Ravelo-Pérez Lidia M, Hernández-Borges Javier, Borges-Miquel Teresa M, Rodríguez-Delgado Miguel Angel
Department of Analytical Chemistry, Nutrition and Food Science, University of La Laguna, Avenida Astrofísico Fco. Sánchez s/n, 38071 La Laguna, Tenerife, Canary Islands, Spain.
J Chromatogr A. 2008 Mar 21;1185(1):151-4. doi: 10.1016/j.chroma.2008.01.069. Epub 2008 Jan 31.
The analysis of a group of seven pesticides (i.e. six fungicides: pyrimethanil, procymidone, nuarimol, fenarimol, benalaxyl and penconazole and one insecticide: pirimicarb) in tomato samples by micellar electrokinetic chromatography is investigated. For this purpose, reversed electrode polarity stacking mode and solid-phase microextraction (SPME) have been used as on-line and off-line preconcentration procedures, respectively. Tomato samples were first homogenized and extracted with acetone. After suitable evaporation and reconstitution of the extract in water, a SPME procedure using poly(dimethylsiloxane)/divinylbenzene fibers was used. Due to the strong influence of the sample matrix in the extraction, a matrix matched calibration of spiked tomato samples was developed. The method was found to be linear between 0.5 and 2.5 mg/kg. Limits of detection achieved are below the maximum residue limits established by the European Union and Spain legislation as well as by the Codex Alimentarius (except for penconazole). The potential of the method was demonstrated by analyzing 12 tomato samples (of ecological and non-ecological production) taken from regional cultivars. No residues of the selected pesticides were detected in any of the samples.
研究了采用胶束电动色谱法分析番茄样品中的一组七种农药(即六种杀菌剂:嘧霉胺、腐霉利、氯苯嘧啶醇、粉锈宁、霜霉威和戊唑醇,以及一种杀虫剂:抗蚜威)。为此,分别采用反向电极极性堆积模式和固相微萃取(SPME)作为在线和离线预浓缩程序。番茄样品首先用丙酮匀浆并萃取。在提取物进行适当蒸发并重新溶解于水中后,使用聚(二甲基硅氧烷)/二乙烯基苯纤维进行SPME程序。由于样品基质在萃取过程中的强烈影响,建立了加标番茄样品的基质匹配校准。该方法在0.5至2.5 mg/kg之间呈线性。所达到的检测限低于欧盟、西班牙法规以及食品法典委员会规定的最大残留限量(戊唑醇除外)。通过分析取自当地品种的12个番茄样品(生态和非生态生产)证明了该方法的潜力。在任何样品中均未检测到所选农药的残留。