Abstract
A new simple, specific, accurate, precise and robust normal phase high performance thin layer chromatography (HPTLC) method were developed and validated for simultaneous estimation of two antihypertensive drugs Amlodipine Besylate (AMB) and Telmisartan (TEL) in pharmaceutical dosage form. Chromatographic separation of the drugs was performed over aluminium plates precoated with silica gel 60F254 as the stationary phase and solvent system comprised of chloroform: methanol: formic acid (8:2.5:0.5 v/v/v). Densitometric evaluation of the separated zones was performed at 251 nm. Analytical performance of the suggested HPTLC method was validated according to the ICH guidelines with respect to the linearity, accuracy, precision, detection and quantitation limits, robustness and specificity. The two drugs were satisfactory resolve with Rf values 0.57 ± 0.02 and 0.77 ± 0.02 for AMB and TEL, respectively. The linearity was studied in the concentration range 100–600 μg/ml for both AMB and TEL with a correlation coefficients (r2) >0.9997 and 0.9999, respectively. Statistical analysis showed that the developed method is repeatable and selective for the estimation of AMB and TEL in its pharmaceutical formulations.
Acknowledgments
The one of the author Trimurti L. Lambat gratefully acknowledges the funding support rendered by the DST, New Delhi for the INSPIRE Fellowship [IF120418]. We are also thanks to the Director, Government Institute of Science, Nagpur for providing good research facilities. We are also thanks to Glenmark pharmaceutical Ltd. Mumbai for providing gift sample of Amlodipine Besylate and Telmisartan and Anchrom Lab., Mumbai for providing the experimental facilities.
Disclosure statement
No potential conflict of interest was reported by the authors.