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Research Journal of Pharmacy and Technology
Year : 2010, Volume : 3, Issue : 4
First page : ( 1227) Last page : ( 1230)
Print ISSN : 0974-3618. Online ISSN : 0974-360X.

HPLC Method Development for Telmisartan and Amlodipine

Chabukswar A.R.1,*, Jagdale S.C.1, Kumbhar S.V.1, Desai D.J.1, Kuchekar B.S.1, Lokhande P.D.2

1MAEER'S Maharashtra Institute of Pharmacy, S.No. 124, MIT Campus, Paud Road, Kothrud, Pune-411038, India

2Département of Chemistry, University of Pune, Pune-411 007

*Corresponding Author E-mail: anigen18@rediffmail.com

Online published on 3 April, 2013.


A simple, rapid, and precise method is developed for the quantitative simultaneous estimation of telmisartan and amlodipine in combined pharmaceutical dosage form. A chromatographic separation of the two drugs was achieved with a Kromasil C18 (250 mm×4.6 mm, 5um) column using Acetonitrile: Methanol: Triethylamine buffer, PH 5.0 adjusted with O-Phosphoric acid. The instrumental settings are flow rate of 1.5 mL/min, and detector wavelength of 237 nm using a variable wavelength detector. The resolution between amlodipine and telmisartan were found to be more than 5. Theoretical plates for amlodipine and telmisartan were 10547 and 6313. Tailing factor for amlodipine and telmisartan was 1.85 and 1.48. The described method shows excellent linearity over a range of 320–480 μg/ml for telmisartan and 50–60 μg/ml for amlodipine. The correlation coefficient for telmisartan and amlodipine are 0.9999. The relative standard deviation for six measurements in two sets of each drug in tablets was always less than 2%. The proposed method was found to be suitable and accurate for quantitative determination of telmisartan and amlodipine in pharmaceutical preparations.



High Performance liquid chromatography, Method validation, Pharmaceutical preparation, amlodipine and telmisartan.


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