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Preparation and characterization of a lutein loading nanoemulsion system for ophthalmic eye drops

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dc.contributor.authorLim, Chaemin-
dc.contributor.authorKim, Da-won-
dc.contributor.authorSim, Taehoon-
dc.contributor.authorNgoc Ha Hoang-
dc.contributor.authorLee, Jun Won-
dc.contributor.authorLee, Eun Seong-
dc.contributor.authorYoun, Yu Seok-
dc.contributor.authorOh, Kyung Teak-
dc.date.available2019-03-08T11:59:16Z-
dc.date.issued2016-12-
dc.identifier.issn1773-2247-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/6392-
dc.description.abstractNanoemulsions (NE) are advantageous nanosized delivery agents for ophthalmic medications because of their ability to penetrate into the ocular structure, as well as their sustained effects. We prepared a NE system composed of isopropyl myristate, triacetin, Tween 80, and ethyl alcohol to increase the solubility and permeability of lutein, an effective medication in macular degeneration. The pseudo-ternary phase diagram was constructed to identify the self-emulsifying region. Eight formulations were selected to characterize each formulation. We examined physical characteristics including particle size, drug solubility, formulation stability, and turbidity. We selected the optimized formulations NE 5 (NE-5) and NE-8, both of which are transparent. The particle size of NE was ca. 10-12 nm with a narrow size distribution. Neither separation nor change in the particle size was observed for 7 days. The lutein loading NEs demonstrated a significant increase in lutein release and sustained release. In contrast, lutein prepared with oil and starch had. limited drug release profiles under 5%. The prepared lutein NE formulation is a potential alternative for lutein delivery systems. (C) 2016 Elsevier B.V. All rights reserved.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCIENCE BV-
dc.titlePreparation and characterization of a lutein loading nanoemulsion system for ophthalmic eye drops-
dc.typeArticle-
dc.identifier.doi10.1016/j.jddst.2016.10.009-
dc.identifier.bibliographicCitationJOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, v.36, pp 168 - 174-
dc.description.isOpenAccessN-
dc.identifier.wosid000390500600020-
dc.identifier.scopusid2-s2.0-84993978558-
dc.citation.endPage174-
dc.citation.startPage168-
dc.citation.titleJOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY-
dc.citation.volume36-
dc.type.docTypeArticle-
dc.publisher.location프랑스-
dc.subject.keywordAuthorNanoemulsion-
dc.subject.keywordAuthorLutein-
dc.subject.keywordAuthorOphthalmic drug delivery system-
dc.subject.keywordAuthorEmulsion morphology-
dc.subject.keywordAuthorPseudo-ternary phase diagram-
dc.subject.keywordAuthorNanosize-
dc.subject.keywordPlusDRUG-DELIVERY SYSTEMS-
dc.subject.keywordPlusMACULAR PIGMENT-
dc.subject.keywordPlusOCULAR IRRITATION-
dc.subject.keywordPlusCYCLOSPORINE-A-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusMICROEMULSIONS-
dc.subject.keywordPlusBIOAVAILABILITY-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusDEGENERATION-
dc.subject.keywordPlusDISSOLUTION-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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