Targeting Cartilage Degradation in Osteoarthritis

被引:23
作者
McClurg, Oliver [1 ]
Tinson, Ryan [1 ]
Troeberg, Linda [1 ]
机构
[1] Univ East Anglia, Norwich Med Sch, Bob Champ Res & Educ Bldg,Rosalind Franklin Rd, Norwich NR4 7UQ, Norfolk, England
关键词
osteoarthritis; cartilage; metalloproteinase; targeting; PLATELET-RICH PLASMA; HUMAN ARTICULAR CHONDROCYTES; FIBROBLAST GROWTH FACTOR-18; ACID REPEAT POLYMORPHISM; IN-VIVO; KNEE-OSTEOARTHRITIS; TGF-BETA; TISSUE INHIBITOR; DRUG-DELIVERY; RAT MODEL;
D O I
10.3390/ph14020126
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Osteoarthritis is a common, degenerative joint disease with significant socio-economic impact worldwide. There are currently no disease-modifying drugs available to treat the disease, making this an important area of pharmaceutical research. In this review, we assessed approaches being explored to directly inhibit metalloproteinase-mediated cartilage degradation and to counteract cartilage damage by promoting growth factor-driven repair. Metalloproteinase-blocking antibodies are discussed, along with recent clinical trials on FGF18 and Wnt pathway inhibitors. We also considered dendrimer-based approaches being developed to deliver and retain such therapeutics in the joint environment. These may reduce systemic side effects while improving local half-life and concentration. Development of such targeted anabolic therapies would be of great benefit in the osteoarthritis field.
引用
收藏
页码:1 / 19
页数:19
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