Asian Journal of Pharmaceutical Analysis

  • Year: 2021
  • Volume: 11
  • Issue: 2

Development and validation of rp-hplc method for analysis of aclidinium bromide and formoterol fumarate in pharmaceuticals

Department of Pharmaceutical Analysis, Koringa College of Pharmacy, Korangi - 533461, Dist - East Godavari, (Andhra Pradesh), India

*Corresponding Author E-mail: devdaspharma@gmail.com

Online published on 8 June, 2021.

Abstract

A fast, sensitive, and reliable RP-HPLC method involving cyberlab HPLC System with PDA detection was developed and validated for the quantification of Aclidinium bromide and Formoterol fumarate in inhalation preparations. Chromatography was performed on the Inertsil -ODS C18 (250 × 4.6mm, 5μ) column using filtered and mixed degassed methanol: buffer (75:25 v/v) as a mobile phase with a flow rate of 1.0mL/min and the column effluent was monitored at 240nm. Retention times for Aclidinium bromide 4.713min and Formoterol fumarate 6.691min. The method obeyed linearity in the concentration range of 20-80μg/mL for the two drugs when validated according to standard procedures.

Keywords

Method Development, Validation, Aclidinium, Formoterol, RP-HPLC