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Optimization and validation of enzyme-linked immunosorbent assay for the determination of endosulfan residues in food samples.

Optimization and validation of enzyme-linked immunosorbent assay for the determination of endosulfan residues in food samples. Research Abstract Details 

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  • Optimization and validation of enzyme-linked immunosorbent assay for the determination of endosulfan residues in food samples. Abstract Text:

    yan zhangYan Zhang,jun w liuJun W Liu,wen j zhengWen J Zheng,lei wangLei Wang,hong y zhangHong Y Zhang,guo z fangGuo Z Fang,shuo wangShuo Wang,yan zhangYan Zhang,jun w liuJun W Liu,wen j zhengWen J Zheng,lei wangLei Wang,hong y zhangHong Y Zhang,guo z fangGuo Z Fang,shuo wangShuo Wang,

    In this study, an enzyme-linked immunosorbent assay (ELISA) was optimized and applied to the determination of endosulfan residues in 20 different kinds of food commodities including vegetables, dry fruits, tea and meat. The limit of detection (IC(15)) was 0.8 mug kg(-1) and the sensitivity (IC(50)) was 5.3 mug kg(-1). Three simple extraction methods were developed, including shaking on the rotary shaker at 250 r min(-1) overnight, shaking on the rotary shaker for 1 h and thoroughly mixing for 2 min. Methanol was used as the extraction solvent in this study. The extracts were diluted in 0.5% fish skin gelatin (FG) in phosphate-buffered saline (PBS) at various dilutions in order to remove the matrix interference. For cabbage (purple and green), asparagus, Japanese green, Chinese cabbage, scallion, garland chrysanthemum, spinach and garlic, the extracts were diluted 10-fold; for carrots and tea, the extracts were diluted 15-fold and 900-fold, respectively. The extracts of celery, adzuki beans and chestnuts, were diluted 20-fold to avoid the matrix interference; ginger, vegetable soybean and peanut extracts were diluted 100-fold; mutton and chicken extracts were diluted 10-fold and for eel, the dilution was 40-fold. Average recoveries were 63.13-125.61%. Validation was conducted by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). The results of this study will be useful to the wide application of an ELISA for the rapid determination of pesticides in food samples.

    Optimization and validation of enzyme-linked immunosorbent assay for the determination of endosulfan residues in food samples. Publishing Authors By Initials

    y zhangY Zhang,jw liuJW Liu,wj zhengWJ Zheng,l wangL Wang,hy zhangHY Zhang,gz fangGZ Fang,s wangS Wang,y zhangY Zhang,jw liuJW Liu,wj zhengWJ Zheng,l wangL Wang,hy zhangHY Zhang,gz fangGZ Fang,s wangS Wang,

    For similar abstracts research abstracts see: abstracts research

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    Optimization and validation of enzyme-linked immunosorbent assay for the determination of endosulfan residues in food samples. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Journal of environmental science and health. Part.

    VOLUME: 43

    Page Numbers: 127-33

    Journal Abbreviation:

    ISSN: 0360-1234

    DAY: 4

    MONTH: Feb

    YEAR: 2008

    Optimization and validation of enzyme-linked immunosorbent assay for the determination of endosulfan residues in food samples. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7607167

    Optimization and validation of enzyme-linked immunosorbent assay for the determination of endosulfan residues in food samples. Keywords Mesh Terms:

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    Grant and Affiliation Information for Optimization and validation of enzyme-linked immunosorbent assay for the determination of endosulfan residues in food samples.

    AFFILIATION: Tianjin Key Laboratory of Food Nutrition and Safety, Tianjin University of Science and Technology, Tianjin, China.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Environ Sci Health B

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