Analytical Method Development and Validation for Simultaneous Estimation of Lercandipine and Atenolol Tablet Dosage Form by RP-HPLC

Journal Title: International Journal of Pharmacy and Analytical Research - Year 2014, Vol 3, Issue 1

Abstract

A rapid high performance liquid chromatographic method has been development and validation for the estimation of Lercanidipine and Atenolol stimultaneously in combined dosage form. A kromosil C-8 column having dimensions of 4.6µmx250mm and particle size of 5µm in isocratic mode , with mobile phase containing a mixture of Di- Potassium Hydrogen Phosphate and Acetonitrile in ratio of (70:30v/v) (pH adjusted to pH 6.5±0.5 using phosphoric acid was used . Detection was done at 215 nm using PDA detector. The mobile phase was pumped at a flow rate of 1.0µl/min and injection volume is10µl. The selected chromatographic conditions were founds to effectively separate Lercandipine (Rt 3.8min)(2) and Atenolol (Rt: 6.1 min) having resolution of 7.8. The method was validated in terms of linearity, accuracy, precision, and specificity, limit of detection and limit of quantitation.

Authors and Affiliations

Mahaboob Subhani Syed

Keywords

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  • EP ID EP656074
  • DOI -
  • Views 44
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How To Cite

Mahaboob Subhani Syed (2014). Analytical Method Development and Validation for Simultaneous Estimation of Lercandipine and Atenolol Tablet Dosage Form by RP-HPLC. International Journal of Pharmacy and Analytical Research, 3(1), 147-156. https://europub.co.uk/articles/-A-656074