Feng Yong-Lai, Zhu Jiping
Chemistry Research Division, Health Canada, Ottawa, Ontario, Canada.
Electrophoresis. 2008 May;29(10):1965-73. doi: 10.1002/elps.200700773.
Electrophoresis characteristics of several monophthalates in the sample zone and EOF variation in a fused-silica capillary column during a constant pressure-assisted electrokinetic injection (PAEKI) in an on-line CE-MS were studied in an effort to reconcile the mobility theory and field amplification with the enhancement achieved in present work. Influences of capillary length on the amount injected using PAEKI were investigated in detail and except for the injection time, the amount injected was found to increase linearly with capillary column length. A longer capillary provides a longer linear increase time range with PAEKI injection. The results show that smaller m/z analytes generate a large enhancement power using PAEKI, which is in agreement with the mobility theory. ACN was used as an example to investigate influences of organic additives on the amount injected and was found to decrease the amount injected with PAEKI injection, which is in agreement with an increase of resistivity in running buffer by organic additives. The peak width obtained with PAEKI injection proved to be independent of the amount injected. The band size of the sample zone was estimated by comparison with conventional hydrodynamic injection. A 240 s PAEKI injection achieved the same size of sample zone as a 2 s of hydrodynamic injection. Existance of two ion layers around the boundary of the buffer and sample solutions in sample zone was hypothesized to contribute the narrow sample zone with a long time of PAEKI injection. With a 240 s on-line PAEKI injection in CZE-MS, five monophthalates were enriched several hundred times without compromise in their separation efficiency and peak shape. With appropriate sample cleanup, PAEKI was applied to the analysis of monophthalates in urine samples, achieving detection limits ranging between 0.53 and 1.3 ng/mL.
为了使迁移率理论和场放大与当前工作中实现的增强效果相协调,研究了在线毛细管电泳-质谱联用(CE-MS)中恒压辅助电动进样(PAEKI)过程中样品区几种单邻苯二甲酸酯的电泳特性以及熔融石英毛细管柱中电渗流(EOF)的变化。详细研究了毛细管长度对使用PAEKI进样量的影响,结果发现,除进样时间外,进样量与毛细管柱长度呈线性增加。较长的毛细管在PAEKI进样时提供更长的线性增加时间范围。结果表明,较小质荷比(m/z)的分析物在使用PAEKI时具有较大的增强功率,这与迁移率理论一致。以乙腈(ACN)为例研究了有机添加剂对进样量的影响,发现其会降低PAEKI进样的进样量,这与有机添加剂使运行缓冲液电阻率增加一致。PAEKI进样获得的峰宽被证明与进样量无关。通过与传统的流体动力学进样比较来估计样品区的谱带大小。240 s的PAEKI进样获得的样品区大小与2 s的流体动力学进样相同。假设在样品区缓冲液和样品溶液边界周围存在两个离子层,这有助于在长时间PAEKI进样时形成狭窄的样品区。在毛细管区带电泳-质谱联用(CZE-MS)中进行240 s的在线PAEKI进样时,五种单邻苯二甲酸酯被富集了数百倍,同时其分离效率和峰形不受影响。经过适当的样品净化后,PAEKI被应用于尿液样品中单邻苯二甲酸酯的分析,检测限在0.53至1.3 ng/mL之间。