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Pluronics: Intelligent building units for targeted cancer therapy and molecular imaging

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dc.contributor.authorUl Khaliq, Nisar-
dc.contributor.authorPark, Dal Yong-
dc.contributor.authorYun, Byeong Min-
dc.contributor.authorYang, Da Hye-
dc.contributor.authorJung, Yong Woo-
dc.contributor.authorSeo, Jae Hong-
dc.contributor.authorHwang, Chang Soon-
dc.contributor.authorYuk, Soon Hong-
dc.date.accessioned2021-09-01T19:06:21Z-
dc.date.available2021-09-01T19:06:21Z-
dc.date.created2021-06-19-
dc.date.issued2019-02-10-
dc.identifier.issn0378-5173-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/67645-
dc.description.abstractPluronics are triblock copolymers, in which two hydrophilic poly (ethylene oxide) (PEO) blocks are connected via a hydrophobic poly propylene oxide (PPO) block. Because of their low molecular weight and high content of PEO, Pluronics have demonstrated the micellization phenomenon, which is dependent on temperature and/or concentration. With an understanding of micellization phenomenon in more detail, information on the morphology, micelle core radius, aggregation behavior with critical micelle concentration (CMC) and critical micelle temperature (CMT) and so on has been revealed. Based on this acquired information, various studies have been performed for biomedical applications such as drug delivery systems, tissue regeneration scaffolders, and biosurfactants. This review discusses the delivery of small molecules and macromolecules using Pluronic-based NPs and their composites.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectSOL-GEL TRANSITION-
dc.subjectOXIDE) TRIBLOCK COPOLYMERS-
dc.subjectBLOCK-COPOLYMERS-
dc.subjectDRUG-DELIVERY-
dc.subjectCORE/SHELL NANOPARTICLES-
dc.subjectMULTILAYER NANOPARTICLES-
dc.subjectMULTIDRUG-RESISTANCE-
dc.subjectIN-VITRO-
dc.subjectSUSTAINED DELIVERY-
dc.subjectPOLYMER MICELLES-
dc.titlePluronics: Intelligent building units for targeted cancer therapy and molecular imaging-
dc.typeArticle-
dc.contributor.affiliatedAuthorJung, Yong Woo-
dc.contributor.affiliatedAuthorSeo, Jae Hong-
dc.contributor.affiliatedAuthorYuk, Soon Hong-
dc.identifier.doi10.1016/j.ijpharm.2018.11.064-
dc.identifier.scopusid2-s2.0-85058220167-
dc.identifier.wosid000455968700004-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF PHARMACEUTICS, v.556, pp.30 - 44-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF PHARMACEUTICS-
dc.citation.titleINTERNATIONAL JOURNAL OF PHARMACEUTICS-
dc.citation.volume556-
dc.citation.startPage30-
dc.citation.endPage44-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusSOL-GEL TRANSITION-
dc.subject.keywordPlusOXIDE) TRIBLOCK COPOLYMERS-
dc.subject.keywordPlusBLOCK-COPOLYMERS-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusCORE/SHELL NANOPARTICLES-
dc.subject.keywordPlusMULTILAYER NANOPARTICLES-
dc.subject.keywordPlusMULTIDRUG-RESISTANCE-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusSUSTAINED DELIVERY-
dc.subject.keywordPlusPOLYMER MICELLES-
dc.subject.keywordAuthorPluronic nanoparticles-
dc.subject.keywordAuthorPhase transition-
dc.subject.keywordAuthorSmall molecules-
dc.subject.keywordAuthorMacromolecules-
dc.subject.keywordAuthorDoxorubicin-
dc.subject.keywordAuthorIn situ gel-
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