An on-line solid phase extraction (SPE) ultra high performance liquid chromatography tandem mass spectrometry method has been developed for the simultaneous identification and determination of thirteen polycyclic aromatic hydrocarbons (PAHs) and twelve aldehydes (derivatized with 2,4-dinitrophenylhydrazine). The chromatographic conditions have been optimized to obtain the maximum of sensitivity and resolution taking into account the different retention interactions and the different ionization conditions of PAHs and derivatized aldehydes. LOD values ranging from 0.028 to 0.768 mu g L(-1) for PAHs and from 0.002 to 0.125 mu g L(-1) for aldehydes were obtained. The resolution permitted the separation of four couples of PAH isomers. Sample pre-treatment and SPE were optimized in order to apply the whole methodology to the analysis of different food matrices as salmon, frankfurter, steak, and pork chop, subjected to different cooking modes (smoked, grilled, cooked in oil or in butter). Particular attention was devoted to the evaluation of matrix effect that was significantly reduced through the on-line SPE treatment. For each food matrix the method detection limits, the method quantitation limits, and the recovery R were evaluated. R was shown not to depend on analyte concentration in the explored concentration range (LOQ - 50.000 mu g L(-1)): the average R percent ranges from 70.6% to 120.0%

Gosetti, F., Chiuminatto, U., Mazzucco, E., Robotti, E., Calabrese, G., Gennaro, M., et al. (2011). Simultaneous determination of thirteen polycyclic aromatic hydrocarbons and twelve aldehydes in cooked food by an automated on-line solid phase extraction ultra high performance liquid chromatography tandem mass spectrometry. JOURNAL OF CHROMATOGRAPHY A, 1218(37), 6308-6318 [10.1016/j.chroma.2011.06.085].

Simultaneous determination of thirteen polycyclic aromatic hydrocarbons and twelve aldehydes in cooked food by an automated on-line solid phase extraction ultra high performance liquid chromatography tandem mass spectrometry

Gosetti, F
;
2011

Abstract

An on-line solid phase extraction (SPE) ultra high performance liquid chromatography tandem mass spectrometry method has been developed for the simultaneous identification and determination of thirteen polycyclic aromatic hydrocarbons (PAHs) and twelve aldehydes (derivatized with 2,4-dinitrophenylhydrazine). The chromatographic conditions have been optimized to obtain the maximum of sensitivity and resolution taking into account the different retention interactions and the different ionization conditions of PAHs and derivatized aldehydes. LOD values ranging from 0.028 to 0.768 mu g L(-1) for PAHs and from 0.002 to 0.125 mu g L(-1) for aldehydes were obtained. The resolution permitted the separation of four couples of PAH isomers. Sample pre-treatment and SPE were optimized in order to apply the whole methodology to the analysis of different food matrices as salmon, frankfurter, steak, and pork chop, subjected to different cooking modes (smoked, grilled, cooked in oil or in butter). Particular attention was devoted to the evaluation of matrix effect that was significantly reduced through the on-line SPE treatment. For each food matrix the method detection limits, the method quantitation limits, and the recovery R were evaluated. R was shown not to depend on analyte concentration in the explored concentration range (LOQ - 50.000 mu g L(-1)): the average R percent ranges from 70.6% to 120.0%
Articolo in rivista - Articolo scientifico
Polycyclic aromatic hydrocarbon, Aldehyde, On-line SPE, UHPLC, Mass spectrometry, Food sample
English
2011
1218
37
6308
6318
reserved
Gosetti, F., Chiuminatto, U., Mazzucco, E., Robotti, E., Calabrese, G., Gennaro, M., et al. (2011). Simultaneous determination of thirteen polycyclic aromatic hydrocarbons and twelve aldehydes in cooked food by an automated on-line solid phase extraction ultra high performance liquid chromatography tandem mass spectrometry. JOURNAL OF CHROMATOGRAPHY A, 1218(37), 6308-6318 [10.1016/j.chroma.2011.06.085].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/253184
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