Fishman H A, Scheller R H, Zare R N
Department of Chemistry, Stanford University, CA 94305.
J Chromatogr A. 1994 Sep 30;680(1):99-107. doi: 10.1016/0021-9673(94)80057-X.
The withdrawal of a capillary structure from a sample solution causes a droplet to be formed at the end of the capillary. Because of the interfacial pressure difference across the curved surface of the droplet, the droplet is driven into the entrance of the capillary, thereby causing injection of the sample. Assuming negligible sample penetration by diffusive or convective mixing, this injection is intrinsically the smallest possible for a capillary. Moreover, the injection volume can be varied by changing the shape of the capillary structure, specifically the outer diameter of the capillary. This injection method eliminates the need for external pressure differences, applied fields across the capillary, or precise timing, thus offering several advantages over conventional procedures. Studies using capillary electrophoresis as the separation procedure show that approximately 3.5 nl (66 microns I.D. capillary) sample volumes can be injected by hand with a reproducibility of 5.8 +/- 0.7% R.S.D. Parameters that affect the variability of the injection are discussed.
从样品溶液中抽出毛细管结构会导致在毛细管末端形成一个液滴。由于液滴弯曲表面上的界面压差,液滴被驱动进入毛细管入口,从而实现样品进样。假设扩散或对流混合导致的样品渗透可忽略不计,这种进样本质上是毛细管所能实现的最小进样量。此外,通过改变毛细管结构的形状,特别是毛细管的外径,可以改变进样体积。这种进样方法无需外部压差、毛细管两端施加的电场或精确计时,因此与传统方法相比具有多个优点。使用毛细管电泳作为分离方法的研究表明,手动进样时大约可进样3.5 nl(内径66微米的毛细管),相对标准偏差(R.S.D.)的重现性为5.8±0.7%。文中讨论了影响进样变异性的参数。