Indian Journal of Pharmacy and Pharmacology
  • Year: 2015
  • Volume: 2
  • Issue: 3

Method Development and Validation for the Estimation of Saroglitazar in Bulk and Pharmaceutical Dosage Form by RP-HPLC

  • Author:
  • K Hanumantha Rao1, A Lakshmana Rao2,, KB Chandra Sekhar3
  • Total Page Count: 5
  • Page Number: 150 to 154

1 Assistant Professor, Department of Pharmacy, Krishna University, Machilipatnam, Andhra Pradesh, India

2Professor and Principle, V. V. Institute of Pharmaceutical Sciences, Gudlavalleru, Andhra Pradesh, India

3Professor, Department of Chemistry, JNTUA, Anantapuramu, Andhra Pradesh, India

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

Online published on 28 July, 2016.

Abstract

A simple, rapid, precise and accurate RP-HPLC method was developed and validated for the determination of Saroglitazar in tablet dosage form. Separation of the drug was achieved on a Kromasil C18 Column (150 mm x 4.6 mm I.D., 5 μm particle size). The method showed a linear response in the concentration range of 10–60 μg/ml using 0.1% orthophosphoric acid buffer: acetonitrile as the mobile phase in the ratio of 45: 55 v/v with detection at 295 nm with a flow rate of 1 ml/min and retention time was 3.430 min. The method was validated as per the ICH guidelines. The method was successfully applied for routine quality control analysis of Saroglitazar in tablet dosage form.

Keywords

Saroglitazar, estimation, UV detection, dosage form