Quality Control and Standardization of Rabeprazole Tablets

Document Type: Research Paper

Authors

1 Department of Pharmacy, Kazan Medical University, Kazan, Russian Federation; JSС Tatchempharmpreparaty, Kazan, Russian Federation

2 JSС «Tatchempharmpreparaty» 260, Belomorskaja st., Kazan, Russia, 420091

3 Department of Analytical Chemistry, Kazan National Research Technological University 68, Karl Marx st., Kazan, Russia, 420015

4 Department of Pharmacy, Kazan Medical University, Kazan, Russian Federation

10.22034/ijps.2020.44033

Abstract

Rabeprazole sodium is a new stable pharmaceutical composition developed by us in tablet form, consisting of rabeprazole sodium as active ingredient, excipients, a separating layer and enteric coating. The manufacturing method involves pressing with preliminary wet granulation. In this work, a method was developed for the quantitative determination of rabeprazole sodium in tablets with simultaneous determination of impurities, using high-performance liquid chromatography with diode-array detection. Chromatographic conditions were established for the separation of rabeprazole and impurities on С18 sorbent, using mobile phase: 0.05 % К2НР04, 0.27 % КН2Р04 with pH 6.8; and acetonitrile in ratio of 70:30 (v/v), using isocratic elution mode. Furthermore, a method was developed for the spectrophotometric determination of rabeprazole sodium and the conditions of its release during dissolution test were optimized. The feasibility of the developed techniques for the analysis of enteric coated rabeprazole tablets was evaluated with the following parameters: specificity, accuracy, stability of solutions, linearity, convergence, and reproducibility. The techniques were confirmed suitable for the determination of impurities in the drug and for its quantitative analysis.

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