Lacassie E, Dreyfuss M F, Daguet J L, Vignaud M, Marquet P, Lachâtre G
Department of Pharmacology and Toxicology, University Hospital, Limoges, France.
J Chromatogr A. 1998 May 1;805(1-2):319-26. doi: 10.1016/s0021-9673(97)01305-8.
This paper describes a rapid, specific and sensitive multiresidue method for the routine analysis of several classes of pesticides used for the treatment of apples and pears, involving a rapid extraction procedure at pH 4.5 with a mixture of acetone-dichloromethane-hexane (50:20:30, v/v/v) and gas chromatography coupled to mass-selective detection, in order to achieve quantitative analysis down to their respective maximum residue limit. Extraction recoveries were between 55 and 98%. Limits of detection and limits of quantitation ranged respectively, from 0.01 to 0.05 mg/kg and from 0.02 to 0.1 mg/kg. Intra-assay relative standard deviation was less than 19% for all compounds. An excellent linearity was observed from these LOQs up to 500 mg/kg. Intermediate (inter-assay) precision and accuracy were satisfactory. The method has been applied to many fruit samples intended for commercialisation.
本文描述了一种快速、特异且灵敏的多残留方法,用于常规分析用于苹果和梨处理的几类农药。该方法包括在pH 4.5下用丙酮 - 二氯甲烷 - 己烷(50:20:30,v/v/v)混合物进行快速萃取程序,以及气相色谱 - 质量选择检测,以实现低至各自最大残留限量的定量分析。萃取回收率在55%至98%之间。检测限和定量限分别为0.01至0.05 mg/kg和0.02至0.1 mg/kg。所有化合物的批内相对标准偏差均小于19%。从这些定量限到500 mg/kg观察到极佳的线性。中间精密度(批间精密度)和准确度令人满意。该方法已应用于许多用于商业化的水果样品。