Wang Dongli, Atkinson Shannon, Hoover-Miller Anne, Shelver Weilin L, Li Qing X
Department of Molecular Biosciences and Bioengineering, University of Hawaii at Manoa, Honolulu, HI 96822, USA.
Rapid Commun Mass Spectrom. 2008;22(5):647-56. doi: 10.1002/rcm.3410.
Bromodiphenyl ethers (BDEs) are a class of synthetic flame retardants and are widely present in the environment. Analysis of higher BDE congeners has proven to be a challenge. We report the development of a method that enhances their analysis by splitting the eluent of a gas chromatograph (GC) between an electron capture detector (ECD) and an ion trap mass spectrometer (ITMS): 1:10, ECD:ITMS. This allowed the quantitation of the lower molecular weight (MW) BDE congeners (Br1-Br7) with the ITMS and of the higher MW BDEs (Br8-Br10) with the highly sensitive ECD. The IT temperature, ionization mode, and MS/MS parameters (excitation amplitude and stability parameter) were optimized. This method took the advantages of the best detector for the different BDE homologues and was suitable for the analysis of BDEs in environmental and biological samples. Average recoveries were 52-112% for BDEs from spiked sand samples and 57-126% from spiked lard samples after accelerated solvent extraction followed by silica gel and alumina column clean-up. Average recoveries ranged from 51% to 130% for 13C-labeled BDEs spiked in the real and in matrix samples. The method detection limits for specific congeners were 0.18-120 pg/g of the BDEs in animal tissue samples, and 0.05-40 pg/g in soil and indoor dust samples. The utility of the method was demonstrated by analyzing actual harbor seal blubber, indoor dust and soil samples. The concentration of each BDE ranged from non-detectable (nd) to 41 ng/g in the dry soil sample, nd to 1042 ng/g in the indoor dust, nd to 15 ng/g wet weight in the Alaskan harbor seal blubber sample, and 0.02 to 11 ng/microL of the identified 23 of the 42 breakdown products from BDE-209 after zerovalent iron treatment. Finally, an interlaboratory comparison showed high correspondence between the GC/ITMS-ECD method and a GC high-resolution MS system for the analysis of BDEs in soil samples.
溴代二苯醚(BDEs)是一类合成阻燃剂,广泛存在于环境中。对高溴代二苯醚同系物的分析已被证明是一项挑战。我们报告了一种方法的开发,该方法通过在电子捕获检测器(ECD)和离子阱质谱仪(ITMS)之间分流气相色谱(GC)的洗脱液来增强对它们的分析:ECD:ITMS为1:10。这使得能够用ITMS对低分子量(MW)的溴代二苯醚同系物(Br1-Br7)进行定量,并用高灵敏度的ECD对高分子量的溴代二苯醚(Br8-Br10)进行定量。对离子阱温度、电离模式和串联质谱参数(激发幅度和稳定性参数)进行了优化。该方法利用了针对不同溴代二苯醚同系物的最佳检测器的优势,适用于环境和生物样品中溴代二苯醚的分析。加标砂样中溴代二苯醚的平均回收率为52-112%,加标猪油样经加速溶剂萃取后再经硅胶和氧化铝柱净化,平均回收率为57-126%。在实际样品和基质样品中加标的13C标记溴代二苯醚的平均回收率为51%至130%。动物组织样品中特定同系物的方法检测限为0.18-120 pg/g溴代二苯醚,土壤和室内灰尘样品中为0.05-40 pg/g。通过分析实际的海豹脂肪、室内灰尘和土壤样品证明了该方法的实用性。在干燥土壤样品中,每种溴代二苯醚的浓度范围为未检出(nd)至41 ng/g,室内灰尘中为nd至1042 ng/g,阿拉斯加海豹脂肪湿重样品中为nd至15 ng/g,零价铁处理后BDE-209的42种分解产物中已鉴定出的23种的浓度为0.02至11 ng/μL。最后,一项实验室间比较表明,GC/ITMS-ECD方法与用于分析土壤样品中溴代二苯醚的GC高分辨率质谱系统之间具有高度一致性。