TY - JOUR
T1 - 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
AU - Gosetti, Fabio
AU - Chiuminatto, Ugo
AU - Mazzucco, Eleonora
AU - Robotti, Elisa
AU - Calabrese, Giorgio
AU - Gennaro, Maria Carla
AU - Marengo, Emilio
PY - 2011/9/16
Y1 - 2011/9/16
N2 - 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 0.768μgL-1 for PAHs and from 0.002 to 0.125μgL-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 - 50.000μgL-1): the average R percent ranges from 70.6% to 120.0%.
AB - 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 0.768μgL-1 for PAHs and from 0.002 to 0.125μgL-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 - 50.000μgL-1): the average R percent ranges from 70.6% to 120.0%.
KW - Aldehyde
KW - Food sample
KW - Mass spectrometry
KW - On-line SPE
KW - Polycyclic aromatic hydrocarbon
KW - UHPLC
UR - http://www.scopus.com/inward/record.url?scp=80051869415&partnerID=8YFLogxK
U2 - 10.1016/j.chroma.2011.06.085
DO - 10.1016/j.chroma.2011.06.085
M3 - Article
SN - 0021-9673
VL - 1218
SP - 6308
EP - 6318
JO - Journal of Chromatography A
JF - Journal of Chromatography A
IS - 37
ER -