The authors would like to thank T. Pond, research support specialist at the Department of Chemical Engineering of The Pennsylvania State University (Penn State), the Nanofabrication Lab staff at Penn State, and Dr. J. de Rutte from Partillion Bioscience for the help and discussion regarding nanofabrication processes. A. Sheikhi acknowledges the support of the Materials Research Institute (MRI) and the College of Engineering Materials Matter at the Human Level seed grants, the Convergence Center for Living Multifunctional Material Systems (LiMC2) and the Cluster of Excellence Living, Adaptive and Energy-autonomous Materials Systems (livMatS) Living Multifunctional Materials Collaborative Research Seed Grant Program, and the startup fund from Penn State. Research reported in this publication was partially supported by the National Institute of Biomedical Imaging and Bioengineering (NIBIB) of the National Institutes of Health (NIH) under award number R56EB032672.

NOTE: See the Table of Materials for details related to all materials, instruments, and reagents used in this protocol.
1. GelMA synthesis
NOTE: GelMA synthesis should be conducted in a chemical fume hood, and proper personal protective equipment (PPE) should be used all the time.
<ol>
	<li>Add 200 mL of Dulbecco&#39;s phosphate buffered saline (DPBS, 1x) to an Erlenmeyer flask and heat the solution until it reaches 50 &#176;C. Co...

<ol>
	<li>Feng, Q., Li, D., Li, Q., Cao, X., Dong, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Microgel+assembly:+Fabrication,+characteristics+and+application+in+tissue+engineering+and+regenerative+medicine.">Microgel assembly: Fabrication, characteristics and application in tissue engineering and regenerative medicine.</a> Bioactive Materials. 9, 105-119 (2022).</li><li>Daly, A. C., Riley, L., Segura, T., Burdick, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hydrogel+microparticles+for+biomedical+applications.">Hydrogel microparticles for biomedical applications.</a> Nature Reviews Materials. 5 (1), 20-43 (2020).</li><li>Griffin, D. R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Activating+an+adaptive+immune+response+from+a+hydrogel+scaffold+imparts+regenerative+wound+healing.">Activating an adaptive immune response from a hydrogel scaffold imparts regenerative wound healing.</a> Nature Materials. 20 (4), 560-569 (2021).</li><li>Griffin, D. R., Weaver, W. M., Scumpia, P. O., Di Carlo, D., Segura, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Accelerated+wound+healing+by+injectable+microporous+gel+scaffolds+assembled+from+annealed+building+blocks.">Accelerated wound healing by injectable microporous gel scaffolds assembled from annealed building blocks.</a> Nature Materials. 14 (7), 737-744 (2015).</li><li>Ding, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Jammed+micro-flake+hydrogel+for+four-dimensional+living+cell+bioprinting.">Jammed micro-flake hydrogel for four-dimensional living cell bioprinting.</a> Advanced Materials. 34 (15), 2109394 (2022).</li><li>Muir, V. G., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Sticking+together:+injectable+granular+hydrogels+with+increased+functionality+via+dynamic+covalent+inter-particle+crosslinking.">Sticking together: injectable granular hydrogels with increased functionality via dynamic covalent inter-particle crosslinking.</a> Small. 18 (36), 2201115 (2022).</li><li>Sideris, E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Particle+hydrogels+based+on+hyaluronic+acid+building+blocks.">Particle hydrogels based on hyaluronic acid building blocks.</a> ACS Biomaterials Science and Engineering. 2 (11), 2034-2041 (2016).</li><li>Molley, T. G., Hung, T., Kilian, K. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cell-laden+gradient+microgel+suspensions+for+spatial+control+of+differentiation+during+biofabrication.">Cell-laden gradient microgel suspensions for spatial control of differentiation during biofabrication.</a> Advanced Healthcare Materials. , 2201122 (2022).</li><li>Zoratto, N., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=In+situ+forming+microporous+gelatin+methacryloyl+hydrogel+scaffolds+from+thermostable+microgels+for+tissue+engineering.">In situ forming microporous gelatin methacryloyl hydrogel scaffolds from thermostable microgels for tissue engineering.</a> Bioengineering and Translational. 5 (3), (2020).</li><li>Yuan, Z., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=In+situ+fused+granular+hydrogels+with+ultrastretchability,+strong+adhesion,+and+mutli-bioactivities+for+efficient+chronic+wound+care.">In situ fused granular hydrogels with ultrastretchability, strong adhesion, and mutli-bioactivities for efficient chronic wound care.</a> Chemical Engineering Journal. 450, 138076 (2022).</li><li>Ataie, Z., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nanoengineered+granular+hydrogel+bioinks+with+preserved+interconnected+microporosity+for+extrusion+bioprinting.">Nanoengineered granular hydrogel bioinks with preserved interconnected microporosity for extrusion bioprinting.</a> Small. 18 (37), 2202390 (2022).</li><li>Annabi, N., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=25th+anniversary+article:+rational+design+and+applications+of+hydrogels+in+regenerative+medicine.">25th anniversary article: rational design and applications of hydrogels in regenerative medicine.</a> Advanced Materials. 26 (1), 85-124 (2014).</li><li>Rajabi, N., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Recent+advances+on+bioprinted+gelatin+methacrylate-based+hydrogels+for+tissue+repair.">Recent advances on bioprinted gelatin methacrylate-based hydrogels for tissue repair.</a> Tissue Engineering. Part A. 27 (11-12), 679-702 (2021).</li><li>Sheikhi, A., Di Carlo, D., Khademhosseini, A., De Rutte, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Methods+for+fabricating+modular+hydrogels+from+macromolecules+with+orthogonal+physico-chemical+responsivity.">Methods for fabricating modular hydrogels from macromolecules with orthogonal physico-chemical responsivity.</a> U.S. Patent Application. , (2021).</li><li>Sheikhi, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Microfluidic-enabled+bottom-up+hydrogels+from+annealable+naturally-derived+protein+microbeads.">Microfluidic-enabled bottom-up hydrogels from annealable naturally-derived protein microbeads.</a> Biomaterials. 192, 560-568 (2019).</li><li>Hinton, T. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Three-dimensional+printing+of+complex+biological+structures+by+freeform+reversible+embedding+of+suspended+hydrogels.">Three-dimensional printing of complex biological structures by freeform reversible embedding of suspended hydrogels.</a> Science Advances. 1 (9), (2015).</li><li>Seymour, A. J., Shin, S., Heilshorn, S. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=3D+printing+of+microgel+scaffolds+with+tunable+void+fraction+to+promote+cell+infiltration.">3D printing of microgel scaffolds with tunable void fraction to promote cell infiltration.</a> Advanced Healthcare Materials. 10 (18), 2100644 (2021).</li><li>Lee, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=3D+bioprinting+of+collagen+to+rebuild+components+of+the+human+heart.">3D bioprinting of collagen to rebuild components of the human heart.</a> Science. 365 (6452), 482-487 (2019).</li><li>de Rutte, J. M., Koh, J., Di Carlo, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Scalable+high-throughput+production+of+modular+microgels+for+in+situ+assembly+of+microporous+tissue+scaffolds.">Scalable high-throughput production of modular microgels for in situ assembly of microporous tissue scaffolds.</a> Advanced Functional Materials. 29 (25), 1900071 (2019).</li><li>Sheikhi, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Modular+microporous+hydrogels+formed+from+microgel+beads+with+orthogonal+thermo-chemical+responsivity:+Microfluidic+fabrication+and+characterization.">Modular microporous hydrogels formed from microgel beads with orthogonal thermo-chemical responsivity: Microfluidic fabrication and characterization.</a> MethodsX. 6, 1747-1752 (2019).</li><li>Van Den Bulcke, A. I., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Structural+and+rheological+properties+of+methacrylamide+modified+gelatin+hydrogels.">Structural and rheological properties of methacrylamide modified gelatin hydrogels.</a> Biomacromolecules. 1 (1), 31-38 (2000).</li><li>Qazi, T. H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Anisotropic+rod-shaped+particles+influence+injectable+granular+hydrogel+properties+and+cell+invasion.">Anisotropic rod-shaped particles influence injectable granular hydrogel properties and cell invasion.</a> Advanced Materials. 34 (12), 2109194 (2022).</li><li>Highley, C. B., Song, K. H., Daly, A. C., Burdick, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Jammed+microgel+inks+for+3d+printing+applications.">Jammed microgel inks for 3d printing applications.</a> Advanced Science. 6 (1), 1801076 (2019).</li><li>Claa&#223;en, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Quantification+of+substitution+of+gelatin+methacryloyl:+best+practice+and+current+pitfalls.">Quantification of substitution of gelatin methacryloyl: best practice and current pitfalls.</a> Biomacromolecules. 19 (1), 42-52 (2018).</li><li>Sheikhi, A., Di Carlo, D., Khademhosseini, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Methods+for+converting+colloidal+systems+to+resuspendable/redispersable+powders+that+preserve+the+original+properties+of+the+colloids.">Methods for converting colloidal systems to resuspendable/redispersable powders that preserve the original properties of the colloids.</a> U.S. Patent Application. , (2022).</li><li>Sheikhi, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Microengineered+emulsion-to-powder+technology+for+the+high-fidelity+preservation+of+molecular,+colloidal,+and+bulk+properties+of+hydrogel+suspensions.">Microengineered emulsion-to-powder technology for the high-fidelity preservation of molecular, colloidal, and bulk properties of hydrogel suspensions.</a> ACS Applied Polymer Materials. 1 (8), 1935-1941 (2019).</li><li>Lee, S., de Rutte, J., Dimatteo, R., Koo, D., Di Carlo, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Scalable+fabrication+and+use+of+3d+structured+microparticles+spatially+functionalized+with+biomolecules.">Scalable fabrication and use of 3d structured microparticles spatially functionalized with biomolecules.</a> ACS Nano. 16 (1), 38-49 (2022).</li><li>Charlet, A., Bono, F., Amstad, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mechanical+reinforcement+of+granular+hydrogels.">Mechanical reinforcement of granular hydrogels.</a> Chemical Science. 13 (11), 3082-3093 (2022).</li></ol>

The authors declare no conflicts of interest.

Gelatin and its derivatives are the most commonly used protein-based biomaterials for HMP fabrication. The challenge of throughput versus particle size monodispersity trade-off can be overcome using step-emulsification microfluidic devices. These devices are capable of forming more than 40 million droplets per hour, with a coefficient of variation less than 5%27. In this article, we discussed the microfabrication of droplets containing GelMA solutions, followed by converting them to GelMA HMPs, po...

Assembling HMP building blocks to form tissue engineering scaffolds has gained tremendous attention in the past few years1. GHS, fabricated via HMP assembly, have unique properties compared with their bulk counterparts, including cell-scale microporosity originating from the void spaces among the discrete building blocks. Additional properties, such as injectability, modularity, and decoupled stiffness from porosity, render GHS&#160;a promising platform to enhance tissue repair and regeneration2. Different biomaterials have been used for GHS fabrication, including synthetic PEG-based polymers3,4 and polysaccharides, such as alginate5 and hyaluronic acid6,7. Among naturally derived polymers, the most common protein-based biopolymer for GHS fabrication is GelMA8,9,10,11, a crosslinkable, biocompatible, bioadhesive, and biodegradable biomaterial12,13.
HMPs may be fabricated via batch emulsification8, flow-focusing14,15 or step-emulsification9,11 microfluidic devices, blending16, or complex coacervation17,18. Usually, there is a trade-off between the fabrication throughput and HMP monodispersity. For instance, the blending technique yields irregularly shaped and highly polydispersed HMPs. Batch emulsification or complex coacervation enables the production of large volumes of polydispersed spherical HMPs. Flow-focusing microfluidic devices have been used to fabricate highly monodispersed droplets with a coefficient of variation of &#60;5%, however the throughput is significantly low. In step-emulsification microfluidic devices, the highly parallelized steps enable the high-throughput fabrication of monodispersed HMPs19.
Methacryloyl-modified gelatin (GelMA) HMP building blocks are thermoresponsive and (photo)chemically crosslinkable, enabling facile GHS fabrication20. Upon cooling below the upper critical solution temperature (UCST)21 (e.g., at 4 &#176;C), droplets containing a GelMA solution are converted to physically crosslinked HMPs. These HMP building blocks are then packed using external forces (e.g., via centrifugation) to yield jammed microgel suspensions. Interparticle linkages are established between adjacent HMPs via (photo)chemical crosslinking to form mechanically robust GHS14. One of the most important properties of GHS&#160;is microporosity, enabling facile cell penetration in vitro11 and enhanced tissue ingrowth in vivo22. Three-dimensional (3D) bioprinting of HMPs is conventionally performed using tightly packed microgel suspensions, compromising microporosity23.
We have recently developed a novel class of granular bioinks based on the interfacial nanoengineering of GelMA microgels via the adsorption of heterogeneously charged nanoparticles, followed by nanoparticle reversible self-assembly. This strategy renders loosely packed microgels shear-yielding and extrusion 3D bioprintable, which preserves the microscale porosity of additively manufactured GHS11. This article presents the methods for high-throughput GelMA droplet fabrication, converting these droplets to physically crosslinked HMPs, fabricating GelMA HMPs using resuspendable powder, GelMA GHS formation, GelMA nanoengineered granular bioink (NGB) preparation, and 3D bioprinting.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>1H,1H-perfluoro-1-octanol</td>
			<td>Alfa Aesar, MA, USA</td>
			<td>B20156-18</td>
			<td>98% purity</td>
		</tr>
		<tr>
			<td>Biopsy punch</td>
			<td>Integra Miltex, NY, USA</td>
			<td>33-31A-P/25</td>
			<td>1.5 mm Biopsy Punch with Plunger System</td>
		</tr>
		<tr>
			<td>Blunt needle</td>
			<td>SANANTS</td>
			<td>30-002-25</td>
			<td>25 G</td>
		</tr>
		<tr>
			<td>Bruker Avance NEO 400 MHz</td>
			<td>400 MHz Bruker NEO, MA, USA</td>
			<td></td>
			<td>NMR device</td>
		</tr>
		<tr>
			<td>Centrifuge</td>
			<td>Eppendorf, Germany</td>
			<td>5415 C</td>
			<td></td>
		</tr>
		<tr>
			<td>Centrifuge tube</td>
			<td>Celltreat, MA ,USA</td>
			<td>229423</td>
			<td></td>
		</tr>
		<tr>
			<td>Coffee filters</td>
			<td>BUNN, IL, USA</td>
			<td>20104.0006</td>
			<td>BUNN 8-12 Cup Coffee Filters, 6 each, 100 ct</td>
		</tr>
		<tr>
			<td>Desiccator</td>
			<td>Thermo Scientific</td>
			<td>5311-0250</td>
			<td>Nalgene Vacuum Desiccator, PC Cover and Body, 280 mm OD</td>
		</tr>
		<tr>
			<td>Deuterium oxide</td>
			<td>Sigma, MA, USA</td>
			<td>151882</td>
			<td></td>
		</tr>
		<tr>
			<td>Dialysis membrane (12-14 kDa)</td>
			<td>Spectrum Laboratories, NJ, USA</td>
			<td>08-667E</td>
			<td></td>
		</tr>
		<tr>
			<td>Dulbecco&#39;s phosphate buffered saline (DPBS, 1x)</td>
			<td>Sigma, MA, USA</td>
			<td>56064C-10L</td>
			<td>dry powder, without calcium, without magnesium, suitable for cell culture</td>
		</tr>
		<tr>
			<td>Erlenmeyer flask</td>
			<td>Corning, NY, USA</td>
			<td>4980</td>
			<td>Corning PYREX&#160;</td>
		</tr>
		<tr>
			<td>Ethanol</td>
			<td>VWR, PA, USA</td>
			<td>89125-188</td>
			<td>Koptec 200 proof</td>
		</tr>
		<tr>
			<td>External thread cryogenic vials (cryovials)</td>
			<td>Corning, NY, USA</td>
			<td>430659</td>
			<td></td>
		</tr>
		<tr>
			<td>Freeze dryer</td>
			<td>Labconco, MO, USA</td>
			<td>71042000</td>
			<td>Equipped with vacuum pump (Catalog# 7587000)</td>
		</tr>
		<tr>
			<td>Gelatin powder</td>
			<td>Sigma, MA, USA</td>
			<td>G1890-5100G</td>
			<td>Type A from porcine skin, gel strength ~300 g Bloom</td>
		</tr>
		<tr>
			<td>Glass microscope slides</td>
			<td>VWR, PA, USA</td>
			<td>82027-788</td>
			<td></td>
		</tr>
		<tr>
			<td>Hotplate</td>
			<td>FOUR E&#39;S SCIENTIFIC</td>
			<td>MI0102003</td>
			<td>5 inch Magnetic Hotplate Stirrer Max Temp 280 &#176;C/536 &#176;F&#160;</td>
		</tr>
		<tr>
			<td>Kimwipes</td>
			<td>Fischer scientific, MA, USA</td>
			<td>06-666</td>
			<td></td>
		</tr>
		<tr>
			<td>KMPR 1000 negative photoresist series</td>
			<td>Kayaku Advanced Materials, MA, USA</td>
			<td>121619</td>
			<td>KMPR1025 and KMP1035 are included</td>
		</tr>
		<tr>
			<td>LAPONITE XLG</td>
			<td>BYK USA Inc., CT, USA</td>
			<td>2344265</td>
			<td></td>
		</tr>
		<tr>
			<td>Lithium phenyl-2,4,6-trimethylbenzoylphosphinate (LAP)</td>
			<td>Sigma, MA, USA</td>
			<td>900889-1G</td>
			<td>&#62;95%</td>
		</tr>
		<tr>
			<td>Luer-Lok connector</td>
			<td>BD, NJ, USA</td>
			<td>BD 302995&#160;</td>
			<td></td>
		</tr>
		<tr>
			<td>MA/BA Gen4-Serie Mask- und Bond-Aligner</td>
			<td>S&#220;SS MicroTeck, German</td>
			<td></td>
			<td>Nanofabrication device</td>
		</tr>
		<tr>
			<td>Methacylate anhydride</td>
			<td>Sigma, MA, USA</td>
			<td>276685-100ML</td>
			<td>contains 2,000&#160;ppm topanol A as inhibitor, 94%</td>
		</tr>
		<tr>
			<td>Milli-Q water</td>
			<td>Millipore Corporation, MA, USA</td>
			<td>ZRQSVR5WW</td>
			<td>electrical resistivity &#8776; 18 M&#937; at 25 &#176;C, Direct-Q 5 UV Remote Water Purification System</td>
		</tr>
		<tr>
			<td>Novec 7500 engineering fluid</td>
			<td>3M, MN, USA</td>
			<td></td>
			<td>3M ID&#160;7100003723</td>
		</tr>
		<tr>
			<td>Oven</td>
			<td>VWR, PA, USA</td>
			<td>VWR-1410</td>
			<td>1410 Vacuum Oven</td>
		</tr>
		<tr>
			<td>Parafilm</td>
			<td>Fischer scientific, MA, USA</td>
			<td>HS234526C</td>
			<td></td>
		</tr>
		<tr>
			<td>Pasteur pipette</td>
			<td>VWR, PA, USA</td>
			<td>14673-010</td>
			<td></td>
		</tr>
		<tr>
			<td>Petri dish</td>
			<td>VWR, PA, USA</td>
			<td>25384-092</td>
			<td>polystyrene</td>
		</tr>
		<tr>
			<td>Pico-Surf</td>
			<td>Sphere Fluidics, UK</td>
			<td>C022</td>
			<td>(5% (w/w) in Novec 7500)</td>
		</tr>
		<tr>
			<td>Pipette</td>
			<td>VWR, PA, USA</td>
			<td>89079-970</td>
			<td></td>
		</tr>
		<tr>
			<td>Pipette tips</td>
			<td>VWR, PA, USA</td>
			<td>87006-060</td>
			<td></td>
		</tr>
		<tr>
			<td>Plasma cleaner chamber</td>
			<td>Harrick Plasma, NY, USA</td>
			<td>PDC-001-HP&#160;</td>
			<td></td>
		</tr>
		<tr>
			<td>Polydimethylsiloxane</td>
			<td>Dow Corning, MI, USA</td>
			<td>&#160;2065623</td>
			<td>SYLGARD 184 Silicone Elastomer Kit</td>
		</tr>
		<tr>
			<td>Positive displacement pipette</td>
			<td>Microman E M100E, Gilson, OH, USA</td>
			<td>M100E</td>
			<td></td>
		</tr>
		<tr>
			<td>Silicon wafers</td>
			<td>UniversityWafer, MA, USA</td>
			<td>452/1196</td>
			<td>4-inch mechanical grade</td>
		</tr>
		<tr>
			<td>Spatula</td>
			<td>VWR, PA, USA</td>
			<td>231-0104</td>
			<td>Disposable</td>
		</tr>
		<tr>
			<td>SU-8&#160;</td>
			<td>Kayaku Advanced Materials, MA, USA</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Syringe pump</td>
			<td>Harvard Apparatus, MA, USA</td>
			<td>70-2001</td>
			<td>PHD 2000</td>
		</tr>
		<tr>
			<td>Trichloro(1H,1H,2H,2H-perfluorooctyl)silane</td>
			<td>Millipore Sigma, MA, USA</td>
			<td>448931-10G</td>
			<td>97%</td>
		</tr>
		<tr>
			<td>Tygon tubings</td>
			<td>Saint-globain, PA, USA</td>
			<td>AAD04103&#160;</td>
			<td></td>
		</tr>
		<tr>
			<td>UV light&#160;</td>
			<td>QUANS</td>
			<td></td>
			<td>Voltage: 85 V-265 V AC / Power: 20 W</td>
		</tr>
		<tr>
			<td>Vacuum filtration unit</td>
			<td>VWR, PA, USA</td>
			<td>10040-460</td>
			<td>0.20 &#181;m</td>
		</tr>
		<tr>
			<td>Vortex</td>
			<td>Fischer scientific, USA</td>
			<td>14-955-151</td>
			<td>Mini Vortex Mixer</td>
		</tr>
	</tbody>
</table>

gelatin methacryloyl granular hydrogel scaffolds: high-throughput microgel fabrication, lyophilization, chemical assembly, and 3d bioprinting

The emergence of granular hydrogel scaffolds (GHS), fabricated via assembling hydrogel microparticles (HMPs), has enabled microporous scaffold formation in situ. Unlike conventional bulk hydrogels, interconnected microscale pores in GHS facilitate degradation-independent cell infiltration as well as oxygen, nutrient, and cellular byproduct transfer. Methacryloyl-modified gelatin (GelMA), a (photo)chemically crosslinkable, protein-based biopolymer containing cell adhesive and biodegradable moieties, has widely been used as a cell-responsive/instructive biomaterial. Converting bulk GelMA to GHS&#160;may open a plethora of opportunities for tissue engineering and regeneration. In this article, we demonstrate the procedures of high-throughput GelMA microgel fabrication, conversion to resuspendable dry microgels (micro-aerogels), GHS formation via the chemical assembly of microgels, and granular bioink fabrication for extrusion bioprinting. We show how a sequential physicochemical treatment via cooling and photocrosslinking enables the formation of mechanically robust GHS.&#160;When light is inaccessible (e.g., during deep tissue injection), individually crosslinked GelMA HMPs may be bioorthogonally assembled via enzymatic crosslinking using transglutaminases. Finally, three-dimensional (3D) bioprinting of microporous GHS&#160;at low HMP packing density is demonstrated via the interfacial self-assembly of heterogeneously charged nanoparticles.

GelMA was synthesized through the reaction of gelatin with MA, as presented in Figure 1A. By tailoring the reaction conditions, such as MA concentration, different degrees of MA substitution were obtained. To quantify the degree of MA substitution, GelMA was assessed via&#160;1H NMR spectroscopy (Figure 1B). Vinyl functional groups with representative peaks at the chemical shifts of ~5-6 ppm confirmed the successful GelMA synthesis from gelat...

Watch this Scientific Journal Video about Gelatin Methacryloyl Granular Hydrogel Scaffolds: High-throughput Microgel Fabrication, Lyophilization, Chemical Assembly, and 3D Bioprinting at JoVE.com

Gelatin Methacryloyl Granular Hydrogel Scaffolds: High-throughput Microgel Fabrication, Lyophilization, Chemical Assembly, and 3D Bioprinting

This article describes protocols for high-throughput gelatin methacryloyl microgel fabrication using microfluidic devices, converting microgels to resuspendable powder (micro-aerogels), the chemical assembly of microgels to form granular hydrogel scaffolds, and developing granular hydrogel bioinks with preserved microporosity for 3D bioprinting.

The emergence of granular hydrogel scaffolds (GHS), fabricated via assembling hydrogel microparticles (HMPs), has enabled microporous scaffold formation ...

Extracellular matrix or ECM numeric hydrogel microparticles may be used as the building blocks for scaffold fabrication. This protocol demonstrates the fabrication, purification, lyophilization, photo assembly, and 3D bioprinting of gelatin methacryloyl or GelMA hydrogel microparticles. GelMA is a photochemically, crosslinkable, protein-based biopolymer containing cell adhesive and biodegradable moieties which has been widely used as a cell-responsive and instructive biomaterial.In comparison to conventional bulk hydrogel, GelMA granular hydrogel scaffolds are microporous, enabling rapid cell infiltration that can be tailored by the building block size. GelMA granular hydrogel scaffolds may open new opportunities for the 3D bioprinting of thick tissues, organs, and diseases on cheap platforms and regenerative engineering. To begin, add 10 milligrams of LAP to 10 milliliters of DPBS to prepare a 0.1%photoinitiator solution.Protect the solution from light by wrapping it with aluminum foil, and label it. Next, dissolve the desired amount of GelMA in the photoinitiator solution. Place the aluminum-foil-wrapped solution in the 37-degrees-Celsius oven for one hour to get a clear solution.To prepare the oil phase, make a 2%biocompatible surfactant solution in the engineering fluid. Insert the Tygon tubing in the inlets and outlet of the PDMS device, then insert a 25-gauge blunt needle in the other end of Tygon tubing for inlets. Place the device under the microscope, and keep the environment warm at approximately 40 degrees Celsius using a hairdryer or a space heater.Load the aqueous and oil solutions in separate syringes connected to the device. Start the syringe pump for the oil phase with a flow rate of 160 microliters per minute. After oil fills the channel, start the aqueous phase at 80 microliters per minute.Check the droplet formation under the microscope. Collect the droplets in a container, and evaluate them in the imaging chamber by optical microscopy imaging. Keep the droplets at four degrees Celsius overnight while protecting them from light to initiate GelMA microgel's physical crosslinking and convert the droplets to stable microgels.To implement the microengineered emulsion-to-powder, MEtoP, method, collect the physically crosslinked microgels in the engineering fluid using thermally durable microcentrifuge tubes or cryovials. Seal the open tube with a laboratory wipe and tape. Deep-freeze the physically crosslinked microgels in liquid nitrogen for 10 minutes to proceed with lyophilization.After lyophilization, a solid powder will be obtained. Add one milliliter of cooled, 0.1%photoinitiator solution at four degrees Celsius to the lyophilized powder to make microgel suspensions. Centrifuge the vortexed mixture at 3, 000g for 15 seconds.After discarding the supernatant, transfer the packed microgel suspension to a mold using a positive displacement pipette, and expose it to light at 400 nanometers wavelength with an intensity of 15 milliwatts per square centimeter for 60 seconds to form granular hydrogel scaffolds or GHS. For 400 microliters of microgel suspension, add an equal amount of ice-cold PFO solution, 20%in engineering fluid to the physically crosslinked GelMA microgels. Then centrifuge the vortexed mixture at 300g for 15 seconds, and remove the oil phase from the GelMA microgels by pipetting.Then add 400 microliters of ice-cold, 0.1%photoinitiator solution to the microgel suspension. After centrifuging the vortexed solution at 300g for 15 seconds, discard the oil. Repeat the steps of photoinitiator solution addition and centrifugation, but centrifuge at 3, 000g this time and discard the supernatant of packed GelMA microgels.Transfer the packed GelMA microgels to a mold, followed by light exposure to form the GHS. Add 100 milligrams of nanoplatelet powder to three milliliters of ice-cold, ultra-pure water to form a 3.33%nanoparticle dispersion. Vortex the dispersion vigorously inside a four-degrees-Celsius refrigerator for 15 minutes to exfoliate the aggregated nanoparticles.Properly exfoliated nanoparticles yield a clear dispersion. Dissolve 50 milligrams of LAP in five milliliters of ice-cold, ultra-pure water to prepare a 1%photoinitiator stock solution. Then add 333 microliters of 1%photoinitiator solution to the exfoliated nanoparticle dispersion, and wrap it in aluminum foil to protect against the ambient light.Vortex the mixture for one minute to mix the nanoparticle dispersion and the photoinitiator. Add ice-cold PFO, 20%in engineering fluid to the physically crosslinked GelMA microgels at a one-to-one volume ratio. After centrifuging the vortexed mixture at 300g for 15 seconds, discard the oil phase containing the surfactant.Add the ice-cold, LAP-supplemented nanoparticle dispersion to the washed GelMA microgels. After centrifuging at 3, 000g for 15 seconds, discard the remaining oil at the bottom and the supernatant dispersion. Store the suspension at four degrees Celsius while protecting it from light using aluminum foil for one day to yield the product GelMA nanoengineered granular bioink or NGB.The following day, load the NGB into a three-milliliter syringe. Seal the loaded syringe with a cap and parafilm, and do a pulse centrifugation at 200g to remove the trapped air. Transfer the bioink to a three-milliliter cartridge using a female-female Luer lock connector.Centrifuge the cartridge briefly at 200g again to remove the trapped air, and keep the NGB at four degrees Celsius before use. Next, load the prepared murine fibroblast cell suspension into a three-milliliter syringe. Couple the NGB and the cell-loaded syringes using a female-female Luer lock connector, and mix the contents gently by pushing back and forth 40 times.Print the NGB or cell-laden NGB using a proper bioprinter with a standard conical nozzle by loading the nozzle into the three-milliliter printhead. Keep the printing bed temperature below 10 degrees Celsius, and optimize parameters such as speed and back pressure. Select the desirable gcode or STL file.Then select the substrate and the nozzle type for a pneumatic three-milliliter syringe equipped with a standard conical nozzle. Calibrate the bioprinter using the device guidelines, and start printing to obtain the 3D structures. The MEtoP technology yielded resuspendable dried microgel powder by low-pressure freeze-drying while protecting microgels from aggregation and severe deformation.The SEM images showed that the dried GelMA microparticles using this technology retain their spherical shape after lyophilization compared with the aggregation observed with conventional lyophilization. The micropore characterization of GelMA, GHS, and NGB with a high molecular weight fluorescence dye showed the interconnected microscale void spaces. Also, the fluorescence image assessed using a custom-written MATLAB script detected the pores.The void fraction and median pore equivalent diameter measurements showed no significant difference attesting to the availability and interconnectivity of microscale pores in the 3D-printed scaffolds using the NGB. The superiority of NGB scaffolds to tightly and loosely packed GelMA microgels by the hanging filament length measurement revealed that NGB had a greater length than the packed microgels. The loosely packed microgels did not yield filaments.A hollow cylinder was 3D-printed, and the whole construct was exposed to light for photocrosslinking. The printed structure was physically held to show the shape, fidelity, and structural integrity. If the scaffold is used for biological assessment, for example, in cell-laden bioprinting, remember to perform all the steps under certain conditions, under the biological safety cabinet.We hope to democratize the use of granular hydrogel scaffolds as a newly emerged biomaterial platform in biomedicine.

gelatin-methacryloyl-granular-hydrogel-scaffolds-high-throughput

Research

JoVE Journal

Bioengineering

5.8K 조회수.  The Pennsylvania State University. 세포외 기질 또는 ECM 수치 하이드로겔 미세입자는 스캐폴드 제조를 위한 빌딩 블록으로 사용될 수 있습니다. 이 프로토콜은 젤라틴 메타크릴로일 또는 GelMA 하이드로겔 미세입자의 제조, 정제, 동결건조, 사진 조립 및 3D 바이오프린팅을 보여줍니다. GelMA는 세포 반응성 및 유익한 생체 재료로 널리 사용되어 온 세포 접착제 및 생분해성 부분을 포함하는 광화학적으로 가교 가?...