Comparison of single and double detection points Taylor Dispersion Analysis for monodisperse and polydisperse samples

被引:37
作者
Chamieh, Joseph [1 ]
Cottet, Herve [1 ]
机构
[1] Univ Montpellier 2, Univ Montpellier 1, CNRS, IBMM,UMR 5247, F-34095 Montpellier 5, France
关键词
Taylor Dispersion Analysis; Double UV detection points; Integration method; Polydisperse samples; DIFFUSION-COEFFICIENTS; CAPILLARY-ELECTROPHORESIS; LIGHT-SCATTERING; LIQUID-SYSTEMS; MIXTURES; PROTEIN; INSTRUMENT; APPARATUS; POLYMERS; SOLUTE;
D O I
10.1016/j.chroma.2012.03.095
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The purpose of this work was to compare single and double detection points Taylor Dispersion Analysis (TDA) of monodisperse and polydisperse samples for low injected volumes. For that, the hydrodynamic radii of human and bovine serum albumins, a poly(styrene sulfonate) standard and two dendrigraft poly-L-lysines were determined by TDA on a capillary electrophoresis instrument using a modified detection interface allowing the analysis on two detection points. The results were compared to values obtained via a single detection point TDA with adequate corrections for the finite injected volume. The results showed no significant difference between the double and single detection points when Taylor conditions were respected and when the injected volume was less than 1% of the capillary volume till the detection window. The issue of the determination of the peak variance of the Taylorgram in the case of polydisperse sample with non-Gaussian peak is addressed. A criterion is proposed to define the interval of time on which the peak variance is calculated by integration as a function of the signal to noise ratio. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 127
页数:5
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