Sanagi Mohd Marsin, Loh Saw Hong, Wan Ibrahim Wan Aini, Hasan Mohamed Noor, Aboul Enein Hassan Y
Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 Johor Bahru, Johor, Malaysia.
J Chromatogr Sci. 2013 Feb;51(2):112-6. doi: 10.1093/chromsci/bms113. Epub 2012 Jul 9.
In this work, a two-phase hollow fiber liquid-phase microextraction (HF-LPME) method combined with gas chromatography-mass spectrometry (GC-MS) is developed to provide a rapid, selective and sensitive analytical method to determine polycyclic aromatic hydrocarbons (PAHs) in fresh milk. The standard addition method is used to construct calibration curves and to determine the residue levels for the target analytes, fluorene, phenanthrene, fluoranthene, pyrene and benzo[a]pyrene, thus eliminating sample pre-treatment steps such as pH adjustment. The HF-LPME method shows dynamic linearity from 5 to 500 µg/L for all target analytes with R(2) ranging from 0.9978 to 0.9999. Under optimized conditions, the established detection limits range from 0.07 to 1.4 µg/L based on a signal-to-noise ratio of 3:1. Average relative recoveries for the determination of PAHs studied at 100 µg/L spiking levels are in the range of 85 to 110%. The relative recoveries are slightly higher than those obtained by conventional solvent extraction, which requires saponification steps for fluorene and phenanthrene, which are more volatile and heat sensitive. The HF-LPME method proves to be simple and rapid, and requires minimal amounts of organic solvent that supports green analysis.
在本研究中,开发了一种两相中空纤维液相微萃取(HF-LPME)与气相色谱-质谱联用(GC-MS)的方法,以提供一种快速、选择性和灵敏的分析方法来测定鲜牛奶中的多环芳烃(PAHs)。采用标准加入法构建校准曲线并测定目标分析物芴、菲、荧蒽、芘和苯并[a]芘的残留水平,从而省去了诸如pH调节等样品预处理步骤。HF-LPME方法对所有目标分析物在5至500 µg/L范围内呈现动态线性,R(2)范围为0.9978至0.9999。在优化条件下,基于3:1的信噪比,所建立的检测限范围为0.07至1.4 µg/L。在100 µg/L加标水平下测定PAHs的平均相对回收率在85%至110%范围内。相对回收率略高于通过传统溶剂萃取获得的回收率,传统溶剂萃取对于芴和菲需要皂化步骤,而芴和菲更易挥发且对热敏感。HF-LPME方法被证明是简单快速的,并且需要极少量的有机溶剂,支持绿色分析。