<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Duong VT</submitter><funding>NIDDK NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>2401952</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11546089</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>34(36)</volume><pubmed_abstract>Decellularized small intestine submucosa (dSIS) is a promising biomaterial for promoting tissue regeneration. Isolated from the submucosal layer of animal jejunum, SIS is rich in extracellular matrix (ECM) proteins, including collagen, laminin, and fibronectin. Following mild decellularization, dSIS becomes an acellular matrix that supports cell adhesion, proliferation, and differentiation. Conventional dSIS matrix is usually obtained by thermal crosslinking, which yields a soft scaffold with low stability. To address these challenges, dSIS has been modified with methacrylate groups for photocrosslinking into stable hydrogels. However, dSIS has not been modified with clickable handles for orthogonal crosslinking. Here, we report the development of norbornene-modified dSIS, named dSIS-NB, v</pubmed_abstract><journal>Advanced functional materials</journal><pubmed_title>Photo-responsive decellularized small intestine submucosa hydrogels.</pubmed_title><pmcid>PMC11546089</pmcid><funding_grant_id>R01 DK127436</funding_grant_id><funding_grant_id>R01 CA227737</funding_grant_id><pubmed_authors>Luong NH</pubmed_authors><pubmed_authors>Lin CC</pubmed_authors><pubmed_authors>Duong VT</pubmed_authors><pubmed_authors>Chang CY</pubmed_authors><pubmed_authors>Nguyen HD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Photo-responsive decellularized small intestine submucosa hydrogels.</name><description>Decellularized small intestine submucosa (dSIS) is a promising biomaterial for promoting tissue regeneration. Isolated from the submucosal layer of animal jejunum, SIS is rich in extracellular matrix (ECM) proteins, including collagen, laminin, and fibronectin. Following mild decellularization, dSIS becomes an acellular matrix that supports cell adhesion, proliferation, and differentiation. Conventional dSIS matrix is usually obtained by thermal crosslinking, which yields a soft scaffold with low stability. To address these challenges, dSIS has been modified with methacrylate groups for photocrosslinking into stable hydrogels. However, dSIS has not been modified with clickable handles for orthogonal crosslinking. Here, we report the development of norbornene-modified dSIS, named dSIS-NB, v</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2026-05-29T18:46:00.741Z</modification><creation>2026-04-08T05:43:16.511Z</creation></dates><accession>S-EPMC11546089</accession><cross_references><pubmed>39525288</pubmed><doi>10.1002/adfm.202401952</doi></cross_references></HashMap>