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作 者:岳强[1,2] 于志强[1] 王德超[1,2] 盛国英[1] 傅家谟[1]
机构地区:[1]中国科学院广州地球化学研究所有机地球化学国家重点实验室,广东广州510640 [2]中国科学院研究生院,北京100039
出 处:《分析测试学报》2009年第7期859-862,共4页Journal of Instrumental Analysis
摘 要:采用固相萃取、高效液相色谱-质谱/质谱仪同位素稀释技术,建立了尿中双酚A(BPA)和壬基酚(NP)的检测方法。液相色谱分离用C18柱,流动相为甲醇和水,负离子电喷雾模式电离,多反应离子监测方式检测,BPA和NP的定量离子对分别为m/z 226.9/132.9、219.3/118.8,^13C和氘代同位素化合物分别做回收率控制和内标定量。BPA和NP的基质加标回收率分别为86%~106%、90%-114%,定量下限分别为0.97、2.3ug/L。实际尿样的测定验证了该方法的可行性。A liquid chromatography coupled to tandem mass spectrometry(LC -MS/MS) method was developed for the determination of urinary bisphenol A(BPA) and nonylphenol(NP) in human urine sample. The cleanup and enrichment of sample was performed by solid-phase extraction. Identification and quantification of BPA and NP were carried out by MS under negative eleetrospray ionization mode and multiple reaction monitoring(MRM). ^13C- and D-labelled BPA and NP were used for surrogate recovery and internal standard, and m/z 226.9/132.9, 219.3/118.8 were selected as quantification transitions of BPA and NP, respectively. The limits of quantification (LOQ) of BPA and NP were 0.97 ug/L and 2.3 ug/L, respectively. The spiked recoveries of BPA and NP in urine sample were in the range of 86% - 106% for BPA and 90% - 114% for NP. The developed method was further validated in human urines.
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