Taylor dispersion analysis in fused silica capillaries: a tutorial review

被引:19
|
作者
Moser, Meagan R. [1 ,2 ]
Baker, Christopher A. [2 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[2] New Mexico State Univ, Dept Chem & Biochem, MSC 3C,POB 30001, Las Cruces, NM 88003 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
SIZE-BASED CHARACTERIZATION; DYNAMIC LIGHT-SCATTERING; SCANNING-ELECTRON-MICROSCOPY; DIFFUSION-COEFFICIENTS; RAPID-DETERMINATION; GOLD NANOPARTICLES; EXCLUSION CHROMATOGRAPHY; CHARGE CHARACTERIZATION; HYDRODYNAMIC RADIUS; MOLECULAR-WEIGHT;
D O I
10.1039/d1ay00588j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Biological and pharmaceutical analytes like liposomes, therapeutic proteins, nanoparticles, and drug-delivery systems are utilized in applications, such as pharmaceutical formulations or biomimetic models, in which controlling their size is often critical. Many of the common techniques for sizing these analytes require method development, significant sample preparation, large sample quantities, and lengthy analysis times. In other cases, such as DLS, sizing can be biased towards the largest constituents in a mixture. Therefore, there is a need for more rapid, sensitive, accurate, and straightforward analytical methods for sizing macromolecules, especially those of biological origin which may be sample-limited. Taylor dispersion analysis (TDA) is a sizing technique that requires no calibration and consumes only nL to pL sample volumes. In TDA, average diffusion coefficients are determined via the Taylor-Aris equation by characterizing band broadening of an analyte plug under well-controlled laminar flow conditions. Diffusion coefficient can then be interpreted as hydrodynamic radius (R-H) via the Stokes-Einstein equation. Here, we offer a tutorial review of TDA, intended to make the method better understood and more widely accessible to a community of analytical chemists and separations scientists who may benefit from the unique advantages of this versatile sizing method. We first provide a tutorial on the fundamental principles that allow TDA to achieve calibration-free sizing of analytes across a wide range of R-H, with an emphasis on the reduced sample consumption and analysis times that result from utilizing fused silica capillaries. We continue by highlighting relationships between operating parameters and critically important flow conditions. Our discussion continues by looking at methods for applying TDA to sample mixtures via algorithmic approaches and integration of capillary electrophoresis and TDA. Finally, we present a selection of reports that demonstrate TDA applied to complex challenges in bioanalysis and materials science.
引用
收藏
页码:2357 / 2373
页数:17
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