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RP-HPLC Method Development and Validation of Lamotrigine | Abstract

Der Pharma Chemica
Journal for Medicinal Chemistry, Pharmaceutical Chemistry, Pharmaceutical Sciences and Computational Chemistry

ISSN: 0975-413X
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Abstract

RP-HPLC Method Development and Validation of Lamotrigine

Author(s): *Pavan Kumar Puvvada, Vedi Gounder Murugan, S. Vimal Kumar and Pavan Kumar Padarthi

A simple, rapid and precise method was developed for the quantitative determination of lamotrigine in tablets. The method was based on RP-HPLC. Chromatographic separation was performed on a Supelco C18 (25cm X 4.6mm and i.d., 5μm) column using a mobile phase of methanol and 0.05 M potassium dihydrogen orthophosphate (65: 35v/v) adjusted the pH 4.5 with dilute orthophosphoric acid. The following system conditions were maintained throughout development and validation i.e., flow rate 1ml/min, column was maintained at room temperature and the detected by a UV-wave length at 270 nm. The lamotrigine was well resolved on the stationary phase and the retention time was 3.7 minute. The method was validated and shown to be linear for lamotrigine in 20-100 μg /ml. the correlation coefficient for lamotrigine is 0.9998 respectively. The method was validated for Precision, Accuracy, LOD and LOQ were determined to be 15ng/ml and 5 ng/ml respectively.


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