Clark Sonya M, Leaist Derek G, Konermann Lars
Department of Chemistry, The University of Western Ontario, London, Ontario, N6A 5B7, Canada.
Rapid Commun Mass Spectrom. 2002;16(15):1454-62. doi: 10.1002/rcm.732.
This work describes a novel approach for monitoring analyte diffusion in solution that is based on electrospray ionization mass spectrometry (ESI-MS). A mass spectrometer at the end of a laminar flow tube is used to measure the Taylor dispersion of an initially sharp boundary between two solutions of different analyte concentration. This boundary is dispersed by the laminar flow profile in the tube. However, this effect is diminished by analyte diffusion that continuously changes the radial position, and hence the flow velocity of individual analyte molecules. The steepness of the resulting dispersion profile therefore increases with increasing diffusion coefficient of the analyte. A theoretical framework is developed to adapt the equations governing the dispersion process to the case of mass spectrometric detection. This novel technique is applied to determine the diffusion coefficients of choline and cytochrome c. The measured diffusion coefficients, (11.9 +/- 1.0) x 10(-10) m(2) s(-1) and (1.35 +/- 0.08) x 10(-10) m(2) s(-1), respectively, are in agreement with the results of control experiments where the Taylor dispersion of these two analytes was monitored optically. Due to the inherent selectivity and sensitivity of ESI-MS, it appears that the approach described in this work could become a valuable alternative to existing methods for studying diffusion processes, especially for experiments on multicomponent systems.
这项工作描述了一种基于电喷雾电离质谱(ESI-MS)监测溶液中分析物扩散的新方法。层流管末端的质谱仪用于测量两种不同分析物浓度溶液之间初始尖锐边界的泰勒色散。该边界在管中被层流轮廓分散。然而,分析物扩散会不断改变径向位置,从而降低这种影响,进而改变单个分析物分子的流速。因此,所得色散曲线的陡度随分析物扩散系数的增加而增大。开发了一个理论框架,以使控制色散过程的方程适用于质谱检测的情况。这项新技术被用于测定胆碱和细胞色素c的扩散系数。测得的扩散系数分别为(11.9±1.0)×10⁻¹⁰ m² s⁻¹和(1.35±0.08)×10⁻¹⁰ m² s⁻¹,与通过光学监测这两种分析物泰勒色散的对照实验结果一致。由于ESI-MS固有的选择性和灵敏度,本文所述方法似乎可能成为研究扩散过程现有方法的一种有价值的替代方法,特别是对于多组分系统的实验。