Dasgupta Soma, Banerjee Kaushik, Dhumal Kondiba N, Adsule Pandurang G
University of Pune, Department of Environmental Sciences, Pune-411 007, India.
J AOAC Int. 2011 Jan-Feb;94(1):273-85.
This paper describes single-laboratory validation of a multiresidue method for the determination of 135 pesticides, 12 dioxin-like polychlorinated biphenyls, 12 polyaromatic hydrocarbons, and bisphenol A in grapes and wine by GC/time-of-flight MS in a total run time of 48 min. The method is based on extraction with ethyl acetate in a sample-to-solvent ratio of 1:1, followed by selective dispersive SPE cleanup for grapes and wine. The GC/MS conditions were optimized for the chromatographic separation and to achieve highest S/N for all 160 target analytes, including the temperature-sensitive compounds, like captan and captafol, that are prone to degradation during analysis. An average recovery of 80-120% with RSD < 10% could be attained for all analytes except 17, for which the average recoveries were 70-80%. LOQ ranged within 10-50 ng/g, with < 25% expanded uncertainties, for 155 compounds in grapes and 151 in wine. In the incurred grape and wine samples, the residues of buprofezin, chlorpyriphos, metalaxyl, and myclobutanil were detected, with an RSD of < 5% (n = 6); the results were statistically similar to previously reported validated methods.
本文描述了一种多残留方法的单实验室验证,该方法用于通过气相色谱/飞行时间质谱仪在48分钟的总运行时间内测定葡萄和葡萄酒中的135种农药、12种二恶英类多氯联苯、12种多环芳烃和双酚A。该方法基于以1:1的样品与溶剂比例用乙酸乙酯萃取,随后对葡萄和葡萄酒进行选择性分散固相萃取净化。气相色谱/质谱条件针对色谱分离进行了优化,以实现所有160种目标分析物的最高信噪比,包括对温度敏感的化合物,如克菌丹和敌菌丹,这些化合物在分析过程中容易降解。除17种分析物外,所有分析物的平均回收率可达80-120%,相对标准偏差<10%,这17种分析物的平均回收率为70-80%。葡萄中155种化合物和葡萄酒中151种化合物的定量限在10-50 ng/g范围内,扩展不确定度<25%。在实际的葡萄和葡萄酒样品中,检测到了噻嗪酮、毒死蜱、甲霜灵和腈菌唑的残留,相对标准偏差<5%(n = 6);结果在统计学上与先前报道的经过验证的方法相似。