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 mL1, respectively, whereas the method detection and quantitation limit values were in the range of 0.006–0.051 ng g1 and 0.018–0.154 ng g1, 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)

Ceci, Luigi;Carelli, Grazia;
2019

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 mL1, respectively, whereas the method detection and quantitation limit values were in the range of 0.006–0.051 ng g1 and 0.018–0.154 ng g1, 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.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11586/248041
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