Development and validation of RP-HPLC method for simultaneous estimation of allopurinol and alphalipoicacid in bulk and tablet dosage form


Volume :

5

Issue :

4

Abstract :

A new simple ,Rapid selective , precise and accurate gradient reversed phase high performance liquid chromatographic method (RP-HPLC )method has been developed And validated for simultaneous estimation of allopurinol and alphalipoic acid in bulk and tablet dosage form. Chromatographic analysis was performed on a c-18 column (250×4.6×5 µ)at ambient temperature .the column used was as BDS in Isocratic mode, with mobile phase containing tetrabutylammoniumhydroxide buffer and acetonitrile(70:30v/v) Adjusted to Ph 6.6 with dilute orthophosphoric acid solution . The flow rate was 0.8 Ml/min and effluents were monitored at 230nm. The retention times of allopurionol and alpha lipoicacid were found to be 2.33 min and 6.32 min, respectively. The method was validated as per ICH guidelines. The recoveries of allopurinol and alpha lipoic acid were found to be 98.53 to 100.03 and 98.5 to 99.9% respectively. The proposed method was found to be accurate reproducible and consistent. It was successfully applied for the analysis of these drugs in marketed formulations and could be effectively used for the routine analysis of formulations containing any one of the above drugs or a combination, without any alteration in the chromatographic conditions.
Journals Insights Open Access Journal Filmy Knowledge Hanuman Devotee Avtarit Wiki In Hindi Multiple Choice GK