Reverse phase HPLC method for the determination of Pravastatin in tablet dosage forms

Delhi Raj N. (1) , Kumaravel S. (2) , Murugan R. (3) , Sriman Narayanan S. (4) , Vijayalakshmi R. (5)
(1) Department of Pharmaceutical Analysis, Brown’s College of Pharmacy, Khammam, Telangana, India, India ,
(2) Department of Analytical Research Development, Micro Labs Limited, Bangalore, Karnataka, India, India ,
(3) Department of Analytical Chemistry, University of Madras, Chennai, Tamil Nadu, India, India ,
(4) Department of Analytical Chemistry, University of Madras, Chennai, Tamil Nadu, India, India ,
(5) Department of Pharmaceutical Analysis, Gautam College of Pharmacy, Bangalore, Karnataka, India, India

Abstract

A simple RP-HPLC method for the determination of pravastatin in tablet dosage form. Numerous HPLC conditions were tested for the  determination of pravastatin. The best result was achieved by using Phenomenex® Luna 5μm C18( 150x4.6mm) ID column, and a  mobile phase consisting of acetonitrile: potassium dihydrogen orthophosphate (0.02M) (30:70) adjusted to pH 3.0 with  orthophosphoric acid, a flow rate of 1.5ml/min with ultraviolet detection at 240nm.The correlation coefficient for calibration curves  within the detection range of 35.22-65.40μl/ml are 0.9993. The within and between-day precision was determined for both retention  time and peak area.

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Authors

Delhi Raj N.
drj_pharma@rediffmail.com (Primary Contact)
Kumaravel S.
Murugan R.
Sriman Narayanan S.
Vijayalakshmi R.
Delhi Raj N., Kumaravel S., Murugan R., Sriman Narayanan S., & Vijayalakshmi R. (2010). Reverse phase HPLC method for the determination of Pravastatin in tablet dosage forms. International Journal of Research in Pharmaceutical Sciences, 1(2), 187–189. Retrieved from https://ijrps.com/home/article/view/2886

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