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首页> 外文期刊>Forensic science international >Comprehensive two-dimensional gas chromatography with time-of-flight mass spectrometry (GC x GC-TOFMS) for drug screening and confirmation.
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Comprehensive two-dimensional gas chromatography with time-of-flight mass spectrometry (GC x GC-TOFMS) for drug screening and confirmation.

机译:全面的二维气相色谱仪与飞行时间质谱仪(GC x GC-TOFMS)进行药物筛选和确认。

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摘要

Comprehensive two-dimensional gas chromatography ( [Formula: see text] ) is applied to analysis of drug standard mixtures containing 78 drugs of interest in forensic samples. For this study, underivatised drugs were employed. While several of the drugs were not detected at the low concentrations employed in the samples, most could be satisfactorily assigned their first and second dimension retentions in the [Formula: see text] retention plane. For this study, time-of-flight mass spectrometry (TOFMS) detection was used. The enhanced separation possible in [Formula: see text] is demonstrated, and typical linearity and apparatus precision are shown for tramadol, diazepam, olanzapine and desipramine using selected qualifier ions. Mass spectral library search quality for the detection of drugs in a selection of authentic forensic cases, along with retention position in the 2D retention plane, is used to support positive identification of the presence of the drugs. The analysis of 'difficult' drugs paracetamol and phenytoin is shown to produce anomalous chromatographic peak shape in the 2D plane, whereas most drugs gave acceptable peak shapes. The [Formula: see text] technique was applied to screening drugs in forensic samples, with either flame ionisation (FID) or TOFMS detection, and compared favourably with conventional single column GC-MS analysis when tested for diazepam in an authentic forensic study.
机译:综合二维气相色谱法([公式:参见正文])用于分析法医样品中含有78种目标药物的药物标准混合物。在这项研究中,使用了未充分利用的药物。尽管没有以样品中使用的低浓度检测到几种药物,但是大多数药物都可以在[公式:参见文本]保留平面中令人满意地指定其一维和二维保留值。在这项研究中,使用了飞行时间质谱(TOFMS)检测。证明了在[化学式:参见文本]中可能的增强分离,并显示了使用选定的定性离子对曲马多,地西epa,奥氮平和地昔帕明的典型线性和装置精密度。质谱库的搜索质量(用于在某些真实的法医案例中进行检测)以及2D保留平面中的保留位置,用于支持对药物存在的肯定识别。对“难”药物对乙酰氨基酚和苯妥英的分析显示在2D平面中产生异常色谱峰形,而大多数药物给出可接受的峰形。 [公式:参见正文]技术用于火焰法电离(FID)或TOFMS检测法筛查法医样品中的药物,并在可靠的法医研究中对地西epa进行测试时,与常规的单柱GC-MS分析相比具有优势。

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