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Development of a methodology utilizing gas chromatography ion-trap tandem mass spectrometry for the determination of low levels of caffeine in surface marine and freshwater samples

机译:利用气相色谱离子捕获串联质谱法的发展,用于测定表面海洋和淡水样品中低水平的咖啡因

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A methodology for monitoring low level of caffeine in aqueous samples via gas chromatography coupled with an ion-trap tandem mass spectrometry detection system (IT-MS/MS) was developed. Four ITMSMS operating parameters, including the collision-induced dissociation ( CID) voltage, the excitation time (ET), the isolation time ( IT) and the maximum ionization time (MIT) were optimized in order to maximize the sensitivity of the IT-MS/MS technique towards the analyte and its isotope-labeled standard. After optimization, a limit of detection of 500 fg mu l(-1) with S/N= 3 was achieved. Taking into account blank values and the matrix background, a method detection limit of 1.0-2.0 ng l(-1) was derived and applied to all of the samples analyzed in the study. Various mass spectrometric conditions have been applied to caffeine and its trimethyl-C-13-labeled standard to elucidate fragmentation pathways for new and commonly occurring product ions observed in the collision-induced dissociation (CID) spectra produced by the ion trap. Ion structures and fragmentation pathway mechanisms have been proposed and compared with previously published data. An isotope dilution method using C-13-labeled caffeine as a surrogate internal standard was employed to determine and correct the recovery of native caffeine in water samples. The developed methodology has been applied for the determination of caffeine in surface marine and freshwater samples collected on the west coast of Vancouver Island in British Columbia, Canada. The results obtained for the marine water samples indicated a wide variation in the level of caffeine, ranging from 4.5 to 149 ng l(-1), depending on the location of the sampling site within the inlet. The concentrations of caffeine in samples from lakes associated with various residential densities ranged from ND to 6.5, 1.8 to 10.4 and 6.1 to 21.7 ng l(-1) for low, moderate and high residential densities, respectively.
机译:通过气相色谱与离子阱串联质谱检测系统(IT-MS / MS)偶联的气相色谱法监测水性样品中咖啡含量低水平的方法。优化了四个ITMSMS操作参数,包括碰撞感应的解离(CID)电压,激发时间(ET),隔离时间(IT)和最大电离时间(MIT),以最大化IT-MS的灵敏度/ MS技术朝向分析物及其同位素标记标准。优化后,实现了具有S / N = 3的500 fg MU L(-1)的检测限。考虑到空白值和矩阵背景,衍生出1.0-2.0 ng L(-1)的方法检测限,并应用于研究中分析的所有样品。各种质谱条件已经施用于咖啡因及其三甲基-C-13标记标准标准,以阐明在由离子阱产生的碰撞诱导的解离(CID)光谱中观察到的新的和通常发生的产物离子的碎片途径。已经提出了离子结构和碎片途径机制,并与先前公布的数据进行了比较。使用C-13标记的咖啡因作为替代内标的同位素稀释方法,以确定和校正水样中天然咖啡因的回收率。已申请了在加拿大不列颠哥伦比亚省(不列颠哥伦比亚省)在加拿大不列颠哥伦比亚省温哥华岛西海岸收集的咖啡因的咖啡因的测定。为海洋水样得到的结果表明咖啡因水平的宽变化,范围为4.5至149 ng L(-1),这取决于入口内采样点的位置。与各种居住密度相关的湖泊中的样品中咖啡因的浓度分别为低,中等和高的居民密度的Nd至6.5,10.4和6.1至21.7 ng L(-1)。

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