Residual Analysis of Aflatoxins in Spice by HPLC Coupled with Solid-Phase Dispersive Extraction and Solid-Phase Fluorescence Derivatization Method

被引:9
|
作者
Saito, Koichi [1 ]
Ishii, Junki [1 ]
Naniwa, Misaki [1 ]
Ishii, Rie [2 ]
Kato, Mihoko [3 ]
Kondo, Takahide [4 ]
Sakurai, Hikaru [5 ]
Taniguchi, Masaru [6 ]
Hashiguchi, Shigeki [7 ]
Hayashi, Takako [8 ]
Ito, Rie [1 ]
机构
[1] Hoshi Univ, Fac Pharmaceut Sci, Dept Analyt Chem, Shinagawa Ku, 2-4-41 Ebara, Tokyo 1428501, Japan
[2] Saitama Inst Publ Hlth, Saitama, Japan
[3] Frontier Inst Co Ltd, Ishikari, Hokkaido, Japan
[4] Saitama City Inst Hlth Sci & Res, Saitama, Japan
[5] Yokohama City Inst Hlth, Yokohama, Kanagawa, Japan
[6] Nagoya City Publ Hlth, Nagoya, Aichi, Japan
[7] Kawasaki City Inst Publ Hlth, Kawasaki, Kanagawa, Japan
[8] Kanagawa Prefectural Inst Publ Hlth, Chigasaki, Kanagawa, Japan
关键词
IMMUNOAFFINITY COLUMN CLEANUP; LIQUID-CHROMATOGRAPHY; B-1; MYCOTOXINS; DRUGS; G(1); G(2);
D O I
10.1093/jaoacint/qsaa077
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Background: Aflatoxins (AFs) are carcinogenic mycotoxins. A simple, quick, and accurate method for the micro-analysis of AFs in foodstuffs, especially spices, is needed. Objective: A sophisticated pretreatment method that combines solid-phase dispersive extraction (SPDE) and solid-phase fluorescence derivatization using immunoaffinity (IA) gel as the solid phase was developed to analyze AFs in spices simply, quickly, and sensitively by liquid chromatography with fluorescence detection. Method: White and black pepper samples were extracted with a mixed solution of methanol/water (4:1) and then diluted with 7% aqueous solution of Triton-X. The solution was subjected to cleanup by SPDE using IA gel. Trifluoroacetic acid was added to the IA gel for on-site solid-phase fluorescence derivatization. Results: Chromatograms containing well-separated peaks and few interference peaks from contaminants were obtained. The method detection limit of AFs in white and black pepper was 0.15-0.29 ng/g. Repeatability and intermediate precision were <10% and <15%, respectively, and accuracy was 61.7-87.8%. In addition, inter-laboratory precision was <29% and mean recovery was 61.5-76.7%. A favorable z-score of vertical bar Z vertical bar <= 1 was obtained in seven laboratories, although one laboratory gave 2 < vertical bar Z vertical bar < 3. Conclusions: The validity, reliability, practicality, and robustness of the developed method were verified. Highlights: By using SPDE and solid-phase fluorescence derivatization in combination for AF analysis, fluorescence derivatization during cleanup was realized, leading to simplification of the pretreatment operation.
引用
收藏
页码:1521 / 1527
页数:7
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