脂质体
药物输送
生物医学工程
骨关节炎
控制释放
材料科学
纳米技术
化学
生物物理学
医学
病理
生物
替代医学
作者
Jielai Yang,Yuan Zhu,Fei Wang,Liangfu Deng,Xiangyang Xu,Wenguo Cui
标识
DOI:10.1016/j.cej.2020.126004
摘要
Immobilizing liposomes in the hydrogel matrix network has become an effective strategy to protect liposomes against rapid clearance in the body, thus facilitating their localized drug delivery in a controlled and sustained manner for a long period. However, the low efficiency of drug delivery and short joint retention time seriously weaken its therapeutic efficacy. Herein, an efficient delivery platform was designed to anchor liposomes by integrating them with photo-crosslinkable GelMA matrix, rapidly forming monodisperse [email protected] hybrid microgels under ultraviolet light using a one-step innovational microfluidics technology. The liposomes were firmly anchored within microgels by the physical network hindrance and non-covalent interaction. Due to the double impediment from the lipid membrane and the hydrogel matrix network, kartogenin (KGN) encapsulated in [email protected] microgel presented notable extended release kinetics. Compared with KGN-loaded liposomes ([email protected]), KGN-loaded [email protected] microgels ([email protected]@KGN) could extend KGN release for over three weeks and remarkably promote chondrocyte differentiation of bone marrow mesenchymal stem cells (BMSCs) in vitro. Furthermore, the in vivo study demonstrated that [email protected]@KGN, with enhanced joint residence over five weeks, could effectively reduce osteophyte burden and prevent articular cartilage degeneration as well as subchondral bone changes when intraarticularly injected in a surgically induced rat osteoarthritis model. Collectively, [email protected] microgel, as an innovative extended delivery platform, holds tremendous potential for osteoarthritis treatment.
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