Identification of Acepromazine and Its Metabolites in Horse Plasma and Urine by LC–MS/MS and Accurate Mass Measurement

Acepromazine maleate (Sedalin ® ) was administered orally to six thoroughbred horses at a dose of 0.15 mg kg −1 . Urine and blood samples were collected up to 412 h post-administration. Plasma and urine were hydrolysed; plasma samples were then processed using liquid–liquid extraction and urine samp...

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Veröffentlicht in:Chromatographia 2012-06, Vol.75 (11-12), p.635-643
Hauptverfasser: Wieder, M. E., Gray, B. P., Brown, P. R., Hudson, S., Pearce, C. M., Paine, S. W., Hillyer, L.
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Sprache:eng
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Zusammenfassung:Acepromazine maleate (Sedalin ® ) was administered orally to six thoroughbred horses at a dose of 0.15 mg kg −1 . Urine and blood samples were collected up to 412 h post-administration. Plasma and urine were hydrolysed; plasma samples were then processed using liquid–liquid extraction and urine samples using solid-phase extraction. A sensitive tandem mass spectrometric method was developed in this study, achieving a lower limit of quantification for acepromazine of 10 pg mL −1 in plasma and 100 pg mL −1 in urine. Acepromazine, hydroxyethylpromazine, hydroxyacepromazine, hydroxyethylpromazine sulphoxide, hydroxyethylhydroxypromazine, dihydroxyacepromazine and dihydroxyhydroxyethylpromazine were detected in the post-administration samples. The parent drug and its metabolites were identified using a combination of UPLC–MS/MS and accurate mass measurement. Separation of the structural isomers hydroxyethylpromazine sulphoxide and hydroxyethylhydroxypromazine was another significant outcome of this work and demonstrated the advantages to be gained from investing in chromatographic method development.
ISSN:0009-5893
1612-1112
DOI:10.1007/s10337-012-2234-4