原位形成的组织黏附大孔支架促进细胞浸润和组织再生。

Farnoosh Saeedinejad, Fatemeh Alipanah, Steven Toro, Noah Pereira, Delaram Ghanbariamin, Ivan Jozic, Tannin A Schmidt, Elmira Arab-Tehrany, Yu Shrike Zhang, Ali Tamayol, Mohamadmahdi Samandari
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引用次数: 0

摘要

大孔水凝胶在组织工程和再生医学中具有重要的应用前景。然而,传统的大孔支架制造是复杂的,不兼容的现场定制和制造。在这里,我们提出了一种高度翻译的方法,通过双注射器系统将气体微流体均质化成自交联的明胶转谷氨酰胺酶(TG)混合物,在原位形成粘附大孔支架。使用这种策略,可以评估组织缺陷,并且具有所需组合物和体积的前体在原位发泡和施用。tg诱导的交联稳定了孔隙,导致强组织粘附和精确的缺陷几何近似。通过改变发泡参数和交联动力学,通过调节明胶和TG的浓度,我们证明了对孔隙率的精确控制。由此产生的泡沫支架具有可控制的孔隙分布、灵活性、组织粘附性、稳定性、持续的蛋白质释放特征和细胞许可性,与散装水凝胶隔室相比,具有更快的生物降解特征。因此,与散装水凝胶相比,皮下注射泡沫可以增强细胞浸润和减少纤维囊形成。最后,与散装水凝胶相比,支架在治疗小鼠全层皮肤伤口方面表现出显著的愈合速度和质量改善。意义声明:提出了一种高度可转化的方法,通过双注射器系统将气体微流体均质化成自交联水凝胶前体,原位形成组织粘附大孔支架。与散装水凝胶相比,这种方法可以精确控制孔隙度和孔径,促进细胞浸润、组织整合,并改善伤口愈合,突出了它们在再生医学中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Situ-Formed Tissue-Adhesive Macroporous Scaffolds Enhance Cell Infiltration and Tissue Regeneration.

Macroporous hydrogels have shown significant promise in tissue engineering and regenerative medicine. However, conventional macroporous scaffold fabrications are complex and incompatible with in situ customization and fabrication. Here, we propose a highly translational approach for the in situ formation of adhesive macroporous scaffolds through microfluidic homogenization of gas into a self-crosslinkable gelatin and transglutaminase (TG) mixture using a double syringe system. Using this strategy, the tissue defect can be evaluated, and the precursor, with the desired composition and volume, foamed and administered in situ. The TG-induced crosslinking stabilizes the pores, leading to strong tissue adhesion and accurate defect geometry approximation. We demonstrate precise control over the porosity, by changing the foaming parameters, and crosslinking kinetics, by adjusting the concentration of gelatin and TG. The resulting foam scaffolds offer controlled pore distribution, flexibility, tissue adhesion, stability, sustained protein release profile, and cell permissibility, with a faster biodegradation profile compared to bulk hydrogel compartments. Consequently, enhanced cell infiltration and reduced fibrous capsule formation are observed upon subcutaneous injection of foams compared to bulk hydrogels. Finally, the scaffolds demonstrate significant improvements in the rate and quality of the healing compared to the bulk hydrogels for the treatment of full-thickness cutaneous wounds in mice. STATEMENT OF SIGNIFICANCE: A highly translational method is presented for the in situ formation of tissue-adhesive macroporous scaffolds through microfluidic homogenization of gas into a self-crosslinkable hydrogel precursor using a double syringe system. This approach allows precise control over porosity and pore size, facilitating cell infiltration, tissue integration, and improved wound healing compared to bulk hydrogels, highlighting their potential in regenerative medicine.

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