Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/44807
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dc.contributor.authorPhạm, Thị Thanh Thảo-
dc.contributor.authorNguyễn, Đức Tuấn-
dc.date.accessioned2021-02-24T01:12:02Z-
dc.date.available2021-02-24T01:12:02Z-
dc.date.issued2018-
dc.identifier.issn0866-7861-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/44807-
dc.description.abstractThree methods were developed for quantitative determination of sofosbuvir (recently used for better treatment of hepatitis c virus infection, but without relevant official monograph in the current Vietnamese Pharmacopeia and other reference ones, as well): The first, by UV-Vis spectrophotometry; the second, by HPLC; the third, by CE. These three proposed methods were valiadated, each proving wide range of linearity, high selectivity, good accuracy and precision. On practical application, sofosbuvir in some pharmaceuticals on the local market were quantitatively analyzed by these proposed methods. Accordingly, the contents of sofosbuvir ranged from 95 % to 105% (calculated on the labeled contents) and without statistically significant differences between the results of any pair of these three methods (p < 0.05).vi_VN
dc.language.isovivi_VN
dc.relation.ispartofseriesTạp chí Dược học;Số 511 .- Tr.51-56-
dc.subjectSofosbuvirvi_VN
dc.subjectHPLCvi_VN
dc.subjectUV-Visvi_VN
dc.subjectCEvi_VN
dc.titleĐịnh lượng sofosbuvir trong chế phẩm bằng phương pháp quang phổ UV-VIS, HPLC và CEvi_VN
dc.typeArticlevi_VN
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