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Development and validation of a simultaneous quantitative analytical method for two Alternaria toxins and their metabolites in plasma and urine using ultra-high-performance liquid chromatography-tandem mass spectrometry.
Zhang, Dan; Liu, Bolin; Xiao, Tingting; Wang, Yan; Zhao, Ziwei; Xie, Ji'an; Li, Weidong; Li, Rui; Cui, Jie.
Afiliación
  • Zhang D; Department of Inspection and Quarantine, School of Public Health, Anhui Medical University, Hefei, China.
  • Liu B; Physical and Chemical Laboratory, Anhui Provincial Center for Disease Control and Prevention, Hefei, China.
  • Xiao T; Department of Inspection and Quarantine, School of Public Health, Anhui Medical University, Hefei, China.
  • Wang Y; Physical and Chemical Laboratory, Anhui Provincial Center for Disease Control and Prevention, Hefei, China.
  • Zhao Z; Physical and Chemical Laboratory, Anhui Provincial Center for Disease Control and Prevention, Hefei, China.
  • Xie J; Physical and Chemical Laboratory, Anhui Provincial Center for Disease Control and Prevention, Hefei, China.
  • Li W; Physical and Chemical Laboratory, Anhui Provincial Center for Disease Control and Prevention, Hefei, China.
  • Li R; Physical and Chemical Laboratory, Anhui Provincial Center for Disease Control and Prevention, Hefei, China.
  • Cui J; Department of Inspection and Quarantine, School of Public Health, Anhui Medical University, Hefei, China.
J Sep Sci ; 47(12): e2400223, 2024 Jun.
Article en En | MEDLINE | ID: mdl-39031838
ABSTRACT
Much more attention has been paid to the contamination of Alternaria toxins because of food contamination and the threat to human health. In this study, an ultra-high-performance liquid chromatography-tandem mass spectrometry method was developed for the simultaneous detection of the prototypical alternariol, alternariol monomethylether, and the metabolites 4-oxhydryl alternariol, and alternariol monomethylether 3-sulfate ammonium salt of Alternaria toxins. The positive samples were used as matrix samples to optimize the different experimental conditions. 0.01% formic acid solution and acetonitrile were used as the mobile phase, and analytes were scanned in negative electron spray ionization under multiple reaction monitoring, and quantitative determination by isotope internal standard method. Application of this method to samples of human plasma and urine showed the detection of the above analytes. The results showed that the recoveries were from 80.40% to 116.4%, intra-day accuracy was between 0.6% and 8.0%, and inter-day accuracy was between 1.1% and 12.1%. The limit of detection of the four analytes ranged from 0.02 to 0.6 µg/L in urine, and 0.02 to 0.5 µg/L in plasma, respectively. Thus, the developed method was rapid and accurate for the simultaneous detection of analytes and provided a theoretical basis for the risk assessment of Alternaria toxins for human exposure.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Espectrometría de Masas en Tándem / Alternaria / Micotoxinas Límite: Humans Idioma: En Revista: J Sep Sci Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Espectrometría de Masas en Tándem / Alternaria / Micotoxinas Límite: Humans Idioma: En Revista: J Sep Sci Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Alemania