Asian Journal of Pharmacy and Technology
  • Year: 2014
  • Volume: 4
  • Issue: 4

A Validated RP-HPLC Method for Simultaneous Estimation of Pseudoephedrine and Terfinadine in its Bulk and Pharmaceutical Dosage forms

  • Author:
  • G. Kumaraswamy1,, Gandla Lalitha4, K. Swetha2, R. Suthakaran2, G. Ramesh Babu3
  • Total Page Count: 5
  • Page Number: 200 to 204

1Research Scholar, Department of Pharmaceutical Analysis, Jawaharlal Nehru Technological University, Kakinada, Kakinada -533 003-Andhra Pradesh, India

2Department of Pharmaceutical analysis and QA, Teegala Ram Reddy College of Pharmacy, Meerpet, Hyderabad-500097. Telangana

3Chaithanya College of Pharmacy, Markapur, Prakasham (Dist). A.P., India

4Chilkur Balaji College of Pharmacy, Aziz Nagar, Hyderabad, Telangana

*Corresponding Author E-mail: Kumaraswamy.gandla@gmail.com

Online published on 5 February, 2015.

Abstract

The present work deals with the development of a precise, accurate, simple, specific, reliable and less time consuming RP-HPLC method for the estimation of Pseudoephedrine and Terfinadine tablets. The chromatographic separation was achieved on a Inertsil C18 ODS (4.6 x 250mm, 5μm) with a mobile phase combination of methanol and water (50:50) v/v at a flow rate of 1.0 ml/min, and the detection was carried out by using PDA detector at 290 nm. Ambient column temperature has maintained. The total run time was 10mins. The retention time of Pseudoephedrine and Terfinadine were found to be 2.9 min. and 3.5 min. respectively. The performance of the method was validated according to the present ICH guidelines.

Keywords

RP-HPLC Method, Pseudoephedrine and Terfinadine, tablet dosage forms, PDA Detection