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dc.contributor.authorSong, R-
dc.contributor.authorJun, YJ-
dc.contributor.authorKim, JI-
dc.contributor.authorJin, C-
dc.contributor.authorSohn, YS-
dc.date.accessioned2024-01-21T04:42:15Z-
dc.date.available2024-01-21T04:42:15Z-
dc.date.created2021-09-03-
dc.date.issued2005-06-20-
dc.identifier.issn0168-3659-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/136356-
dc.description.abstractA new amphiphilic poly(organophosphazene) was synthesized by stepwise nucleophilic substitutions with a hydrophilic methoxy poly(ethylene glycol) with an average molecular weight of 350 (MPEG350) and a hydrophobic glyCyl-L-glutamate as side groups, and then an antitumor (dach)platinum(II) (dach: trans -(+/-)- 1,2-diaminocyclohexane) moiety was conjugated to the polymer using the dipeptide as a spacer. This polymeric platinum conjugate was found to be accumulated in the tumor tissue to a remarkably greater extent than in the normal tissue (tumor/tissue ratio > 4), probably due to the excellent EPR effect and the long circulating properties of the polymer conjugate (t(1/2 beta)=6.2 h and AUC=4020 nmol h/ml) compared with carboplatin ((1/2 beta) =0.42 h and AUC=120 nmol h/ml). The polymer conjugate also exhibited high in vitro cytotoxicity comparable to cisplatin against several human tumor cells tested. (c) 2005 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectVASCULAR-PERMEABILITY-
dc.subjectANTITUMOR-ACTIVITY-
dc.subjectMOLECULAR-WEIGHT-
dc.subjectDRUG-DELIVERY-
dc.subjectLIPOSOME SIZE-
dc.subjectCOMPLEXES-
dc.subjectPOLYMERS-
dc.subjectBIODISTRIBUTION-
dc.subjectELECTROLYTES-
dc.subjectTHERAPEUTICS-
dc.titleSynthesis, characterization, and tumor selectivity of a polyphosphazene-platinum(II) conjugate-
dc.typeArticle-
dc.identifier.doi10.1016/j.jconrel.2005.03.016-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF CONTROLLED RELEASE, v.105, no.1-2, pp.142 - 150-
dc.citation.titleJOURNAL OF CONTROLLED RELEASE-
dc.citation.volume105-
dc.citation.number1-2-
dc.citation.startPage142-
dc.citation.endPage150-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000230576600013-
dc.identifier.scopusid2-s2.0-20444427224-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusVASCULAR-PERMEABILITY-
dc.subject.keywordPlusANTITUMOR-ACTIVITY-
dc.subject.keywordPlusMOLECULAR-WEIGHT-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusLIPOSOME SIZE-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusPOLYMERS-
dc.subject.keywordPlusBIODISTRIBUTION-
dc.subject.keywordPlusELECTROLYTES-
dc.subject.keywordPlusTHERAPEUTICS-
dc.subject.keywordAuthorpolyphosphazene-
dc.subject.keywordAuthorplatinum conjugate-
dc.subject.keywordAuthoranticancer drug-
dc.subject.keywordAuthortumor selectivity-
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