The accidental ingestion of leaves or cut branches of oleander (Nerium oleander) often results in severe poisoning in cattle. This natural shrub contains oleandrin, a highly toxic cardiac glycoside, which may prove fatal even at very low amounts. For this reason, a highly sensitive ultra-high performance liquid chromatography-tandem mass spectrometry method was developed and validated for in vivo oleandrin determination in bovine blood and serum samples or in bovine liver and heart for post-mortem diagnosis. The method was highly selective as the mass spectrometer worked in selected reaction monitoring mode using the first five most intense m/z transitions of oleandrin. The limits of detection and quantitation were 0.11 and 0.36 ng mL−1, respectively, whereas the method detection and quantitation limit values were in the range of 0.006–0.051 ng g−1 and 0.018–0.154 ng g−1, respectively. The chromatographic run was only 5 min and the time employed for the sample pretreatment (25–30 min) is useful to avoid the presence of matrix effects. All the recovery values were within 62.9–80.5%. The method was successfully used to analyse incurred samples from an accidentally poisoned cow and is expected to be applicable to forensic purposes.

UHPLC-MS/MS determination of oleandrin in blood and tissues of dairy cattle poisoned by oleander (: Nerium oleander)

Nebbia C.;
2019-01-01

Abstract

The accidental ingestion of leaves or cut branches of oleander (Nerium oleander) often results in severe poisoning in cattle. This natural shrub contains oleandrin, a highly toxic cardiac glycoside, which may prove fatal even at very low amounts. For this reason, a highly sensitive ultra-high performance liquid chromatography-tandem mass spectrometry method was developed and validated for in vivo oleandrin determination in bovine blood and serum samples or in bovine liver and heart for post-mortem diagnosis. The method was highly selective as the mass spectrometer worked in selected reaction monitoring mode using the first five most intense m/z transitions of oleandrin. The limits of detection and quantitation were 0.11 and 0.36 ng mL−1, respectively, whereas the method detection and quantitation limit values were in the range of 0.006–0.051 ng g−1 and 0.018–0.154 ng g−1, respectively. The chromatographic run was only 5 min and the time employed for the sample pretreatment (25–30 min) is useful to avoid the presence of matrix effects. All the recovery values were within 62.9–80.5%. The method was successfully used to analyse incurred samples from an accidentally poisoned cow and is expected to be applicable to forensic purposes.
2019
11
43
5562
5567
http://pubs.rsc.org/en/journals/journal/ay
Oleandrin - cattle - analytical methods - LC-MS/MS
Gosetti F.; Nebbia C.; Ceci L.; Carelli G.; Marengo E.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1722312
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