Literature DB >> 26688343

Overcoming bioanalytical challenges associated with the separation and quantitation of GSK1278863, a HIF-prolyl hydroxylase inhibitor, and its 14 stereoisomeric metabolites.

Hermes Licea Perez1, Dana Knecht2, Christopher A Evans2.   

Abstract

GSK1278863 is an investigative drug under investigation for treatment of anemia associated with chronic kidney disease. Its metabolism is primarily metabolized by P450 enzymes where 19 unique metabolic species have been identified. These include multiple products of mono-, di-, and tri-oxygenation. Initially, two separate and complex ultra high performance liquid chromatography (UHPLC) reverse phase methodologies were developed, validated and applied to measure parent and various predominant and circulating metabolites in numerous clinical studies. However, 5 of the 6 oxidative metabolites may exist in different stereoisomeric forms, resulting in 14 separate species; therefore a chiral methodology was required to determine which stereoisomeric forms circulated in human. A variety of conventional approaches were explored, where in the end a supercritical fluid chromatography (SFC) method was required to separate this complex mixture of 14 stereoisomeric metabolites; data from these experiments provided important information on which species circulate in human. The details of these methodologies will be discussed herein.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  GSK1278863; High performance fraction collector LCJet system; Stereoisomeric metabolite separation; Supercritical fluid chromatography (SFC); Ultra high performance liquid chromatography tandem mass spectrometry (UHPLC–MS/MS); Ultra performance convergence chromatography (UPC(2))

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Year:  2015        PMID: 26688343     DOI: 10.1016/j.jchromb.2015.11.057

Source DB:  PubMed          Journal:  J Chromatogr B Analyt Technol Biomed Life Sci        ISSN: 1570-0232            Impact factor:   3.205


  4 in total

Review 1.  Quantitative mass spectrometry methods for pharmaceutical analysis.

Authors:  Glenn Loos; Ann Van Schepdael; Deirdre Cabooter
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2016-10-28       Impact factor: 4.226

2.  The role of hypoxia-inducible factor stabilizers in the treatment of anemia in patients with chronic kidney disease.

Authors:  Hongzhen Zhong; Tianbiao Zhou; Hongyan Li; Zhiqing Zhong
Journal:  Drug Des Devel Ther       Date:  2018-09-18       Impact factor: 4.162

3.  Clinical Pharmacokinetics of Daprodustat: Results of an Absorption, Distribution, and Excretion Study With Intravenous Microtracer and Concomitant Oral Doses for Bioavailability Determination.

Authors:  Kelly M Mahar; Stephen Caltabiano; Susan Andrews; Bandi Ramanjineyulu; Liangfu Chen; Graeme Young; Adrian Pereira; Alistair C Lindsay; Frans van den Berg; Alexander R Cobitz
Journal:  Clin Pharmacol Drug Dev       Date:  2021-10-28

4.  Pharmacokinetics of Daprodustat and Metabolites in Individuals with Normal and Impaired Hepatic Function.

Authors:  Kelly M Mahar; Bonnie C Shaddinger; Bandi Ramanjineyulu; Susan Andrews; Stephen Caltabiano; Alistair C Lindsay; Alexander R Cobitz
Journal:  Clin Pharmacol Drug Dev       Date:  2022-03-30
  4 in total

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