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Self-Assembling Peptide Amphiphile-Based Nanofiber Gel for Bioresponsive Cisplatin Delivery

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dc.contributor.authorKim, Jin-Ki-
dc.contributor.authorAnderson, Joel-
dc.contributor.authorJun, Ho-Wook-
dc.contributor.authorRepka, Michael A.-
dc.contributor.authorJo, Seongbong-
dc.date.accessioned2021-06-23T15:39:27Z-
dc.date.available2021-06-23T15:39:27Z-
dc.date.created2021-01-21-
dc.date.issued2009-05-
dc.identifier.issn1543-8384-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/41263-
dc.description.abstractThe aim of this study is to develop a bioresponsive cisplatin (CDDP) delivery system with a self-assembling peptide amphiphile (PA) comprising a cell-adhesive matrix metalloproteinase-2 (MMP-2)-sensitive GTAGLIGQRGDS and a fatty acid. A biomimetic CDDP-PA gel was spontaneously formed upon incubating a mixture of CDDP and the PA for 5 h at 37 degrees C. CDDP-PA gel formation was confirmed by rheological analysis. The structure of self-assembled CDDP-PA nanofibers inside the gel was determined by transmission electron microscopy (TEM). Bioresponsive drug release from the biomimetic gel was demonstrated by in vitro MMP-2-triggered CDDP release. The MMP-2-sensitive CDDP release was dependent on the enzyme concentration in the medium. Enzymatic degradation of the CDDP-PA gel was confirmed by TEM images of the gel degraded in an MMP-2 containing medium. The MMP-2-triggered CDDP release as well as the presentation of RGDS in the gel would potentially provide a spatially and temporally controlled delivery system for targeted anticancer drug delivery.-
dc.language영어-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.titleSelf-Assembling Peptide Amphiphile-Based Nanofiber Gel for Bioresponsive Cisplatin Delivery-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jin-Ki-
dc.identifier.doi10.1021/mp900009n-
dc.identifier.scopusid2-s2.0-67249114390-
dc.identifier.wosid000266652600033-
dc.identifier.bibliographicCitationMOLECULAR PHARMACEUTICS, v.6, no.3, pp.978 - 985-
dc.relation.isPartOfMOLECULAR PHARMACEUTICS-
dc.citation.titleMOLECULAR PHARMACEUTICS-
dc.citation.volume6-
dc.citation.number3-
dc.citation.startPage978-
dc.citation.endPage985-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusMESENCHYMAL STEM-CELLS-
dc.subject.keywordPlusHYBRID SCAFFOLD-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusTHERAPEUTICS-
dc.subject.keywordPlusSTRATEGIES-
dc.subject.keywordPlusCOMPLEX-
dc.subject.keywordPlusCANCER-
dc.subject.keywordAuthorCisplatin-
dc.subject.keywordAuthormatrix metalloproteinase-2-
dc.subject.keywordAuthornanofiber-
dc.subject.keywordAuthorpeptide amphiphile-
dc.subject.keywordAuthortargeted drug delivery-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/mp900009n-
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