“…For these reasons, several immunoassays, including enzyme‐linked immunosorbent assay (ELISA), flow‐through immunoassays (FIA), lateral flow devices (LFD), and fluorescence polarization immunoassays (FPIA), have been extensively developed for the rapid screening of DON in cereals due to their rapidity, simplicity, and cost effectiveness . In particular, an FPIA for the determination of DON in wheat bran and whole‐wheat flour showed performances, in terms of sensitivity, accuracy, and precision, comparable to those of chromatographic techniques .…”
“…For these reasons, several immunoassays, including enzyme‐linked immunosorbent assay (ELISA), flow‐through immunoassays (FIA), lateral flow devices (LFD), and fluorescence polarization immunoassays (FPIA), have been extensively developed for the rapid screening of DON in cereals due to their rapidity, simplicity, and cost effectiveness . In particular, an FPIA for the determination of DON in wheat bran and whole‐wheat flour showed performances, in terms of sensitivity, accuracy, and precision, comparable to those of chromatographic techniques .…”
“…GC offers some benefits over LC methods such as lower instrument cost as well as lower maintenance, even though analysis of mycotoxins by GC requires derivatization. Ion sources used in LC-MS are also related to ion suppression or enhancement with strong consequences on the accuracy, precision and sensitivity of the methods (Ran et al, 2013).…”
“…3-ADON, 15-ADON and T-2 showed 100% of deacetylation after 24 h of exposure. The Michaelis-Menten (K M ) constant, which shows the affinity of an enzyme for its substrate, revealed that carboxylesterase had a major affinity to 15 The data presented from our work represents a preliminary study, which demonstrated that optimization can be used to provide even more promising degradation values. The use of enzymes with high purification grade and low cost, presented in this work, represents a significant advance to the works mentioned so far, in terms of velocity, time and selectivity in enzymatic action specificity.…”
Section: Trichothecene a And B Biodegradationmentioning
confidence: 84%
“…For trichothecenes, derivatization is performed by silanization, acylation and alkylation reactions. 11,15 The development of a method suitable for multiple mycotoxins, with a common sample preparation procedure, requiring only a final determination is highly desirable. Most analytical techniques used for the determination of trichothecenes proposed their extraction from the food matrix into a solvent.…”
An investigation was conducted to standardize conditions for laccase and lipase activity required to maximize trichothecene degradation. The analytical methods were suitable and validated in model solutions for detection of five analytes (T-2 toxin, deoxynivalenol, nivalenol, 3-acetyldeoxynivalenol and 15-acetyldeoxynivalenol), the methods were then applied in the degradation tests of these trichothecenes. The method of salting-out assisted liquid-liquid extraction (SALLE), using three different NaCl concentration levels, obtained recoveries in the range of 47.4-103.4% at pH 5.0 and 36.6-106.8% at pH 7.0, with an intra-day relative standard deviation under 15% for the majority of the compounds. Quantification limits remained in the region of 0.07 μg mL -1 for 15-acetyldeoxynivalenol and 0.3 μg mL -1 for nivalenol. Finally, the suitable analytical methods were applied in a study of trichothecene degradation by enzymatic action, resulting in a reduction of 12.3% for T-2 toxin, 68.4% for deoxynivalenol, 50.2% for 3-acetyldeoxynivalenol and 45.4% for 15-acetyldeoxynivalenol.
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