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Pitfall in the high-throughput quantification of whole blood cyclosporin A using liquid chromatography-tandem mass spectrometry

  • Michael Vogeser and Ute Spöhrer
Published/Copyright: September 21, 2011

Abstract

In a growing number of laboratories the technique of liquid chromatography-tandem mass spectrometry is used for the quantification of cyclosporin A in whole blood, employing cyclosporin D as the internal standard. Cyclosporin A is extensively metabolized in vivo; in liquid chromatography-tandem mass spectrometry respective metabolites can give rise to both parent and product ions that are isobaric with ions commonly used for the detection of cyclosporin A and cyclosporin D, respectively. In this article it is demonstrated that limited chromatography with co-elution of such metabolites together with cyclosporin A and cyclosporin D can lead to incorrect results.


Corresponding author: Michael Vogeser, Institute of Clinical Chemistry, Hospital of the University of Munich, 81366 Munich, Germany Phone: +49-89-7095-3221, Fax: +49-89-7095-3240,

References

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Received: 2004-10-8
Accepted: 2005-2-3
Published Online: 2011-9-21
Published in Print: 2005-4-1

© by Walter de Gruyter Berlin New York

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