通过非共价到共价键转换可编程的两组合
Kohei Sato, Wei Ji1, Liam C Palmer
1Prometheus, Division of Skeletal Tissue Engineering, and ∥Skeletal Biology and Engineering Research Center, Department of Development and Regeneration, KU Leuven , Leuven 3000, Belgium.
Journal of the American Chemical Society
|June 23, 2017
概括
研究人员通过形成两性单体之间的共价键来控制高分子聚合物长度. 较长的纳米纤维增强了细胞活力,表明了潜在的生物医学应用.
科学领域:
- 超分子化学
- 材料科学
- 生物材料工程
背景情况:
- 在超分子聚合物中控制单体数量是可编程自组件的挑战.
- 通过调整分子间力量, 挫败性增长是限制组装大小的一种策略.
- 氨基为自组装的纳米结构提供了多功能平台.
研究的目的:
- 作为控制超分子纳米纤维长度的机制,研究共价键的形成.
- 评估纤维长度对细胞毒性的影响,用于潜在的生物医学应用.
主要方法:
- 两性的自我组合,随后形成共价键.
- 循环二光学,动态光散射,尺寸排除色谱和传输电子显微镜用于结构分析.
- 使用C2C12前细胞进行细胞毒性测定.
主要成果:
- 协价键形成补偿了静电排斥,使得有控制的纤维延长.
- 纤维中的键通过共价交叉连接得到加强.
- 细胞活力随着纳米纤维长度的增加而增加,表明细胞毒性降低.
结论:
- 共价键的形成是控制超分子纳米纤维长度的有效策略.
- 较长的两纳米纤维具有较低的细胞毒性,可能是由于结尾稳定.
- 这些发现支持用于生物医学应用的两纳米纤维的开发.
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