ISSN

0974-4150 (Online)
0974-4169 (Print)


Author(s): V. Mohan Goud, A. Srinivasa Rao, S.V. Phanindra, S. Pragati Ranjan

Email(s): mohanvanga@yahoo.com

DOI: Not Available

Address: V. Mohan Goud1*, A. Srinivasa Rao2, S.V. Phanindra1, S. Pragati Ranjan1
1Department of Pharmaceutical Chemistry, Joginpally B.R Pharmacy College, Yenkapally, Moinabad, R.R. Dist. A.P.
2Bhaskar Pharmacy College, Yenkapally, Moinabad, R.R. Dist. A.P.
*Corresponding Author

Published In:   Volume - 6,      Issue - 8,     Year - 2013


ABSTRACT:
The present work describes a simple reverse-phase high performance liquid chromatographic method for estimation of the drug Seratrodast in pure and in tablet dosage form. The estimation was carried out on a Thermo Hypersil C 18 (150mm × 4.6 mm i.d., particle size 5µm) column with a mixture of Phosphate buffer, Acetonitrile and Water with a pH 6.8 adjusted with ortho phosphoric acid in the ratio of 50:40:10%v/v. UV detection was performed at 266nm. The retention time was 6.016 min. and the flow rate was 1.0 ml min -1. The calibration curve was linear over the concentration range of 200-600ppm. The LOD and LOQ values were found to be 2.5 and 9.6. The method was validated for accuracy, specificity, limit of quantification, limit of detection, robustness and stability. The results showed that proposed method is successfully applied for the quantitative estimation of Seratrodast in pharmaceutical dosage form.


Cite this article:
V. Mohan Goud, A. Srinivasa Rao, S.V. Phanindra, S. Pragati Ranjan. Development and Validation of RP-HPLC Method for Assay of Seratrodast in Pharmaceutical Dosage Form. Asian J. Research Chem. 6(8): August 2013; Page 749-751.


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