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Development of HPLC-Fluorescence Method for the Determination ofIvermectin Residues in Commercial Milk

机译:高效液相色谱-荧光法测定商品奶中伊维菌素残留的开发

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Objective: A study aimed at the validation of a high performance liquid chromatography (HPLC) method for detection and quantification of ivermectin (IVM) in commercial milk. Method: After a liquid-liquid extraction with acetonitrile and hexane, a derivatization with a mixture of trifluoroacetic acid and trifluoroacetic anhydride was performed. Chromatography conditions were a C8 column, a fluorescent detector (Ex. 360; Em. 470 nm), a run time of 25 minutes and an isocratic elution at 30°C. The methodology was validated in terms of selectivity, linearity, precision, recovery, limit of quantification (LoQ), limit of detection (LoD), and robustness. Results: The method showed an adequate linearity and selectivity (r2=0.999) with an elution time of 13.909 minutes. However, the repeatability and intermediate precision showed RSD values above of 20% and recovery between 37 to 79%. The calculated LoD and LoQ were 2.50 and 5.00 ng/ml respectively. Robustness showed a significant variation on the analytical method with small changes in heating time during the derivatization and flow rate of chromatography system. Conclusion: The HPLC-fluorescence method showed results partially satisfactory and could be the used for IVM detection in commercial milk samples.
机译:目的:一项旨在验证高效液相色谱(HPLC)方法用于检测和定量商业牛奶中伊维菌素(IVM)的研究。方法:用乙腈和己烷液-液萃取后,用三氟乙酸和三氟乙酸酐的混合物进行衍生化。色谱条件为C8柱,荧光检测器(Ex。360; Em。470 nm),运行时间为25分钟和在30°C等度洗脱。该方法论在选择性,线性,精密度,回收率,定量限(LoQ),检测限(LoD)和稳健性方面得到了验证。结果:该方法显示出足够的线性和选择性(r2 = 0.999),洗脱时间为13.909分钟。但是,重复性和中间精度显示RSD值高于20%,回收率介于37%至79%之间。计算的LoD和LoQ分别为2.50和5.00 ng / ml。色谱法的衍生性和流速期间,加热时间的变化很小,因此稳健性显示了分析方法的显着变化。结论:HPLC-荧光法显示部分结果令人满意,可用于商业牛奶样品中的IVM检测。

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