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开发一种创新的“绿色”搅拌棒吸附萃取-热脱附-气相色谱-串联质谱法用于定量分析海洋生物群中的多环芳烃。

Development of an innovative and "green" stir bar sorptive extraction-thermal desorption-gas chromatography-tandem mass spectrometry method for quantification of polycyclic aromatic hydrocarbons in marine biota.

作者信息

Lacroix C, Le Cuff N, Receveur J, Moraga D, Auffret M, Guyomarch J

机构信息

LEMAR - UMR 6539 - Technopôle de Brest-Iroise, 29280 Plouzané, France.

CEDRE - 715, Rue Alain Colas/CS 41836, 29218 Brest Cedex 2, France.

出版信息

J Chromatogr A. 2014 Jul 4;1349:1-10. doi: 10.1016/j.chroma.2014.04.094. Epub 2014 May 4.

Abstract

There is a growing awareness of the need to reduce the negative impact of chemical analyses on the environment and to develop new eco-friendly and sustainable analytical methods without compromising performance. In this study, we developed a "green" analytical method enabling the accurate and simultaneous routine analysis of 21 polycyclic aromatic hydrocarbons (PAHs) in reduced quantities (100mg and 1g wet weight (WW)) of marine biota samples (fish muscle, mussel and oyster tissues) using alkaline digestion combined with stir bar sorptive extraction-thermal desorption-gas chromatography-tandem mass spectrometry (SBSE-GC-MS/MS). The innovative method provides good selectivity and specificity for most compounds. In 1gWW samples, limits of quantification (LOQs) ranged from 1 to 10μg/kgWW in fish muscle and from 0.5 to 10μg/kgWW in mussel tissue. The method enables most analytes to be quantified below the restrictive limits established by the European Commission (2 and 10μg/kgWW in fish muscle and bivalve mollusc, respectively). Higher LOQs were obtained in 100mgWW samples ranging from 1 to 50μg/kgWW. Recovery and linearity were assessed for all analytes. The results were satisfactory for most compounds with recoveries ranging from 94% to 117% in 1gWW mussel samples at spike concentration of 10ng/gWW with standard deviation not exceeding 12%. However, results confirmed that the SBSE efficiency is affected by the complexity of biological matrices, especially for high molecular weight compounds in lipid-rich mussel tissue. Because of the matrix effects, matrix-matched calibrations were carried out. Validation was performed using the standard reference material 1974c with recovery ranging from 71% to 119% except for naphthalene, anthracene and benzo(e)pyrene that were therefore not validated. Overall, the developed method meets analytical validation criteria for most compounds. Thanks to the combination of alkaline digestion and SBSE, which greatly simplifies sample treatment and limits solvent use to ethanol, the developed method followed most green analytical chemistry principles.

摘要

人们越来越意识到需要减少化学分析对环境的负面影响,并开发新的环保且可持续的分析方法,同时不影响性能。在本研究中,我们开发了一种“绿色”分析方法,该方法能够使用碱性消解结合搅拌棒吸附萃取-热脱附-气相色谱-串联质谱法(SBSE-GC-MS/MS),对海洋生物样本(鱼肉、贻贝和牡蛎组织)中减少量(100毫克和1克湿重(WW))的21种多环芳烃(PAHs)进行准确且同时的常规分析。该创新方法对大多数化合物具有良好的选择性和特异性。在1克湿重样本中,鱼肉的定量限(LOQs)范围为1至10微克/千克湿重,贻贝组织中为0.5至10微克/千克湿重。该方法能够对大多数分析物进行定量,且低于欧盟委员会设定的限制水平(鱼肉和双壳贝类分别为2和10微克/千克湿重)。在100毫克湿重样本中获得了更高的定量限,范围为1至50微克/千克湿重。对所有分析物的回收率和线性进行了评估。对于大多数化合物,结果令人满意,在1克湿重贻贝样本中,加标浓度为10纳克/克湿重时,回收率范围为94%至117%,标准偏差不超过12%。然而,结果证实SBSE效率受生物基质复杂性的影响,特别是对于富含脂质的贻贝组织中的高分子量化合物。由于基质效应,进行了基质匹配校准。使用标准参考物质1974c进行了验证,除萘、蒽和苯并(e)芘外,回收率范围为71%至119%,因此这三种物质未经验证。总体而言,所开发的方法满足大多数化合物的分析验证标准。由于碱性消解和SBSE的结合,极大地简化了样品处理,并将溶剂使用限制为乙醇,所开发的方法遵循了大多数绿色分析化学原则。

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