Literature DB >> 1722438

Bile acids and conjugates identified in metabolic disorders by fast atom bombardment and tandem mass spectrometry.

R Libert1, D Hermans, J P Draye, F Van Hoof, E Sokal, E de Hoffmann.   

Abstract

From a study of the collision-activated fragmentation of bile acids, a qualitative analytical method based on negative ion fast atom bombardment tandem mass spectrometry has been developed. The times for sample preparation and analyses are short. Both free and conjugated bile acids are detected as they occur in biological fluids, without derivatization. For identifying bile acids and conjugates, the method offers better specificity and sensitivity than does the fast atom bombardment mass spectrometric technique alone. Specific scan modes have been developed for the selective detection of taurine conjugates, delta 4-unsaturated taurine conjugates, delta 4-3-keto free acids and their glycine conjugates, free acids and glycine conjugates bearing a hydroxyl group at the C-12 position, sulfates of glycine and taurine conjugates, and a C29 dicarboxylic bile acid, specific for generalized peroxisomal disorders. Applications of this technique demonstrate its potential usefulness, principally in the diagnosis of several peroxisomal disorders.

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Year:  1991        PMID: 1722438

Source DB:  PubMed          Journal:  Clin Chem        ISSN: 0009-9147            Impact factor:   8.327


  11 in total

1.  Rapid analysis of conjugated bile acids in plasma using electrospray tandem mass spectrometry: application for selective screening of peroxisomal disorders.

Authors:  A H Bootsma; H Overmars; A van Rooij; A E van Lint; R J Wanders; A H van Gennip; P Vreken
Journal:  J Inherit Metab Dis       Date:  1999-05       Impact factor: 4.982

Review 2.  Electrospray and tandem mass spectrometry in biochemistry.

Authors:  W J Griffiths; A P Jonsson; S Liu; D K Rai; Y Wang
Journal:  Biochem J       Date:  2001-05-01       Impact factor: 3.857

3.  Comparison of high- and low-energy collision-induced dissociation tandem mass spectrometry in the analysis of glycoalkaloids and their aglycons.

Authors:  M Claeys; H Van den Heuvel; S Chen; P J Derrick; F A Mellon; K R Price
Journal:  J Am Soc Mass Spectrom       Date:  1996-02       Impact factor: 3.109

4.  Quantitative-profiling of bile acids and their conjugates in mouse liver, bile, plasma, and urine using LC-MS/MS.

Authors:  Yazen Alnouti; Iván L Csanaky; Curtis D Klaassen
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2008-09-03       Impact factor: 3.205

5.  Distinct signatures of host-microbial meta-metabolome and gut microbiome in two C57BL/6 strains under high-fat diet.

Authors:  Alesia Walker; Barbara Pfitzner; Susanne Neschen; Melanie Kahle; Mourad Harir; Marianna Lucio; Franco Moritz; Dimitrios Tziotis; Michael Witting; Michael Rothballer; Marion Engel; Michael Schmid; David Endesfelder; Martin Klingenspor; Thomas Rattei; Wolfgang Zu Castell; Martin Hrabé de Angelis; Anton Hartmann; Philippe Schmitt-Kopplin
Journal:  ISME J       Date:  2014-06-06       Impact factor: 10.302

6.  Single-step analysis of individual conjugated bile acids in human bile using 1H NMR spectroscopy.

Authors:  G A Nagana Gowda; Omkar B Ijare; B S Somashekar; Ajay Sharma; V K Kapoor; C L Khetrapal
Journal:  Lipids       Date:  2006-06       Impact factor: 1.880

7.  Investigations of novel unsaturated bile salts of male sea lamprey as potential chemical cues.

Authors:  Nicholas S Johnson; Sang-Seon Yun; Weiming Li
Journal:  J Chem Ecol       Date:  2014-10-30       Impact factor: 2.626

8.  Fast-atom bombardment mass spectrometry and low energy collision-induced tandem mass spectrometry of tauroconjugated bile acid anions.

Authors:  V Stroobant; E de Hoffmann; R Libert; F Van Hoof
Journal:  J Am Soc Mass Spectrom       Date:  1995-07       Impact factor: 3.109

Review 9.  Bile acids: analysis in biological fluids and tissues.

Authors:  William J Griffiths; Jan Sjövall
Journal:  J Lipid Res       Date:  2010-01       Impact factor: 5.922

10.  Targeted inactivation of sister of P-glycoprotein gene (spgp) in mice results in nonprogressive but persistent intrahepatic cholestasis.

Authors:  R Wang; M Salem; I M Yousef; B Tuchweber; P Lam; S J Childs; C D Helgason; C Ackerley; M J Phillips; V Ling
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-06       Impact factor: 11.205

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