Bailey C G, Wallenborg S R
Sandia National Laboratories, Livermore, CA 94551, USA.
Electrophoresis. 2000 Sep;21(15):3081-7. doi: 10.1002/1522-2683(20000901)21:15<3081::AID-ELPS3081>3.0.CO;2-R.
Mixtures of nitroaromatic and nitramine explosive compounds and their degradation products were analyzed using electrokinetically driven separations with both indirect laser-induced fluorescence (IDLIF) and UV absorption detection. Complete separations of the 14-component mixture (EPA 8330) were achieved using both capillary electrochromatography (CEC) and micellar electrokinetic chromatography (MEKC). IDLIF detection was performed using an epifluorescence system with excitation provided by a 635 nm diode laser and micromolar concentrations of the dye Cy-5 as the visualizing agent. While the sensitivity of the two detection methods was similar for the nitroaromatic compounds, the nitramines could only be detected using UV absorption due to their low fluorescence quenching efficiency of Cy-5. The detection sensitivity using IDLIF was limited by low frequency oscillations in the fluorescence background. The oscillations increased with higher electric field strength and were attributed to thermal fluctuations caused by Joule heating. Due to the more conductive running buffer and higher separation currents used in MEKC, sensitive IDLIF detection could only be achieved using low (approximately 100 V/cm) field strengths, resulting in long analysis times. CEC separations, which are typically run with low conductivity mobile phases to avoid bubble formation, are less sensitive to this effect. In CEC separations with IDLIF detection a stable fluorescence background using Cy-5 could be established using only a nonporous stationary phase. In capillaries packed with porous silica particles, anomalous migration behavior was observed with charged dye molecules and a stable fluorescence background could not be established under electrokinetic flow. This is the first demonstration of IDLIF in packed channel CEC.
采用电动驱动分离技术,结合间接激光诱导荧光(IDLIF)和紫外吸收检测,对硝基芳香族和硝胺类爆炸化合物及其降解产物的混合物进行了分析。使用毛细管电色谱(CEC)和胶束电动色谱(MEKC)实现了14种成分混合物(EPA 8330)的完全分离。IDLIF检测采用落射荧光系统,由635 nm二极管激光器提供激发光,并使用微摩尔浓度的染料Cy-5作为可视化剂。虽然两种检测方法对硝基芳香族化合物的灵敏度相似,但由于硝胺类化合物对Cy-5的荧光猝灭效率较低,只能通过紫外吸收进行检测。IDLIF的检测灵敏度受荧光背景低频振荡的限制。振荡随着电场强度的增加而增加,这归因于焦耳热引起的热波动。由于MEKC中使用的运行缓冲液导电性更强且分离电流更高,只有在低电场强度(约100 V/cm)下才能实现灵敏的IDLIF检测,这导致分析时间较长。CEC分离通常使用低电导率流动相以避免气泡形成,对这种影响不太敏感。在使用IDLIF检测的CEC分离中,仅使用无孔固定相就可以建立使用Cy-5的稳定荧光背景。在填充有多孔二氧化硅颗粒的毛细管中,观察到带电染料分子出现异常迁移行为,在电动流作用下无法建立稳定的荧光背景。这是在填充通道CEC中首次展示IDLIF。