跳到主要內容區塊

3. Development and Validation of High Performance Liquid Chromatographic Method for The Determination of Esomeprazole in Tablets
| 發布日期:2006-01-03 | 更新日期:2023-03-08 發布單位:

Development and Validation of High Performance Liquid Chromatographic Method for The Determination of Esomeprazole in Tablets

ArmaĞAn ÖNal* and Aysel ÖZtunÇ

Department of Analytical Chemistry, Faculty of Pharmacy, Istanbul University, 34116 Istanbul, Turkey

(Received: May 3, 2005; Accepted: September 20, 2005)

Abstract

   A simple, selective and accurate high performance liquid chromatographic (HPLC) method was developed and validated for the analysis of esomeprazole magnesium trihydrate (ES) in tablets.  Chromatographic separation was achieved isocratically on a C18 column utilizing a mobile phase of acetonitrile/phosphate buffer (60:40, v/v, pH 7) at a flow rate of 1.0 mL/min with UV detection at 205 nm.  Lansoprazole was used as an internal standard (IS).  The calibration curve of ES was linear in the range of 100~1000 ng/mL (r = 0.9992, n = 4).  The RSD values for intra- and inter-day precision were 0.66~0.86% and 0.84~1.11%, respectively.  The proposed method was successfully applied to the determination of ES in tablets.  The mean recovery for ES from the tablets ranged between 97.82~98.22%.  ES was subjected to neutral, acid and alkali hydrolysis as well as oxidation, dry heat treatment and photodegradation.  Being simple, accurate and selective, the method can be used for routine quality control analysis.

Key words: esomeprazole, HPLC, stability-indicating, validation, tablet assay

檔案下載