Key result
Validated reversed-phase HPLC method simultaneously quantifies clopidogrel, aspirin, and atorvastatin in rat plasma.
A simple and robust HPLC method was successfully developed and validated for the simultaneous quantitation of clopidogrel, aspirin, and atorvastatin in rat plasma and pharmaceutical formulations.
May aid rat pharmacokinetic studies of these agents; leaves open human validation and clinical translation.
A simple and robust analytical reversed-phase high-performance liquid chromatography method was developed and validated for simultaneous chromatographic elution of three cardiovascular drugs, namely clopidogrel, aspirin (ASP) and atorvastatin. The method was developed in rat plasma and dosage formulation with high-quality chromatographic separation between the drug peaks by using a stainless steel analytical column thermo beta-basic, C18 (25 × 0.46 cm, 5 µm). The system was operated at 25°C using a mobile phase consisting of acetonitrile and phosphate buffer (pH 3.0) in the gradient ratio at a flow rate of 1 mL min(-1) with ultraviolet detection monitored at 232 nm. The parametric statistics, i.e., correlation coefficient of 0.999, was assessed for all the drugs having linearity over the tested concentration range (10-10,000 ng mL(-1)) in rat plasma using an unweighted calibration curve. The accuracy of samples for six replicate measurements at lower limit of quantitation level was within limit. The method was applicable for the quality control of the mentioned drugs in raw material, bulk drug and pharmaceutical formulations as well as in pharmacokinetic studies.
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Porwal et al. (2015) studied this question. Reversed-phase high-performance liquid chromatography method was evaluated on Simultaneous chromatographic elution and quantitation of clopidogrel, aspirin, and atorvastatin. A reversed-phase HPLC method was successfully developed and validated for the simultaneous quantitation of clopidogrel, aspirin, and atorvastatin in rat plasma with high linearity (r=0.999).
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