Locally delivered lovastatin nanoparticles enhance fracture healing in rats

被引:78
作者
Garrett, I. R.
Gutierrez, G. E.
Rossini, G.
Nyman, J.
McCluskey, B.
Flores, A.
Mundy, G. R.
机构
[1] OsteoScreen Ltd, San Antonio, TX 78023 USA
[2] Univ Texas, Hlth Sci Ctr, San Antonio, TX 78285 USA
关键词
lovastatin; bone formation; nanoparticles; HMG-CoA reductase inhibitors;
D O I
10.1002/jor.20391
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Statins stimulate bone formation in vitro and in vivo and, when given in large doses or by prolonged infusions, stimulate biomechanical strength of murine long bones with healing fractures. However, administration of statins by large oral doses or prolonged infusions to a fracture site is not a feasible therapeutic approach to hasten healing of human fractures. We administered lovastatin in biodegradable polymer nanobeads of poly(lactic-co-glycolide acid) to determine if lovastatin delivered in low doses in nanoparticles of a therapeutically acceptable scaffold could increase rates of healing in a standard preclinical model of femoral fracture. We found that these nanobeads: (1) stimulated bone formation in vitro at 5 ng/mL, (2) increased rates of healing in femoral fractures when administered as a single injection into the fracture site, and (3) decreased cortical fracture gap at 4 weeks as assessed by microcomputed tomography. These preclinical results suggest that lovastatin administered in a nanobead preparation may be therapeutically useful in hastening repair of human fractures. (c) 2007 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.
引用
收藏
页码:1351 / 1357
页数:7
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