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

机译:致密包装的生长因子封装的壳聚糖微凝胶的可注射和微孔支架

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摘要

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 16 kPa 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.
机译:在这项工作中,开发了一种乳液交联方法来生产壳聚糖-Genipin微凝胶,该凝胶可用作可注射的微孔支架。通过光散射和水滴定法表征了壳聚糖的pH值。通过密集包装的微凝胶溶液的溶胀,光散射和流变学对其微凝胶进行表征。结果表明,随着壳聚糖在pKa以上变得越来越去质子化,排斥力减弱,分子间吸引力导致pH响应链聚集。导致微凝胶-微凝胶聚集。当在pH 7.4下凝结为微凝胶糊剂时,壳聚糖最多且交联剂最少的微凝胶表现出最高的屈服应力和16 kPa的储能模量。可以将两种带相反电荷的生长因子封装到微凝胶中,并且内皮细胞能够增殖到3D微凝胶支架中。这项工作激发了壳聚糖微凝胶支架作为可注射和微孔支架在再生医学中的应用的进一步研究。

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