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dc.contributor.authorOh, Keun Sang-
dc.contributor.authorLee, Sangmin-
dc.contributor.authorNa, Jin Hee-
dc.contributor.authorKim, Jeong-Yeon-
dc.contributor.authorKim, Dong-Eog-
dc.contributor.authorKim, Kwangmeyung-
dc.contributor.authorKwon, Ick Chan-
dc.contributor.authorYuk, Soon Hong-
dc.contributor.authorJeong, Seo Young-
dc.date.accessioned2024-01-20T13:33:05Z-
dc.date.available2024-01-20T13:33:05Z-
dc.date.created2021-09-04-
dc.date.issued2012-11-01-
dc.identifier.issn0378-5173-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/128668-
dc.description.abstractMultifunctional nanoparticles (NPs) were prepared based on temperature-induced phase transition in a molten mixture of Lipiodol (R), Tween 80, paclitaxel (PTX), and Pluronic F-68, wherein the Lipiodol (R)/Tween 80 mixture is used as a solubilizer for PTX, and Pluronic F-68 is used for the stabilization of the molten mixture. The morphology and size distribution of optimized multifunctional NPs were observed using transmittance electron microscopy (TEM) and a particle size analyzer. In the optical imaging of tumor-bearing mice using a near-infrared fluorescence (NIRF) imaging system, the multifunctional NPs were evaluated in terms of a time-dependent excretion profile, in vivo biodistribution and tumor-targeting capability compared to free fluorescence dye. In addition, the prolonged circulation of multifunctional NPs was confirmed by enhancement of the blood-pool in live animals using a micro-CT imaging system, because iodine-containing Lipiodol (R) has an X-ray enhancement property. Finally, the anti-tumor efficacy of multifunctional NPs was monitored by injecting the multifunctional NPs into the tail veins of tumor-bearing mice. The multifunctional NPs showed excellent tumor targetability and anti-tumor efficacy in tumor-bearing mice, caused by the enhanced permeation and retention (EPR) effect. (C) 2012 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectLOADED PLURONIC NANOPARTICLES-
dc.subjectNONIONIC CONTRAST-MEDIUM-
dc.subjectPOLYMERIC NANOPARTICLES-
dc.subjectTUMOR-
dc.subjectPACLITAXEL-
dc.subjectDRUG-
dc.subjectHYPERSENSITIVITY-
dc.subjectPERMEABILITY-
dc.subjectDOXORUBICIN-
dc.subjectTRAFFICKING-
dc.titleBlood-pool multifunctional nanoparticles formed by temperature-induced phase transition for cancer-targeting therapy and molecular imaging-
dc.typeArticle-
dc.identifier.doi10.1016/j.ijpharm.2012.08.028-
dc.description.journalClass1-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF PHARMACEUTICS, v.437, no.1-2, pp.192 - 202-
dc.citation.titleINTERNATIONAL JOURNAL OF PHARMACEUTICS-
dc.citation.volume437-
dc.citation.number1-2-
dc.citation.startPage192-
dc.citation.endPage202-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000309115300022-
dc.identifier.scopusid2-s2.0-84866740903-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusLOADED PLURONIC NANOPARTICLES-
dc.subject.keywordPlusNONIONIC CONTRAST-MEDIUM-
dc.subject.keywordPlusPOLYMERIC NANOPARTICLES-
dc.subject.keywordPlusTUMOR-
dc.subject.keywordPlusPACLITAXEL-
dc.subject.keywordPlusDRUG-
dc.subject.keywordPlusHYPERSENSITIVITY-
dc.subject.keywordPlusPERMEABILITY-
dc.subject.keywordPlusDOXORUBICIN-
dc.subject.keywordPlusTRAFFICKING-
dc.subject.keywordAuthorMultifunctional nanoparticles-
dc.subject.keywordAuthorLipiodol (R)-
dc.subject.keywordAuthorPluronic F-68-
dc.subject.keywordAuthorTemperature-induced phase transition-
dc.subject.keywordAuthorCancer-targeting therapy-
dc.subject.keywordAuthorMolecular imaging-
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