Serôdio P, Nogueira J M F
Chemistry and Biochemistry Department, University of Lisbon, Campo Grande Ed. C8, 1749-016 Lisbon, Portugal.
Anal Bioanal Chem. 2005 Jun;382(4):1141-51. doi: 10.1007/s00216-005-3210-8. Epub 2005 Jun 4.
Stir-bar-sorptive extraction followed by liquid desorption and large-volume injection capillary gas chromatography with mass spectrometric detection (SBSE-LD-LVI-GC-MS), had been applied for the determination of ultra-traces of eight pyrethroid pesticides (acrinathrin, cypermethrin, deltamethrin, esfenvalerate, fenpropathrin, fenvalerate, and permethrin cis and trans isomers) in water samples. Instrumental calibration for selected-ion monitoring acquisition and conditions that could affect the SBSE-LD efficiency are fully discussed. By performing systematic assays on 30-mL water samples spiked at the 0.10 microg L(-1) level it was established that stir-bars coated with 47 microL polydimethylsiloxane, an equilibrium time of 60 min (750 rpm), 5% methanol as organic modifier, and acetonitrile as back-extraction solvent, provided the best analytical performance to monitor pyrethroid pesticides in water matrices. Good accuracy (81.8-105.0%) and remarkable reproducibility (<11.7%) were obtained, and the experimental recovery data were in good agreement with the theoretical equilibrium described by octanol-water partition coefficients (log K(O/W)), with the exception of acrinathrin for which lower yields were measured. Excellent linear dynamic ranges between 25 and 400 ng L(-1) (r2>0.994), low quantification (3.0-7.5 ng L(-1)) and detection (1.0-2.5 ng L(-1)) limits were also achieved for the eight pyrethroid pesticides studied. The method was successfully used for analysis of tap-water and groundwater matrices spiked at the 0.10 microg L(-1), revealing the suitability of the method for determination of pyrethroid pesticides in real samples. The method was shown be reliable and sensitive and a small volume of sample was required to monitor pyrethroids at ultra-trace levels, in compliance with international regulatory directives on water quality.
搅拌棒吸附萃取结合液体解吸和大体积进样毛细管气相色谱-质谱检测(SBSE-LD-LVI-GC-MS)已用于测定水样中痕量的8种拟除虫菊酯类农药(氟丙菊酯、氯氰菊酯、溴氰菊酯、乙氰菊酯、甲氰菊酯、氰戊菊酯以及顺式和反式氯菊酯异构体)。文中充分讨论了选择离子监测采集的仪器校准以及可能影响SBSE-LD效率的条件。通过对加标浓度为0.10 μg L⁻¹的30 mL水样进行系统分析,确定涂覆47 μL聚二甲基硅氧烷的搅拌棒、60 min(750 rpm)的平衡时间、5%甲醇作为有机改性剂以及乙腈作为反萃取溶剂,能为监测水基质中的拟除虫菊酯类农药提供最佳分析性能。获得了良好的准确度(81.8 - 105.0%)和出色的重现性(<11.7%),实验回收率数据与由正辛醇-水分配系数(log K(O/W))描述的理论平衡相符,但氟丙菊酯的回收率较低。对于所研究的8种拟除虫菊酯类农药,还实现了25至400 ng L⁻¹之间出色的线性动态范围(r²>0.994)、较低的定量限(3.0 - 7.5 ng L⁻¹)和检测限(1.0 - 2.5 ng L⁻¹)。该方法成功用于分析加标浓度为0.10 μg L⁻¹的自来水和地下水基质,表明该方法适用于实际样品中拟除虫菊酯类农药的测定。该方法可靠且灵敏,只需少量样品就能监测超痕量水平的拟除虫菊酯,符合国际水质监管指令要求。