首页> 外文期刊>Journal of the American Society for Mass Spectrometry >Quantitative MALDI-MSn Analysis of Cocaine in the Autopsied Brain of a Human Cocaine User Employing a Wide Isolation Window and Internal Standards
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Quantitative MALDI-MSn Analysis of Cocaine in the Autopsied Brain of a Human Cocaine User Employing a Wide Isolation Window and Internal Standards

机译:使用宽隔离窗口和内标物的可卡因使用者尸体解剖脑中可卡因的定量MALDI-MSn分析

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摘要

Detection of drugs in tissue typically requires extensive sample preparation in which the tissue is first homogenized, followed by drug extraction, before the extracts are finally analyzed by LC/MS. Directly analyzing drugs in intact tissue would eliminate any complications introduced by sample pretreatment. A matrix-assisted laser desorption/ionization tandem mass spectrometry (MALDI-MS") method as been developed for the quantification of cocaine present in postmortem brain tissue of a chronic human cocaine user. It is shown that tandem mass spectrometry (MS2 and MS3 increase selectivity, which is critical for differentiating analyte ions from background ions such as matrix clusters and endogenous compounds found in brain tissue. It is also shown that the use of internal standards corrects for signal variability during quantitative MALDI, which can be caused by inhomogeneous crystal formation, inconsistent sample preparation, and laser shot-to-shot variability. The MALDI-MS" method developed allows for a single MS3 experiment that uses a wide isolation window to isolate both analyte and internal standard target ions. This method is shown to provide improved precision [similar to 10-20 times reduction in percent relative standard deviation (%RSD)] for quantitative analysis compared to using two alternating MS3 experiments that separately isolate the target analyte and internal standard ions.
机译:组织中药物的检测通常需要大量的样品前处理,其中首先将组织匀浆,然后进行药物提取,然后再通过LC / MS对提取物进行最终分析。直接分析完整组织中的药物将消除样品预处理带来的任何并发症。建立了一种矩阵辅助激光解吸/电离串联质谱(MALDI-MS“)方法,用于定量分析可卡因在慢性人类用户中的死后脑组织中的可卡因含量。结果表明,串联质谱(MS2和MS3)有所增加选择性,这对于将分析物离子与背景离子(例如脑组织中的基质簇和内源性化合物)区分开来至关重要,并且还表明,使用内标校正了定量MALDI过程中的信号变异性,这可能是由于晶体形成不均引起的,样品制备不一致以及激光的逐次变化性。开发的MALDI-MS“方法允许进行单个MS3实验,该实验使用宽的隔离窗口来分离分析物和内标目标离子。与usin相比,定量分析的精度[类似于相对标准偏差百分比(%RSD)降低10-20倍] g两个交替的MS3实验,分别分离目标分析物和内标离子。

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