Journal :   Asian Journal of Research in Chemistry

Volume No. :   6

Issue No. :  1

Year :  2013

Pages :   19-23

ISSN Print :  0974-4169

ISSN Online :  0974-4150


Registration

Allready Registrered
Click to Login

Method Development and Validation of Aliskiren Hemifumarate and Valsartan in bulk drug by RP-HPLC method



Address:   Somsubhra Ghosh1*, B. Anusha1, Santhoshi1, David Banji1, Y. Chaithanya Kumar1, P. Raghavendra1, Subhadip Roy2
1Nalanda College of Pharmacy, Nalgonda, Andhra Pradesh, India, 508001.
2Mylan Laboratories Ltd, Hyderabad, Andhra Pradesh, India.
*Corresponding Author
DOI No:

ABSTRACT:
A new simple, accurate, rapid and precise isocratic High Performance Liquid Chromatographic (HPLC) method was developed and validated for the determination of Aliskiren Hemifumarate (ALSK) and Valsartan (VAL) in bulk drug. The Method employs Waters HPLC system on C8 Column (4.6 x 250 mm, 5 µm) and flow rate of 1 ml/min with a load of 10µl. The Detection was carried out at 220 nm. mobile phase used as Acetonitrile and Phosphate buffer and Methanol was used as mobile phase in the composition of 45:40:15 , phosphate buffer (0.02Mm) adjusted the pH to 4 with Orthophosphoric acid within a short runtime of 8 min. The retention times of Aliskiren (ALSK) was 3.407 min, Valsartan (VAL) was 4.268 min. The method was validated according to the regulatory guidelines with respect to specificity, precision, accuracy, linearity and robustness etc.
KEYWORDS:
Aliskiren Hemifumarate, Valsartan, HPLC, Validation.
Cite:
Somsubhra Ghosh, B. Anusha, Santhoshi, David Banji, Y. Chaithanya Kumar, P. Raghavendra, Subhadip Roy. Method Development and Validation of Aliskiren Hemifumarate and Valsartan in bulk drug by RP-HPLC method. Asian J. Research Chem. 6(1): January 2013; Page 19-23.
[View HTML]      [View PDF]



Visitor's No. :   126254