Literature DB >> 22222607

LC-ESI-MS/MS method for quantification of ambrisentan in plasma and application to rat pharmacokinetic study.

Ramakrishna Nirogi1, Vishwottam Kandikere, Prashanth Komarneni, Raghupathi Aleti, Nagasuryaprakash Padala, Ilayaraja Kalaikadhiban.   

Abstract

A sensitive high-performance liquid chromatography-positive ion electrospray tandem mass spectrometry method was developed and validated for the quantification of ambrisentan in plasma. The analyte and the internal standard (armodafinil) were extracted from plasma by acetonitrile precipitation and they were separated on a reversed-phase C(18) column with a gradient program. The MS acquisition was performed with multiple reaction monitoring mode using the respective [M + H](+) ions, m/z 379-347 for ambrisentan and m/z 274-167 for the IS. The assay exhibited a linear dynamic range of 1-2000 ng/mL for ambrisentan in plasma. Acceptable precision (<10%) and accuracy (100 ± 8%) were obtained for concentrations over the standard curve range. The method was successfully applied to quantify ambrisentan concentrations in a rodent pharmacokinetic study after a single oral administration of ambrisentan at 2.5 mg/kg to rats. Following oral administration the maximum mean concentration in plasma (C(max) ; 1197 ± 179 ng/mL) was achieved at 1.0 ± 0.9 h (T(max) ), and the area under the curve (AUC) was 6013 ± 997 ng h/mL. Therefore, development of such a simple and sensitive method in rat plasma should translate into a method for ambrisentan in human plasma for clinical trials.
Copyright © 2012 John Wiley & Sons, Ltd.

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Year:  2012        PMID: 22222607     DOI: 10.1002/bmc.2670

Source DB:  PubMed          Journal:  Biomed Chromatogr        ISSN: 0269-3879            Impact factor:   1.902


  3 in total

1.  Extractive spectrophotometric determination of ambrisentan.

Authors:  Namasani Santhosh Kumar; Avula Prameela Rani; Telu Visalakshi; Chandra Bala Sekharan
Journal:  Adv Pharm Bull       Date:  2013-02-07

2.  Evaluation of herb-drug interaction of ambrisentan with shikonin based on UPLC-MS/MS.

Authors:  Tian Lan; Ping Fang; Xuemei Ye; Xia Lan; Ren-Ai Xu
Journal:  Pharm Biol       Date:  2021-12       Impact factor: 3.503

3.  Stability-Indicating RP-HPLC Method for the Determination of Ambrisentan and Tadalafil in Pharmaceutical Dosage Form.

Authors:  Jayvadan K Patel; Nilam K Patel
Journal:  Sci Pharm       Date:  2014-05-22
  3 in total

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