Kowalczewski Christine J, Saul Justin M
U.S. Army Institute of Surgical Research, San Antonio, TX, United States.
Department of Chemical, Paper and Biomedical Engineering, Miami University, Oxford, OH, United States.
Front Pharmacol. 2018 May 29;9:513. doi: 10.3389/fphar.2018.00513. eCollection 2018.
Bone fracture followed by delayed or non-union typically requires bone graft intervention. Autologous bone grafts remain the clinical "gold standard". Recently, synthetic bone grafts such as Medtronic's Infuse Bone Graft have opened the possibility to pharmacological and tissue engineering strategies to bone repair following fracture. This clinically-available strategy uses an absorbable collagen sponge as a carrier material for recombinant human bone morphogenetic protein 2 (rhBMP-2) and a similar strategy has been employed by Stryker with BMP-7, also known as osteogenic protein-1 (OP-1). A key advantage to this approach is its "off-the-shelf" nature, but there are clear drawbacks to these products such as edema, inflammation, and ectopic bone growth. While there are clinical challenges associated with a lack of controlled release of rhBMP-2 and OP-1, these are among the first clinical examples to wed understanding of biological principles with biochemical production of proteins and pharmacological principles to promote tissue regeneration (known as regenerative pharmacology). After considering the clinical challenges with such synthetic bone grafts, this review considers the various biomaterial carriers under investigation to promote bone regeneration. This is followed by a survey of the literature where various pharmacological approaches and molecular targets are considered as future strategies to promote more rapid and mature bone regeneration. From the review, it should be clear that pharmacological understanding is a key aspect to developing these strategies.
骨折后出现延迟愈合或不愈合通常需要进行骨移植干预。自体骨移植仍然是临床“金标准”。最近,诸如美敦力公司的Infuse骨移植产品等合成骨移植材料为骨折后的骨修复带来了药理学和组织工程策略的可能性。这种临床可用策略使用可吸收胶原海绵作为重组人骨形态发生蛋白2(rhBMP - 2)的载体材料,史赛克公司在其产品中也采用了类似策略,只不过使用的是骨形态发生蛋白7(BMP - 7),也称为成骨蛋白 - 1(OP - 1)。这种方法的一个关键优势在于其“现货供应”的特性,但这些产品也存在明显的缺点,如水肿、炎症和异位骨生长。虽然与rhBMP - 2和OP - 1缺乏控释相关存在临床挑战,但这些是将生物学原理的理解与蛋白质的生化生产以及促进组织再生的药理学原理相结合(即再生药理学)的首批临床实例之一。在考虑了此类合成骨移植材料的临床挑战后,本综述探讨了正在研究的各种用于促进骨再生的生物材料载体。随后对文献进行了综述,其中考虑了各种药理学方法和分子靶点作为促进更快速和成熟骨再生的未来策略。从该综述中可以清楚地看出,药理学理解是开发这些策略的关键方面。