Jiangsu Key Laboratory of Pesticide Science, College of Science, Nanjing Agricultural University, Nanjing 210095, China.
Arch Environ Contam Toxicol. 2011 Oct;61(3):359-67. doi: 10.1007/s00244-010-9626-y. Epub 2010 Dec 3.
A new and efficient analytic methodology based on cloud point extraction (CPE) was developed for determination of pesticide residues of metsulfuron-methyl (MSM), chlorsulfuron (CS), and bensulfuron-methyl (BSM) in water, soil, and rice grain by high-performance liquid chromatography (HPLC). Multiple experimental conditions that affected CPE efficiency-including surfactant type and concentration, equilibration temperature and duration, ionic strength, and solution pH were identified. CPE conditions were optimized as follows: 1.5% Triton X-114 (w/v), 12% Na(2)SO(4) (w/v) solution (pH 2.0), and heat-assisted at 50 °C for 15 min. The calibration curves for all analytes were linear, ranging from 0.05 to 4.0 mg L(-1), with the correlation coefficients >0.9995 by HPLC-ultraviolet detector and were linear, ranging from 0.004 to 2.0 mg L(-1), with correlation coefficients >0.9983 by CPE-HPLC. The average recoveries at the three spiked levels using CPE ranged from 86.0% to 94.5% for water samples with relative SDs (RSDs) of 0.4% to approximately 7.8%; from 85.6% to 94.8% for soil samples with RSDs of 1.2% to approximately 9.5%; and from 81.9% to 91.3% for rice samples with RSDs of 1.7% to approximately 5.8%. The proposed CPE-HPLC method can be successfully used to analyze MSM, CS, and BSM residues from contaminated water, soil, and rice grain samples.
建立了一种基于浊点萃取(CPE)的新的、高效的分析方法,用于高效液相色谱(HPLC)测定水中、土壤中和水稻中的甲磺隆(MSM)、氯磺隆(CS)和苄嘧磺隆(BSM)农药残留。确定了影响 CPE 效率的多个实验条件,包括表面活性剂类型和浓度、平衡温度和时间、离子强度和溶液 pH 值。优化的 CPE 条件如下:1.5%Triton X-114(w/v),12%Na2SO4(w/v)溶液(pH 2.0),加热至 50°C 并保持 15 min。所有分析物的校准曲线均呈线性,范围为 0.05 至 4.0 mg/L,HPLC-紫外检测器的相关系数>0.9995;CPE-HPLC 的线性范围为 0.004 至 2.0 mg/L,相关系数>0.9983。使用 CPE 时,在三个加标水平下,水样品的平均回收率为 86.0%至 94.5%,相对标准偏差(RSD)为 0.4%至约 7.8%;土壤样品的平均回收率为 85.6%至 94.8%,RSD 为 1.2%至约 9.5%;水稻样品的平均回收率为 81.9%至 91.3%,RSD 为 1.7%至约 5.8%。该方法可成功用于分析受污染的水、土壤和水稻样品中的 MSM、CS 和 BSM 残留。