Kwon Sun-Myung, Shin Ho-Sang
Department of Environmental Science, Kongju National University, Kongju, 314-701, South Korea.
Department of Environmental Education, Kongju National University, Kongju 314-701, South Korea.
J Chromatogr A. 2015 Aug 14;1407:216-21. doi: 10.1016/j.chroma.2015.06.066. Epub 2015 Jul 2.
A simple and convenient method to detect fluoride in biological samples was developed. This method was based on derivatization with 2-(bromomethyl)naphthalene, headspace solid phase microextraction (HS-SPME) in a vial, and gas chromatography-tandem mass spectrometric detection. The HS-SPME parameters were optimized as follows: selection of CAR/PDMS fiber, 0.5% 2-(bromomethyl)naphthalene, 250 mg/L 15-crown-5-ether as a phase transfer catalyst, extraction and derivatization temperature of 95 °C, heating time of 20 min and pH of 7.0. Under the established conditions, the lowest limits of detection were 9 and 11 μg/L in 1.0 ml of plasma and urine, respectively, and the intra- and inter-day relative standard deviation was less than 7.7% at concentrations of 0.1 and 1.0 mg/L. The calibration curve showed good linearity of plasma and urine with r=0.9990 and r=0.9992, respectively. This method is simple, amenable to automation and environmentally friendly.
开发了一种简单便捷的生物样品中氟化物检测方法。该方法基于用2-(溴甲基)萘进行衍生化、在小瓶中进行顶空固相微萃取(HS-SPME)以及气相色谱-串联质谱检测。HS-SPME参数优化如下:选择CAR/PDMS纤维、0.5% 2-(溴甲基)萘、250 mg/L 15-冠-5-醚作为相转移催化剂、萃取和衍生化温度为95℃、加热时间为20分钟以及pH为7.0。在既定条件下,1.0 ml血浆和尿液中的最低检测限分别为9和11 μg/L,在0.1和1.0 mg/L浓度下,日内和日间相对标准偏差均小于7.7%。校准曲线显示血浆和尿液具有良好的线性,r分别为0.9990和0.9992。该方法简单、适合自动化且环保。