Research Article

Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Teneligliptin Hydrobromide Hydrate in Synthetic Mixture

Volume: 10 Number: 4 November 11, 2023
EN

Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Teneligliptin Hydrobromide Hydrate in Synthetic Mixture

Abstract

For the quantitative measurement of Dapagliflozin propanediol monohydrate and Teneligliptin hydrobromide hydrate in synthetic mixture form in the presence of its degradants, precise, accurate, robust, cost-effective, and isocratic stability indicating RP-HPLC method was developed and validated. The mobile phase comprises [Methanol: 20 mM Ammonium formate (70:30 v/v)] at a flow rate of 1.0 ml/min, injection volume of 20 µl, and UV detection at 225 nm. Separation was accomplished using Gemini, C18 column. Teneligliptin hydrobromide hydrate and Dapagliflozin propanediol monohydrate were eluted with retention times of 6.65 minutes and 4.20 minutes, respectively. This procedure was approved following ICH guideline Q2 (R1). The calibration plots for Dapagliflozin propanediol monohydrate and Teneligliptin hydrobromide hydrate have correlation coefficients of 0.9995 and 0.9996 over the concentration ranges of 5-100 µg/ml and 10-200 µg/ml respectively. For Dapagliflozin propanediol monohydrate and Teneligliptin hydrobromide hydrate, accuracy ranged from 99.81-100.78% and 99.13-100.69%, respectively. For Dapagliflozin propanediol monohydrate and Teneligliptin hydrobromide hydrate, the LOD was found to be 0.947 µg/ml and 1.355 µg/ml. In contrast, the LOQ was 2.869 µg/ml and 4.107 µg/ml, respectively. The findings demonstrated the applicability of the devised approach for routine analysis of Teneligliptin hydrobromide hydrate and Dapagliflozin propanediol monohydrate in a synthetic mixture form with its degradants.

Keywords

Thanks

The authors are grateful to MERRIL PHARMA PVT. LTD. for providing standard samples of Dapagliflozin propanediol monohydrate and teneligliptin hydrobromide hydrate and B.K. MODY GOVERNMENT PHARMACY COLLEGE, RAJKOT, and SAURASHTRA UNIVERSITY to offer facilities to work.

References

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Details

Primary Language

English

Subjects

Analytical Chemistry

Journal Section

Research Article

Publication Date

November 11, 2023

Submission Date

April 26, 2023

Acceptance Date

August 17, 2023

Published in Issue

Year 2023 Volume: 10 Number: 4

APA
Hıteksha, D., & Chotaliya, U. (2023). Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Teneligliptin Hydrobromide Hydrate in Synthetic Mixture. Journal of the Turkish Chemical Society Section A: Chemistry, 10(4), 1025-1034. https://doi.org/10.18596/jotcsa.1288000
AMA
1.Hıteksha D, Chotaliya U. Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Teneligliptin Hydrobromide Hydrate in Synthetic Mixture. JOTCSA. 2023;10(4):1025-1034. doi:10.18596/jotcsa.1288000
Chicago
Hıteksha, Dobarıya, and Urvi Chotaliya. 2023. “Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Teneligliptin Hydrobromide Hydrate in Synthetic Mixture”. Journal of the Turkish Chemical Society Section A: Chemistry 10 (4): 1025-34. https://doi.org/10.18596/jotcsa.1288000.
EndNote
Hıteksha D, Chotaliya U (November 1, 2023) Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Teneligliptin Hydrobromide Hydrate in Synthetic Mixture. Journal of the Turkish Chemical Society Section A: Chemistry 10 4 1025–1034.
IEEE
[1]D. Hıteksha and U. Chotaliya, “Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Teneligliptin Hydrobromide Hydrate in Synthetic Mixture”, JOTCSA, vol. 10, no. 4, pp. 1025–1034, Nov. 2023, doi: 10.18596/jotcsa.1288000.
ISNAD
Hıteksha, Dobarıya - Chotaliya, Urvi. “Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Teneligliptin Hydrobromide Hydrate in Synthetic Mixture”. Journal of the Turkish Chemical Society Section A: Chemistry 10/4 (November 1, 2023): 1025-1034. https://doi.org/10.18596/jotcsa.1288000.
JAMA
1.Hıteksha D, Chotaliya U. Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Teneligliptin Hydrobromide Hydrate in Synthetic Mixture. JOTCSA. 2023;10:1025–1034.
MLA
Hıteksha, Dobarıya, and Urvi Chotaliya. “Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Teneligliptin Hydrobromide Hydrate in Synthetic Mixture”. Journal of the Turkish Chemical Society Section A: Chemistry, vol. 10, no. 4, Nov. 2023, pp. 1025-34, doi:10.18596/jotcsa.1288000.
Vancouver
1.Dobarıya Hıteksha, Urvi Chotaliya. Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Teneligliptin Hydrobromide Hydrate in Synthetic Mixture. JOTCSA. 2023 Nov. 1;10(4):1025-34. doi:10.18596/jotcsa.1288000

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