DISSOLUTION TEST IN QUALITY ASSESSMENT OF TABLETS CONTAINING 11-DEOXYMISOPROSTOL
https://doi.org/10.25207/1608-6228-2018-25-1-129-132
Abstract
Aim. Development of the dissolution test method of 11-deoxymisoprostol tablets.
Materials and methods. The research was carried out on a "paddle apparatus". The media dissolution temperature is 37±0,5 degrees, the stirring rate is 50 rpm, the sampling time is 45 minutes, the dissolution media volume is 500 ml. The method of quantitative determination of 11-deoxymisoprostol in sample solution – HPLC with UV-detection, reverse phase chromatography. Chromatograph "Shimadzu Prominence LC-20" (Japan) with a matrix photodiode detector SPD20, column Discovery C18 (5 μm; 150 mm x 4.6 mm), mobile phase: water-acetonitrile (50:50), isocratic elution, detection at a wavelength of 195 nm.
Results. All tested tablet samples meet the requirements of the State Pharmacopoeia in terms of "Dissolution test".
Conclusion. A dissolution test method of 11-deoxyimisoprostol tablets has been developed.
About the Authors
A. A. FEDOTOVARussian Federation
Pushkin str., 96/98, Ufa, 450008.
A. G. YALKAEV
Russian Federation
Pushkin str., 96/98, Ufa, 450008.
V. A. KATAEV
Russian Federation
Pushkin str., 96/98, Ufa, 450008.
R. A. KHALIKOV
Russian Federation
Pushkin str., 96/98, Ufa, 450008.
F. Kh. KILDIYAROV
Russian Federation
Pushkin str., 96/98, Ufa, 450008.
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Review
For citations:
FEDOTOVA A.A., YALKAEV A.G., KATAEV V.A., KHALIKOV R.A., KILDIYAROV F.Kh. DISSOLUTION TEST IN QUALITY ASSESSMENT OF TABLETS CONTAINING 11-DEOXYMISOPROSTOL. Kuban Scientific Medical Bulletin. 2018;25(1):129-132. (In Russ.) https://doi.org/10.25207/1608-6228-2018-25-1-129-132