<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(32)</volume><submitter>Dhand AP</submitter><pubmed_abstract>Light-mediated manipulation of hydrogel physicochemical properties is attractive for numerous applications, yet the processing of such hydrogels via vat photopolymerization [e.g., digital light processing (DLP)] is challenging as photoresponsive chemistries may be consumed during printing. Here, we report a facile strategy to DLP print hydrogels that combines short light exposures to set the shape of a printed object and complementary dark polymerization to continue the reaction of macromers without disturbing photoresponsive groups. Postprinting, hydrogels are then programmed using single- or multiphoton light and photoinitiator-free reactions: tetrazole-alkene click reaction (for photofunctionalization), dithiolane ring-opening polymerization (for photostiffening), and o-nitrobenzyl clea</pubmed_abstract><journal>Science advances</journal><pagination>eadw9262</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12333685</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Digital light processing of photoresponsive and programmable hydrogels.</pubmed_title><pmcid>PMC12333685</pmcid><pubmed_authors>Kirkpatrick BE</pubmed_authors><pubmed_authors>Dhand AP</pubmed_authors><pubmed_authors>Meurer-Zeman B</pubmed_authors><pubmed_authors>Mandal A</pubmed_authors><pubmed_authors>Anseth KS</pubmed_authors><pubmed_authors>Bowman CN</pubmed_authors><pubmed_authors>Nelson BR</pubmed_authors><pubmed_authors>Lee JS</pubmed_authors><pubmed_authors>Miksch CE</pubmed_authors><pubmed_authors>Cione J</pubmed_authors><pubmed_authors>Burdick JA</pubmed_authors><pubmed_authors>Garay-Sarmiento M</pubmed_authors><pubmed_authors>Zlotnick HM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Digital light processing of photoresponsive and programmable hydrogels.</name><description>Light-mediated manipulation of hydrogel physicochemical properties is attractive for numerous applications, yet the processing of such hydrogels via vat photopolymerization [e.g., digital light processing (DLP)] is challenging as photoresponsive chemistries may be consumed during printing. Here, we report a facile strategy to DLP print hydrogels that combines short light exposures to set the shape of a printed object and complementary dark polymerization to continue the reaction of macromers without disturbing photoresponsive groups. Postprinting, hydrogels are then programmed using single- or multiphoton light and photoinitiator-free reactions: tetrazole-alkene click reaction (for photofunctionalization), dithiolane ring-opening polymerization (for photostiffening), and o-nitrobenzyl clea</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-01T08:49:51.018Z</modification><creation>2026-04-07T16:46:26.272Z</creation></dates><accession>S-EPMC12333685</accession><cross_references><pubmed>40779636</pubmed><doi>10.1126/sciadv.adw9262</doi></cross_references></HashMap>