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pH sensitive polyelectrolyte complex micelles for highly effective combination chemotherapy

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dc.contributor.authorRamasamy, Thiruganesh-
dc.contributor.authorKim, Jeong Hwan-
dc.contributor.authorChoi, Ju Yeon-
dc.contributor.authorTuan Hiep Tran-
dc.contributor.authorChoi, Han-Gon-
dc.contributor.authorYong, Chul Soon-
dc.contributor.authorKim, Jong Oh-
dc.date.accessioned2021-06-23T01:44:47Z-
dc.date.available2021-06-23T01:44:47Z-
dc.date.issued2014-07-
dc.identifier.issn2050-7518-
dc.identifier.issn2050-750X-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/25906-
dc.description.abstractThe co-encapsulation of two or more drugs in the same carrier affords synergistic therapeutic effects and enhanced therapeutic potency. For this, polyethylene oxide-b-polyacrylic acid di-block polymer based-smart pH-sensitive di-block polyelectrolyte complex (PEC) micelles were designed to encapsulate mitoxantrone (MTX) and doxorubicin (DOX) with high payload capacity and precise drug ratio. Three molar ratios (MTX/DOX: 2 : 1, 1 : 1, 1 : 2) of the drug-loaded PECs were prepared with high payload capacity and evaluated for various physicochemical characteristics. The dual drug combination exhibited a synergistic cytotoxic activity against both sensitive (MCF-7 and A-549) and resistant cancer cell lines (MDA-MB-231), unlike the individual drugs. Dual drug-loaded nanosystems (MTX/DOX-M) prolonged the blood circulation of drugs, and a synergic ratio was maintained throughout the study period. MTX/DOX-M exhibited superior therapeutic efficacy in xenograft models; by contrast, the free drug cocktail caused a significant loss of body weight in mice. Taken together, our results suggest that PEC micelles have great potential as nano-scaled therapeutic delivery systems for combination chemotherapy.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherROYAL SOC CHEMISTRY-
dc.titlepH sensitive polyelectrolyte complex micelles for highly effective combination chemotherapy-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/c4tb00867g-
dc.identifier.scopusid2-s2.0-84907075319-
dc.identifier.wosid000341457500018-
dc.identifier.bibliographicCitationJOURNAL OF MATERIALS CHEMISTRY B, v.2, no.37, pp 6324 - 6333-
dc.citation.titleJOURNAL OF MATERIALS CHEMISTRY B-
dc.citation.volume2-
dc.citation.number37-
dc.citation.startPage6324-
dc.citation.endPage6333-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusBLOCK IONOMER COMPLEXES-
dc.subject.keywordPlusDRUG-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusPHARMACOKINETICS-
dc.subject.keywordPlusDOXORUBICIN-
dc.subject.keywordPlusANTICANCER-
dc.subject.keywordPlusPACLITAXEL-
dc.subject.keywordAuthorDRUG-
dc.subject.keywordAuthorNANOPARTICLES-
dc.subject.keywordAuthorTHERAPY-
dc.subject.keywordAuthorPHARMACOKINETICS-
dc.subject.keywordAuthorANTICANCER-
dc.subject.keywordAuthorDOXORUBICIN-
dc.subject.keywordAuthorBLOCK IONOMER COMPLEXES-
dc.subject.keywordAuthorCANCER-
dc.subject.keywordAuthorDELIVERY-
dc.subject.keywordAuthorPACLITAXEL-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2014/TB/C4TB00867G-
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