Literature DB >> 21489890

Determination of 3-methoxysalicylamine levels in mouse plasma and tissue by liquid chromatography-tandem mass spectrometry: application to in vivo pharmacokinetics studies.

Irene Zagol-Ikapitte1, Venkataraman Amarnath, Satyawan Jadhav, John A Oates, Olivier Boutaud.   

Abstract

We report the development of a sensitive liquid chromatography-tandem mass spectrometric assay to quantitate 3-methoxysalicylamine (3-MoSA) in biological samples. Derivatization with 1,1'-thiocarbonyldiimidazole followed by C(18) reverse-phase chromatography allowed the detection of both analyte and internal standard (hexylsalicylamine) using electrospray ionization and selected reaction monitoring (SRM) in positive ion mode. We monitored the transitions from m/z 196.7 to 65.1 and from m/z 250.1 to 77.1 for 3-MoSA and HxSA, respectively. The method is validated with respect to linearity (r(2)=0.995), precision (<17% RSD), recovery (100% for 3-MoSA and HxSA), and stability (77% after storage up to 7 month at -80°C). The LOD and LOQ were 16.12 and 48.87 μg/l, respectively and the LLOQ of 1 pg/ml. In addition, we used this assay to analyze the pharmacokinetics of 3-MoSA in mouse plasma and tissues following both intraperitoneal and oral administration, providing new information regarding the distribution of this compound in vivo.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21489890      PMCID: PMC3091354          DOI: 10.1016/j.jchromb.2011.03.026

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


  21 in total

1.  Isolevuglandin-protein adducts in humans: products of free radical-induced lipid oxidation through the isoprostane pathway.

Authors:  R G Salomon; E Batyreva; K Kaur; D L Sprecher; M J Schreiber; J W Crabb; M S Penn; A M DiCorletoe; S L Hazen; E A Podrez
Journal:  Biochim Biophys Acta       Date:  2000-05-31

2.  Identification of extremely reactive gamma-ketoaldehydes (isolevuglandins) as products of the isoprostane pathway and characterization of their lysyl protein adducts.

Authors:  C J Brame; R G Salomon; J D Morrow; L J Roberts
Journal:  J Biol Chem       Date:  1999-05-07       Impact factor: 5.157

3.  Isolevuglandins, a novel class of isoprostenoid derivatives, function as integrated sensors of oxidant stress and are generated by myeloperoxidase in vivo.

Authors:  Eugenia Poliakov; Marie-Luise Brennan; Jennifer Macpherson; Renliang Zhang; Wei Sha; Laura Narine; Robert G Salomon; Stanley L Hazen
Journal:  FASEB J       Date:  2003-12       Impact factor: 5.191

Review 4.  Protein lipidation.

Authors:  Marissa J Nadolski; Maurine E Linder
Journal:  FEBS J       Date:  2007-09-24       Impact factor: 5.542

5.  Selection of experimental conditions for the accurate determination of blood--brain transfer constants from single-time experiments: a theoretical analysis.

Authors:  R G Blasberg; C S Patlak; J D Fenstermacher
Journal:  J Cereb Blood Flow Metab       Date:  1983-06       Impact factor: 6.200

6.  Characterization of covalent adducts of nucleosides and DNA formed by reaction with levuglandin.

Authors:  Erica J Carrier; Venkataraman Amarnath; John A Oates; Olivier Boutaud
Journal:  Biochemistry       Date:  2009-11-17       Impact factor: 3.162

7.  Characterization of bis(levuglandinyl) urea derivatives as products of the reaction between prostaglandin H2 and arginine.

Authors:  Irene Zagol-Ikapitte; Nathalie Bernoud-Hubac; Venkataraman Amarnath; L Jackson Roberts; Olivier Boutaud; John A Oates
Journal:  Biochemistry       Date:  2004-05-11       Impact factor: 3.162

8.  Levuglandin E2 crosslinks proteins.

Authors:  R S Iyer; S Ghosh; R G Salomon
Journal:  Prostaglandins       Date:  1989-04

9.  Characterization of scavengers of gamma-ketoaldehydes that do not inhibit prostaglandin biosynthesis.

Authors:  Irene Zagol-Ikapitte; Venkataraman Amarnath; Manju Bala; L Jackson Roberts; John A Oates; Olivier Boutaud
Journal:  Chem Res Toxicol       Date:  2010-01       Impact factor: 3.739

10.  Levuglandinyl adducts of proteins are formed via a prostaglandin H2 synthase-dependent pathway after platelet activation.

Authors:  Olivier Boutaud; Junyu Li; Irene Zagol; Elizabeth A Shipp; Sean S Davies; L Jackson Roberts; John A Oates
Journal:  J Biol Chem       Date:  2003-03-11       Impact factor: 5.157

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  3 in total

1.  On-tissue chemical derivatization of 3-methoxysalicylamine for MALDI-imaging mass spectrometry.

Authors:  Almary Chacon; Irene Zagol-Ikapitte; Venkataraman Amarnath; Michelle L Reyzer; John A Oates; Richard M Caprioli; Olivier Boutaud
Journal:  J Mass Spectrom       Date:  2011-08       Impact factor: 1.982

Review 2.  Isolevuglandins as mediators of disease and the development of dicarbonyl scavengers as pharmaceutical interventions.

Authors:  Sean S Davies; Linda S May-Zhang; Olivier Boutaud; Venkataraman Amarnath; Annet Kirabo; David G Harrison
Journal:  Pharmacol Ther       Date:  2019-10-16       Impact factor: 12.310

3.  Levuglandin forms adducts with histone h4 in a cyclooxygenase-2-dependent manner, altering its interaction with DNA.

Authors:  Erica J Carrier; Irene Zagol-Ikapitte; Venkataraman Amarnath; Olivier Boutaud; John A Oates
Journal:  Biochemistry       Date:  2014-04-11       Impact factor: 3.162

  3 in total

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