High-performance liquid chromatographic determination of pesticides in tomatoes using laboratory-made NH2 and C18 solid-phase extraction materials

被引:60
作者
Melo, LFC
Collins, CH
Jardim, ICSF
机构
[1] Univ Estadual Campinas, Inst Chem, BR-13084971 Campinas, SP, Brazil
[2] Univ Estadual Campinas, Sch Chem Engn, BR-13084971 Campinas, SP, Brazil
关键词
sample preparation; solid-phase extraction; multiclass pesticide analysis; tomatoes; method validation;
D O I
10.1016/j.chroma.2004.09.043
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A method for high-performance liquid chromatographic (HPLC) multiresidue determination of six pesticides in tomatoes was developed and validated. Silica-based C-18 (octadecyl) and NH2 (aminopropyl) solid-phase extraction (SPE) sorbents, made in our laboratory, were used for sample preparation. The SPE materials were obtained by thermal immobilization of appropriate polysiloxanes onto 40 mu m silica surfaces and were used in sample preparation for multiresidue analysis of the following pesticides: tebuthiuron and diuron (urea herbicides), simazine, atrazine and ametryn (triazines herbicides) and benomyl (benzimidazol fungicide). The results were compared with similar commercial materials. Reversed-phase high-performance liquid chromatography (RP-HPLC) using a Purospher RP- 18 5 mu m column and ACN: 0.01% aqueous NH4OH, pH 8.4 (35:65, v/v) as mobile phase, at 0.7 ml min(-1), with 235 nm UV detection, was used for separation and quantification of the pesticides. Method validation was performed at three fortification levels (100, 200, 1000 mu g l(-1)). Limits of detection and quantification show that the methods developed can be used to detect the pesticides in concentrations below the maximum residue levels (MRL) established by the Codex Alimentarius, USA, European Union and Brazilian legislations. The results showed that aminopropyl materials have a better performance than the octadecyl sorbents. Laboratory-made materials give results similar to commercial sorbents, with recoveries and precisions in agreement with directives for method validation in residue analysis. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 81
页数:7
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