<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(6)</volume><submitter>Gevrek TN</submitter><pubmed_abstract>Multifunctionalizable hydrogel coatings on titanium interfaces are useful in a wide range of biomedical applications utilizing titanium-based materials. In this study, furan-protected maleimide groups containing multi-clickable biocompatible hydrogel layers are fabricated on a titanium surface. Upon thermal treatment, the masked maleimide groups within the hydrogel are converted to thiol-reactive maleimide groups. The thiol-reactive maleimide group allows facile functionalization of these hydrogels through the thiol-maleimide nucleophilic addition and Diels-Alder cycloaddition reactions, under mild conditions. Additionally, the strained alkene unit in the furan-protected maleimide moiety undergoes radical thiol-ene reaction, as well as the inverse-electron-demand Diels-Alder reaction with </pubmed_abstract><journal>Polymers</journal><pagination>E1211</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7362003</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Multifunctional and Transformable 'Clickable' Hydrogel Coatings on Titanium Surfaces: From Protein Immobilization to Cellular Attachment.</pubmed_title><pmcid>PMC7362003</pmcid><pubmed_authors>Gevrek TN</pubmed_authors><pubmed_authors>Degirmenci A</pubmed_authors><pubmed_authors>Sanyal A</pubmed_authors><pubmed_authors>Sanyal R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multifunctional and Transformable 'Clickable' Hydrogel Coatings on Titanium Surfaces: From Protein Immobilization to Cellular Attachment.</name><description>Multifunctionalizable hydrogel coatings on titanium interfaces are useful in a wide range of biomedical applications utilizing titanium-based materials. In this study, furan-protected maleimide groups containing multi-clickable biocompatible hydrogel layers are fabricated on a titanium surface. Upon thermal treatment, the masked maleimide groups within the hydrogel are converted to thiol-reactive maleimide groups. The thiol-reactive maleimide group allows facile functionalization of these hydrogels through the thiol-maleimide nucleophilic addition and Diels-Alder cycloaddition reactions, under mild conditions. Additionally, the strained alkene unit in the furan-protected maleimide moiety undergoes radical thiol-ene reaction, as well as the inverse-electron-demand Diels-Alder reaction with </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 May</publication><modification>2025-04-22T19:28:31.856Z</modification><creation>2025-04-06T02:47:44.778Z</creation></dates><accession>S-EPMC7362003</accession><cross_references><pubmed>32466521</pubmed><doi>10.3390/polym12061211</doi></cross_references></HashMap>