2011
DOI: 10.1016/j.foodchem.2010.10.009
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Analysis of fumonisins B1, B2 and their hydrolysed metabolites in pig liver by LC–MS/MS

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Cited by 29 publications
(34 citation statements)
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“…Recently, determination of fumonisins by LC/MS was significantly developed because of the high sensitivity and selectivity of the mass spectrometer (Gazzotti et al, 2011;Monbaliu et al, 2010;Ş enyuva & Gilbert, 2008). Fumonisins are detected by electrospray ionization (ESI) with such analyzers as singlequadrupole, triple-quadrupole, ion-trap and time-of-flight (Gazzotti et al, 2009;Li, Herrman, & Dai, 2010;Ş enyuva & Gilbert, 2008).…”
Section: Analytical Methods For Identification Of Fumonisinsmentioning
confidence: 99%
“…Recently, determination of fumonisins by LC/MS was significantly developed because of the high sensitivity and selectivity of the mass spectrometer (Gazzotti et al, 2011;Monbaliu et al, 2010;Ş enyuva & Gilbert, 2008). Fumonisins are detected by electrospray ionization (ESI) with such analyzers as singlequadrupole, triple-quadrupole, ion-trap and time-of-flight (Gazzotti et al, 2009;Li, Herrman, & Dai, 2010;Ş enyuva & Gilbert, 2008).…”
Section: Analytical Methods For Identification Of Fumonisinsmentioning
confidence: 99%
“…Also, in rat liver microsomes FB1 was scarcely metabolized (Merrill, Nikolova‐Karakashian, Schmelz, Morgan, & Stewart, ). As in the case of pigs (Gazzotti et al., ), there was a small conversion rate of FB1 to HFB1 (<1%), indicating that this process was not important during metabolism (Fodor et al., ) (Table ).…”
Section: Fumonisins (Fb)mentioning
confidence: 96%
“…FB incubation pinpointed a high stability in vitro in pigs and cows. In pig liver microsomes, only traces of HFB1 and HFB2 were observed (Gazzotti et al., ), while in bovine liver microsomes FB1 was not degraded or transformed to other compounds (Spotti, Pompa, & Caloni, ). Also, in rat liver microsomes FB1 was scarcely metabolized (Merrill, Nikolova‐Karakashian, Schmelz, Morgan, & Stewart, ).…”
Section: Fumonisins (Fb)mentioning
confidence: 99%
“…Among the published methods for mycotoxin determination in biological samples, including HPLC [20,31,32], GC-MS/MS [33], LC-MS [34,35], LC-MS/MS [4,18,36,37], and LC-HRMS [38], LC-MS/MS provides remarkable selectivity, accuracy and sensitivity. Most of the methods were applied to detect common regulated mycotoxins [4,5,8,19,32,37,[39][40][41][42], employing various sample preparation strategies such as the "dilute and shoot" approach [4,5,37,41], QuEChERS [15], liquid-liquid extraction (LLE) [20], immunoaffinity (IAC) columns [41,42], solid phase extraction (SPE) [18], and various combinations of these techniques [13]. However, only a few methods targeted for Alternaria and emerging Fusarium mycotoxins, including ENNB [38,43], AOH [3], AOH and AME [15], TeA [44], ENNs, and BEA [7], for human biomonitoring.…”
Section: Introductionmentioning
confidence: 99%