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Skin protein-derived peptide-conjugated vesicular nanocargos for selected skin cell targeting and consequent activation

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dc.contributor.authorCho, Jung Hyeon-
dc.contributor.authorKang, Jeong Yi-
dc.contributor.authorKim, Seulgi-
dc.contributor.authorBaek, Hwi Ra-
dc.contributor.authorKim, Junoh-
dc.contributor.authorJang, Kwang-Suk-
dc.contributor.authorKim, Jin Woong-
dc.date.accessioned2024-04-17T06:00:24Z-
dc.date.available2024-04-17T06:00:24Z-
dc.date.issued2021-06-
dc.identifier.issn2050-750X-
dc.identifier.issn2050-7518-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/118793-
dc.description.abstractSeveral studies have reported that a drug nanocarrier conjugated with ligands having cell binding ability improves drug delivery performance, but multiple cell-targeting and the resultant activation in designated cells has not been investigated yet. This study reports a skin cell multi-targeting vesicular nanocargo system. We selectively conjugated several skin protein-derived cell-targeting peptides (CTPs), including KTTKS, NAP-amide, and Lam332, to amphiphilic polymer-reinforced lipid nanovesicles (PLNVs) to specifically target fibroblasts, melanocytes, and keratinocytes, respectively, through effective association with the corresponding cell membrane receptors. We then showed that CTP-conjugated PLNVs specifically bind to the designated skin cells, even in a mixture of different types of skin cells, eventually leading to skin cell multi-targeting and consequent activation. These results highlight that this CTP-conjugated PLNV system has significant potential for developing an intelligent cellular drug delivery technology for dermatological applications. © The Royal Society of Chemistry 2021.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherRoyal Society of Chemistry-
dc.titleSkin protein-derived peptide-conjugated vesicular nanocargos for selected skin cell targeting and consequent activation-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/d1tb00935d-
dc.identifier.scopusid2-s2.0-85108677844-
dc.identifier.wosid000659474800001-
dc.identifier.bibliographicCitationJournal of Materials Chemistry B, v.9, no.24, pp 4956 - 4962-
dc.citation.titleJournal of Materials Chemistry B-
dc.citation.volume9-
dc.citation.number24-
dc.citation.startPage4956-
dc.citation.endPage4962-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusTISSUE-
dc.subject.keywordPlusKERATINOCYTES-
dc.subject.keywordPlusTHERAPEUTICS-
dc.subject.keywordPlusULTRAVIOLET-
dc.subject.keywordPlusPET-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2021/tb/d1tb00935d-
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ERICA 공학대학 (ERICA 에너지바이오학과)
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