Simultaneous Determination of Aflatoxins and Ochratoxin A in Bee Pollen by Low-Temperature Fat Precipitation and Immunoaffinity Column Cleanup Coupled with LC-MS/MS

A simple and sensitive method has been developed for simultaneous determination of aflatoxins (AFB1, AFB2, AFG1, and AFG2) and ochratoxin A (OTA) in bee pollen. The analytes in the sample were extracted with a mixture of acetonitrile/water (60:40, v / v ), using low temperature for fat precipitation...

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Published inFood analytical methods Vol. 7; no. 3; pp. 690 - 696
Main Authors Xue, XiaoFeng, Selvaraj, Jonathan Nimal, Zhao, Liuwei, Dong, Haimin, Liu, Fengmao, Liu, Yang, Li, Yi
Format Journal Article
LanguageEnglish
Published Boston Springer US 01.03.2014
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Abstract A simple and sensitive method has been developed for simultaneous determination of aflatoxins (AFB1, AFB2, AFG1, and AFG2) and ochratoxin A (OTA) in bee pollen. The analytes in the sample were extracted with a mixture of acetonitrile/water (60:40, v / v ), using low temperature for fat precipitation, followed by immunoaffinity column cleanup of extracts. The mycotoxins were quantified using liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) with an electrospray ionization (ESI) and a triple quadrupole (QqQ) analyzer. Matrix effect, accuracy, and precision were evaluated and achieved good results calculated by matrix-matched calibration standards which reduced the influence of matrix effect. Recoveries at three levels were in the range of 74.3–96.5 % with RSD less than 10.0 %. The correlation coefficients ( r 2 ) of the five mycotoxins were higher than 0.997. The method showed high sensitivity with LOD below 0.05 μg/kg.
AbstractList A simple and sensitive method has been developed for simultaneous determination of aflatoxins (AFB1, AFB2, AFG1, and AFG2) and ochratoxin A (OTA) in bee pollen. The analytes in the sample were extracted with a mixture of acetonitrile/water (60:40, v / v ), using low temperature for fat precipitation, followed by immunoaffinity column cleanup of extracts. The mycotoxins were quantified using liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) with an electrospray ionization (ESI) and a triple quadrupole (QqQ) analyzer. Matrix effect, accuracy, and precision were evaluated and achieved good results calculated by matrix-matched calibration standards which reduced the influence of matrix effect. Recoveries at three levels were in the range of 74.3–96.5 % with RSD less than 10.0 %. The correlation coefficients ( r 2 ) of the five mycotoxins were higher than 0.997. The method showed high sensitivity with LOD below 0.05 μg/kg.
Author Selvaraj, Jonathan Nimal
Zhao, Liuwei
Liu, Fengmao
Liu, Yang
Dong, Haimin
Li, Yi
Xue, XiaoFeng
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  organization: Bee Research Institute, Chinese Academy of Agricultural Sciences, Risk Assessment Laboratory for Bee Products Quality and Safety of Ministry of Agriculture
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  givenname: Jonathan Nimal
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  givenname: Yi
  surname: Li
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  email: liyibqsitc@163.com
  organization: Bee Research Institute, Chinese Academy of Agricultural Sciences, Risk Assessment Laboratory for Bee Products Quality and Safety of Ministry of Agriculture
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Keywords Aflatoxins
Immunoaffinity column
Bee pollen
Ochratoxin A
Low-temperature fat precipitation
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Snippet A simple and sensitive method has been developed for simultaneous determination of aflatoxins (AFB1, AFB2, AFG1, and AFG2) and ochratoxin A (OTA) in bee...
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springer
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StartPage 690
SubjectTerms Analytical Chemistry
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Food Science
Microbiology
Title Simultaneous Determination of Aflatoxins and Ochratoxin A in Bee Pollen by Low-Temperature Fat Precipitation and Immunoaffinity Column Cleanup Coupled with LC-MS/MS
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