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dc.contributor.authorXie, Sheng-Xue
dc.contributor.authorSong, Linyong
dc.contributor.authorYuca, Esra
dc.contributor.authorBoone, Kyle
dc.contributor.authorSarikaya, Rizacan
dc.contributor.authorVanOosten, Sarah Kay
dc.contributor.authorMisra, Anil
dc.contributor.authorYe, Qiang
dc.contributor.authorSpencer, Paulette
dc.contributor.authorTamerler, Candan
dc.date.accessioned2022-01-20T16:13:21Z
dc.date.available2022-01-20T16:13:21Z
dc.date.issued2020-03-13
dc.identifier.citationXie, S. X., Song, L., Yuca, E., Boone, K., Sarikaya, R., VanOosten, S. K., Misra, A., Ye, Q., Spencer, P., & Tamerler, C. (2020). Antimicrobial Peptide-Polymer Conjugates for Dentistry. ACS applied polymer materials, 2(3), 1134–1144. https://doi.org/10.1021/acsapm.9b00921en_US
dc.identifier.urihttp://hdl.handle.net/1808/32458
dc.descriptionThis document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Polymer Materials, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see doi.org/10.1021/acsapm.9b00921.en_US
dc.description.abstractBacterial adhesion and growth at the composite/adhesive/tooth interface remain the primary cause of dental composite restoration failure. Early colonizers, including Streptococcus mutans, play a critical role in the formation of dental caries by creating an environment that reduces the adhesive’s integrity. Subsequently, other bacterial species, biofilm formation, and lactic acid from S. mutans demineralize the adjoining tooth. Because of their broad spectrum of antibacterial activity and low risk for antibiotic resistance, antimicrobial peptides (AMPs) have received significant attention to prevent bacterial biofilms. Harnessing the potential of AMPs is still very limited in dentistry—a few studies have explored peptide-enabled antimicrobial adhesive copolymer systems using mainly nonspecific adsorption. In the current investigation, to avoid limitations from nonspecific adsorption and to prevent potential peptide leakage out of the resin, we conjugated an AMP with a commonly used monomer for dental adhesive formulation. To tailor the flexibility between the peptide and the resin material, we designed two different spacer domains. The spacer-integrated antimicrobial peptides were conjugated to methacrylate (MA), and the resulting MA–AMP monomers were next copolymerized into dental adhesives as AMP–polymer conjugates. The resulting bioactivity of the polymethacrylate-based AMP conjugated matrix activity was investigated. The antimicrobial peptide conjugated to the resin matrix demonstrated significant antimicrobial activity against S. mutans. Secondary structure analyses of conjugated peptides were applied to understand the activity differential. When mechanical properties of the adhesive system were investigated with respect to AMP and cross-linking concentration, resulting AMP–polymer conjugates maintained higher compressive moduli compared to hydrogel analogues including polyHEMA. Overall, our result provides a robust approach to develop a fine-tuned bioenabled peptide adhesive system with improved mechanical properties and antimicrobial activity. The results of this study represent a critical step toward the development of peptide-conjugated dentin adhesives for treatment of secondary caries and the enhanced durability of dental composite restorations.en_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsCopyright © 2020 American Chemical Societyen_US
dc.subjectBioconjugationen_US
dc.subjectAntimicrobial peptidesen_US
dc.subjectDental adhesivesen_US
dc.subjectStreptococcus mutansen_US
dc.subjectMechanical propertyen_US
dc.subjectBioactivityen_US
dc.titleAntimicrobial Peptide–Polymer Conjugates for Dentistryen_US
dc.typeArticleen_US
kusw.kuauthorXie, Sheng-Xue
kusw.kuauthorSong, Linyong
kusw.kuauthorYuca, Esra
kusw.kuauthorBoone, Kyle
kusw.kuauthorSarikaya, Rizacan
kusw.kuauthorVanOosten, Sarah Kay
kusw.kuauthorMisra, Anil
kusw.kuauthorYe, Qiang
kusw.kuauthorSpencer, Paulette
kusw.kuauthorTamerler, Candan
kusw.kudepartmentBioengineeringen_US
kusw.kudepartmentMechanical Engineeringen_US
dc.identifier.doi10.1021/acsapm.9b00921en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0002-1960-2218en_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC8026165en_US
dc.rights.accessrightsopenAccessen_US


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