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采用超高效液相色谱和混合四极杆飞行时间质谱对全氟烷基物质进行定量分析。

Quantitative profiling of perfluoroalkyl substances by ultrahigh-performance liquid chromatography and hybrid quadrupole time-of-flight mass spectrometry.

作者信息

Picó Yolanda, Farré Marinella, Barceló Damià

机构信息

Food and Environmental Safety Research Group (SAMA-UV), Facultat de Farmàcia, Universitat de València, Av, Vicent Andrés s/n, 46100, Burjassot, València, Spain,

出版信息

Anal Bioanal Chem. 2015 Jun;407(15):4247-59. doi: 10.1007/s00216-015-8459-y. Epub 2015 Jan 30.

Abstract

The accurate determination of perfluoroalkyl substances (PFSAs) in water, sediment, fish, meat, and human milk was achieved by ultrahigh-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UHPLC-QqTOF-MS) with an ABSciex Triple TOF®. A group of 21 PFSAs was selected as target to evaluate the quantitative possibilities. Full scan MS acquisition data allows quantification at relevant low levels (0.1-50 ng L(-1) in water, 0.05-2 ng g(-1) in sediments, 0.01-5 ng g(-1) in fish and meat, and 0.005-2 ng g(-1) in human milk depending on the compound). Automatic information dependent acquisition product ion mass spectrometry (IDA-MS/MS) confirms the identity even for those compounds that presented only one product ion. The preparation of a homemade database using the extracted ion chromatogram (XIC) Manager of the software based upon retention time, accurate mass, isotopic pattern, and MS/MS library searching achieves not only the successful identification of PFSAs but also of some pharmaceuticals, such as acetaminophen, ibuprofen, salicylic acid, and gemfibrozid. Mean recoveries and relative standard deviation (RSD) were 67-99% (9-16% RSD) for water, 62-103% (8-18% RSD) for sediment, 60-95% (8-17% RSD) for fish, 64-95% (8-15% RSD) for meat, and 63-95% (8-16%) for human milk. The quantitative data obtained for 60 samples by UHPLC-QqTOF-MS agree with those obtained by LC-MS/MS with a triple quadrupole (QqQ).

摘要

采用配备ABSciex Triple TOF®的超高效液相色谱-四极杆飞行时间质谱仪(UHPLC-QqTOF-MS)实现了对水、沉积物、鱼类、肉类和人乳中全氟烷基物质(PFSA)的准确测定。选择了一组21种PFSA作为目标物来评估定量的可能性。全扫描MS采集数据能够在相关低水平下进行定量(水中为0.1 - 50 ng L⁻¹,沉积物中为0.05 - 2 ng g⁻¹,鱼类和肉类中为0.01 - 5 ng g⁻¹,人乳中为0.005 - 2 ng g⁻¹,具体取决于化合物)。自动信息依赖采集产物离子质谱(IDA-MS/MS)即使对于那些仅呈现一个产物离子的化合物也能确认其身份。使用基于保留时间、精确质量、同位素模式和MS/MS库搜索的软件中的提取离子色谱图(XIC)管理器制备自制数据库,不仅成功鉴定了PFSA,还鉴定了一些药物,如对乙酰氨基酚、布洛芬、水杨酸和吉非贝齐。水的平均回收率和相对标准偏差(RSD)为67 - 99%(RSD为9 - 16%),沉积物为62 - 103%(RSD为8 - 18%),鱼类为60 - 95%(RSD为8 - 17%),肉类为64 - 95%(RSD为8 - 15%),人乳为63 - 95%(RSD为8 - 16%)。通过UHPLC-QqTOF-MS获得的60个样品的定量数据与通过配备三重四极杆(QqQ)的LC-MS/MS获得的数据一致。

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