材料科学
泊洛沙姆
体内
生物医学工程
基因传递
软骨
遗传增强
生物材料
生物物理学
纳米技术
生物
医学
解剖
聚合物
生物化学
基因
共聚物
复合材料
生物技术
作者
Henning Madry,Liang Gao,Ana Rey‐Rico,Jagadeesh K. Venkatesan,Kathrin Müller‐Brandt,Xiaoyu Cai,Lars Goebel,Gertrud Schmitt,Susanne Speicher‐Mentges,David Zurakowski,Michael D. Menger,Matthias W. Laschke,Magali Cucchiarini
标识
DOI:10.1002/adma.201906508
摘要
Advanced biomaterial-guided delivery of gene vectors is an emerging and highly attractive therapeutic solution for targeted articular cartilage repair, allowing for a controlled and minimally invasive delivery of gene vectors in a spatiotemporally precise manner, reducing intra-articular vector spread and possible loss of the therapeutic gene product. As far as it is known, the very first successful in vivo application of such a biomaterial-guided delivery of a potent gene vector in an orthotopic large animal model of cartilage damage is reported here. In detail, an injectable and thermosensitive hydrogel based on poly(ethylene oxide) (PEO)-poly(propylene oxide) (PPO)-PEO poloxamers, capable of controlled release of a therapeutic recombinant adeno-associated virus (rAAV) vector overexpressing the chondrogenic sox9 transcription factor in full-thickness chondral defects, is applied in a clinically relevant minipig model in vivo. These comprehensive analyses of the entire osteochondral unit with multiple standardized evaluation methods indicate that rAAV-FLAG-hsox9/PEO-PPO-PEO hydrogel-augmented microfracture significantly improves cartilage repair with a collagen fiber orientation more similar to the normal cartilage and protects the subchondral bone plate from early bone loss.
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