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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of biomarkers of tobacco smoke exposure in oral fluid using solid-phase extraction and gas chromatography-tandem mass spectrometry
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Determination of biomarkers of tobacco smoke exposure in oral fluid using solid-phase extraction and gas chromatography-tandem mass spectrometry

机译:固相萃取-气相色谱-串联质谱法测定口腔液中烟草烟雾暴露的生物标志物

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摘要

A new, simple and sensitive method was described for the simultaneous determination of nicotine, cotinine and trans-3'-hydroxycotinine in oral fluid samples using solid-phase extraction and gas chromatography/tandem mass spectrometry (GC-MS/MS). This technique was developed using only 0.2. mL of sample, and deuterated analogues were used as internal standards. The method was found to be linear between 0.5 and 1000. ng/mL, with determination coefficients higher than 0.996 for all analytes. Intra- and interday precision and accuracy were in conformity with the criteria normally accepted in bioanalytical method validation. All analytes were stable in the samples for at least 24. h at room temperature, for at least 72. h at 25 °C in processed samples and for at least three freeze/thaw cycles. Absolute recoveries ranged from 89 to 92% for all analytes. GC-MS/MS has demonstrated to be a powerful tool for the simultaneous quantitation of the analytes, providing adequate selectivity and sensitivity. In addition, its performance characteristics allow its routine use in the analysis of biomarkers of tobacco smoke exposure, extending the window of analyte detection in nicotine cessation programs, using a sample amount as low as 0.2. mL of human oral fluid.
机译:描述了一种使用固相萃取和气相色谱/串联质谱法(GC-MS / MS)同时测定口腔液样品中烟碱,可替宁和反式3'-羟基烟碱的新方法,该方法简单,灵敏。此技术仅使用0.2进行开发。毫升样品和氘代类似物用作内标。发现该方法在0.5至1000 ng / mL之间是线性的,所有分析物的测定系数均高于0.996。盘中和盘中的精确度和准确性符合生物分析方法验证中通常接受的标准。样品中的所有分析物在室温下至少稳定24小时,在处理过的样品中至少在25°C下稳定72小时,并至少进行三个冷冻/融化循环。所有分析物的绝对回收率在89%到92%之间。 GC-MS / MS被证明是同时定量分析物的强大工具,具有足够的选择性和灵敏度。此外,它的性能特点使其可以常规用于分析烟草烟雾暴露的生物标志物,从而扩展了尼古丁戒烟计划中分析物检测的范围,使用的样品量低至0.2。毫升人类口服液。

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