dc.contributor.author |
Xin, Rui-hua |
|
dc.contributor.author |
Liang, Ge |
|
dc.contributor.author |
Zheng, Ji-fang |
|
dc.date.accessioned |
2022-11-03T10:25:54Z |
|
dc.date.available |
2022-11-03T10:25:54Z |
|
dc.date.issued |
2017-03 |
|
dc.identifier.citation |
Xin, 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.uri |
http://142.54.178.187:9060/xmlui/handle/123456789/13942 |
|
dc.description.abstract |
The 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.iso |
en_US |
en_US |
dc.publisher |
Faculty of Pharmacy & Pharmaceutical Sciences |
en_US |
dc.subject |
Genhuang dispersible tablet |
en_US |
dc.subject |
orthogonal design |
en_US |
dc.subject |
disintegration time |
en_US |
dc.subject |
content determination |
en_US |
dc.title |
Design and content determination of Genhuang dispersible tablet herbal formulation |
en_US |
dc.type |
Article |
en_US |