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High-performance liquid chromatography and Enzyme-Linked Immunosorbent Assay techniques for detection and quantification of aflatoxin B1 in feed samples: a comparative study

机译:高效液相色谱法和酶联免疫吸附测定技术检测和定量分析饲料样品中的黄曲霉毒素B1:一项比较研究

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摘要

ObjectiveComparison was done between high-performance liquid chromatography (HPLC) and a competitive enzyme-linked immunosorbent assay (ELISA) for detection and quantification of aflatoxin B1 (AFB1) in feed samples. The two procedures were standardized and validated before the actual experiment. Five concentrations (0, 5, 10, 20 and 30 ppb) of feed samples were used for both methods. For the HPLC technique, the samples were extracted in acetonitrile/water (90/10) solution, cleaned-up using solid phase extraction (SPE) column, and derivatized by water/trifluoroacetic acid/glacial acetic acid (35/10/5) solution before instrument analysis. The samples were extracted in 70% methanol for the ELISA technique.
机译:目的比较高效液相色谱(HPLC)和竞争性酶联免疫吸附测定(ELISA),用于检测和定量饲料样品中的黄曲霉毒素B1(AFB1)。在实际实验之前,对这两个程序进行了标准化和验证。两种方法均使用五种浓度(0、5、10、20和30 ppb)的饲料样品。对于HPLC技术,将样品在乙腈/水(90/10)溶液中萃取,使用固相萃取(SPE)柱进行净化,然后用水/三氟乙酸/冰醋酸(35/10/5)衍生化仪器分析之前的解决方案。样品用70%甲醇提取,用于ELISA技术。

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