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[采用高效液相色谱-串联质谱联用多壁碳纳米管固相萃取法测定食品接触材料中双酚二缩水甘油醚的迁移量]

[Determination of the migration of bisphenol diglycidyl ethers from food contact materials by high performance chromatography-tandem mass spectrometry coupled with multi-walled carbon nanotubes solid phase extraction].

作者信息

Wu Xinhua, Ding Li, Li Zhonghai, Zhang Yanli, Liu Xiaoxia, Wang Libing

机构信息

Hunan Academy of Inspection and Quarantine, Technology Center of Hunan Entry-Exit Inspection and Quarantine Bureau, Hunan Key Laboratory of Food Safety Science & Technology, Changsha 410004, China.

出版信息

Se Pu. 2010 Nov;28(11):1094-8.

Abstract

A comprehensive analytical method based on high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was developed for measuring 6 exogenous endocrine disruptors--bisphenol diglycidyl ethers, including bisphenol A diglycidyl ether (BADGE), bisphenol A glycidyl (2,3-dihydroxypropyl) ether (BADGE x H2O), bisphenol A glycidyl (3-chloro-2-hydroxypropyl) ether ( BADGE x HCl), bisphenol A (3-chloro-2-hydroxypropyl) (2,3-dihydroxypropyl) ether (BADGE x H2O x HCl), bisphenol F diglycidyl ether (BFDGE) and bisphenol F bis (3-chloro-2-hydroxypropyl) ether (BFDGE x 2HCl). The samples were extracted with methyl tert-butyl ether (MTBE) by ultrasonic wave assistant extraction. The extracts were cleaned up and concentrated on multi-walled carbon nanotubes (MWCNTs). The target compounds were analyzed by HPLC-MS/MS under positive ion mode using a COSMOSIL C18 column as analytical column. Under the optimal conditions, the calibration curves showed a good linearity in the concentration range of 1.0-100.0 microg/L for 6 target compounds. The correlation coefficients (r2) were higher than 0.999 1. Recoveries of 6 analytes at three spiked levels ranged from 78.6% to 89.9%, with relative standard deviations (RSDs) less than 10%. The detection limits of the method ranged from 0.5 to 1.5 microg/L. The method is sensitive and simple, and is suitable for the rapid determination of the migration of bisphenol diglycidyl ethers from food contact materials.

摘要

建立了一种基于高效液相色谱 - 串联质谱法(HPLC - MS/MS)的综合分析方法,用于测定6种外源性内分泌干扰物——双酚二缩水甘油醚,包括双酚A二缩水甘油醚(BADGE)、双酚A缩水甘油(2,3 - 二羟基丙基)醚(BADGE x H2O)、双酚A缩水甘油(3 - 氯 - 2 - 羟基丙基)醚(BADGE x HCl)、双酚A(3 - 氯 - 2 - 羟基丙基)(2,3 - 二羟基丙基)醚(BADGE x H2O x HCl)、双酚F二缩水甘油醚(BFDGE)和双酚F双(3 - 氯 - 2 - 羟基丙基)醚(BFDGE x 2HCl)。样品采用甲基叔丁基醚(MTBE)通过超声波辅助萃取法进行萃取。萃取液经多壁碳纳米管(MWCNTs)净化和浓缩。以COSMOSIL C18柱为分析柱,在正离子模式下通过HPLC - MS/MS对目标化合物进行分析。在最佳条件下,6种目标化合物的校准曲线在1.0 - 100.0 μg/L浓度范围内呈良好线性。相关系数(r2)高于0.999 1。6种分析物在3个加标水平下的回收率为78.6%至89.9%,相对标准偏差(RSDs)小于10%。该方法的检测限为0.5至1.5 μg/L。该方法灵敏、简便,适用于快速测定食品接触材料中双酚二缩水甘油醚的迁移量。

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