Department of Analytical and Bioanalytical Sciences and Miniaturization (LSABM), ESPCI ParisTech, UMR PECSA 7195 (CNRS - UPMC - ESPCI ParisTech), 10 rue Vauquelin, 75231 Paris CEDEX 05, France.
Department of Analytical and Bioanalytical Sciences and Miniaturization (LSABM), ESPCI ParisTech, UMR PECSA 7195 (CNRS - UPMC - ESPCI ParisTech), 10 rue Vauquelin, 75231 Paris CEDEX 05, France.
J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Feb 15;949-950:16-23. doi: 10.1016/j.jchromb.2013.11.051. Epub 2013 Dec 15.
Considering the important complexity of biological samples, a molecularly imprinted polymer (MIP) was applied to the selective extraction of cocaine and its two main metabolites, benzoylecgonine and ecgonine methyl ester from biological samples. The MIP was imprinted with cocaine and it was synthesized in acetonitrile with methacrylic acid as a functional monomer and ethylene glycol dimethacrylate as a crosslinker. The selectivity of the MIP was first assessed for the three target analytes in acetonitrile with recoveries higher than 80% on the MIP and lower than 30% on the non-imprinted polymer (NIP). The MIP was then evaluated for the selective extraction of these targets from real aqueous media, i.e. serum and urine samples. The pH adjustment of the sample as well as the optimization of the washing step led to a very selective extraction of cocaine from these media. A LOQ of 0.5ng/mL was obtained for cocaine in urine. Concerning cocaine metabolites, benzoylecgonine and ecgonine methyl ester, they were first extracted from urine by liquid-liquid extraction and the resulting extract was purified on the MIP. The results obtained with the MIP as compared to the LLE alone showed the great potential of the MIP extraction for the clean-up of the biological matrix. This procedure was tested for the extraction of the analytes from urine samples, leading to a very selective protocol with LOQs of 0.09ng/mL, 0.4ng/mL and 1.1ng/mL for cocaine, benzolecgonine and ecgonine methyl ester respectively in urine samples.
考虑到生物样本的重要复杂性,应用分子印迹聚合物(MIP)从生物样本中选择性提取可卡因及其两种主要代谢物苯甲酰可卡因和甲基育亨宾。MIP 是用可卡因印迹合成的,在乙腈中用甲基丙烯酸作为功能单体和乙二醇二甲基丙烯酸酯作为交联剂合成。首先在乙腈中评估 MIP 对三种目标分析物的选择性,在 MIP 上的回收率高于 80%,在非印迹聚合物(NIP)上的回收率低于 30%。然后,评估 MIP 从真实水介质(即血清和尿液样本)中选择性提取这些目标物的能力。样品的 pH 值调整以及洗涤步骤的优化导致从这些介质中非常选择性地提取可卡因。在尿液中可卡因的 LOQ 为 0.5ng/mL。关于可卡因代谢物苯甲酰可卡因和甲基育亨宾,它们首先通过液-液萃取从尿液中提取,然后将得到的提取物在 MIP 上进行纯化。与单独的 LLE 相比,MIP 获得的结果显示了 MIP 萃取对生物基质净化的巨大潜力。该程序用于从尿液样品中提取分析物,导致在尿液样品中可卡因、苯甲酰可卡因和甲基育亨宾的 LOQs 分别为 0.09ng/mL、0.4ng/mL 和 1.1ng/mL 的非常选择性方案。