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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/13942
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dc.contributor.authorXin, Rui-hua-
dc.contributor.authorLiang, Ge-
dc.contributor.authorZheng, Ji-fang-
dc.date.accessioned2022-11-03T10:25:54Z-
dc.date.available2022-11-03T10:25:54Z-
dc.date.issued2017-03-
dc.identifier.citationXin, R. H., Liang, G., & Zheng, J. F. (2017). Design and content determination of Genhuang dispersible tablet herbal formulation. Pakistan Journal of Pharmaceutical Sciences, 30.en_US
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/13942-
dc.description.abstractThe aim of the present study was to optimize the shaping technology of the traditional herbal formula Genhuang dispersible tablets, and also establish a method for content determination. The optimal formulation of Genhuang dispersible tablets was determined based on the results of single factor test and orthogonal design test. The disintegration was used as the main study indicator. The proportion of each adjuvant in the optimal formulation consisted of 40% MCC as bulking agent, 15% PVPP and 7% L-HPC as disintegrant, ethanol as adhesive, CSD as lubricant, preparing the dispersible tablets with wet granulation. The content of baicalin in Genhuang dispersible tablets was determined by RP-HPLC method, the C18 column (150×4.6 mm, 10μm) was used, the mobile phase was methanol- water-phosphoric acid (47: 53: 0.2) with the flow rate of 1mL/min, the detection wavelength was at 280 nm and the column temperature was 30.en_US
dc.language.isoen_USen_US
dc.publisherFaculty of Pharmacy & Pharmaceutical Sciencesen_US
dc.subjectGenhuang dispersible tableten_US
dc.subjectorthogonal designen_US
dc.subjectdisintegration timeen_US
dc.subjectcontent determinationen_US
dc.titleDesign and content determination of Genhuang dispersible tablet herbal formulationen_US
dc.typeArticleen_US
Appears in Collections:No.2(Supplementary),March 2017

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