剪切诱导的循环逆转导致剪切薄化和自主自我愈合在可注射,保持形状的原凝中
Mahsa Jamadi Khiabani1, Sareh Soroushzadeh2, Ardeshir Talebi2
1Macromolecular Chemistry, Department of Chemistry─Ångström Laboratory, Uppsala University, Box 538, 751 21 Uppsala, Sweden.
ACS applied materials & interfaces
|October 8, 2024
概括
这项研究引入了一种新的基于原的可注射水凝,用于组织工程. 这种先进的生物材料提供了扩展的注射能力,自主自我愈合和稳定的形状保留,解决了该领域的关键局限性.
科学领域:
- 生物材料科学 生物材料科学
- 组织工程是组织工程.
- 再生医学是一种再生医学.
背景情况:
- 可以注射的水凝对于组织工程中的细胞封装至关重要.
- 当前的水凝往往缺乏足够的注射时间窗口,自我愈合能力和形状稳定性.
- 细胞外基质 (ECM) 衍生水凝非常理想,但面临着挑战.
研究的目的:
- 开发一种可注射的,基于原的水凝,具有用于组织工程应用的增强性质.
- 克服当前注射水凝的局限性,特别是注射性,自我愈合性和形状保持性.
- 为了创建一个多功能生物材料用于体内应用.
主要方法:
- 开发一种以原为基础的水凝,通过 furan-maleimide 循环添加进行交联.
- 在延长时间窗口 (长达48小时) 中评估可注射性.
- 在注射后评估自主自我愈合特性.
- 在水性条件下测试形状和尺寸的保留.
- 使用原酶进行降解研究.
- 在细胞培养体内生物相容性测试.
- 在动物体内皮下植入大鼠以评估可吸收性和炎症.
主要成果:
- 开发的水凝可在制备后长达48小时内进行注射.
- 在注射后观察到水凝完全自主自我愈合.
- 这种水凝在缓冲中多年表现出极好的形状和尺寸保留.
- 在原酶治疗后几个小时内迅速降解.
- 通过体外细胞培养证实了生物相容性.
- 在未引起炎症的老鼠中,完全的in vivo可吸收性.
结论:
- 这种基于原的新型水凝成功满足了先进组织工程的关键标准.
- 这种生物材料为细胞封装提供了一个有前途的解决方案,可改善注射性,自我愈合性和稳定性.
- 水凝的生物相容性和可再吸收性使其适用于体内应用.
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