Gros Meritxell, Pizzolato Tânia-Mara, Petrović Mira, de Alda Maria José López, Barceló Damià
Department of Environmental Chemistry, IIQAB-CSIC, c/Jordi Girona 18-26, 08034 Barcelona, Spain.
J Chromatogr A. 2008 May 2;1189(1-2):374-84. doi: 10.1016/j.chroma.2007.10.052. Epub 2007 Oct 23.
This paper describes the development of an analytical methodology to determine eight beta-blockers in waste waters using molecularly imprinted polymers (MIPs) as extraction and pre-concentration material, followed by liquid chromatography-quadrupole-linear ion trap mass spectrometry (LC-QqLIT MS). The advantages offered by MIPs, in terms of selectivity and specificity, were compared with the most commonly polymeric materials used (the lipophilic-hydrophilic balanced Oasis HLB cartridges). Even though recoveries achieved with both sorbents were similar, ranging from 50 to 110% for sewage treatment plant (STP) effluent and 40-110 for STP influent, respectively, MIPs provided lower method detection limits than Oasis HLB, due to their specificity for target analytes and closely related analogues. Method detection limits (MDL) achieved using MIPs ranged from 0.2 to 6.4 ng/L for STP effluent and from 0.4 to 6.5 ng/L for STP influent. To highlight the advantages of MIPs against conventional polymeric cartridges, a detailed matrix effects study as well as cross reactivity tests were performed. For the latter purpose, the extraction efficiency of some pharmaceuticals and pesticides belonging to different therapeutic classes was assessed. LC-QqLIT MS, used for quantification and confirmation, proved to be a powerful analytical tool, as instrumental detection limits (IDL) achieved ranged from 0.2 to 2.7 pg injected (in multiple reaction monitoring mode (MRM)). In addition the inclusion of high sensitive MS/MS scans for each compound when working in Information Dependent Acquisition mode (IDA) provided extra confirmation for unequivocal identification of target compounds in complex environmental matrices.
本文描述了一种分析方法的开发,该方法使用分子印迹聚合物(MIP)作为萃取和预浓缩材料,结合液相色谱-四极杆-线性离子阱质谱(LC-QqLIT MS)来测定废水中的8种β受体阻滞剂。将MIP在选择性和特异性方面的优势与最常用的聚合材料(亲脂-亲水平衡的Oasis HLB柱)进行了比较。尽管两种吸附剂的回收率相似,污水处理厂(STP)出水的回收率分别为50%至110%,进水的回收率为40%至110%,但由于MIP对目标分析物及其密切相关类似物具有特异性,其方法检测限低于Oasis HLB。使用MIP获得的污水处理厂出水的方法检测限(MDL)为0.2至6.4 ng/L,进水的方法检测限为0.4至6.5 ng/L。为了突出MIP相对于传统聚合物柱的优势,进行了详细的基质效应研究以及交叉反应测试。对于后一个目的,评估了一些属于不同治疗类别的药物和农药的萃取效率。用于定量和确证的LC-QqLIT MS被证明是一种强大的分析工具,因为在多反应监测模式(MRM)下获得的仪器检测限(IDL)为0.2至2.7 pg进样量。此外,在信息依赖采集模式(IDA)下工作时,对每种化合物进行高灵敏度的MS/MS扫描,为在复杂环境基质中明确鉴定目标化合物提供了额外的确证。