溴化阻燃劑如：十溴二苯醚 (Decabromodiphenyl ether, decaBDE)、六溴環十二烷 (Hxabromocyclododecane, HBCD)，已是市面上被常用來添加於防火材料中，主要是此兩種化合物在防火部分相較於其他鹵素，僅需少量添加，便可有良好的阻燃效果。這類溴化阻燃劑因具有持久性與高親脂性 (log Kow>5)，因此在食物鏈中會累積放大。目前在許多人類常食用的水產中已檢測出含有此類物質。 本研究主要開發一套簡單、有效且可快速檢測這兩種溴化阻燃劑的樣品前處理方法，應用在不同種類生物樣品中。實驗的萃取方法是使用基質固相分散萃取法 (Matrix solid-phase dispersion, MSPD) 來進行樣品前處理，並利用氣相層析質譜儀結合電子捕捉負離子化學游離法 (GC-ECNI-MS) 進行偵測。最佳化的萃取條件為將1 g經由冷凍乾燥的生物樣品和2 g的SiO2，放入震盪器中快速均勻混合。把混合物轉移到含有1 g 30 % 酸性SiO2與1.5 g SiO2的玻璃管柱中，並以20 mL Hexane： DCM=1： 1的比例進行沖提，之後再將萃取液轉移至與上面相同淨化粉末的管柱中，再以10 mL 相同比例進行沖提，最後將萃取液旋濃乾燥。回溶後取1 μL利用GC-ECNI-MS進行檢測分析。 本研究結果顯示萃取回收率在81-108 %之間，其相對標準偏差 (RSDs) 皆小於10 %，顯示此方法具有良好的再現性與穩定性。而decaBDE與HBCD的偵測極限 (LOD) 分別為0.05 ng/g與0.03 ng/g；在真實樣品部分，市售的水產中分別可檢測出decaBDE: 0.34-2.11 ng/g與HBCD: 0.17-0.5 ng/g。;Brominated flame retardants, such as decabromodiphenyl ether (decaBDE),and hxabromocyclododecane (HBCD), are used to add in the fire protection materials. Comparing to other halogen fire section, they have good flame retardant effect by adding only small amount. Because brominated flame retardants are persistent and highly lipophilic (log Kow> 5), they can be bio-accumulated and bio-magnificated in the food chain. Currently in many human regular consumption of biota products have detected containing such substances. This study was to develop a simple, effective and rapid sample pretreatment of two brominated flame retardants and apply to different types of biological samples. Experimental extraction method involves the use of vortex-homogenization matrix solid-phase dispersion (VHMSPD) extraction for sample pretreatment, and determination by gas chromatography- electron capture negative ion mass spectrometry (GC-ECNI-MS). The optimal extraction conditions involved dispersing of freeze-dried biota sample (1 g) with 2 g of SiO2 by a vigorous shaking to obtain a homogenous mixture. The mixture was transferred to a glass column containing 1 g 30% acidic SiO2 and 1.5 g SiO2 as the clean-up co-sorbent.The target analytes were then eluted with 20 mL of Hexane: DCM = 1: 1.The extract was transferred to the same column described above, and eluted with 10 mL of the same solvent. The extract was adjusted to 1 μL and then determined by GC-ECNI-MS. The findings show that the extraction recovery was obtained about 81-108% and relative standard deviations (RSDs) are less than 10 %, respectively. It indicats that the method shows good reproducibility and stability. The detection limit of decaBDE and HBCD were 0.05 ng / g and 0.03 ng / g respectively. In real sample section, decaBDE can be detected between 0.34-2.11 ng / g and HBCD can be dected detween 0.17- 0.5 ng / g in marketed sea food samples.
