Institute of Chemical Sciences, University of Peshawar, Khyber Pakhtunkhwa, Pakistan.
Department of Chemistry, University of Malakand, Khyber Pakhtunkhwa, Pakistan.
Environ Toxicol Chem. 2019 Dec;38(12):2614-2620. doi: 10.1002/etc.4589. Epub 2019 Nov 16.
An accurate and sensitive method has been developed for determination of the herbicide isoproturon using the Quick Easy Cheap Effective Rugged Safe (QuEChERS) extraction-spectrofluorimetric technique. The method involves the reaction of 2-cyanoacetamide with isoproturon in basic medium (NH ; 15 mol/L). The resulting fluorescent product was found to show maximum emission at 378 nm and maximum excitation at 333 nm. Fluorescence intensity under the influence of different parameters was investigated. The linear range of analyte concentrations was found to be 0.5 to 15 µg/mL, with a limit of detection of 0.144 µg/mL, a limit of quantification of 0.437 µg/mL (signal to noise ratio = 3), and a regression coefficient of 0.9991, under optimized conditions. The proposed method was effectively applied for determination of isoproturon in different matrices; the percentage of recovery varied from 85.00 ± 1.2% to 96.00 ± 0.5%. The method was also applied for residue analysis of isoproturon in real soil samples collected from a pilot field. For extraction of isoproturon, the QuEChERS extraction approach was used, and the average residue in the soil samples was found to be 0.81 ± 0.07 µg/g. To show the potential of this approach, our results were compared with those of other methods reported in the literature. Environ Toxicol Chem 2019;38:2614-2620. © 2019 SETAC.
一种使用快速、简单、便宜、有效、耐用、安全(QuEChERS)萃取-荧光光度法测定除草剂异丙隆的准确灵敏的方法已经建立。该方法涉及在碱性介质(NH 15 mol/L)中 2-氰基乙酰胺与异丙隆的反应。结果表明,荧光产物在 378nm 处具有最大发射,在 333nm 处具有最大激发。研究了不同参数对荧光强度的影响。在优化条件下,分析物浓度的线性范围为 0.5 至 15μg/mL,检测限为 0.144μg/mL,定量限为 0.437μg/mL(信噪比=3),回归系数为 0.9991。该方法有效地应用于不同基质中异丙隆的测定,回收率在 85.00±1.2%至 96.00±0.5%之间变化。该方法还应用于从试点田间采集的实际土壤样品中异丙隆的残留分析。对于异丙隆的提取,采用了 QuEChERS 提取方法,土壤样品中的平均残留量为 0.81±0.07μg/g。为了展示这种方法的潜力,我们将结果与文献中报道的其他方法进行了比较。Environ Toxicol Chem 2019;38:2614-2620. © 2019 SETAC。