Particle Diffusion in Polymeric Hydrogels with Mixed Attractive and Repulsive Interactions

被引:36
|
作者
Hansing, Johann [1 ]
Duke, Joseph R., III [2 ]
Fryman, Emily B. [2 ]
DeRouchey, Jason E. [2 ]
Netz, Roland R. [1 ]
机构
[1] Free Univ Berlin, Fachbereich Phys, D-14195 Berlin, Germany
[2] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
基金
美国国家科学基金会;
关键词
Diffusion; hydrogels; mucus; biological barriers; Langevin simulations; FLUORESCENCE CORRELATION SPECTROSCOPY; NANOPARTICLE DIFFUSION; EXTRACELLULAR-MATRIX; MUCUS; CHARGE; GELS; TRANSPORT; SIZE; MACROMOLECULES; DIAGNOSTICS;
D O I
10.1021/acs.nanolett.8b02218
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
All biogels are heterogeneous, consisting of functional groups with different biophysical properties arrayed on spatially disordered polymer networks. Nanoparticles diffusing in such biogels experience a mixture of attractive and repulsive interactions. Here, we present experimental and theoretical studies of charged particle diffusion in gels with a random distribution of attractive and repulsive electrostatic interaction sites inside the gel In addition to interaction disorder, we theoretically investigate the effect of spatial disorder of the polymer network Our coarse-grained simulations reveal that attractive interactions primarily determine the diffusive behavior of the particles in systems with mixed attractive and repulsive interactions. As a consequence, charged particles of either sign are immobilized in mixed catiomc/anionic gels because they are trapped near oppositely charged interaction sites, whereas neutral particles diffuse rapidly.Even small fractions of oppositely charged interaction sites lead to strong trapping of a charged particle .ranslational diffusion coefficients of charged probe molecules in gels consisting of mixed catiomc and anionic dextran polymers are determined by fluorescence correlation spectroscopy and quantitatively confirm our theoretical predictions
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页码:5248 / 5256
页数:9
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