Identification and quantification of the atypical metabolite ornithine-lactam in human plasma by liquid chromatography–tandem mass spectrometry (LC–MS/MS)

In the late 1970s the atypical metabolite of ornithine, ornithine-lactam, has been observed in urine samples of patients suffering from hyperornithinemia. However, not least due to insufficient analytical methods, until now there are no data available about ornithine-lactam in human plasma. Here, we...

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Veröffentlicht in:Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2009-08, Vol.877 (23), p.2284-2289
Hauptverfasser: Martens-Lobenhoffer, Jens, Becker, Achim, Freude, Horst, Bode-Böger, Stefanie M.
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Sprache:eng
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Zusammenfassung:In the late 1970s the atypical metabolite of ornithine, ornithine-lactam, has been observed in urine samples of patients suffering from hyperornithinemia. However, not least due to insufficient analytical methods, until now there are no data available about ornithine-lactam in human plasma. Here, we describe a new method, which is, for the first time, suitable to identify and quantify ornithine-lactam in human EDTA-plasma. The method was validated according to the requirements of the FDA guidance for bioanalytical method validation. The analytes were extracted on mixed mode cation exchange SPE columns, separated on a silica analytical HPLC column working in the HILIC mode and detected on a tandem mass spectrometer equipped with an ESI ion source. As internal standard newly synthesized stable isotope labeled D 6-ornithine-lactam was used. The calibration function was linear in the range of 0.1–5 μM. Intra- and inter-day precision and accuracy was better than 14% at all concentration levels. In EDTA-plasma samples from 30 volunteers ornithine-lactam concentrations ranging from 0.136 to 0.653 μM were determined. These concentrations correlated significantly ( p < 0.001, R 2 = 0.784) to those of ornithine in EDTA-plasma.
ISSN:1570-0232
1873-376X
DOI:10.1016/j.jchromb.2009.01.031