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Cited 27 time in webofscience Cited 34 time in scopus
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Targeting delivery of tocopherol and doxorubicin grafted-chitosan polymeric micelles for cancer therapy: In vitro and in vivo evaluation

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dc.contributor.authorNam, Joung-Pyo-
dc.contributor.authorLee, Kyeong-Jae-
dc.contributor.authorChoi, Joung-Woo-
dc.contributor.authorYun, Chae-Ok-
dc.contributor.authorNah, Jae-Woon-
dc.date.accessioned2021-08-02T17:54:26Z-
dc.date.available2021-08-02T17:54:26Z-
dc.date.issued2015-09-
dc.identifier.issn0927-7765-
dc.identifier.issn1873-4367-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/24876-
dc.description.abstractIn this study, we report the development of a novel, redox-sensitive chitosan-based targeted drug delivery system, containing two drugs. We determined whether the synthesized polymeric micelles (HPTOC-DOX) were suitable as a drug carrier. The formation of HPTOC-DOX micelles was confirmed by H-1 NMR. HPTOC-DOX formed micelles of approximately 151.9 similar to 311.2 nm in size in aqueous solution. Analysis of the drug release profile of HPTOC-DOX in different pH conditions (pH 5.2, 6.2, and 7.4) indicated that DOX was released from HPTOC-DOX micelles at acidic pH (5.2 or 6.2), while almost no DOX was released at pH 7.4. In vitro cell cytotoxicity and hemolysis assays indicated that HPTOC-DOX micelles safely deliver anti-cancer drugs and decrease the cytotoxicity of DOX. In vitro anti-cancer activity assays, confocal laser scanning microscopy analysis of SK-BR-3 cells, and in vivo anti-tumor activity in SK-BR-3-derived tumor-bearing mice were used to evaluate synergistic drug effects and the effect of the targeting peptide (anti-human epidermal growth factor receptor 2 [HER2] target peptide, epitope form; LTVSPWY) on receptor-mediated endocytosis. (C) 2015 Elsevier B.V. All rights reserved.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleTargeting delivery of tocopherol and doxorubicin grafted-chitosan polymeric micelles for cancer therapy: In vitro and in vivo evaluation-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.colsurfb.2015.06.018-
dc.identifier.scopusid2-s2.0-84934927558-
dc.identifier.wosid000359172600031-
dc.identifier.bibliographicCitationColloids and Surfaces B: Biointerfaces, v.133, pp 254 - 262-
dc.citation.titleColloids and Surfaces B: Biointerfaces-
dc.citation.volume133-
dc.citation.startPage254-
dc.citation.endPage262-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusVITAMIN-E-
dc.subject.keywordPlusMULTIDRUG-RESISTANCE-
dc.subject.keywordPlusCOPOLYMER MICELLES-
dc.subject.keywordPlusBLOCK-COPOLYMER-
dc.subject.keywordPlusGENE DELIVERY-
dc.subject.keywordPlusSTEARIC ACID-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusSUCCINATE-
dc.subject.keywordPlusCARRIERS-
dc.subject.keywordAuthorChitosan-
dc.subject.keywordAuthorDoxorubicin-
dc.subject.keywordAuthorpH-sensitive-
dc.subject.keywordAuthorTargeted delivery-
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