Literature DB >> 22374454

Mussel-inspired silver-releasing antibacterial hydrogels.

Dominic E Fullenkamp1, José G Rivera, Yong-Kuan Gong, K H Aaron Lau, Lihong He, Rahul Varshney, Phillip B Messersmith.   

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. Copyright Â
© 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22374454      PMCID: PMC3367767          DOI: 10.1016/j.biomaterials.2012.02.027

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  26 in total

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Authors:  Lihong He; Dominic E Fullenkamp; José G Rivera; Phillip B Messersmith
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  30 in total

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8.  Electrochemical-Mediated Gelation Of Catechol-Bearing Hydrogels Based On Multimodal Crosslinking.

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Review 9.  Nanoparticle-hydrogel superstructures for biomedical applications.

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Review 10.  Nanoparticle-Hydrogel: A Hybrid Biomaterial System for Localized Drug Delivery.

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