Zhang Haijing, Lin Shaobin
Se Pu. 2014 Jul;32(7):730-4. doi: 10.3724/sp.j.1123.2014.02026.
A solid phase extraction coupled with high performance liquid chromatography-tandem mass spectrometry (SPE-HPLC-MS/MS) method was developed for the determination of eight bisphenol diglycidyl ethers, including bisphenol A diglycidyl ether (BADGE), bisphenol A (3-chloro-2-hydroxypropyl) glycidyl ether (BADGE x HCl), bisphenol A bis (3-chloro-2-hydroxypropyl) ether (BADGE x 2HCl), bisphenol A (2, 3-dihydroxypropyl) glycidyl ether (BADGE x H2O), bisphenol A bis(2,3-dihydroxypropyl) ether (BADGE x 2H2O), bisphenol A (3-chloro-2-hydroxypropyl) (2,3-dihydroxypropyl) ether (BADGE x HCl x H2O), bisphenol F diglycidyl ether (BFDGE) and bisphenol F bis (3-chloro-2-hydroxypropyl) ether (BFDGE 2HCl) in water. A total of ten samples were collected from the leaching of the coatings for drinking water supply system. Then, 200 mL exposure water was preconcentrated on C18 solid-phase extraction cartridge. The eight compounds were analyzed by liquid chromatography-tandem mass spectrometry method on a C18 column by the gradient elution with methanol, water and 5 mmol/L ammonium acetate as mobile phases in the multiple reaction monitoring (MRM) scan mode. The external matrix standard solutions were used for the quantitative determination and the calibration curves of the eight compounds showed good linearity in the range of 0.007-5.00 microg/L with the correlation coefficients more than 0.999 0. The limits of quantification (LOQs) of the method were 7-91 ng/L. The spiked recoveries ranged from 79.1% to 101% with the relative standard deviations of 4.0% - 12%. The method is sensitive and accurate, and is applicable to the determination of bisphenol diglycidyl ethers in water.
建立了一种固相萃取-高效液相色谱-串联质谱(SPE-HPLC-MS/MS)法,用于测定水中的8种双酚二缩水甘油醚,包括双酚A二缩水甘油醚(BADGE)、双酚A(3-氯-2-羟丙基)缩水甘油醚(BADGE x HCl)、双酚A双(3-氯-2-羟丙基)醚(BADGE x 2HCl)、双酚A(2,3-二羟丙基)缩水甘油醚(BADGE x H2O)、双酚A双(2,3-二羟丙基)醚(BADGE x 2H2O)、双酚A(3-氯-2-羟丙基)(2,3-二羟丙基)醚(BADGE x HCl x H2O)、双酚F二缩水甘油醚(BFDGE)和双酚F双(3-氯-2-羟丙基)醚(BFDGE 2HCl)。从饮用水供应系统涂层的浸出液中总共采集了10个样品。然后,将200 mL暴露水在C18固相萃取柱上进行预浓缩。采用液相色谱-串联质谱法,以甲醇、水和5 mmol/L醋酸铵为流动相,在C18柱上进行梯度洗脱,在多反应监测(MRM)扫描模式下对8种化合物进行分析。采用外标基质标准溶液进行定量测定,8种化合物的校准曲线在0.007 - 5.00 μg/L范围内线性良好,相关系数大于0.999 0。该方法的定量限(LOQs)为7 - 91 ng/L。加标回收率在79.1%至101%之间,相对标准偏差为4.0% - 12%。该方法灵敏、准确,适用于水中双酚二缩水甘油醚的测定。