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首页> 外文期刊>Journal of Chromatography, Biomedical Applications >Determination of acrolein by headspace solid-phase microextraction gas chromatography and mass spectrometry
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Determination of acrolein by headspace solid-phase microextraction gas chromatography and mass spectrometry

机译:顶空固相微萃取气相色谱-质谱法测定丙烯醛

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We developed a heads pace solid-phase microextraction (headspace SPME)method to measure acrolein in human urine. This new technique resolves some problems with the headspace gas chromatography and mass spectrometry (GC-MS) method which we developed previously. With the original method, a column and a filament were damaged by the injection of air. A 0.5-ml urine (or phosphate-buffered saline) sample in a glass vial containing propionaldehyde as an internal standard was heated for 5 min. The SPME fiber (65 #mu#m carbonwax-divinylbenzene fiber) was exposed to the headspace and then Inserted into a GC-MS instrument in which a DB-WAX capillary column (30 m * 0.32 mm, film thickness 0.5 #mu#m) was installed. The total analysis time was 15 min. The inter-assay and intra-assay coefficients of variation were 10.07 and 5..79%, respectively. The calibration curve demonstrated good linearity throughout concentrations ranging from 1 to 10 000 nM .The headspace SPME method exhibits high sensitivity and requires a short analysis time as well as the previous method. We conclude that this method is useful to measure urinary acrolein.
机译:我们开发了一种头部固相微萃取(顶空SPME)方法来测量人尿中的丙烯醛。这项新技术解决了我们之前开发的顶空气相色谱和质谱分析(GC-MS)方法的一些问题。使用原始方法,空气注入会损坏色谱柱和细丝。将装有丙醛作为内标的玻璃小瓶中的0.5毫升尿液(或磷酸盐缓冲盐水)加热5分钟。将SPME纤维(65#mu#m碳蜡-二乙烯基苯纤维)暴露在顶部空间,然后插入GC-MS仪器中,在该仪器中使用DB-WAX毛细管柱(30 m * 0.32 mm,膜厚0.5#mu#m )已安装。总分析时间为15分钟。批间和批内变异系数分别为10.07和5..79%。校准曲线在从1到10000 nM的整个浓度范围内均显示出良好的线性。顶空SPME方法与以前的方法相比具有较高的灵敏度,并且分析时间短。我们得出的结论是,该方法对测量尿中的丙烯醛很有用。

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