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Simultaneous determination of five Alternaria toxins in cereals using QuEChERS-based methodology.
Zhou, Jian; Xu, Jiao-Jiao; Cai, Zeng-Xuan; Huang, Bai-Fen; Jin, Mi-Cong; Ren, Yi-Ping.
Affiliation
  • Zhou J; Lab of Physicochemical Research, Department of Physicochemical & Toxicology, Zhejiang Provincial Center for Disease Control and Prevention, Zhejiang 310051, China; Zhejiang Provincial Key Lab of Health Risk Appraisal for Trace Toxic Chemicals, Ningbo Municipal Center for Disease Control and Prev
  • Xu JJ; Lab of Physicochemical Research, Department of Physicochemical & Toxicology, Zhejiang Provincial Center for Disease Control and Prevention, Zhejiang 310051, China. Electronic address: jjxucdc@163.com.
  • Cai ZX; Lab of Physicochemical Research, Department of Physicochemical & Toxicology, Zhejiang Provincial Center for Disease Control and Prevention, Zhejiang 310051, China.
  • Huang BF; Lab of Physicochemical Research, Department of Physicochemical & Toxicology, Zhejiang Provincial Center for Disease Control and Prevention, Zhejiang 310051, China.
  • Jin MC; Zhejiang Provincial Key Lab of Health Risk Appraisal for Trace Toxic Chemicals, Ningbo Municipal Center for Disease Control and Prevention, Ningbo 315010, China.
  • Ren YP; National Center for Food Safety Risk Assessment Application Technology Cooperation Center, Yangtze Delta Region Institute of Tsinghua University, Zhejiang 314006, China. Electronic address: renyiping@263.net.
J Chromatogr B Analyt Technol Biomed Life Sci ; 1068-1069: 15-23, 2017 Nov 15.
Article in En | MEDLINE | ID: mdl-29028614
Two analytical approaches, including ultra-high performance liquid chromatograph linked with photo-diode array/fluorescence detector, and ultra-high performance liquid chromatography-tandem mass spectrometry, have been proposed for simultaneous determination of five Alternaria toxins in cereals, which both based on QuEChERS strategy. After QuEChERS extraction and salting out, the collected supernatant was subjected to an extra dispersive liquid-liquid microextraction step prior to quantitative analysis. Response surface methodology based on central composite design was employed to optimize the micro-extraction conditions. During photo-diode array/fluorescence detector method validation, satisfactory analytical characteristics, in terms of selectivity, recovery (72.7%-109.1%), precision (inter-day RSDs <9.6%), sensitivity (limits of quantification ranged from 2.1µgkg-1 to 120.0µgkg-1) and linearity (R2 all higher than 0.9984), were achieved. Mass spectrometry method was employed as a certified method for accuracy. The two methodologies were successfully applied to 71 samples including three different matrices and the quantitative results were compared. As the result of non-parametric test shown, the established two analytical approach exhibited comparable quantitative accuracy to each other.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatography, High Pressure Liquid / Alternaria / Liquid Phase Microextraction / Mycotoxins Type of study: Prognostic_studies Language: En Journal: J Chromatogr B Analyt Technol Biomed Life Sci Journal subject: ENGENHARIA BIOMEDICA Year: 2017 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatography, High Pressure Liquid / Alternaria / Liquid Phase Microextraction / Mycotoxins Type of study: Prognostic_studies Language: En Journal: J Chromatogr B Analyt Technol Biomed Life Sci Journal subject: ENGENHARIA BIOMEDICA Year: 2017 Document type: Article Country of publication: