Wu Qiuhua, Zhou Xin, Li Yuemin, Zang Xiaohuan, Wang Chun, Wang Zhi
Key Laboratory of Bioinorganic Chemistry, College of Sciences, Agricultural University of Hebei, Baoding, 071001, China.
Anal Bioanal Chem. 2009 Mar;393(6-7):1755-61. doi: 10.1007/s00216-009-2625-z. Epub 2009 Feb 13.
A rapid and sensitive method has been established for the determination of four carbamate pesticides (carbofuran, carbaryl, pirimicarb, and diethofencarb) in water samples by using dispersive liquid-liquid microextraction coupled with high-performance liquid chromatography-diode array detection. Parameters that affect the extraction efficiency, such as the kind and volume of the extraction and disperser solvent, extraction time, and salt addition, were investigated and optimized. Under the optimum conditions, the enrichment factors were in the range between 101 and 145. The linearity of the method was obtained in the range of 5-500 ng mL(-1) with the correlation coefficients (r) ranging from 0.9978 to 0.9997. The method detection limits were 0.4-1.0 ng mL(-1). The relative standard deviations varied from 4.7% to 6.5% (n = 5). The relative recoveries of the four carbamates from water samples at spiking levels of 5.0 and 20.0 ng mL(-1) were 84.0-92.0% and 86.5-94.0%, respectively. The proposed method has been successfully applied to the analysis of target carbamate residues in river, rain, well, and tap water samples with satisfactory results.
建立了一种快速灵敏的方法,采用分散液液微萃取结合高效液相色谱 - 二极管阵列检测法测定水样中的四种氨基甲酸酯类农药(克百威、西维因、抗蚜威和乙霉威)。研究并优化了影响萃取效率的参数,如萃取溶剂和分散剂溶剂的种类及体积、萃取时间和加盐量。在最佳条件下,富集因子在101至145之间。该方法在5 - 500 ng mL⁻¹范围内呈线性,相关系数(r)在0.9978至0.9997之间。方法检出限为0.4 - 1.0 ng mL⁻¹。相对标准偏差在4.7%至6.5%之间(n = 5)。水样中5.0和20.0 ng mL⁻¹加标水平下四种氨基甲酸酯的相对回收率分别为84.0 - 92.0%和86.5 - 94.0%。所提出的方法已成功应用于河流、雨水、井水和自来水样中目标氨基甲酸酯残留的分析,结果令人满意。