LC-MS/MS Based Quantitative Analysis of Remogliflozin in Rat Plasma: A Kinetic Study Approach

Authors

  • Smit J. Patel
  • Hiralben Mehta
  • Basheer Shaikh
  • Nadeem Khan

Keywords:

Remogliflozin, Rat Plasma, UPLC-MS/MS, Isocratic Elution, Bixafen

Abstract

This research utilized high-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method to quantitatively measure concentration of remogliflozin in rat plasma using bixafen as the internal standard. Samples were prepared by aqueous acetonitrile-based protein precipitation technique. Remogliflozin was then analysed by isocratic elution chromatography with a mobile phase consisting of 0.1% formic acid in milli-Q water (20): acetonitrile (80). Remogliflozin was monitored by m/z 451.4→289.4 transition for quantification and m/z 451.4→111.2 transition for qualification, and bixafen was determined by m/z 414.0→ 394 by multiple reaction monitoring (MRM) in positive ion electrospray ionization (ESI) source. Method exhibited good linearity in the range of 15 ng/mL to 2009 ng/mL. During pharmacokinetic experiments involving oral administration of remogliflozin in rat, the time to reach maximum concentration (Tmax) was found to 0.5 h in both males and females. The maximum concentration (Cmax) was found to be 201 ng/mL in males and 293 ng/mL in females while the last area under the concentration-time curve (AUClast) was determined to be 448 ng*h/mL for males and 297 ng*h/mL for females.

Downloads

Download data is not yet available.

References

M.R. Tammisetty, B.R. Challa, S.B. Puttagunta, Turkish Journal of Pharmaceutical Sciences, 18(3) (2021), doi: 10.4274/tjps.galenos.2020.39699

American Diabetes Association Professional Practice Committee; 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Care in Diabetes 2024. Diabetes Care, 2024; 47 (Supplement-1): S158–S178, doi: https://doi.org/10.2337/dc24-S009

M.A Abdul-Ghani, L. Norton, R.A DeFronzo, American Journal of Physiology Renal Physiology, 309(11) (2015), doi:10.1152/ajprenal.00267.2015

R. Maccari, R. Ottanà, Journal of Medicinal Chemistry, 65(16) (2022), doi:10.1021/acs.jmedchem.2c00867

T. Madaan, M. Akhtar, A.K Najmi, European Journal of Pharmaceutical Sciences, 93, (2016), doi:10.1016/j.ejps.2016.08.025

A. Markham, Drugs, 79(10) (2019), doi:10.1007/s40265-019-01150-9

M. Tandrima, K.S. Gubbiyappa, Rasayan Journal of Chemistry, 16(2) (2023), doi: http://doi.org/10.31788/RJC.2023.1628240

E. D. L. Putra, N. Nazliniwaty, F. R. Harun, N. Nerdy, Rasayan Journal of Chemistry, 13(2), 968(2020), http://dx.doi.org/10.31788/RJC.2020.1325645

I. Sopyan, D. Dwiputri, M. Muchtarid, Rasayan Journal of Chemistry, 13(4) (2020), http://dx.doi.org/10.31788/RJC.2020.1346045

K. Chandrasekhar, A. Manikandan, Rasayan Journal of Chemistry, 14(2) (2021), http://dx.doi.org/10.31788/RJC.2021.1425740

S.J. Patel , B. Chauhan, B. Shaikh, P. Chavan, N. Khan, Research Journal of Pharmacy and Technology, 17(10) (2024), doi: 10.52711/0974-360X.2024.0077

U. Jisha, S.S Prasanth, M.K Sibina, P.K. Sanooja, K.T. Akshara, R. Rajan, M. Farooq, A. A. Ajay, International Journal of pharmaceutical sciences, 2(8) (2024) doi: https://doi.org/10.5281/zenodo.13376811

V.H Herck, V. Baumans, C.J. Brandt, H.A Boere, A.P Hesp, H.A van Lith, M. Schurink, A.C Beynen, Laboratory Animals, 35(2) (2001), doi: 10.1258/0023677011911499

https://www.fda.gov/files/drugs/published/Bioanalytical-Method-Validation-Guidance-for-Industry.pdf

Downloads

Published

2025-06-21

How to Cite

1.
Patel SJ, Mehta H, Shaikh B, Khan N. LC-MS/MS Based Quantitative Analysis of Remogliflozin in Rat Plasma: A Kinetic Study Approach. J Neonatal Surg [Internet]. 2025Jun.21 [cited 2025Oct.10];14(8):503-8. Available from: https://www.jneonatalsurg.com/index.php/jns/article/view/7586