D. Narmada, P.V. Murali Krishna, Shaik Mohammad Yusuf, B. Ranganayakulu, K. Uday Praveen, P. Raja Abhilash
D. Narmada1*, P.V. Murali Krishna1, Shaik Mohammad Yusuf1, B. Ranganayakulu1,
K. Uday Praveen1 and P. Raja Abhilash2
1Srinivasa Institute of Pharmaceutical Sciences, Proddatur, A.P.
2S.V.S. Group of Institutions, School of Pharmacy, Bhemaram, Hanamkonda, Telangana.
Volume - 4,
Issue - 3,
Year - 2014
The prime aim of the current work is to develop and validate a novel, sensitive, reverse phase High Performance Liquid Chromatography (RP-HPLC) technique for the estimation of Glibenclamide in dosage form. Chromatographic separation was achieved on a Chromosil column, (150mm×4.6mm x5µ) using an isocratic method with mobile phase composed of Potassium di-hydrogen phosphate buffer (pH 4.5) : Acetonitrile in the ratio 60:40 v/v. The flow rate was 1 ml/min, temperature of the column was maintained at ambient and detection was made at 233 nm. The run time was 12 min. The developed method was validated according to the International Conference on Harmonization (ICH) guidelines with respect to linearity, accuracy, precision, specificity and robustness. The developed method was linear for Glibenclamide from 10 - 50 µg/ml and the linear regression obtained was > 0.999. Precision, evaluated by intra- and inter-day assays had relative standard deviation (R.S.D) values within 1.5 %. Recovery data were in the range 98.2% to 100.9% with R.S.D. values < 1.5 %. The method is precise, accurate, linear, robust and fast. The short retention time allows the analysis of a large number of samples in a short period of time and, therefore, should be cost-effective for routine Quality Control in the pharmaceutical industry.
Cite this article:
D. Narmada, P.V. Murali Krishna, Shaik Mohammad Yusuf, B. Ranganayakulu, K. Uday Praveen, P. Raja Abhilash. RP-HPLC method development and validation for estimation of Glibenclamide in tablet dosage form. Asian J. Pharm. Ana. 4(3): July-Sept 2014; Page 125-128.