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可注射的、由紧密堆积的、包裹生长因子的壳聚糖微凝胶组成的微孔支架。

Injectable and microporous scaffold of densely-packed, growth factor-encapsulating chitosan microgels.

作者信息

Riederer Michael S, Requist Brennan D, Payne Karin A, Way J Douglas, Krebs Melissa D

机构信息

Department of Chemical & Biological Engineering, Colorado School of Mines, 1613 Illinois Street, Golden, CO 80401, United States.

Department of Orthopedics, University of Colorado Anschutz Medical Campus, 12800 E. 19th Avenue, Aurora, CO 80045, United States.

出版信息

Carbohydr Polym. 2016 Nov 5;152:792-801. doi: 10.1016/j.carbpol.2016.07.052. Epub 2016 Jul 18.

Abstract

In this work, an emulsion crosslinking method was developed to produce chitosan-genipin microgels which acted as an injectable and microporous scaffold. Chitosan was characterized with respect to pH by light scattering and aqueous titration. Microgels were characterized with swelling, light scattering, and rheometry of densely-packed microgel solutions. The results suggest that as chitosan becomes increasingly deprotonated above the pKa, repulsive forces diminish and intermolecular attractions cause pH-responsive chain aggregation; leading to microgel-microgel aggregation as well. The microgels with the most chitosan and least cross-linker showed the highest yield stress and a storage modulus of 16kPa when condensed as a microgel paste at pH 7.4. Two oppositely-charged growth factors could be encapsulated into the microgels and endothelial cells were able to proliferate into the 3D microgel scaffold. This work motivates further research on the applications of the chitosan microgel scaffold as an injectable and microporous scaffold in regenerative medicine.

摘要

在这项工作中,开发了一种乳液交联方法来制备壳聚糖-京尼平微凝胶,其作为一种可注射的微孔支架。通过光散射和水溶液滴定对壳聚糖进行了pH表征。通过微凝胶的溶胀、光散射以及紧密堆积的微凝胶溶液的流变学对微凝胶进行了表征。结果表明,当壳聚糖在pKa以上变得越来越去质子化时,排斥力减小,分子间吸引力导致pH响应性链聚集;这也导致了微凝胶-微凝胶聚集。当在pH 7.4下浓缩成微凝胶糊剂时,壳聚糖含量最高且交联剂含量最低的微凝胶表现出最高的屈服应力和16kPa的储能模量。两种带相反电荷的生长因子可以被包裹在微凝胶中,并且内皮细胞能够在三维微凝胶支架中增殖。这项工作推动了对壳聚糖微凝胶支架作为可注射微孔支架在再生医学中的应用的进一步研究。

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