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微凝胶在透明 PEG 水凝胶的 3D 多孔结构内的动力学。

Microgel dynamics within the 3D porous structure of transparent PEG hydrogels.

机构信息

Department of Chemistry "Ugo Schiff" and CSGI, University of Florence, via della Lastruccia, 3 - Sesto Fiorentino, FI I-50019, Italy.

Department of Chemistry "Ugo Schiff" and CSGI, University of Florence, via della Lastruccia, 3 - Sesto Fiorentino, FI I-50019, Italy.

出版信息

Colloids Surf B Biointerfaces. 2023 Jan;221:112938. doi: 10.1016/j.colsurfb.2022.112938. Epub 2022 Oct 18.

Abstract

We report an investigation on the effects of the confinement imposed by application-relevant poly(ethylene glycol) (PEG) hydrogel matrices with controlled porosity on the dynamics of soft microgels. Through a detailed characterization of the internal structure of the hydrogels at the nano and microscale, we were able to link the microgel dynamics, measured by particle tracking, to the 3D geometrical confinement imposed by the porous matrices. PEG hydrogels with a high degree of transparency and tunable pore sizes and volume fractions were obtained using freeze-thawing. We found that the porosity of the hydrogel networks is characterized by elongated channels having asymmetric sections, with the average size decreasing from about 7 to about 2 particle diameters, and the size distribution becoming narrower with increasing PEG content in the pre-reaction mixture. The microgel dynamics slowdown and change from diffusive to sub-diffusive as a result of the increasing confinement. The observed decrease in diffusivity is consistent with models of diffusion in cylindrical pores and can be attributed to hydrodynamic and steric effects in addition to geometrical constriction. A dependence of the effective diffusion coefficient on the pore volume fraction, which is unusually pronounced, suggests the presence of microgel-hydrogel interactions. Our results demonstrate that a detailed characterization of the 3D geometry of the porous network is of primary importance for the understanding of transport properties in complex, random porous media.

摘要

我们报告了一项关于应用相关的聚乙二醇(PEG)水凝胶基质的受限效应的研究,该水凝胶基质具有受控的孔隙率,对软微凝胶的动力学有影响。通过在纳米和微米尺度上对水凝胶的内部结构进行详细的表征,我们能够将通过粒子追踪测量的微凝胶动力学与多孔基质施加的 3D 几何限制联系起来。使用冻融法获得了具有高透明度和可调孔径和体积分数的 PEG 水凝胶。我们发现,水凝胶网络的孔隙率由具有不对称截面的拉长通道来表征,平均尺寸从约 7 个粒子直径减小到约 2 个粒子直径,并且随着预反应物混合物中 PEG 含量的增加,尺寸分布变得更窄。由于限制的增加,微凝胶动力学减慢并从扩散变为亚扩散。观察到的扩散系数的降低与圆柱孔中的扩散模型一致,除了几何收缩外,还可以归因于流体动力学和空间位阻效应。有效扩散系数对孔体积分数的依赖性非常显著,表明存在微凝胶-水凝胶相互作用。我们的结果表明,对多孔网络的 3D 几何形状进行详细的表征对于理解复杂随机多孔介质中的传输性质至关重要。

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