Asian Journal of Research in Chemistry

  • Year: 2010
  • Volume: 3
  • Issue: 3

Development and Validation of RP-HPLC Method for the Estimation of Sitagliptin Phosphate in Tablet Dosage Form.

  • Author:
  • Sachin Patil1,, B Ramesh1, AR Hareesh1, Kiran Patil2, Ashok Dhokane2
  • Total Page Count: 3
  • DOI:
  • Page Number: 653 to 655

1Shri Adichunchunagiri College of Pharmacy, B. G. Nagara, Tal: Nagmangala Dist: Mandya, Karnataka, India

2Government College of Pharmacy, Vidyanagar, Karad, Dist-Satara, Maharashtra-415 124, India

Abstract

Simple, precise, sensitive and reproducible quantitative reverse phase HPLC method has been developed for estimation of Sitagliptin phosphate in pharmaceutical dosage form. The method was carried out on a Phenomenex RP 18 (2) Column (250×4.6mm i.d; particle size 5 μm) column with a mobile phase consisting of (60:40 v/v Acetonitrile: water) at a flow rate of 1.0 ml/min. The eluents were monitored at 272 nm. The retention time of Sitagliptin phosphate was found out to be 5.062. The developed method was validated in terms of accuracy, precision, linearity, limit of detection and limit of quantification. The proposed method can be used for the estimation of this drug in pharmaceutical dosage forms.

Keywords

Sitagliptin phosphate, Validation, Estimation