自愈水凝胶
材料科学
甲基丙烯酸酯
纳米复合材料
纳米技术
肌发生
组织工程
原位
各向异性
生物医学工程
聚合物
化学
单体
高分子化学
复合材料
体外
有机化学
物理
医学
量子力学
生物化学
作者
Kevin J. De France,Kevin G. Yager,Katelyn J. W. Chan,Brandon Corbett,Emily D. Cranston,Todd Hoare
出处
期刊:Nano Letters
[American Chemical Society]
日期:2017-09-28
卷期号:17 (10): 6487-6495
被引量:128
标识
DOI:10.1021/acs.nanolett.7b03600
摘要
While injectable in situ cross-linking hydrogels have attracted increasing attention as minimally invasive tissue scaffolds and controlled delivery systems, their inherently disorganized and isotropic network structure limits their utility in engineering oriented biological tissues. Traditional methods to prepare anisotropic hydrogels are not easily translatable to injectable systems given the need for external equipment to direct anisotropic gel fabrication and/or the required use of temperatures or solvents incompatible with biological systems. Herein, we report a new class of injectable nanocomposite hydrogels based on hydrazone cross-linked poly(oligoethylene glycol methacrylate) and magnetically aligned cellulose nanocrystals (CNCs) capable of encapsulating skeletal muscle myoblasts and promoting their differentiation into highly oriented myotubes in situ. CNC alignment occurs on the same time scale as network gelation and remains fixed after the removal of the magnetic field, enabling concurrent CNC orientation and hydrogel injection. The aligned hydrogels show mechanical and swelling profiles that can be rationally modulated by the degree of CNC alignment and can direct myotube alignment both in two- and three-dimensions following coinjection of the myoblasts with the gel precursor components. As such, these hydrogels represent a critical advancement in anisotropic biomimetic scaffolds that can be generated noninvasively in vivo following simple injection.
科研通智能强力驱动
Strongly Powered by AbleSci AI