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采用离子对液相色谱-串联质谱法测定加利福尼亚州人体尿液中有机磷酸酯阻燃剂四种二酯代谢物的分析方法。

Analytical methodology using ion-pair liquid chromatography-tandem mass spectrometry for the determination of four di-ester metabolites of organophosphate flame retardants in California human urine.

作者信息

Petropoulou Syrago-Styliani E, Petreas Myrto, Park June-Soo

机构信息

Environmental Chemistry Laboratory, Department of Toxic Substances Control, 700 Heinz Ave., Suite 100, Berkeley, CA 94710, United States.

Environmental Chemistry Laboratory, Department of Toxic Substances Control, 700 Heinz Ave., Suite 100, Berkeley, CA 94710, United States.

出版信息

J Chromatogr A. 2016 Feb 19;1434:70-80. doi: 10.1016/j.chroma.2016.01.020. Epub 2016 Jan 14.

Abstract

Alkyl- and aryl-esters of phosphoric acid (both halogenated and non-halogenated) are mainly used as flame retardants (FRs), among other applications, in furniture and consumer products and they are collectively known as organophosphate flame retardants (OPFRs). The absorption, biotransformation or elimination of many of these chemicals in humans and their possible health effects are not yet well known. A major reason for the limited information is the nature of these compounds, which causes several technical difficulties in their isolation and sensitive determination. A novel analytical liquid chromatography tandem mass spectrometry (LC-MS/MS) method for the accurate and sensitive determination of four urinary OPFR metabolites: bis(1,3-dichloro-2-propyl) phosphate (BDCIPP), bis(2-chloroethyl) phosphate (BCEP), bis(1-chloro-2-propyl) phosphate (BCIPP), and diphenyl phosphate (DPhP), using mixed-mode solid phase extraction and isotope. For the first time all four analytes can be identified in one chromatographic run. An extensive investigation of method development parameters (enzymatic hydrolysis, matrix effects, process efficiency, sources of background interferences, linearity, accuracy, precision, stabilities and limits of detection and quantification) was performed in order to address previously reported method inconsistencies and select a process with the highest accuracy and sensitivity. Chromatographic separation was achieved on a Luna C18 (2) (2.00 mm × 150 mm, 3 μm) with mobile phase 80:20 v/v water: MeOH and MeOH: water 95:5 v/v, both containing 1mM tributylamine and 1mM acetic acid. Limits of detection were 0.025 ng mL(-1) for BDCIPP and BCIPP and 0.1 ng mL(-1) for DPhP and BCEP. Absolute recoveries of all four analytes and their labeled compounds were in the range of 88-107%. The method was tested on 13 adult California urine samples. BCEP was detected at 0.4-15 ng mL(-1) with a geometric mean (GM): 1.9 ng mL(-1); BDCIPP at 0.5-7.3 ng mL(-1), (GM: 2.5 ng mL(-1)) and DPhP at <MDL-5.6 ng mL(-1), (GM: 1.7 ng mL(-1)). BCIPP was detected for the first time in US samples in 92.3% of the samples with two to three times lower values (range <MDL-3.5 ng mL(-1) and GM: 0.4 ng mL(-1)) than the other OPFRs.

摘要

磷酸的烷基酯和芳基酯(包括卤代和非卤代的)主要用作阻燃剂,在家具和消费品等其他应用中使用,它们统称为有机磷酸酯阻燃剂(OPFRs)。这些化学物质在人体中的吸收、生物转化或消除及其可能的健康影响尚未完全清楚。信息有限的一个主要原因是这些化合物的性质,这在其分离和灵敏测定方面造成了一些技术困难。一种新颖的分析液相色谱串联质谱(LC-MS/MS)方法,用于准确灵敏地测定四种尿中OPFR代谢物:双(1,3-二氯-2-丙基)磷酸酯(BDCIPP)、双(2-氯乙基)磷酸酯(BCEP)、双(1-氯-2-丙基)磷酸酯(BCIPP)和二苯基磷酸酯(DPhP),采用混合模式固相萃取和同位素。首次可以在一次色谱运行中鉴定出所有四种分析物。对方法开发参数(酶促水解、基质效应、过程效率、背景干扰源、线性、准确性、精密度、稳定性以及检测和定量限)进行了广泛研究,以解决先前报道的方法不一致问题,并选择具有最高准确性和灵敏度的方法。在Luna C18(2)(2.00 mm×150 mm,3μm)色谱柱上进行色谱分离,流动相为80:20 v/v水:甲醇以及甲醇:水95:5 v/v,二者均含有1 mM三丁胺和1 mM乙酸。BDCIPP和BCIPP的检测限为0.025 ng mL-1,DPhP和BCEP的检测限为0.1 ng mL-1。所有四种分析物及其标记化合物的绝对回收率在88 - 107%范围内。该方法在13份加利福尼亚成年尿液样本上进行了测试。检测到BCEP的浓度为0.4 - 15 ng mL-1,几何平均值(GM):1.9 ng mL-1;BDCIPP的浓度为0.5 - 7.3 ng mL-1,(GM:2.5 ng mL-1),DPhP的浓度为<MDL - 5.6 ng mL-1,(GM:1.7 ng mL-1)。在美国样本中首次检测到BCIPP,92.3%的样本中其含量比其他OPFR低两到三倍(范围<MDL - 3.5 ng mL-1,GM:0.4 ng mL-1)。

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