Simple and rapid HPLC method for simultaneous determination of atenolol and chlorthalidone in spiked human plasma

A simple, sensitive and rapid chromatographic method was developed and validated for the simultaneous quantification of atenolol and chlorthalidone in human plasma using hydrochlorothiazide as internal standard (IS). The method utilized proteins precipitation with acetonitril as the only sample preparation involved prior to reverse phase-HPLC. The analytes were chromatographed on Shimpack cyanopropyl column with isocratic elution with 10 mM KH2PO4 (pH 6.0) – methanol (70:30, v/v) at ambient temperature with flow rate of 1 mL min ^-1 and UV detection at 225 nm. The chromatographic run time was less than 10 min for the mixture. The calibration curves were linear over the range of 0.1–10 µgmL ^-1. The method was validated in terms of accuracy, precision, absolute recovery, freeze–thaw stability, bench-top stability and reinjection reproducibility. The within-and between-day accuracy and precision were found to be within acceptable limits 15%. The analytes were stable after three freeze–thaw cycles (deviation 15%). The proposed method was specific for the simultaneous determination of atenolol and chlorthalidone in human plasma where there was no interference from endogenous biological substances.