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Layer-by-layer coated lipid-polymer hybrid nanoparticles designed for use in anticancer drug delivery

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dc.contributor.authorRamasamy, Thiruganesh-
dc.contributor.authorTuan Hiep Tran-
dc.contributor.authorChoi, Ju Yeon-
dc.contributor.authorCho, Hyuk Jun-
dc.contributor.authorKim, Jeong Hwan-
dc.contributor.authorYong, Chul Soon-
dc.contributor.authorChoi, Han-Gon-
dc.contributor.authorKim, Jong Oh-
dc.date.accessioned2021-06-23T00:03:26Z-
dc.date.available2021-06-23T00:03:26Z-
dc.date.issued2014-02-
dc.identifier.issn0144-8617-
dc.identifier.issn1879-1344-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/23704-
dc.description.abstractPolyelectrolyte multilayers created via sequential adsorption of complimentary materials may be useful in the delivery of small molecules such as anti-cancer drugs. In this study, layer-by-layer (LbL) nanoarchitectures were prepared by step-wise deposition of naturally derived chitosan and hyaluronic acid on negatively charged hybrid solid lipid nanoparticles (SLNs). A doxorubicin/dextran sulfate complex was incorporated into the SLNs. This resulted in the production of spherical nanoparticles similar to 265 nm in diameter, with a zeta potential of approximately -12 mV. The nanoparticles were physically stable and exhibited controlled doxorubicin (DOX) release kinetics. Further pharmacokinetic manipulations revealed that in comparison with both free DOX and uncoated DOX-loaded SLNs, LbL-functionalized SLNs remarkably enhanced the circulation half-life and decreased the elimination rate of the drug. Cumulatively, our results suggest that this novel LbL-coated system, with a pH-responsive shell and molecularly targeted entities, has the potential to act as a vehicle to deliver medication to targeted tumor regions. (C) 2013 Elsevier Ltd. All rights reserved.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCI LTD-
dc.titleLayer-by-layer coated lipid-polymer hybrid nanoparticles designed for use in anticancer drug delivery-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.carbpol.2013.11.009-
dc.identifier.scopusid2-s2.0-84893844350-
dc.identifier.wosid000331779600086-
dc.identifier.bibliographicCitationCARBOHYDRATE POLYMERS, v.102, pp 653 - 661-
dc.citation.titleCARBOHYDRATE POLYMERS-
dc.citation.volume102-
dc.citation.startPage653-
dc.citation.endPage661-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusPOLYELECTROLYTE MULTILAYER FILMS-
dc.subject.keywordPlusHYALURONIC-ACID-
dc.subject.keywordPlusCHITOSAN-
dc.subject.keywordPlusDOXORUBICIN-
dc.subject.keywordPlusALGINATE-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusCYTOTOXICITY-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordPlusSURFACE-
dc.subject.keywordPlusCORE-
dc.subject.keywordAuthorLayer-by-layer-
dc.subject.keywordAuthorPolyelectrolyte multilayer-
dc.subject.keywordAuthorHybrid solid lipid nanoparticles-
dc.subject.keywordAuthorChitosan-
dc.subject.keywordAuthorHyaluronic acid-
dc.subject.keywordAuthorDoxorubicin-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0144861713011405?via%3Dihub-
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