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首页> 外文期刊>Poljoprivreda i Sumarstvo: Agriculture and Forestry >DETERMINATION OF MALATHION IN PESTICIDE FORMULATION BY HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY
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DETERMINATION OF MALATHION IN PESTICIDE FORMULATION BY HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY

机译:高效液相色谱法测定农药制剂中的马拉硫磷

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摘要

A new, simple, fast and reliable high-performance liquid chromatography (HPLC) method for determination of an active ingredient malathion in the pesticide formulation has been developed. Successful separation and quantification of malathion were achieved using Purospher STAR RP-18e (30 x 4 mm, 3 μm) and isocratic elution with mobile phase consisted of acetonitrile/water (47/53, V/V), flow rate of 1 mL/min, constant column temperature at 25 °C and UV detection at 220 nm. The specificity, selectivity, linearity, precision, accuracy, limit of detection (LOD) and quantification (LOQ) were tested for the method validation according to the CIPAC and SANCO guidelines. The obtained values for multiple correlation coefficients (R2 0.99), relative standard deviation (RSD) of retention times and peak areas (RSD ≤ 0.64%), and recoveries ranged from 101.04 to 101.84 %, revealed that the developed method has an excellent linearity, precision of retention time and peak area and accuracy. The proposed method was successfully applied for determination of an active ingredient malathion in the emulsifiable concentrate (EC) “Etiol techni” for a run time of 4 min.
机译:已经开发出一种新的,简单,快速可靠的高效液相色谱(HPLC)方法,用于测定农药配方中的活性成分畸变。使用净化器之星RP-18E(30×4mm,3μm)和具有流动相的异形洗脱,由乙腈/水(47/53,v / v)组成,实现了乙腈/水(47/53,v / v)的成功分离和定量。流速/分钟,25℃的恒定柱温度和220nm处的UV检测。根据CIPAC和SANCO指南测试了方法验证测试了特异性,选择性,线性,精度,准确度,检测极限(LOD)和定量(LOQ)。所获得的多个相关系数(R2> 0.99)的值,保留时间和峰面积的相对标准偏差(RSD)(RSD≤0.64%),以及回收率为101.04至101.84%,显示出开发方法具有优异的线性度保留时间和峰面积精度和精度的精度。该方法成功地应用于测定乳化浓缩物(EC)“Etiol Techni”的活性成分少于4分钟的运行时间。

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