2013
DOI: 10.1016/j.jchromb.2012.12.016
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Simultaneous determination of carbamate insecticides and mycotoxins in cereals by reversed phase liquid chromatography tandem mass spectrometry using a quick, easy, cheap, effective, rugged and safe extraction procedure

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Cited by 26 publications
(8 citation statements)
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“…Similar LOD and LOQ values obtained for fusarin C, fusaric acid, FB 1 , FB 2 and FB 3 were 0.1 and 0.3 ng mL −1 , respectively. These limits were lower than those obtained by Kleigrewe et al (2011) and Zhang et al (2013), indicating that the sensitivity of the present method is high.…”
Section: Sample Preparation and Preliminary Methods Characterisationcontrasting
confidence: 74%
See 1 more Smart Citation
“…Similar LOD and LOQ values obtained for fusarin C, fusaric acid, FB 1 , FB 2 and FB 3 were 0.1 and 0.3 ng mL −1 , respectively. These limits were lower than those obtained by Kleigrewe et al (2011) and Zhang et al (2013), indicating that the sensitivity of the present method is high.…”
Section: Sample Preparation and Preliminary Methods Characterisationcontrasting
confidence: 74%
“…Based on the quick, easy, cheap, effective, rugged and safe (QuEChERS) protocol adapted for the analysis of aflatoxins, ochratoxin A, enniatin A, citrinin, fusarin C and FB1 (Frenich et al 2011;Arroyo-Manzanares et al 2013;Zhang et al 2013), the present study did not use the primary and secondary amine (PSA) as the base sorbent for removing the impurities of the sample solutions (for sample purification) since it can remove FB 1 , FB 2 and FB 3 from extracts due to ion exchange.…”
Section: Sample Preparation and Preliminary Methods Characterisationmentioning
confidence: 99%
“…However, Zhang et al [62] observed that, during the simultaneous analysis of mycotoxins and pesticides, the signal related to fumonisins (B1 and B2) dramatically decreased when Acquity HSS T3 was used, but they obtained better results using conventional Acquity BEH C18. Moreover, they observed that better responses were obtained when water/methanol was used as mobile phase instead of water/acetonitrile, and formic acid and ammonium acetate were added to the mobile phase in order to get suitable signal for both types of compounds (carbamate pesticides and mycotoxins).…”
Section: Multi-class/multi-residue Methodsmentioning
confidence: 99%
“…It comprises two steps: (i) an extraction based on partitioning via salting-out, involving the equilibrium between an aqueous and an organic layer; (ii) a dispersive SPE (dSPE) for further clean-up using combinations of MgSO 4 and different sorbents, such as C 18 or primary and secondary amine (PSA). QuEChERS-based methods have been recently reported for the extraction of different mycotoxins in cereal products [39][40][41], bread [42], eggs [43], or spices [44] and in the multiresidue extraction of different contaminants (including mycotoxins) in foods [45,46]. Also, we proposed this methodology for the determination of OTA in wine samples by capillary HPLC-LIF [18].…”
Section: Current Analytical Methods For Determination Of Mycotoxins Imentioning
confidence: 99%