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Determination of azoxystrobin and its impurity in pesticide formulations by liquid chromatography

机译:液相色谱法测定氮杂氧杂环蛋白及其在农药制剂中的杂质

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摘要

A method was developed for the simultaneous qualitative and quantitative determination of azoxystrobin and its relevant impurity (Z)-azoxystrobin using high performance liquid chromatography with diode array detector (HPLC-DAD) in suspension concentrate (SC) pesticide formulations, with the aim of the product quality control. Method validation was realized according to SANCO/3030/99 rev. 5. The proposed method was characterized by acceptable accuracy and precision. The repeatability expressed as ratio standard deviation (%RSD) to relative standard deviation (%RSDr) was lower than 1, whereas individual recoveries were in the range of 97-103% and 90-110% for azoxystrobin and (Z)-azoxystrobin, respectively. The limit of quantification (LOQ) for the impurity ((Z)-azoxystrobin) amounted to 0.3 mu g mL(-1)and was acceptable because it was lower than the maximum permitted level according to Commission Implementing Regulation (EU) No 703/2011 of 20 July 2011 for the active substance (azoxystrobin) being 25 g kg(-1)of the azoxystrobin content found. The method described in this paper is simple, precise, accurate and selective as well as represents a new and reliable way of simultaneous determination of azoxystrobin and its relevant impurity in formulated products.
机译:用于使用高效液相色谱法同时进行定性和定量测定偶氮氧杂菌素(HPLC-DAD)的同时定性和定量测定偶氮氧杂环蛋白及其相关杂质(Z) - 唑氧基萘,其目的是产品质量控制。根据Sanco / 3030/99 Rever实现了方法验证。该方法的特征在于可接受的精度和精度。表达为与相对标准偏差(%RSD)的比率标准偏差(%RSD)表示的可重复性低于1,而偶氮素和(Z)-AxOxystrobin,个体回收率为97-103%和90-110%,分别。杂质((Z) - 唑氧键)的定量限量为0.3μgmm(-1),并且是可接受的,因为它根据委员会实施规则(欧盟)的最大允许水平低703 / 2011年7月20日为2011年7月20日为活性物质(氮杂氧杂歧板)25克kg(-1)发现的偶氮素含量。本文中描述的方法简单,精确,准确和选择,以及同时测定制剂产品中同时测定偶氮氧素及其相关杂质的新方法。

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