Stability-Indicating RP-UPLC Method for Simultaneous Determination of Azilsartan Medoxomil and Chlorthalidone in Tablets in the Presence of Its Degradation Products

J Chromatogr Sci. 2019 Mar 1;57(3):213-219. doi: 10.1093/chromsci/bmy102.

Abstract

Azilsartan Medoxomil (AZL) angiotensin II receptor blocker and chlorthalidone (CLT) were determined by ultraperformance liquid chromatography (UPLC) method in their combined dosage form, they were both subjected to forced degradation studies under extensive stress conditions. The method is a stability indicating by resolving the investigated drugs from their degradation products. Moreover, the degradation products for both drugs obtained from forced degradation were subjected to LC-MS for structure elucidation. The UPLC technique depends on the measurement of spectra for AZL and CLT at 254 nm. Linearity, accuracy and intermediate precision were acceptable over the concentration range of 67.2-268.8 and 40-160 μg/mL for AZL and CLT, respectively. The method was applied for the determination of the studied drugs in their dosage forms. The UPLC method is inexpensive, simple and considered as green chemistry method for the routine analysis and quality control of both drugs in their combined dosage form.

MeSH terms

  • Benzimidazoles / analysis*
  • Benzimidazoles / chemistry*
  • Chlorthalidone / analysis*
  • Chlorthalidone / chemistry*
  • Chromatography, High Pressure Liquid / methods*
  • Drug Stability
  • Linear Models
  • Oxadiazoles / analysis*
  • Oxadiazoles / chemistry*
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Tablets

Substances

  • Benzimidazoles
  • Oxadiazoles
  • Tablets
  • azilsartan medoxomil
  • Chlorthalidone