Beijing Higher Institution Engineering Research Center of Food Additives and Ingredients, Beijing Technology and Business University, NO. 11 Fucheng Road, Beijing, 100048, China.
Beijing Centre for Physical and Chemical Analysis, Beijing, 100089, China.
Mikrochim Acta. 2019 Jul 23;186(8):560. doi: 10.1007/s00604-019-3651-y.
A simple and fast method is described for the extraction of polycyclic aromatic hydrocarbons (PAHs) from complex samples. It is based on the use of a nanoferrofluid modified with a ternary hydrophobic deep eutectic solvent. A predictive model was used for the selection of the optimal eutectic mixture. The entire microextraction only takes a few minutes for completion. Under the optimal extraction conditions (by using menthol, borneol and camphor in a molar ratio of 5:1:4; 80 mg of nanoferrofluid), it offers marked improvements in terms of selectivity and sensitivity. The limits of detection range between 0.31 and 5.9 ng·L, and recoveries from spiked samples between 91.3 and 121%. In addition, the strong interactions between PAHs and the extractant were supported by quantum mechanical calculations. This results in a better insight into the microextraction mechanism, providing a fast, environmentally friendly and effective route for the optimization of pretreatment parameters. The method was successfully applied to the determination of the PAHs naphthalene, acenaphthylene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, chrysene, benzo[b]fluoranthene, benzo[a]pyrene, dibenzo[a,h]anthracene, benzo[g,h,i]perylene and indeno[1,2,3-c,d]pyrene in 12 kinds of coffee samples after different roasting conditions. Graphical abstract Schematic presentation of nanoferrofluid modified with ternary hydrophobic deep eutectic solvent and their application for selective microextraction of ultra-trace polycyclic aromatic hydrocarbons in coffee prior to HPLC analysis.
一种简单快速的方法用于从复杂样品中提取多环芳烃(PAHs)。它基于使用纳米铁流体修饰的三元疏水性深共晶溶剂。使用预测模型选择最佳共晶混合物。整个微萃取仅需几分钟即可完成。在最佳萃取条件下(使用薄荷醇、龙脑和莰烯摩尔比为 5:1:4;80mg 纳米铁流体),在选择性和灵敏度方面有显著提高。检测限范围在 0.31 到 5.9ng·L 之间,加标样品的回收率在 91.3%到 121%之间。此外,量子力学计算支持 PAHs 和萃取剂之间的强相互作用。这使得对微萃取机制有了更好的了解,为预处理参数的优化提供了一种快速、环保和有效的途径。该方法成功应用于 12 种不同烘焙条件下咖啡样品中萘、苊烯、苊、芴、菲、蒽、荧蒽、芘、䓛、苯并[b]荧蒽、苯并[a]芘、二苯并[a,h]蒽、苯并[g,h,i]苝和茚并[1,2,3-c,d]芘的测定。