Prousalis Konstantinos P, Polygenis Dimitris A, Syrokou Alexandra, Lamari Fotini N, Tsegenidis Theodore
Department of Chemistry, Section of Organic Chemistry, Biochemistry and Natural Products, University of Patras, 26500 Patras, Greece.
Anal Bioanal Chem. 2004 Jun;379(3):458-63. doi: 10.1007/s00216-004-2614-1. Epub 2004 Apr 17.
An efficient analytical method is presented involving effective sample clean-up with solid-phase extraction and HPLC-UV analysis for the simultaneous determination of carbendazim, thiabendazole, and o-phenylphenol residues in lemons. Sample preparation involves extraction with acetonitrile acidified with trifluoroacetic acid and an ethyl acetate/petroleum ether mixture. Purification of the crude extract was carried out with liquid-liquid partitioning after addition of an aqueous ammonia solution. Final clean-up was performed on polymeric reversed-phase cartridges pretreated with sodium dodecyl sulfate. Chromatographic analysis was performed on a reversed-phase HPLC column isocratically eluted with an acetonitrile/water/ammonia mixture and UV detection at 254 nm. The chromatographic method is repeatable, reproducible, and sensitive. Fungicide recoveries from lemon samples fortified at levels of 5 and 1 mg kg(-1) were 81-85% for carbendazim, 96-98% for thiabendazole, and 81-106% for o-phenylphenol with coefficients of variation of 2.5-7.4%. Detection limits for carbendazim, thiabendazole, and o-phenylphenol in lemons were 0.21, 0.27, and 0.51 mg kg(-1), respectively.
本文提出了一种高效的分析方法,该方法采用固相萃取进行有效的样品净化,并结合高效液相色谱-紫外检测法,用于同时测定柠檬中的多菌灵、噻菌灵和邻苯基苯酚残留量。样品制备包括用三氟乙酸酸化的乙腈和乙酸乙酯/石油醚混合物进行萃取。在加入氨水溶液后,通过液-液分配对粗提物进行纯化。最终净化在经十二烷基硫酸钠预处理的聚合物反相柱上进行。色谱分析在反相高效液相色谱柱上进行,用乙腈/水/氨混合物等度洗脱,并在254 nm处进行紫外检测。该色谱方法具有可重复性、重现性和灵敏性。在添加水平为5和1 mg kg(-1)的柠檬样品中,多菌灵的杀菌剂回收率为81-85%,噻菌灵为96-98%,邻苯基苯酚为81-106%,变异系数为2.5-7.4%。柠檬中多菌灵、噻菌灵和邻苯基苯酚的检测限分别为0.21、0.27和0.51 mg kg(-1)。