G. Ianiri, Cristina Di Fiore, S. Passarella, Ivan Notardonato, Alessia Iannone, Fabiana Carriera, Virgilio Stillittano, V. De Felice, M. V. Russo, P. Avino
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引用次数: 0
摘要
本研究开发了一种简单、快速、有效的方法,用于检测和定量自动售货机使用的一次性容器中热饮中可能释放的七种邻苯二甲酸盐。采用模型溶液,确定了从热饮中提取7种邻苯二甲酸酯(DMP、DEP、DBP、DiBP、DEHP、DNOP和DDP)各步骤的最佳条件。采用超声-涡辅助分散液液微萃取(UVA-DLLME) -气相色谱法提取富集,回收率为66.7% ~ 101.2%,精密度<6.3%,重现性<11.1%。研究了从调配饮料到实际消费的等待时间对分子提取的影响,获得了分子量较高的PAEs的时间释放曲线,分子量较低的PAEs的时间释放曲线反之亦然。此外,还确定了提取液分析时的最佳仪器参数。使用GC-FID进行优化,而实际样品的分析使用GC-IT/MS进行超痕量分析;检出限为0.8 ~ 15.4 ng mL−1,定量限为1.6 ~ 35.8 ng mL−1,均低于FID。
Methodology for Determining Phthalate Residues by Ultrasound–Vortex-Assisted Dispersive Liquid–Liquid Microextraction and GC-IT/MS in Hot Drink Samples by Vending Machines
In this study, a simple, fast, and effective methodology has been developed for the detection and quantification of seven phthalates potentially released in hot drinks from disposable containers used in vending machines. The authors determined the optimal conditions to be applied during the various steps of extraction of seven phthalates (DMP, DEP, DBP, DiBP, DEHP, DNOP, and DDP) from hot beverages using a model solution. The extraction and preconcentration technique used was ultrasound–vortex-assisted dispersive liquid–liquid microextraction (UVA-DLLME) followed by gas chromatographic analysis obtaining recoveries from 66.7% to 101.2% with precision and reproducibility <6.3% and <11.1%, respectively. The influence of waiting time, from the dispensing of the drink to its actual consumption, for the extraction of molecules was investigated, obtaining a temporal release profile slightly shifted towards the PAEs with higher molecular weight and vice versa for those with low molecular weight. In addition, the best instrumental parameters to be applied during the analysis of the extracts obtained were established. This optimization was carried out using GC-FID, whereas the analysis of real samples was carried out by means of GC-IT/MS for ultra-trace analysis purposes; limits of detection (LODs) ranging between 0.8 ng mL−1 and 15.4 ng mL−1 and limits of quantification (LOQs) from 1.6 ng mL−1 to 35.8 ng mL−1, both of them lower than those found by FID, were obtained.