Volume : 10, Issue : 10, October – 2023

Title:

SIMULTANEOUS ESTIMATION OF FUROSEMIDE & TRIAMTERENE IN PURE AND PHARMACEUTICAL DOSAGE FORM BY USING RP-HPLC METHOD.

Authors :

G.Bhavani*, Dr.Nihar Ranjan Das, Dr.K.Balaji

Abstract :

A new, simple, precise, accurate and reproducible RP-HPLC method for Simultaneous estimation of Triamterene and Furosemide in bulk and pharmaceutical formulations. Separation of Triamterene and Furosemide was successfully achieved on a Phenomenex Luna C18 (4.6×250mm, 5µm) particle size or equivalent in an isocratic mode utilizing Acetonitrile: Phosphate Buffer (pH-4.6) (45:55 v/v) at a flow rate of 1.0mL/min and eluates was monitored at 245nm, with a retention time of 2.102 and 3.537 minutes for Triamterene and Furosemide respectively. The method was validated and the response was found to be linear in the drug concentration range of 6µg/mL to 14µg/mL for Triamterene and 18µg/mL to 42µg/mL for Furosemide. The values of the slope and the correlation coefficient were found to be 77824 and 0.999 for Triamterene and 10515 and 0.999 for Furosemide respectively. The LOD and LOQ for Triamterene were found to be 0.6µg/mL and 1.8µg/mL respectively. The LOD and LOQ for Furosemide were found to be 0.8 µg/mL and 2.4µg/mL respectively. This method was found to be good percentage recovery for Triamterene and Furosemide were found to be 100.351 and 100.93 respectively indicates that the proposed method is highly accurate. The specificity of the method shows good correlation between retention times of standard with the sample so, the method specifically determines the analytes in the sample without interference from excipients of tablet dosage forms. The method was extensively validated according to ICH guidelines for Linearity, Range, Accuracy, Precision, Specificity and Robustness.
Keywords: Triamterene and Furosemide, High performance liquid chromatography, Validation.

Cite This Article:

Please cite this article in press G.Bhavani et al, Simultaneous Estimation Of Furosemide & Triamterene In Pure And Pharmaceutical Dosage Form By Using Rp-Hplc Method, Indo Am. J. P. Sci, 2023; 10 (10).

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References:

BIBLIOGRAPHY:
1. Dr. Kealey and P.J Haines, Analytical Chemistry, 1stedition, Bios Publisher, (2002), PP 1-7.
2. A.BraithWait and F.J.Smith, Chromatographic Methods, 5thedition, Kluwer Academic Publisher, (1996), PP 1-2.
3. Andrea Weston and Phyllisr. Brown, HPLC Principle and Practice, 1st edition, Academic press, (1997), PP 24-37.
4. Yuri Kazakevich and Rosario Lobrutto, HPLC for Pharmaceutical Scientists, 1stedition, Wiley Interscience A JohnWiley & Sons, Inc., Publication, (2007), PP 15-23.
5. Chromatography, (online). URL:http://en.wikipedia.org/wiki/Chromatography.
6. Meyer V.R. Practical High-Performance Liquid Chromatography, 4th Ed. England, John Wiley & Sons Ltd, (2004), PP 7-8.
7. Sahajwalla CG a new drug development, vol 141, Marcel Dekker Inc., New York, (2004), PP 421–426.
8. D. H. Shewiy, E. Kaale, P. G. Risha, B. Dejaegher, J. S. Verbeke, Y. V. Heyden, Journal Pharmaceut. Biomed. Anal, 66, 2012, 11-23.
9. M. D. Rockville, General Tests, Chapter 621 – Chromatography System Suitability, United States Pharmacopeial Convention (USP), USP 31, 2009.
10. FDA Guidance for Industry-Analytical Procedures and Method Validation, Chemistry, Manufacturing, and Controls Documentation, Center for Drug Evaluation and Research (CDER) and Center for Biologics Evaluation and Research (CBER), 2000.
11. Korany MA, Mahgoub H, Ossama TF, Hadir MM. Application of artifcial neural networks for response surface modelling in HPLC method development. J Adv Res, 3, 2012, 53-63.
12. Swartz ME, Jone MD, Fowler P, Andrew MA. Automated HPLC method development and transfer. Lc Gc N. Am, 75, 2002, 49-50.
13. Synder LR, Kirkland JJ, Glajach JL. X. In Practical HPLC Methods Development. John Wiley , New York, 295, 1997, 643-712.
14. Swartz M, Murphy MB. New Fronties in Chromatography. Am Lab, 37, 2005, 22-27.
15. Dolan JW. Peak tailing and resolution. Lc Gc N. Am, 20, 2002, 430-436.
16. Chan CC, Leo YC, Lam H. Analytical method validation and Instrument Perfomance Validation. Vol-I, Wiley Interscince, 2004.
17. Shabir GA, Lough WJ., Arain SA, Bradshaw TK. Evaluation and application of best practice in analytical method validation. J Chromatogr RT, 30, 2007, 311-333.
18. Miller JN, Miller JC, Statistics and chemometrics for analytical chemistry Harlow, Pearson Prentice Hall, 2005, 263.
19. Huber L. Validation of HPLC methods. BioPharm. Int, 12, 1999, 64-66.