<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fullenkamp DE</submitter><funding>NIBIB NIH HHS</funding><funding>NIDCR NIH HHS</funding><funding>NHLBI NIH HHS</funding><pagination>3783-91</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3367767</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(15)</volume><pubmed_abstract>A silver-releasing antibacterial hydrogel was developed that simultaneously allowed for silver nanoparticle formation and gel curing. Water-soluble polyethylene glycol (PEG) polymers were synthesized that contain reactive catechol moieties, inspired by mussel adhesive proteins, where the catechol containing amino acid 3,4-dihydroxyphenylalanine (DOPA) plays an important role in the ability of the mussel to adhere to almost any surface in an aqueous environment. We utilized silver nitrate to oxidize polymer catechols, leading to covalent cross-linking and hydrogel formation with simultaneous reduction of Ag(I). Silver release was sustained for periods of at least two weeks in PBS solution. Hydrogels were found to inhibit bacterial growth, consistent with the well-known antibacterial properties of silver, while not significantly affecting mammalian cell viability. In addition, thin hydrogel films were found to resist bacterial and mammalian cell attachment, consistent with the antifouling properties of PEG. We believe these materials have a strong potential for antibacterial biomaterial coatings and tissue adhesives, due to the material-independent adhesive properties of catechols.</pubmed_abstract><journal>Biomaterials</journal><pubmed_title>Mussel-inspired silver-releasing antibacterial hydrogels.</pubmed_title><pmcid>PMC3367767</pmcid><funding_grant_id>R01 EB005772-04</funding_grant_id><funding_grant_id>R01 DE014193</funding_grant_id><funding_grant_id>R01 EB005772</funding_grant_id><funding_grant_id>R01 EB005772-02S1</funding_grant_id><funding_grant_id>F30 HL096292</funding_grant_id><funding_grant_id>R01 DE014193-04</funding_grant_id><funding_grant_id>F30 HL096292-03</funding_grant_id><funding_grant_id>R37 DE014193</funding_grant_id><pubmed_authors>Fullenkamp DE</pubmed_authors><pubmed_authors>Gong YK</pubmed_authors><pubmed_authors>Lau KH</pubmed_authors><pubmed_authors>Messersmith PB</pubmed_authors><pubmed_authors>Rivera JG</pubmed_authors><pubmed_authors>Varshney R</pubmed_authors><pubmed_authors>He L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mussel-inspired silver-releasing antibacterial hydrogels.</name><description>A silver-releasing antibacterial hydrogel was developed that simultaneously allowed for silver nanoparticle formation and gel curing. Water-soluble polyethylene glycol (PEG) polymers were synthesized that contain reactive catechol moieties, inspired by mussel adhesive proteins, where the catechol containing amino acid 3,4-dihydroxyphenylalanine (DOPA) plays an important role in the ability of the mussel to adhere to almost any surface in an aqueous environment. We utilized silver nitrate to oxidize polymer catechols, leading to covalent cross-linking and hydrogel formation with simultaneous reduction of Ag(I). Silver release was sustained for periods of at least two weeks in PBS solution. Hydrogels were found to inhibit bacterial growth, consistent with the well-known antibacterial properties of silver, while not significantly affecting mammalian cell viability. In addition, thin hydrogel films were found to resist bacterial and mammalian cell attachment, consistent with the antifouling properties of PEG. We believe these materials have a strong potential for antibacterial biomaterial coatings and tissue adhesives, due to the material-independent adhesive properties of catechols.</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 May</publication><modification>2020-10-31T09:24:53Z</modification><creation>2019-03-27T00:54:10Z</creation></dates><accession>S-EPMC3367767</accession><cross_references><pubmed>22374454</pubmed><doi>10.1016/j.biomaterials.2012.02.027</doi></cross_references></HashMap>