Determination of aflatoxins B1, B2, G1, G2 and ochratoxin A in animal feed by ultra high-performance liquid chromatography–tandem mass spectrometry
✍ Scribed by Sergio José López Grío; Antonia Garrido Frenich; José Luis Martínez Vidal; Roberto Romero-González
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 192 KB
- Volume
- 33
- Category
- Article
- ISSN
- 1615-9306
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A rapid and simple method was developed to determine aflatoxins B1, B2, G1, G2 and ochratoxin A in animal feed and pet foods by UHPLC–MS/MS. Because the complexity of the evaluated matrices, the proposed method is based on sonication extraction using an ACN/water mixture (80:20 v/v) followed by a clean‐up step utilising C~18~ as sorbent. Performance parameters of the method were evaluated, including linearity, trueness, precision and LOQ. Good linearity was found for all mycotoxins, with determination coefficients higher than 0.99 in the range considered, using matrix‐matched calibration for quantification purposes. Recoveries ranged from 84 to 113%, with RSD lower than 20%, whereas LOQs were 5 μg/kg for the assayed mycotoxins. Finally, the method was successfully applied to the analysis of 19 real samples, detecting aflatoxin G2 in two samples at 13 and 17 μg/kg respectively, whereas the other mycotoxins were detected at trace levels (
📜 SIMILAR VOLUMES
## Abstract A reliable isotope dilution method for simultaneous determination of fumonisin B1, fumonisin B2 and fumonisin B3 in traditional Chinese medicines by ultra‐high‐performance LC‐MS/MS was developed, and a special focus was placed on the optimization of extraction, cleanup, ultra‐high‐perfo
## Abstract A photodegradation study of Aflatoxin B~1~ (AFB~1~) in water solution was performed under UV irradiation at different AFB~1~ initial concentrations and UV irradiation intensities. The effect of UV intensity on the AFB~1~ photodegradation ratio is dominative, when compared with AFB~1~ in
## Abstract A high‐performance liquid chromatographic–tandem mass spectrometric (HPLC‐MS‐MS) method was developed and validated to determine simultaneously coumafuryl and coumateralyl in animal tissues using warfarin as an internal standard (IS). Animal tissue samples were extracted with ethyl acet