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STABILITY INDICATING RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF PREGABALIN AND EPALRESTAT
Uriti Sri Venkatesh*, Chintakayala Chandrasekhar, Regeti Suneetha and Dharmavarapu Keerthana
ABSTRACT A simple, precise, accurate, rapid, robust and economical RP-HPLC method was developed and validated for the assay of Epalrestat and Pregabalin in tablet formulation. This method yielded high recoveries with good linearity and precision. The method was developed using WATERS HPLC 2965 SYSTEM with Auto Injector and PDA 2996 Detector. Software used is Empower 2. Discovery (250 x 4.6mm, 5μ) column is used as stationary phase with mobile phase containing mixture of buffer: acetonitrile, 50:50 (v/v). The eluted compound was monitored at 241nm. The developed method was validated for parameters of Specificity, Linearity, Precision, Accuracy, Limit of Detection, Limit of Quantification and Robustness as per approved ICH guidelines. The results obtained after the analysis of drug by the proposed validation parameters were highly reproducible and reliable. The % Assay of Epalrestat and Pregabalin by the proposed method wasfound to be 98.0% - 99.0%. The % RSD of the drug was found to be 0.7 & 0.6 which are within limit. The validation parameters results of the drug were found to be within limit. Keywords: . [Download Article] [Download Certifiate] |
