Lambropoulou Dimitra A, Konstantinou Ioannis K, Albanis Triantafyllos A
Laboratory of Environmental Technology, Department of Chemistry, University of Ioannina, Ioannina 45110, Greece.
J Chromatogr A. 2006 Aug 18;1124(1-2):97-105. doi: 10.1016/j.chroma.2006.05.044. Epub 2006 Jun 14.
A simple and reliable sample methodology based on simultaneous ultrasonic extraction, sulfuric acid clean-up and headspace solid-phase microextraction (SPME)-gas chromatography-mass spectrometry has been developed as an advantageous analytical tool for the determination of seven polychlorinated biphenyl congeners in bird livers at low levels. The influence of several parameters on the efficiency of the proposed method was systematically investigated. The clean-up efficiency of sulfuric acid treatment was tested and compared with those of column chromatography (Flosiril, silica gel and alumina) and solid-phase extraction (SPE) (Supelclean ENVI-Carb cartridge) procedures. The use of sulfuric acid in the clean-up step prior to headspace solid-phase microextraction analysis allows the removal of interfering matrix compounds present in the liver extracts that would otherwise cause severe ionization suppression of the polychlorinated biphenyls (PCBs) during the ionization process. The optimized method had good linearity (R2>0.99) over the range studied (5-500 ng/g wet weight) and showed satisfactory level of precision, with RSD values lower than 10.6%. The obtained relative recoveries ranged between 63 and 94%. The limits of detection (0.06-0.63 ng/g wet weight) were low enough to check for harmful levels of polychlorinated biphenyls in biological samples, and were well below most of the restrictive limits established by European Union regulations. The method was found to be reliable under the operational conditions proposed and was applied successfully to the analysis of individual polychlorinated biphenyls in liver tissues. The results obtained from five bird species from Greece revealed the presence of the target compounds in all samples analyzed, at levels ranging between 0.54 and 39.45 ng/g wet weight.
基于同时进行超声提取、硫酸净化和顶空固相微萃取(SPME)-气相色谱-质谱联用技术,开发了一种简单可靠的样品处理方法,作为一种优势分析工具用于测定鸟类肝脏中低含量的7种多氯联苯同系物。系统研究了几个参数对所提方法效率的影响。测试了硫酸处理的净化效率,并与柱色谱法(弗罗里硅土、硅胶和氧化铝)及固相萃取(SPE)法(Supelclean ENVI-Carb柱)的净化效率进行了比较。在顶空固相微萃取分析之前的净化步骤中使用硫酸,可以去除肝脏提取物中存在的干扰基质化合物,否则这些化合物会在电离过程中导致多氯联苯(PCBs)出现严重的电离抑制。优化后的方法在所研究的范围内(5 - 500 ng/g湿重)具有良好的线性(R2>0.99),精密度令人满意,相对标准偏差(RSD)值低于10.6%。获得的相对回收率在63%至94%之间。检测限(0.06 - 0.63 ng/g湿重)足够低,能够检测生物样品中多氯联苯的有害水平,且远低于欧盟法规规定的大多数限制水平。该方法在所提出的操作条件下被证明是可靠的,并成功应用于肝脏组织中单个多氯联苯的分析。从希腊的5种鸟类获得的结果表明,在所有分析样品中均均目标化合物均有存在,含量范围在0.54至39.45 ng/g湿重之间。