HPLC method development for the analysis of bisoprolol in combined dosage form containing bisoprolol and enalapril and in vitro dissolution studied

dc.contributor.authorLogoyda, L.
dc.contributor.authorKovalenko, S.
dc.contributor.authorAbdel-Megied, A. М.
dc.contributor.authorZhulkevych, I.
dc.contributor.authorDrapak, I.
dc.contributor.authorDemchuk, I.
dc.contributor.authorNetsyuk, O.
dc.contributor.authorКоваленко, Сергій Іванович
dc.date.accessioned2021-11-16T08:38:17Z
dc.date.available2021-11-16T08:38:17Z
dc.date.issued2019
dc.description.abstractA simple, rapid and reproducible HPLC method was developed for the determination of bisoprolol in experimental combined dosage forms containing bisoprolol and enalapril and for drug dissolution studies.uk_UK
dc.identifier.citationHPLC method development for the analysis of bisoprolol in combined dosage form containing bisoprolol and enalapril and in vitro dissolution studied / L. Logoyda, S. Kovalenko, A. M. Abdel-Megied, I. Zhulkevych, I. Drapak, I. Demchuk, O. Netsyuk // International Journal of Applied Pharmaceutic. - 2019. - Vol.11, N 3. - P. 196-194. - https://doi.org/10.22159/ijap.2019v11i3.32391uk_UK
dc.identifier.urihttps://zsmu.rosbai.com/handle/123456789/15427
dc.language.isoenuk_UK
dc.subjectbisoprololuk_UK
dc.subjecthigh-performance liquid chromatographyuk_UK
dc.subjectvalidationuk_UK
dc.subjectdissolution studyuk_UK
dc.titleHPLC method development for the analysis of bisoprolol in combined dosage form containing bisoprolol and enalapril and in vitro dissolution studieduk_UK
dc.typeArticleuk_UK

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