<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lian L</submitter><funding>NIBIB NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>Brigham Research Institute</funding><funding>National Institutes of Health</funding><funding>Chan Zuckerberg Initiative</funding><funding>Foundation for the National Institutes of Health</funding><funding>NCI NIH HHS</funding><funding>Army Research Office</funding><funding>NIAMS NIH HHS</funding><funding>AFOSR</funding><funding>Air Force Office of Scientific Research</funding><funding>NIH HHS</funding><funding>ARO</funding><funding>National Science Foundation</funding><pagination>e2304846</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11260906</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>36(34)</volume><pubmed_abstract>Decellularized extracellular matrix (dECM)-based hydrogels are widely applied to additive biomanufacturing strategies for relevant applications. The extracellular matrix components and growth factors of dECM play crucial roles in cell adhesion, growth, and differentiation. However, the generally poor mechanical properties and printability have remained as major limitations for dECM-based materials. In this study, heart-derived dECM (h-dECM) and meniscus-derived dECM (Ms-dECM) bioinks in their pristine, unmodified state supplemented with the photoinitiator system of tris(2,2-bipyridyl) dichlororuthenium(II) hexahydrate and sodium persulfate, demonstrate cytocompatibility with volumetric bioprinting processes. This recently developed bioprinting modality illuminates a dynamically evolving li</pubmed_abstract><journal>Advanced materials (Deerfield Beach, Fla.)</journal><pubmed_title>Rapid Volumetric Bioprinting of Decellularized Extracellular Matrix Bioinks.</pubmed_title><pmcid>PMC11260906</pmcid><funding_grant_id>CISE-IIS-2225698</funding_grant_id><funding_grant_id>R01AR070975</funding_grant_id><funding_grant_id>P41 EB027062</funding_grant_id><funding_grant_id>R01EB028143</funding_grant_id><funding_grant_id>CBET‐EBMS‐1936105</funding_grant_id><funding_grant_id>R01HL166522</funding_grant_id><funding_grant_id>R01 CA282451</funding_grant_id><funding_grant_id>R01HL165176</funding_grant_id><funding_grant_id>P41EB027062</funding_grant_id><funding_grant_id>1541959</funding_grant_id><funding_grant_id>R01 EB028143</funding_grant_id><funding_grant_id>R01 HL165176</funding_grant_id><funding_grant_id>CBET-EBMS-1936105</funding_grant_id><funding_grant_id>FA9550‐20‐1‐0363</funding_grant_id><funding_grant_id>W911NF2120130</funding_grant_id><funding_grant_id>2022‐316712</funding_grant_id><funding_grant_id>R01 HL166522</funding_grant_id><funding_grant_id>R01CA282451</funding_grant_id><funding_grant_id>FA9550-20-1-0363</funding_grant_id><funding_grant_id>R21EB030257</funding_grant_id><funding_grant_id>CISE‐IIS‐2225698</funding_grant_id><funding_grant_id>R01 AR070975</funding_grant_id><funding_grant_id>R21 EB030257</funding_grant_id><funding_grant_id>2022-316712</funding_grant_id><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Maharjan S</pubmed_authors><pubmed_authors>Sahoo JK</pubmed_authors><pubmed_authors>Mu X</pubmed_authors><pubmed_authors>Kaplan DL</pubmed_authors><pubmed_authors>Luo Z</pubmed_authors><pubmed_authors>Mei X</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Xie M</pubmed_authors><pubmed_authors>Abril Manjarrez Rivera V</pubmed_authors><pubmed_authors>Cai L</pubmed_authors><pubmed_authors>Gonzalez FZ</pubmed_authors><pubmed_authors>Kuang X</pubmed_authors><pubmed_authors>Tang G</pubmed_authors><pubmed_authors>Lian L</pubmed_authors><pubmed_authors>Garciamendez-Mijares CE</pubmed_authors><pubmed_authors>Guo J</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Zhang YS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rapid Volumetric Bioprinting of Decellularized Extracellular Matrix Bioinks.</name><description>Decellularized extracellular matrix (dECM)-based hydrogels are widely applied to additive biomanufacturing strategies for relevant applications. The extracellular matrix components and growth factors of dECM play crucial roles in cell adhesion, growth, and differentiation. However, the generally poor mechanical properties and printability have remained as major limitations for dECM-based materials. In this study, heart-derived dECM (h-dECM) and meniscus-derived dECM (Ms-dECM) bioinks in their pristine, unmodified state supplemented with the photoinitiator system of tris(2,2-bipyridyl) dichlororuthenium(II) hexahydrate and sodium persulfate, demonstrate cytocompatibility with volumetric bioprinting processes. This recently developed bioprinting modality illuminates a dynamically evolving li</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-03-16T08:18:10.97Z</modification><creation>2025-08-15T03:06:17.887Z</creation></dates><accession>S-EPMC11260906</accession><cross_references><pubmed>38252896</pubmed><doi>10.1002/adma.202304846</doi></cross_references></HashMap>