首页> 外文期刊>Journal of Environmental Science and Health. Part B, Pesticides, Food Contaminants and Agricultural Wastes >Determination of azoxystrobin, topramezone, acetamiprid, fluometuron and folpet in their commercially available pesticide formulations by liquid chromatography
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Determination of azoxystrobin, topramezone, acetamiprid, fluometuron and folpet in their commercially available pesticide formulations by liquid chromatography

机译:通过液相色谱法测定其市售农药制剂中的偶氮氧杂蛋白,TOPRAMEZONE,acetamiprid,Fluometuron和FOFPET

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摘要

A rapid, simple, precise and accurate high performance liquid chromatographic (HPLC) analytical method was developed and validated for the determination of the active substances (a.s.) azoxystrobin, topramezone, acetamiprid, fluometuron and folpet in their respective commercially available formulations. The method was used for the analysis of samples under the frame of the national quality control program of plant protection products in the Greek market. Chromatographic separation of the active substances from additives and co-formulants is achieved using isocratic elution with acetonitrile and 0.1% phosphoric acid solution (60∶40 v/v) at a flow rate of 0.4 mL min~(-1) on a C_(18) monolithic column (Chromolith Performance-RP18e 100×4.6 mm) and UV detection at 230 nm. Validation parameters of the method fulfilled acceptability criteria. Recovery of all individual compounds was in the range 97.8-100.9%. Precision expressed as relative standard deviation was lower than the theoretical values of the modified Horwitz equation. Correlation coefficients of linearity of response were better than 0.999. The benefits of the proposed method are significant reduction in analysis time and total cost since all analytes were determined with the same extraction procedures and chromatographic system. Analysis of real samples for all active ingredients confirmed fitness for purpose of the suggested method.
机译:开发出快速,简单,精确和精确的高性能液相色谱(HPLC)分析方法并验证用于测定它们各自的市售制剂中的活性物质(A.S.)偶氮氧基蛋白,TOPRAMEZONE,ACETAMIPRID,FLUORTURON和FOFPET。该方法用于在希腊市场植物保护产品框架框架下分析样品。通过用乙腈和0.1%磷酸溶液(60:40 v / v)在C_( 18)单片柱(ChromoLith Performance-RP18E 100×4.6mm)和230nm的UV检测。该方法的验证参数满足可接受性标准。所有单个化合物的回收率在97.8-100.9%的范围内。作为相对标准偏差表示的精度低于改进的Horwitz方程的理论值。响应线性度的相关系数优于0.999。所提出的方法的益处是分析时间和总成本的显着降低,因为所有分析物用相同的提取程序和色谱系统测定。对所有活性成分的真实样品分析确认了建议方法的适用性。

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