[Determination of 22 organophosphates and their metabolites and 11 phthalate metabolites in human whole blood by ultra performance liquid chromatography-tandem mass spectrometry].

Fei-Yun Shi, Hao-Yu Xu, Jun-Hong Li, Meng-Yuan Xu
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引用次数: 0

Abstract

Organic phosphate esters (OPEs) and phthalate esters (PAEs) are two classes of synthetic compounds widely incorporated into various industrial and consumer products as flame retardants and plasticizers. Both exhibit multi-organ cumulative toxicity. In this study, an ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed for the determination of 22 OPEs and their diester metabolites (mOPEs) and 11 phthalate ester metabolites (mPAEs) in whole blood. The whole blood samples were extracted with 0.1% formic acid-acetonitrile by liquid-liquid extraction for protein precipitation, and then purified by HMR S-micro BIO 96-well solid phase extraction column. The filtrate was blown to near dryness with nitrogen, and reconstituted with 0.1% formic acid-acetonitrile solution. The target compounds were detected by UPLC-MS/MS. A Ghost Trap DS-HP chromatographic column (30 mm×2.1 mm) was used as the background ghost peak trap column, and an ACQUITY UPLC® BEH C18 chromatographic column (150 mm×2.1 mm, 1.7 μm) was used as the analytical column. Methanol and 0.5 mmol/L ammonium acetate were used as mobile phase for gradient elution. Electrospray ionization (ESI) was used for MS detection, with both positive and negative ion scanning in the multiple reaction monitoring (MRM) mode. Isotope internal standard method was used for quantification. The results showed that 33 target compounds could be separated within 15 min, and good linear relationships were observed for all target compounds across their respective mass concentration ranges (r=0.993 3-0.999 8). The limits of detection were 0.003-0.31 ng/mL and the limits of quantification were 0.01-1.02 ng/mL. The spiked recoveries of 33 targets in whole blood samples ranged from 60.5% to 138.3%, with relative standard deviations (RSDs) from 1.6% to 11.0%. The detection rates of tris-(2-chloroisopropyl)phosphate (TCiPP), triphenyl phosphate (TPHP), 2-ethylhexyl diphenyl (EHDPP), mono(2-ethyl-5-hydroxyhexyl) phthalate (MEHHP), mono-n-butyl phthalate (MNBP) and mono-n-octyl phthalate (MOP) were 100% in 14 whole blood samples, and the highest detection amount of TPHP was 10.04 ng/mL. The developed method is simple to operate, sensitive, accurate, requires small sample volumes, and is cost-effective on reagents. It is suitable for human biomonitoring, and provides a theoretical basis for monitoring organic phosphate and phthalic ester substances in the population.

超高效液相色谱-串联质谱法测定人全血中22种有机磷及其代谢物和11种邻苯二甲酸盐代谢物
有机磷酸酯(OPEs)和邻苯二甲酸酯(PAEs)是两类合成化合物,作为阻燃剂和增塑剂广泛应用于各种工业和消费品中。两者都表现出多器官累积毒性。本研究建立了超高效液相色谱-串联质谱(UPLC-MS/MS)测定全血中22种OPEs及其二酯代谢物(mOPEs)和11种邻苯二甲酸酯代谢物(mPAEs)的方法。全血样品采用0.1%甲酸-乙腈液-液萃取法进行蛋白质沉淀,然后采用HMR S-micro BIO 96孔固相萃取柱纯化。滤液用氮气吹至近干,用0.1%甲酸-乙腈溶液复溶。目的化合物采用UPLC-MS/MS检测。Ghost Trap DS-HP色谱柱(30 mm×2.1 mm)作为背景鬼峰陷阱柱,ACQUITY UPLC®BEH C18色谱柱(150 mm×2.1 mm, 1.7 μm)作为分析柱。以甲醇和0.5 mmol/L乙酸铵为流动相进行梯度洗脱。质谱检测采用电喷雾电离法(ESI),在多反应监测(MRM)模式下进行正离子和负离子扫描。采用同位素内标法定量。结果表明,33个目标化合物均可在15 min内分离,且在质量浓度范围内均具有良好的线性关系(r=0.993 ~ 0.999 8)。检测限为0.003 ~ 0.31 ng/mL,定量限为0.01 ~ 1.02 ng/mL。33个标靶在全血样品中的加标回收率为60.5% ~ 138.3%,相对标准偏差(rsd)为1.6% ~ 11.0%。14份全血样品中三-(2-氯异丙基)磷酸(TCiPP)、磷酸三苯基(TPHP)、2-乙基己基二苯基(EHDPP)、邻苯二甲酸单(2-乙基-5-羟基己基)酯(MEHHP)、邻苯二甲酸单正丁酯(MNBP)和邻苯二甲酸单正辛酯(MOP)的检出率均为100%,TPHP最高检出量为10.04 ng/mL。该方法操作简单、灵敏、准确、样本量小、试剂成本低。适用于人体生物监测,为人群中有机磷和邻苯二甲酸酯类物质的监测提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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