Ding Xiaochu, Wang Yadong
Department of Bioengineering and the McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Department of Surgery, University of Pittsburgh, Pittsburgh, PA 15260, USA.
J Mater Chem B. 2017 Feb 7;5(5):887-906. doi: 10.1039/C6TB03052A. Epub 2016 Dec 16.
Here we define hydrogels crosslinked by weak bonds as physical hydrogels. They possess unique features including reversible bonding, shear thinning and stimuli-responsiveness. Unlike covalently crosslinked hydrogels, physical hydrogels do not require triggers to initiate chemical reactions for gelation. The drug can be fully loaded in a pre-formed hydrogel for delivery with minimal cargo leakage during injection. These benefits make physical hydrogels useful as delivery vehicles for applications in biomedical engineering. This review focuses on recent advances of physical hydrogels crosslinked by weak bonds: hydrogen bonds, ionic interactions, host-guest chemistry, hydrophobic interactions, coordination bonds and π-π stacking interactions. Understanding the principles and the state of the art of gels with these dynamic bonds may give rise to breakthroughs in many biomedical research areas including drug delivery and tissue engineering.
在这里,我们将通过弱键交联的水凝胶定义为物理水凝胶。它们具有独特的特性,包括可逆键合、剪切变稀和刺激响应性。与共价交联水凝胶不同,物理水凝胶不需要引发剂来启动化学反应以实现凝胶化。药物可以完全负载在预先形成的水凝胶中以便递送,在注射过程中货物泄漏最小。这些优点使物理水凝胶作为递送载体在生物医学工程应用中很有用。本综述重点关注通过弱键交联的物理水凝胶的最新进展:氢键、离子相互作用、主客体化学、疏水相互作用、配位键和π-π堆积相互作用。了解具有这些动态键的凝胶的原理和技术现状可能会在包括药物递送和组织工程在内的许多生物医学研究领域带来突破。