自愈水凝胶
边界润滑
材料科学
润滑
润滑油
脂质体
透明质酸
剪切(地质)
骨关节炎
生物医学工程
药物输送
化学工程
化学
复合材料
纳米技术
高分子化学
遗传学
替代医学
医学
病理
工程类
生物
作者
Yiting Lei,Xingkuan Wang,Junyi Liao,Jieliang Shen,Yuling Li,Zhengwei Cai,Ning Hu,Xiaoji Luo,Wenguo Cui,Wei Huang
标识
DOI:10.1016/j.bioactmat.2022.02.016
摘要
Lipid-based boundary layers formed on liposome-containing hydrogels can facilitate lubrication. However, these boundary layers can be damaged by shear, resulting in decreased lubrication. Here, a shear-responsive boundary-lubricated drug-loaded hydrogel is created by incorporating celecoxib (CLX)-loaded liposomes within dynamic covalent bond-based hyaluronic acid (HA) hydrogels (CLX@Lipo@HA-gel). The dynamic cross-linked network enables the hydrogel to get restructured in response to shear, and the HA matrix allows the accumulation of internal liposome microreservoirs on the sliding surfaces, which results in the formation of boundary layers to provide stable lubrication. Moreover, hydration shells formed surrounding the hydrogel can retard the degradation process, thus helping in sustaining lubrication. Furthermore, in vitro and in vivo experiments found that CLX@Lipo@HA-gels can maintain anabolic-catabolic balance, alleviate cartilage wear, and attenuate osteoarthritis progression by delivering CLX and shear-responsive boundary lubrication. Overall, CLX@Lipo@HA-gels can serve as shear-responsive boundary lubricants and drug-delivery vehicles to alleviate friction-related diseases like osteoarthritis.
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