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Pluronic-Based Core/Shell Nanoparticles for Drug Delivery and Diagnosis

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dc.contributor.authorJung, Yong Woo-
dc.contributor.authorLee, Hwanbum-
dc.contributor.authorKim, Jae Yeon-
dc.contributor.authorKoo, Eun Jin-
dc.contributor.authorOh, Keun Sang-
dc.contributor.authorYuk, Soon Hong-
dc.date.accessioned2021-09-05T22:00:32Z-
dc.date.available2021-09-05T22:00:32Z-
dc.date.created2021-06-14-
dc.date.issued2013-09-
dc.identifier.issn0929-8673-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/102231-
dc.description.abstractPluronic-based core/shell nanoparticles (NPs) were formed using various strategies such as self-assembly and temperature induced-phase transition. To improve their functionality as a nanomedicine for diagnosis and therapy, the vesicle fusion and layer by layer approach were employed. Because of the hydrophilic nature of the Pluronic shell and the relatively small size, Pluronic-based core/shell NPs were used in order to improve their pharmacokinetic behaviors in drugs and in imaging agents. This review will introduce various types of Pluronic-based core/shell NPs according to their preparation method and formation mechanism. The focus will be on the Pluronic-based core/shell NPs for tumor targeting, stimulated release of proteins, and cancer imaging capabilities.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherBENTHAM SCIENCE PUBL LTD-
dc.subjectCORE VESICLE NANOPARTICLES-
dc.subjectTRIBLOCK COPOLYMER MELTS-
dc.subjectINDUCED PHASE-TRANSITION-
dc.subjectGH-DEFICIENT PATIENTS-
dc.subjectBLOOD-BRAIN-BARRIER-
dc.subjectGROWTH-HORMONE GH-
dc.subjectBLOCK-COPOLYMERS-
dc.subjectIN-VIVO-
dc.subjectCANCER-THERAPY-
dc.subjectAQUEOUS-SOLUTION-
dc.titlePluronic-Based Core/Shell Nanoparticles for Drug Delivery and Diagnosis-
dc.typeArticle-
dc.contributor.affiliatedAuthorJung, Yong Woo-
dc.contributor.affiliatedAuthorYuk, Soon Hong-
dc.identifier.doi10.2174/09298673113209990036-
dc.identifier.scopusid2-s2.0-84883286953-
dc.identifier.wosid000322573700006-
dc.identifier.bibliographicCitationCURRENT MEDICINAL CHEMISTRY, v.20, no.28, pp.3488 - 3499-
dc.relation.isPartOfCURRENT MEDICINAL CHEMISTRY-
dc.citation.titleCURRENT MEDICINAL CHEMISTRY-
dc.citation.volume20-
dc.citation.number28-
dc.citation.startPage3488-
dc.citation.endPage3499-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusCORE VESICLE NANOPARTICLES-
dc.subject.keywordPlusTRIBLOCK COPOLYMER MELTS-
dc.subject.keywordPlusINDUCED PHASE-TRANSITION-
dc.subject.keywordPlusGH-DEFICIENT PATIENTS-
dc.subject.keywordPlusBLOOD-BRAIN-BARRIER-
dc.subject.keywordPlusGROWTH-HORMONE GH-
dc.subject.keywordPlusBLOCK-COPOLYMERS-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusCANCER-THERAPY-
dc.subject.keywordPlusAQUEOUS-SOLUTION-
dc.subject.keywordAuthorAntitumor efficacy-
dc.subject.keywordAuthorcancer targetability-
dc.subject.keywordAuthorchitosan/heparin composite-
dc.subject.keywordAuthorcore/shell nanoparticles-
dc.subject.keywordAuthorenhanced permeability and retention effect-
dc.subject.keywordAuthorlayer-by-layer approach-
dc.subject.keywordAuthormolecular imaging agent-
dc.subject.keywordAuthorPluornics-
dc.subject.keywordAuthorPluronic/liposome composite nanoparticles-
dc.subject.keywordAuthorpolyethylene glycol-
dc.subject.keywordAuthorprotein drug-
dc.subject.keywordAuthorself-assembly-
dc.subject.keywordAuthortemperature-induced phase transition-
dc.subject.keywordAuthorvesicle fusion-
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