Author(s): Bankar R.R., Modha N.

Email(s): Email ID Not Available

DOI: Not Available

Address: Bankar R.R.*, Modha N.
Department of Quality Assurance, Shivam Pharmaceutical Studies and Research Centre, Valasan-Aanad, India.
*Corresponding Author

Published In:   Volume - 6,      Issue - 7,     Year - 2013


ABSTRACT:
A simple, precise and accurate stability indicating RP-HPLC method has been developed andsubsequently validated for simultaneous estimation of Amlodipine Besylate (AML) and Lisinopril(LSN) from their combination dosage form. A Shimadzu’s HPLC (LC-2010-HT, Shimadzu, Singapore) equipped with UV-Visible and Diode Array detectors, with Class-VP software was used. Column used was Hypersil BDS RP18, 5 micrometer, 150 mm × 4.6 mm i.d., at 25° C. Mobile phase consisted mixture of solution A (0.05 M Sodium dihydrogen phosphate) and solution B (Acetonitrile) in ratio of 50:50 v/v with flow rate of 1.0 mL/ min and UV detection was carried out at 258 nm for AML and LSN, respectively. LSN, AML and their combined dosage form were exposed to thermal, oxidative, acid-base hydrolytic stress conditions, the stressed samples were analyzed by proposed method. Peak purity results suggested no other co-eluting, interfering peaks from excipients, impurities, or degradation products due to variable stress condition, and the method is specific for the estimation of AML and LSN in presence of their degradation products and impurities. The method was validated with respect to linearity, precision, accuracy, system suitability, and robustness. The described method was linear over the range of 12.5-37.5 micrometer/mL for AML and LSN both. The mean recoveries were in the range of 100.06-100.13 % for AML and 99.61-100.31 % for LSN, respectively. The intermediate precision data were obtained under different experimental conditions and calculated value of the coefficient of variation (CV, %) was found to be less than critical value. The proposed method can be useful in the quality control of pharmaceuticals.


Cite this article:
Bankar R.R., Modha N. A Validated Stability Indicating RP-HPLC Method for Estimation of Amlodipine Besylate and Lisinopril in Pharmaceutical dosage Forms. Research J. Pharm. and Tech 6(7): July 2013; Page 784-789.

Cite(Electronic):
Bankar R.R., Modha N. A Validated Stability Indicating RP-HPLC Method for Estimation of Amlodipine Besylate and Lisinopril in Pharmaceutical dosage Forms. Research J. Pharm. and Tech 6(7): July 2013; Page 784-789.   Available on: https://rjptonline.org/AbstractView.aspx?PID=2013-6-7-10


Recomonded Articles:

Research Journal of Pharmacy and Technology (RJPT) is an international, peer-reviewed, multidisciplinary journal.... Read more >>>

RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 

1.3
2021CiteScore
 
56th percentile
Powered by  Scopus


SCImago Journal & Country Rank


Recent Articles




Tags


Not Available