Xu Zhongqi, Doi Takayuki, Timerbaev Andrei R, Hirokawa Takeshi
Department of Applied Chemistry, Graduate School of Engineering, Hiroshima University, 1-4-1 Kagamiyama 1, Higashi-hiroshima 739-8527, Japan.
Talanta. 2008 Oct 19;77(1):278-81. doi: 10.1016/j.talanta.2008.06.017. Epub 2008 Jun 22.
A transient isotachophoresis-capillary electrophoresis (tITP-CE) system for the determination of minor inorganic anions in saliva is described. The complete separation and quantification of bromide, iodide, nitrate, nitrite, and thiocyanate has been achieved with only centrifugation and dilution of the saliva sample. In-line tITP preconcentration conditions, created by introduction of the plugs of 5 mM dithionic acid (leading electrolyte) and 10 mM formic acid (terminating electrolyte) before and after the sample zone, respectively, allowed the limits of direct UV absorption detection (at 200 nm) to be up to 50-fold improved as compared with CE without tITP. As a result, nitrate and thiocyanate were still detectable at 4.6 and 3.8 microgl(-1), respectively, in 1000 times diluted saliva. The daily variations of anionic concentrations in saliva samples taken from a smoking health volunteer were discussed based on the results of tITP-CE analysis. It was confirmed that the thiocyanate concentration in saliva noticeably increased after smoking. This is apparently the first report on simultaneous quantification of more than four anionic salivary constituents using CE.
本文描述了一种用于测定唾液中微量无机阴离子的瞬态等速电泳-毛细管电泳(tITP-CE)系统。仅通过对唾液样品进行离心和稀释,就实现了溴离子、碘离子、硝酸根、亚硝酸根和硫氰酸根的完全分离和定量。通过分别在样品区前后引入5 mM连二亚硫酸(前导电解质)和10 mM甲酸(终止电解质)的塞子来创建在线tITP预浓缩条件,与没有tITP的CE相比,直接紫外吸收检测(在200 nm处)的检测限提高了50倍。结果,在稀释1000倍的唾液中,硝酸根和硫氰酸根仍分别可在4.6和3.8 μg mL-1时被检测到。基于tITP-CE分析结果,讨论了从一名吸烟健康志愿者采集的唾液样品中阴离子浓度的每日变化。证实吸烟后唾液中的硫氰酸根浓度显著增加。这显然是第一篇关于使用CE同时定量四种以上唾液阴离子成分的报告。