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Science 4 November 1994:
Vol. 266. no. 5186, pp. 773 - 776
DOI: 10.1126/science.266.5186.773

Articles

Use of Taylor-Aris Dispersion for Measurement of a Solute Diffusion Coefficient in Thin Capillaries

Michael S. Bello 1, Roberta Rezzonico 2, and Pier Giorgio Righetti 2

1 Institute of Macromolecular Compounds, Russian Academy of Sciences, St. Petersburg, Bolshoi 31, 199004, Russia
2 Faculty of Pharmacy and Department of Biomedical Sciences and Technologies, University of Milan, Via G. Celoria 2, Milan, 20133, Italy

A method for the fast measurement of the diffusion coefficients of both small and large molecules in thin capillaries is reported. The method relies on Taylor-Aris dispersion theory and uses standard instrumentation for capillary zone electrophoresis. With this equipment, which consists of thin capillaries (50 to 100 micrometers in inner diameter), an injection system, detector ports, and computer data acquisition, a sample plug is pumped through the capillary at known velocity and the peak dispersion coefficient (D*) is measured. With the experimentally measured values of D* and flow velocity, and knowledge of the inner diameter of the capillary, the molecular diffusion coefficient (D) can be rapidly derived. For example, for ovalbumin a D value of 0.759 x 10-6 square centimeter per second is found versus a tabulated value of 0.776 x 10-6 square centimeter per second (error, 2 percent). For hemoglobin a D value of 0.676 x 10-6 square centimeter per second is obtained versus a literature value of 0.690 x 10-6 square centimeter per second (error, 1.5 percent).

Submitted on May 27, 1994
Accepted on September 15, 1994


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
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