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一种新的液相色谱-串联质谱法,采用常压光离子化,用于同时测定荷兰河流沉积物中的氮杂芳烃和氮杂酮。

A new liquid chromatography-tandem mass spectrometry method using atmospheric pressure photo ionization for the simultaneous determination of azaarenes and azaarones in Dutch river sediments.

机构信息

Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, The Netherlands.

出版信息

J Chromatogr A. 2013 Jun 14;1294:33-40. doi: 10.1016/j.chroma.2013.03.079. Epub 2013 Apr 17.

Abstract

A new method for the analysis of azaarenes and their degradation products (azaarones) was developed, optimized and validated using liquid chromatography coupled with atmospheric pressure photo ionization tandem mass spectrometric detection (LC-APPI/MS/MS). Seventeen compounds including 4 PAHs (naphthalene, anthracene, phenanthrene, benz[a]anthracene), 7 azaarenes (quinoline, acridine, phenanthridine, 5,6-benzoquinoline and 7,8-benzoquinoline, benzo[a]acridine, benzo[c]acridine), and 6 azaarones (2-OH-quinoline, 4-OH-quinoline, 5-OH-quinoline, 6-OH-quinoline, 9(10H)-acridone, 6(5H)phenanthridinone) were analyzed in sediment samples from Dutch rivers. All compounds were analyzed simultaneously in multi reaction monitoring (MRM) mode. Soxhlet extraction was used for the extraction of analytes from sediments. The limits of quantification of azaarenes and azaarones varied from 0.21 to 1.12μg/l and from 0.23 to 1.58μg/l, respectively. The limits of quantification for PAHs varied from 32 to 769μg/l. Matrix-independent recoveries of sediment samples were in the range 85-110%; matrix-dependent recoveries were in the range 73-148%, respectively. The method was tested on real sediment samples and the results were compared with a previous study in which GC/MS/MS was used for the simultaneous measurement of azaarenes and azaarones. 4-, 5- and 6-OH-quinolines and naphthalene, anthracene and phenanthrene were not present or below detection limits in some samples. All other analytes were present in samples in the concentration range 0.2-1200ng/g (dw). To our knowledge, this is the first report showing the possibility of measurement non-polar polyaromatic hydrocarbons together with polar azaarenes and their degradation products azaarones simultaneously with sufficient sensitivity and accuracy using LC/MS/MS.

摘要

开发了一种新的分析氮杂芳烃及其降解产物(氮杂酮)的方法,该方法使用液相色谱与大气压光电离串联质谱检测(LC-APPI/MS/MS)进行了优化和验证。该方法分析了来自荷兰河流沉积物样本中的 17 种化合物,包括 4 种多环芳烃(萘、蒽、菲、苯并[a]蒽)、7 种氮杂芳烃(喹啉、吖啶、菲啶、5,6-苯并喹啉和 7,8-苯并喹啉、苯并[a]吖啶、苯并[c]吖啶)和 6 种氮杂酮(2-OH-喹啉、4-OH-喹啉、5-OH-喹啉、6-OH-喹啉、9(10H)-吖啶酮、6(5H)菲啶酮)。所有化合物均在多反应监测(MRM)模式下同时分析。索氏提取用于从沉积物中提取分析物。氮杂芳烃和氮杂酮的定量限范围分别为 0.21-1.12μg/l 和 0.23-1.58μg/l。多环芳烃的定量限范围为 32-769μg/l。沉积物样品的基质独立回收率范围为 85-110%;基质依赖性回收率范围分别为 73-148%。该方法在实际沉积物样品中进行了测试,并将结果与先前使用 GC/MS/MS 同时测量氮杂芳烃和氮杂酮的研究进行了比较。在一些样本中,4-、5-和 6-OH-喹啉以及萘、蒽和菲不存在或低于检测限。所有其他分析物在样品中的浓度范围为 0.2-1200ng/g(dw)。据我们所知,这是首次报道使用 LC/MS/MS 以足够的灵敏度和准确性同时测量非极性多环芳烃与极性氮杂芳烃及其降解产物氮杂酮的可能性。

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