Department of Analytical Chemistry and Organic Chemistry, Universitat Rovira i Virgili, Tarragona, Spain.
J Sep Sci. 2011 May;34(10):1091-101. doi: 10.1002/jssc.201100043. Epub 2011 Apr 13.
A solid-phase extraction and liquid chromatography-tandem mass spectrometry (SPE/LC-MS-MS) method was developed and validated for the simultaneous determination of nicotine, five drugs of abuse (morphine, cocaine, codeine, methadone, and 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine) and four metabolites (dihydrocodeine, 6-acetylmorphine, 11-nor-carboxy-Δ(9)-tetrahydrocannabinol, and benzoylecgonine) in water samples. A Fused-Core™ particle column was used as an alternative to sub-2-μm particles in chromatographic separations to work with low backpressures and high efficiencies in short analysis times. Drugs were extracted from waste and surface water with SPE using Oasis MCX cartridges. Electrospray (ESI) in positive and negative mode and tandem MS selected reaction monitoring mode were used for identification and quantification. Calibration by linear regression analysis with deuterated internal standards was used to compensate the matrix effects. Limits of detection were found as low as 0.5-1 ng/L (surface water) and 1-50 ng/L (wastewater). The method was applied to the analysis of different kinds of samples. Wastewater from a sewage treatment plant was collected from three sampling points (after primary, secondary, and tertiary treatments) for a week. The analysis of the samples revealed a significant presence of these drugs in samples from primary treatments, where maximum concentrations of nicotine (1105 ng/L) and benzoylecgonine (3336 ng/L) were found. Most of the compounds showed values between <LOQ and 52 ng/L after tertiary treatment. When surface waters from the Ebro River were analyzed, only benzoylecgonine showed levels between 19 and 35 ng/L.
建立并验证了固相萃取-液相色谱串联质谱法(SPE/LC-MS-MS),用于同时测定水样中的尼古丁、五种滥用药物(吗啡、可卡因、可待因、美沙酮和 2-亚乙基-1,5-二甲基-3,3-二苯基吡咯烷)和四种代谢物(二氢可待因、6-乙酰吗啡、11-去甲羧基-Δ(9)-四氢大麻酚和苯甲酰爱康宁)。采用核壳型颗粒柱替代亚 2μm 颗粒柱进行色谱分离,以实现低压、高效率、短分析时间。采用 Oasis MCX 萃取小柱通过固相萃取法从废水和地表水样品中提取药物。采用电喷雾(ESI)正、负离子模式和串联质谱选择反应监测模式进行鉴定和定量。采用内标法进行线性回归分析校准,以补偿基质效应。检测限低至 0.5-1ng/L(地表水)和 1-50ng/L(废水)。该方法已应用于不同类型样品的分析。从污水处理厂的三个采样点(一级、二级和三级处理后)收集一周的废水。对样品的分析表明,这些药物在一级处理样品中大量存在,其中尼古丁(1105ng/L)和苯甲酰爱康宁(3336ng/L)的浓度最高。大多数化合物在三级处理后,浓度值介于<LOQ 和 52ng/L 之间。对埃布罗河地表水进行分析时,仅检测到苯甲酰爱康宁的浓度在 19-35ng/L 之间。