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Method Development and Validation for the Quantification of Abametapir in Biological Matrices by LC-ESI-MS/MS

1, 2,3, 3

  1. 1Department of Chemistry, Bir Tikandrajit University, Canchipur, Imphal West, Manipur, INDIA.
  2. 2Department of Pharmacy, Bir Tikandrajit University, Canchipur, Imphal West, Manipur, INDIA.
  3. 3Department of Pharmaceutical Analysis, TRR College of Pharmacy, Meerpet, Hyderabad, Telangana, INDIA.

CORRESPONDENCE

Dr. Darna Bhikshapathi

Department of Pharmacy, Bir Tikandrajit University, Canchipur, Imphal West, Manipur, INDIA.,

dbpathi71@gmail.com

Received: 02-03-2023; Accepted: 12-05-2024.

Volume 58, Issue 3s (Supplement) · pp. s1028-s1033 · 2024 · DOI: 10.5530/ijper.58.3s.102

ABSTRACT

Aim: A precise, linear and specific liquid chromatography-tandem mass spectrometry procedure was executed and subjected for validation for the quantification of plasma.Materials and Methods: The chromatography elution was carried out using a C18-Discovery column of 15 cm in length and 2.1 mm in internal diameter, packed with stationary phase particles of 5 μm size, at a flow rate of 0.80 mL/min. An isocratic elution process was conducted with a mobile phase solution consisting of methanol and 0.10% V/V HCOOH in a ratio of 90:10. The separation of Abametapir and Metformin was achieved by a liquid-liquid extraction process using ethyl acetate as the solvent.Results: A triple quadrupole mass spectrometer was used for the measurement of ions. Electrospray ionization is a technology that ionizes positively, and it was used in Multiple Reaction Monitoring (MRM) with parent/product ionic transitions m/z 185.1→106.06 for Abametapir and 130.1→60.20 for the Metformin internal standard. A calibration graph was constructed with values ranging from 2.05 to 82.00 ng/mL, resulting in the equation y=0.0149x+0.00221, with a r2 value above 0.99. The recovery values of Abametapir exceeded 94.27%, with its accuracy assessed in terms of relative error ranging from -4.04% to 6.52%.Conclusion: The accuracy, recovery and sensitivity values of Abametapir in the plasma sample, as shown by the established approach, highlight its significance in pharmacokinetic and bioequivalence research.

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    Krishnan, V. S., Bhikshapathi, D., & Cheruku, S. (2024). Method Development and Validation for the Quantification of Abametapir in Biological Matrices by LC-ESI-MS/MS. Indian Journal of Pharmaceutical Education and Research, 58(3s), s1028-s1033. https://doi.org/10.5530/ijper.58.3s.102

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    © 2024 Author(s)

    This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. CC BY 4.0