Original ArticleIndian Journal of Pharmaceutical Education and ResearchVol. 51 | Issue 2 | 2017 | pp. 343–348Open access
Simultaneous Determination of Sartans by High Performance Liquid Chromatography with Ultra Violet Detection
- 1*,
- 2,
- 3,
- 1
- 1 Department of Chemistry, Faculty of Pharmacy, Medical University-Sofia, BULGARIA.
- 2 Pharmaceutical Company Berlin Chemie, BULGARIA.
- 3 Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Medical University-Sofia, BULGARIA.
Published in Indian Journal of Pharmaceutical Education and Research
Correspondence: Vania Maslarska
Department of Chemistry, Faculty of Pharmacy, Medical University-Sofia, BULGARIA.
Email: vmaslarska@mail.bg
Copyright: © 2017 Manuscript Technomedia. This is an open access article.
- Published:
- Jan 1, 2017
- Received:
- Aug 30, 2016
- Accepted:
- Nov 23, 2016
- DOI:
- 10.5530/ijper.51.2.41
How to cite
Maslarska, V., Yankov, V., Obreshkova, D., & Bozhanov, S. (2017). Simultaneous Determination of Sartans by High Performance Liquid Chromatography with Ultra Violet Detection. Indian Journal of Pharmaceutical Education and Research, 51(2), 343–348. https://doi.org/10.5530/ijper.51.2.41
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
Subject
Article metadata
| Title | Simultaneous Determination of Sartans by High Performance Liquid Chromatography with Ultra Violet Detection |
|---|---|
| Authors | Vania Maslarska; Vladimir Yankov; Danka Obreshkova; Stanislav Bozhanov |
| Affiliations | Department of Chemistry, Faculty of Pharmacy, Medical University-Sofia, BULGARIA.; Pharmaceutical Company Berlin Chemie, BULGARIA.; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Medical University-Sofia, BULGARIA. |
| Corresponding author | vmaslarska@mail.bg |
| Journal | Indian Journal of Pharmaceutical Education and Research |
| Volume / Issue | Vol. 51, Issue 2 (2017) |
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