 mbar and 40 °C. Purify the pale yellow, viscous liquid by distillation under reduced pressure at 2.3 Torr and 96 °C.
8. Monitor the success of the synthesis using the following ¹H NMR peaks. ¹H NMR (400 MHz, CDCl₃, δ[ppm]): 4.75-4.68 (m, 1H, CHClCO), 4.37-4.26 (m, 1H, CH₂O), 4.18-4.05 (m, 1H, CH₂O), and 2.06-1.58 (m, 6H, −CH₂−)^6,27.

2. Synthesis of α-Three-arm Star Block Copolymer (SBC-αCl) by Ring Opening Copolymerization (Sharma et al.⁶ and Amsden et al.²⁹)

1. Before synthesis, silanize a 20-mL ampoule by filling it with a 2% (v/v) solution of 1H,1H, 2H,2H-perfluorooctyltriethoxysilane in toluene and stirring for about 24 h. Rinse with isopropyl alcohol and dry it by placing it in an oven at 140 °C for 30 min.
2. Add 3.64 g of distilled ε-caprolactone, 0.5 g of α-chloro-ε-caprolactone, and 0.25 mL of glycerol to the ampoule. Mix using a vortex for 1 min.
3. Add 4.90 g of D,L-lactide to the ampoule and purge it with nitrogen. Place the ampoule in an oven at 120 °C to melt the D,L-lactide; this process typically takes about 2 h. Mix again using a vortex to make sure that all contents are well mixed and add 66 µL of tin(II)2-ethylhexanoate (Sn(Oct)₂) to the ampoule.
   NOTE: D,L-lactide will cool down during this process and will need to be re-heated in the oven to melt.
4. Vigorously mix one last time using the vortex and flush with nitrogen.
5. Close the ampoule with a rubber stopper. Place a needle connected to a vacuum tube (the house vacuum is usually enough) through the rubber stopper. Turn on the vacuum and, using a flame, melt the long neck of the glass, twisting slowly until the glass collapses on itself. Be careful to not melt the rubber stopper. Once the ampoule is flame-sealed, place it in a sand bath, an oven, or appropriate heating element at 140 °C for 48 h.
6. Take out the ampoule and let it cool at room temperature.
7. Break the ampoule at the sealed mark and dissolve the highly viscous liquid by adding 10 mL of dichloromethane. Transfer the solution to a separatory funnel.
8. Prepare a flask containing 100 mL of cold methanol (chilled using a dry ice/acetone bath at a temperature around -78 °C). Fix the separatory funnel (step 2.7) on top of the flask. Adjust the opening of the separatory funnel so that about two drops fall every other second (dropwise).
9. Collect the white precipitate by filtration (using a paper filter) and dry it in a vacuum oven between 50 and 60 °C.
10. Monitor the success of the synthesis using the following ¹H NMR and FT-IR peaks. ¹H NMR (400 MHz, CDCl₃, δ [ppm]): 5.29-5.03 (m, COCHCH₃), 4.43-4.25 (m, CHCl), 4.24-4.12 (m, CH₂O), 4.11-4.03 (t, J = 4.6 Hz, CH₂O), 3.80-3.68 (m, CHCH₂), 3.09-2.64 (broad, s, OH), 2.39 (t, J = 4.5 Hz, α-H), 2.33 (t, J = 5.1 Hz, α-H), and 1.77-1.25 (m, CH₂, CH₃); FT-IR (1/λ [cm^-1]): 2,932 (s), 2,869 (m), 1,741 (s), 961 (s), 866, and 735 (m)^6,27.
    Note: To prepare a more hydrophilic 3D LCE, prepare a linear block copolymer (LBC) instead of an SBC, following the ring opening copolymerization (ROP) procedure described above.
    1. Add 0.3 g of polyethylene glycol (PEG), 3.15 g ε-caprolactone, 1.0 g of α-chloro-ε-caprolactone, and 5.0 g of D,L-lactide to the silanized vial mix.

3. Synthetic Modification of α-Cl-Three Arm SBC to α-N₃-Three Arm SBC (SBC-αN₃) (According to Sharma et al.⁶)

1. In a round-bottom flask and under nitrogen, dissolve 5 g of SBC-αCl in 30 mL of dry N,N'-dimethylformamide.
2. Add 0.22 g of sodium azide and allow to react overnight at room temperature.
   Caution: Sodium azide is toxic; wear appropriate personal protective clothing (PPE).
3. Remove the N,N'-dimethylformamide under reduced pressure using a rotary evaporator at 11 mbar and 40 °C. Dissolve the mixture in 30 mL of toluene. Centrifuge the solution thrice at 2,800 x g for 15 min to remove the salt formed. Evaporate the toluene under reduced pressure using a rotary evaporator at 77 mbar and 40 °C.
4. Monitor the success of the azide substitution using ¹H NMR and FT-IR peaks.
   NOTE: ¹H NMR spectrum was similar to the parent SBC-αCl, with the exception of the appearance of a peak at 3.90 ppm related to the azide group; FT-IR (1/λ [cm^-1]): 2,928, 2,108 (s, azide), 1,754 (s), 1,450 (s), 960 (m), 865 (s), 733 (s), and 696 (m).

4. Synthesis of Cholesteryl 5-Hexynoate (LC Moiety) (According to Sharma et al.⁶ and Donaldson et al.³⁰)

1. In a round-bottom flask, mix 3 g of 5-hexynoic acid and 130 mL of dichloromethane. Cool to 0 °C using an ice bath.
2. In another round-bottom flask, mix 8.28 g of N,N'-dicyclohexylcarbodiimide, 10.3 g of cholesterol, and 0.2 g of 4-dimethylaminopyridine.
3. Transfer the 5-hexynoic acid solution dropwise to the flask containing the cholesterol mixture and maintain the final mixture at 0 °C for 1 h.
4. Allow the mixture to warm up to room temperature overnight.
5. Remove the resulting dicyclohexylurea precipitate by filtration using a grade 415 paper filter and discard it.
6. Concentrate the filtrate under reduced pressure using a rotary evaporator at 850 mbar and 40 °C. Dissolve the collected residue in 150 mL of hexane.
7. Evaporate the solvent under reduced pressure using a rotary evaporator at 335 mbar and 40 °C. Add 350 mL of ethanol to the oily residue to collect the final product. Wash the off-white solid formed with ethanol and dry the solid product under vacuum at 50 °C.
8. Monitor the synthesis using the following ¹H NMR and FT-IR peaks. ¹H NMR (400 MHz, CDCl₃, δ [ppm]): 5.39 (d, J = 4.7 Hz, 1H, CH=C), 4.70-4.58 (m, 1H, CHOCO), 2.44 (t, J = 2.5 Hz, 2H, CH₂CO), 2.34 (m, 2H, CH₂-CH=), 2.31 (m, 2H, CH₂CH₂-COO), 2.28 (s, 1H, HC≡C), 2.27 (d, J = 2.3 Hz, 2H, ≡C-CH₂), 2.07-1.06 (m, 2H, CH₂, CH), 0.94 (s, 3H, CH₃), 0.89 (d, J = 1.8 Hz, 3H, CH₃CH), and 0.88 (d, J = 1.8 Hz, 6H, CH₃-CH), 0.67 (s, 3H, CH₃). FT-IR (1/λ [cm^-1]): 2,830-2,990 (broad and strong peak), 2,104 (m), 1,695 (s), 1,428 (m), 1,135 (m), 999 (s), 798 (s), and 667 (s).

5. Synthetic Modification of α-N₃-Three Arm SBC to α-Cholesteryl-Three Arm SBC (SBC-αCLC) via an Azide-Alkyne Huisgen Cyclo-addition Reaction ("Click" Reaction) to Obtain SBC-Chol (According to Sharma et al.⁶)

1. In a round-bottom flask, dissolve 1 molar equivalent of SBC-αN₃ (1.5 g) in 100 mL of freshly distilled tetrahydrofuran (THF). Add 1.2 molar equivalent of cholesteryl 5-hexynoate (1.94 g), 0.1 molar equivalent of copper(I)iodide (0.06 g), and 0.1 molar equivalent of triethylamine (0.03 g). Stir the mixture overnight at 35 °C under nitrogen.
2. Evaporate the solvent under reduced pressure using a rotary evaporator at 357 mbar and 40 °C.
3. Dissolve the residual mixture in 80 mL of dichloromethane and centrifuge for 5 min at 2,800 x g at room temperature to remove unreacted materials and side products.
4. Monitor the synthesis using the following ¹H NMR and FT-IR peaks. ¹H NMR (400 MHz, CDCl₃, δ [ppm]): 7.54 (s, CH=C-triazole), 5.43-5.34 (m, C=CH cholesterol), 5.10-5.06 (m, COCHCH₃), 4.68-4.55 (m, O-CH cholesterol), 4.24-4.19 (m, CH₂O), 4.18-4.13 (t, J=5.0 Hz, CH₂O), 4.11-4.05 (t, J=4.4 Hz, CH₂O), 2.47-2.41 (t, J=4.9 Hz, COCH₂), 2.31-2.25 (m, COCH₂), 2.07-1.02 (m, CH₂, CH₃), 1.05-1.03 (s, CH₂, CH₃), 0.96-0.92 (d, J=3.3 Hz, CH₂, CH₃), 0.91-0.87 (dd, J=1.9 Hz, J=1.8 Hz, CH₃), and 0.71-0.68 (s, CH₃). FT-IR (1/λ [cm^-1]): 3,260 (s), 2,920 (s), 1,710 (s), 1,460 (s), 1,370 (s), 1,240 (m), 1,190 (s), 733 (s), and 668 (s).

6. Synthesis of 2,2-Bis(1-caprolactone-4-yl)propane (Crosslinker, BCP) (According to Gao et al.²⁷ and Albertsson et al.³¹)

1. In a round-bottom flask, prepare a solution containing 10.8 g of 2-bis(4-hydroxy-cyclohexyl)propane and 52 mL of acetic acid.
2. Prepare a solution containing 11 g of chromium trioxide in 50 mL of acetic acid and 8 mL of distilled water. Add this solution dropwise to the solution prepared in step 6.1 while maintaining the mixture temperature between 17 and 20 °C (e.g., in a water bath); this dropwise process takes 2 h. Once the process is complete, allow the solution to stir for about 30 min.
3. Add 50 mL of 2-propanol. Stir the solution overnight at room temperature.
4. Concentrate the dark purple solution under reduced pressure using a rotary evaporator at 137 mbar and 40 °C. Add 300 mL of distilled water to precipitate; the precipitate should be light purple.
5. Filtrate the crude product using a grade 415 paper filter. Wash the solid material with ~ 250 mL of distilled water or until the solid becomes white.
6. Dissolve the solid material in 15 mL of benzene at 40 °C and let it recrystallize at 25 °C.
7. Add 8.34 g of dry diketone dissolved in dry dichloromethane and a solution containing 6.0 g of 3-chloroperbenzoic acid in 75 mL of dichloromethane to the flask.
8. Reflux the solution at 40 °C for 24 h.
9. Cool the reaction mixture to -20 °C for 10 min to precipitate the m-chlorobenzoic acid byproduct.
10. Remove m-chlorobenzoic acid by filtration (using a paper filter) and concentrate the solution under reduced pressure.
11. Wash the viscose crude product with 200 mL of 2-heptanone and dry the precipitate under vacuum at 50 °C overnight.
12. Monitor the synthesis using the following ¹H NMR and FT-IR peaks. ¹H NMR (400 MHz, CDCl₃, δ [ppm]): 4.42-4.37 (dd, J = 14.2, 7.4 Hz, 2H, CH₂OC=O), 4.21-4.15 (t, 2H, J = 11.3 Hz, CH₂OC=O), 2.80-2.75 (ddt, J = 14.3, 6.5, 1.6 Hz, 2H, CH₂COO), 2.63-2.57 (tt, J = 13.3, 2.1 Hz, 2H, CH₂COO), 2.04-1.93 (M, 4H, -CH₂CH₂OC=O), 1.70-1.56 (m, 4H, -CH₂ CH₂COO), 1.48-1.38 (m, 2H, -CHC(CH₃)₂), and 0.84 (s, 6H, CH₃C-).

7. Creation of Porous 3D Elastomer Scaffold Using either Hexamethylene Diisocyanate (HDI) or 2,2-Bis(1-caprolactone-4-yl)propane (BCP)²⁷ as Crosslinkers (According to Gao et al.²⁷)

1. Prepare three-arm elastomer mixture using 0.75 g of SBC-αCLC by adding 0.25 mL of HDI (or 0.45 mL of BCP) and 0.24 mL of distilled ε-caprolactone monomer. Add 60 µL of Sn(Oct)₂. If using BCP instead of HDI, mix SBC-αCLC and BCP using a vortex and place them in an oven at 140 °C until the BCP fully melts and dissolves (this step can take up to 2 h). Once the BCP has been dissolved, take it out of the oven and, the Sn(Oct)₂, and vortex.
2. Prepare a "sacrificial" nickel foam template by cutting a 1 x 4 cm metal piece. Roll it from one of the short ends so that the final roll is approximately a 1 x 1 cm metal piece (see Figure 4).
3. Put the nickel foam in a glass vial or aluminum foil pack and pour the mixture prepared in step 7.1 to fully cover the foam for 2 min. Remove the excess mixture with a Pasteur pipet. Leave it in an oven overnight at 80 °C.
4. Peel off the aluminum foil or break the glass. Using a razor blade, shave the elastomer around the metal foam to expose the nickel metal.
5. Prepare 1 M iron(III)chloride (FeCl₃) solution in 100 mL of water. Place the foam in a flask and add 70 mL of FeCl₃ solution. Stir for three days at room temperature and change the FeCl₃ solution every day. Before each change, stir the foam with ionized water for 0.5 h.
   NOTE: The etching process is typically completed after three days. To ensure that the etching process is completed, perform tactile compression tests until the foams feel soft. Foam resistance to tactile compression tests indicates the presence of a residual metal template.
6. Rinse the elastomer foam with ethanol and place in a vacuum oven overnight at 40 °C.
7. Characterize the materials using scanning electron microscopy (SEM), differential scanning calorimetry (DSC), mechanical compression tests, and thermal gravimetric analysis (TGA)²⁷.
   NOTE: For preparing a more hydrophilic 3D LCE, replace the SBC with LBC (making sure that the LBC also contains an LC moiety) following the steps described in step 7.5.

8. Seeding of Elastomer Scaffold with SH-SY5Y Neuroblastoma Cells and Culture Using Sterile Techniques

1. Sterilize the elastomer by washing it twice with 1 mL of 70% ethanol. Perform UV irradiation for 10 min and wash with 1 mL of 70% ethanol. Rinse it twice with 1 mL of sterile water and 1 mL of phosphate-buffered saline (PBS). Place the elastomers in 24-well culture plates.
2. Prepare cell growth medium for SH-SY5Y containing 90% Dulbecco Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum (FBS) and 1% Penicillin-Streptomycin (Pen-Strep).
3. After counting the cells using a hematocytometer, prepare 1.5 x 10⁵ SH-SY5Y cells suspended in 100 μL of growth medium (seed solution). Add the solution on top of the elastomers, making sure to form a drop.
4. Incubate the seeded elastomers at 37 °C and 5% CO₂ for 2 h to promote cell adhesion. Add 0.5 mL of growth medium. Incubate again at 37 °C with 5% CO₂.
5. Change the medium every other day after washing with 1 mL of PBS.

9. Microscopic Imaging of Elastomer Construct

1. Fix the cells grown on elastomers with 4% paraformaldehyde (PFA) in PBS for 15 min. Rinse with 3 mL of PBS three times for 5 min each and place the elastomer with the fixed cells in a culture dish with an attached coverslip.
   Caution: PFA is toxic. Wear appropriate personal protective clothing (PPE).
2. Stain the fixed samples with 0.1% of 4',6-diamidino-2-phenylindole (DAPI) in 500 µL of PBS for 10 min and rinse twice with 1 mL of PBS for 5 min.
3. Immediately image the elastomers using confocal microscopy with DAPI fluorescence, acquiring image stacks that span the sample.
   NOTE: Here, image stacks were acquired using a 20X objective and a 60X objective.
4. Analyze the optical confocal image stacks using ImageJ³².

Results

This report shows the preparation method of a porous 3D LCE as a scaffold for cell culture using a nickel metal template. The obtained 3D LCE demonstrates a complex interconnected channel network that allows for easy cell infiltration, as well as more suitable mass transport²⁷. It was found that cells are able to fully penetrate the interconnected channel network and are also able to align within the LCE. Here, a metal nickel foam (99% Ni, density of 860 g/cm^2...

Discussion

Liquid crystalline elastomers have recently been studied as biocompatible cell scaffolds due to their stimuli responsiveness. They have been proven to be ideal platforms as cell scaffolds. However, an important factor to keep in mind when preparing and designing a new LCE scaffold is porosity. The incorporation of leachable solids²³ or gases does not always result in homogeneous porosity or fully interconnected pores. The use of a metal template that can be etched out not only offers the opportuni...

Materials

Name	Company	Catalog Number	Comments
1H, 1H, 2H, 2H-perfluorooctyltriethoxysilane	Alfa Aesar	L16606	Silanizing agent
2-bis(4-hydroxy-cyclohexyl)propane	TCI	B0928	Reagent
2-chlorohexanone	Alfa Aesar	A18613	Reagent
2-heptanone	Sigma Aldrich	W254401	Solvent
2-propanol	Sigma Aldrich	278475	Solvent
3-chloroperbenzoic acid, m-CPBA	Sigma Aldrich	273031	Reagent
4-dimethylaminopyridine	Alfa Aesar	A13016	Reagent
4',6-diamidino-2-phenylindole, DAPI	Invitrogen	D1306	Nuclear Stain
5-hexynoic acid	Alfa Aesar	B25132-06	Reagent
Acetic acid	VWR	36289	Solvent
Acetone	Sigma Aldrich	34850	Solvent
Alcohol 200 proof ACS Grade	VWR	71001-866	Reagent
Benzene	Alfa Aesar	AA33290	Solvent
ε-caprolactone	Alfa Aesar	A10299-0E	Reagent
Chloroform	VWR	BDH1109	Solvent
Cholesterol	Sigma Aldrich	C8503	Reagent
Chromium(VI) oxide	Sigma Aldrich	232653	Reagent
Copper(I) iodide	Strem Chemicals	100211-060	Reagent
D,L-Lactide	Alfa Aesar	L09026	Reagent
Dichloromethane	Sigma Aldrich	320269	Solvent
Diethyl ether	Emd Millipore	EX0190	Solvent
N,N-Dimethylformamide	Sigma Aldrich	270547	Solvent
Dulbecco’s modified Eagle medium, DEME	CORNING Cellgo	10-013	Cell Media
Ethanol	Alfa Aesar	33361	Solvent
Formaldehyde	SIGMA Life Science	F8775	Fixative
Fetal bovine serum, FBS	HyClone	SH30071.01	Media Component
Filter paper, Grade 415, qualitative, crepe	VWR	28320	Filtration
Glycerol	Sigma Aldrich	G5516	Central node (3-arm)
Hexamethylene diisocyanate, HDI	Sigma Aldrich	52649	Crosslinker
Iron(III) chloride	Alfa Aesar	12357	Etching agent
Isopropyl alcohol	VWR	BDH1133	Solvent
Methanol	Alfa Aesar	L13255	Solvent
N,N'-dicyclohexylcarbodiimide	Aldrich	D80002	Solvent
N,N-Dimethylformamide	Sigma Aldrich	270547	Solvent
Nickel metal template	American Elements	Ni-860	Foam template
Neuroblastomas cells (SH-SY5Y)	ATCC	CRL-2266	Cell line
Penicillin streptomycin	Thermo SCIENTIFIC	15140122	Antibiotics
Polyethylene glycol 2000, PEG	Alfa Aesar	B22181	Reagent
Sodium azide	VWR	97064-646	Reagent
Sodium bicarbonate	AMRESCO	865	Drying salt
Sodium chloride	BDH	BDH9286	Drying salt
Sodium phosphate dibasic heptahydrate	Fisher Scientific	S-374	Drying salt
Sodium phosphate monobasic monohydrate	Sigma Aldrich	S9638	Drying salt
Sodium sulfate	Sigma Aldrich	239313	Drying salt
Tetrahydrofuran	Alfa Aesar	41819	Solvent
Thiosulfate de sodium	AMRESCO	393	Drying salt
Tin(II) 2-ethylhexanoate	Aldrich	S3252	Reagent
Toluene	Alfa Aesar	22903	Solvent
Triethylamine	Sigma Aldrich	471283	Reagent
Trypsin	HyClone	SH30042.01	Cell Detachment
Olympus FV1000