Development and validation of high performance liquid chromatographic method for the determination of esomeprazole in tablets
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.
Önal, A. and Öztunç, A.
"Development and validation of high performance liquid chromatographic method for the determination of esomeprazole in tablets,"
Journal of Food and Drug Analysis: Vol. 14
, Article 8.
Available at: https://doi.org/10.38212/2224-6614.2503