Department of Food Science and Technology/National Nutrition and Food Technology Research Institute, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
J Chromatogr A. 2012 May 11;1237:30-6. doi: 10.1016/j.chroma.2012.02.078. Epub 2012 Mar 10.
A simple and efficient method was developed using microwave-assisted extraction (MAE) and dispersive liquid-liquid microextraction (DLLME) coupled with gas chromatography-mass spectrometry (GC-MS) for the extraction and quantification of 16 polycyclic aromatic hydrocarbons (PAHs) in smoked fish. Benzo[a]pyrene, chrysene and pyrene were employed as model compounds and spiked to smoked fish to assess the extraction procedure. Several parameters, including the nature and volume of hydrolysis, extracting and disperser solvents, microwave time and pH, were optimized. In the optimum condition for MAE, 1g of fish sample was extracted in 12 mL KOH (2M) and ethanol with a 50:50 ratio in a closed-vessel system. For DLLME, 500 μL of acetone (disperser solvent) containing 100 μL of ethylene tetrachloride (extraction solvent) was rapidly injected by syringe into 12 mL of the sample extract solution (previously adjusted to pH 6.5), thereby forming a cloudy solution. Phase separation was performed by centrifugation and a volume of 1.5 μL of the sedimented phase was analyzed by GC-MS in select ion monitoring (SIM) mode. Satisfactory results were achieved when this method was applied to analyze the PAHs in smoked fish samples. The MAE-DLLME method coupled with GC-MS provided excellent enrichment factors (in the range of 244-373 for 16 PAHs) and good repeatability (with a relative standard deviation between 2.8 and 9%) for spiked smoked fish. The calibration graphs were linear in the range of 1-200 ng g(-1), with the square of the correlation coefficient (R(2))>0.981 and detection limits between 0.11 and 0.43 ng g(-1). The recoveries of those compounds in smoked fish were from 82.1% to 105.5%. A comparison of this method with previous methods demonstrated that the proposed method is an accurate, rapid and reliable sample-pretreatment method that gives very good enrichment factors and detection limits for extracting and determining PAHs from smoked fish.
建立了一种采用微波辅助萃取(MAE)和分散液-液微萃取(DLLME)与气相色谱-质谱联用(GC-MS)相结合的方法,用于提取和定量分析熏鱼中的 16 种多环芳烃(PAHs)。将苯并[a]芘、屈和芘作为模型化合物添加到熏鱼中,以评估提取程序。优化了几个参数,包括水解、萃取和分散溶剂的性质和体积、微波时间和 pH 值。在 MAE 的最佳条件下,1g 鱼样在封闭系统中用 12mL KOH(2M)和乙醇(50:50 比例)提取。对于 DLLME,通过注射器迅速将 500μL 丙酮(分散溶剂)注入 12mL 样品萃取溶液(先前调节至 pH 6.5)中,含有 100μL 四氯乙烯(萃取溶剂),从而形成混浊溶液。通过离心进行相分离,用 GC-MS 在选择离子监测(SIM)模式下分析 1.5μL 沉淀相。将该方法应用于分析熏鱼样品中的多环芳烃,得到了令人满意的结果。MAE-DLLME 方法与 GC-MS 结合,为 16 种多环芳烃提供了优异的富集因子(范围为 244-373)和良好的重复性(加标熏鱼的相对标准偏差在 2.8-9%之间)。校准曲线在 1-200ng g(-1)范围内呈线性,相关系数(R(2))>0.981,检测限在 0.11-0.43ng g(-1)之间。这些化合物在熏鱼中的回收率为 82.1%-105.5%。与以往方法的比较表明,该方法是一种准确、快速、可靠的样品预处理方法,对从熏鱼中提取和测定多环芳烃具有非常好的富集因子和检测限。