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IJPER · Lens · Simultaneous Determination of Sartans by High Performance Liquid Chromatography with Ultra Violet Detection

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Article · Volume 51, Issue 2 · pp. 343–348

Simultaneous Determination of Sartans by High Performance Liquid Chromatography with Ultra Violet Detection

Vania Maslarska1, Vladimir Yankov2, Danka Obreshkova3, Stanislav Bozhanov1

  1. 1Department of Chemistry, Faculty of Pharmacy, Medical University-Sofia, BULGARIA.
  2. 2Pharmaceutical Company Berlin Chemie, BULGARIA.
  3. 3Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Medical University-Sofia, BULGARIA.

Abstract

Objective: A high performance liquid chromatographic method with ultra violet detection for simultaneous analysis of three sartans (Valsartan, Irbesartan and Telmisartan) has been developed for quality control. Method and Results: Isocratic elution on a LiChrospher C18 column (250 × 4 mm, particle size 5 μm) at the temperature 30ºC with a mobile phase consisting of 10mM phosphate buffer: acetonitrile (65:35 v/v) at a flow rate 1.0 ml/min has been done. The column eluent was monitored with a UV detector at 225 nm. This allowed a rapid detection and identification as well as quantitation of the eluting peaks. Method Validation: Calibration curves for all drugs were in the range of 5- 40 μg/ml and the linear regression coefficients were more than 0.995. Recovery rates for the sartans were in the range 96.5% to 103.1%. The limits of detection were calculated between 0.04- 0.06 μg/ ml. Also, the limits of quantification were 0.12- 0.16 μg/ml. Within-day and between-day coefficient of variation for all sartans at all concentrations in the range of 0.83 - 3.79% was calculated.Conclusion: The procedure can provide a simple, sensitive and fast method for the quality control of the three sartans in bulk and tablets.

Keywords: Drug analysis; Sartans; HPLC; Quality control; Hypertension; Heart failure

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