DETERMINATION OF AZOXYSTROBIN AND DIFENOCONAZOLE IN PESTICIDE PRODUCTS.

S Lazić, D Šunjka
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Abstract

In this study a high performance liquid chromatographic (HPLC-DAD) procedure has been developed for the simultaneous determination of azoxystrobin and difenoconazole in suspension concentrate pesticide formulations, with the aim of the product quality control. Azoxystrobin, strobilurin fungicide and difenoconazole (cis,trans-3-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-2-yl]phenyl 4-chlorophenyl ether), triazole fungicide, are used for the protection of plants from wide spectrum of fungal diseases. For the analysis LC system an Agilent Technologies 1100 Series was used. Good separation was achieved on a Zorbax SB-C18 column (5 μm, 250 mm x 3 mm internal diameter) using a mobile phase consisting of acetonitrile/ultrapure water (90:10, v/v), at a flow rate of 0.9 ml/minute and UV detection at 218 nm. Column temperature was 25 degrees C, injected volume was 1 μl. Retention times for azoxystrobin and difenoconazole were 2.504 min and 1.963 min, respectively. This method is validated according to the requirements for new methods, which include linearity, precision, accuracy and selectivity. The method demonstrates good linearity with r2 > 0.997. The repeatability of the method, expressed as relative standard deviation (RSD, %), was found to be 1.9% for azoxystrobin and 0.5% for difenoconazole. The precision of the method was also considered to be acceptable as the experimental repeatability relative standard deviation (RSD) was lower than the RSD calculated using the Horwitz equation of 1.7% and 1.4% for azoxystrobin and difenoconazole, respectively. The accuracy of the proposed method was determined from recovery experiments through standard addition procedure. The average recoveries of the three fortification levels were 101.9% for azoxystrobin and 103.2% for difenoconazole with RSDs of 1.1% and 1.2%. The method described in this paper is simple, precise, accurate and selective and represents a new and reliable way of simultaneous determination of azoxystrobin and difenoconazole in formulated products.

农药产品中嘧菌酯和异虫康唑的测定。
建立了高效液相色谱(HPLC-DAD)同时测定悬浮液浓缩农药制剂中嘧菌酯和异虫康唑的方法,并对其进行了质量控制。三唑类杀菌剂偶氮嘧菌酯和二苯唑类杀菌剂(顺式,反式,3-氯-4-[4-甲基-2-(1h -1,2,4-三唑-1-甲基)-1,3-二恶唑-2-基]苯基-4-氯苯醚)用于防治广谱真菌病。用于分析的LC系统是Agilent Technologies 1100系列。采用Zorbax SB-C18色谱柱(5 μm, 250 mm × 3 mm内径),流动相为乙腈/超纯水(90:10,v/v),流速为0.9 ml/min,紫外检测波长为218 nm,获得了良好的分离效果。柱温25℃,进样量1 μl。氮嘧菌酯和异虫康唑的保留时间分别为2.504 min和1.963 min。根据新方法的线性度、精密度、准确度和选择性要求,对该方法进行了验证。方法线性良好,r2 > 0.997。方法的重复性以相对标准偏差(RSD, %)表示,偶氮虫胺为1.9%,异苯康唑为0.5%。实验可重复性相对标准偏差(RSD)低于Horwitz方程计算的RSD(分别为1.7%和1.4%),该方法的精密度也可接受。通过标准加成程序进行回收率实验,确定了该方法的准确性。三种添加水平的平均加样回收率分别为101.9%和103.2%,rsd分别为1.1%和1.2%。该方法简便、精密度高、准确度高、选择性好,为同时测定制剂中嘧菌酯和异虫康唑的含量提供了一种可靠的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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