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Investigation of an active film coating to prepare new fixed-dose combination tablets for treatment of diabetes

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dc.contributor.authorKim, Ju-Young-
dc.contributor.authorKim, Dong-Wook-
dc.contributor.authorKuk, Yun-Mo-
dc.contributor.authorPark, Chun-Woong-
dc.contributor.authorRhee, Yun-Seok-
dc.contributor.authorOh, Tack-Oon-
dc.contributor.authorWeon, Kwon-Yeon-
dc.contributor.authorPark, Eun-Seok-
dc.date.accessioned2022-12-27T01:47:22Z-
dc.date.available2022-12-27T01:47:22Z-
dc.date.issued2012-05-10-
dc.identifier.issn0378-5173-
dc.identifier.issn1873-3476-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/22179-
dc.description.abstractThe aim of the present study was to formulate new fixed-dose combination tablets (FCTs) by coating a glimepiride (GLM) immediate-release (IR) layer on a metformin hydrochloride (MTF) extended-release (ER) core tablet using perforated film coating equipment. Composition of GLM-IR coating suspension for homogeneity was studied and application of near-infrared spectroscopy (NIR) to determine the end-point of the coating process was also investigated. The final product was administered to healthy male volunteers and its pharmacokinetic parameters were analyzed. GLM-IR coating suspension was prepared with a ratio of SLS to GLM at 0.75 for homogeneity. An inert mid-layer was introduced to prevent contact between MTF-ER core tablet and GLM-IR layer, which led to an increased release rate of GLM in pH 7.8 medium. The proportional correlation was confirmed between analytical results of GLM determined by NIRS and those by HPLC-UV. Thus, the end-point of the GLM coating process was determined by NIRS, the fast and non-destructive method. New FCTs were confirmed to be bioequivalent to the marketed product. (C) 2012 Elsevier B.V. All rights reserved.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER-
dc.titleInvestigation of an active film coating to prepare new fixed-dose combination tablets for treatment of diabetes-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.ijpharm.2012.01.057-
dc.identifier.scopusid2-s2.0-84862818425-
dc.identifier.wosid000302364500008-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF PHARMACEUTICS, v.427, no.2, pp 201 - 208-
dc.citation.titleINTERNATIONAL JOURNAL OF PHARMACEUTICS-
dc.citation.volume427-
dc.citation.number2-
dc.citation.startPage201-
dc.citation.endPage208-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusPROCESS ANALYTICAL TECHNOLOGY-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusHUMAN PLASMA-
dc.subject.keywordPlusGLIMEPIRIDE-
dc.subject.keywordPlusRELEASE-
dc.subject.keywordPlusMETFORMIN-
dc.subject.keywordPlusSPECTROSCOPY-
dc.subject.keywordPlusMONOTHERAPY-
dc.subject.keywordPlusSUSPENSIONS-
dc.subject.keywordPlusTHICKNESS-
dc.subject.keywordAuthorActive film coating-
dc.subject.keywordAuthorGlimepiride-
dc.subject.keywordAuthorFixed-dose combination tablets-
dc.subject.keywordAuthorNear-infrared spectroscopy-
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