1 Institute for BioNanotechnology in Medicine, Northwestern University , Chicago, Illinois.
Tissue Eng Part A. 2013 Dec;19(23-24):2664-73. doi: 10.1089/ten.TEA.2012.0667. Epub 2013 Aug 6.
We report here the use of novel self-assembling collagen-hyaluronic acid (HyA) membranes to deliver bone morphogenetic protein-2 (BMP-2) for orthopedic applications. Prior work has demonstrated that collagen-HyA membranes are formed initially through electrostatic interactions between the oppositely charged collagen and HyA molecules, and that membrane growth is driven by osmotic pressure imbalances between the collagen and HyA solutions. The purpose of this study was to investigate the potential of incorporating charged growth factors such as BMP-2 within the membrane for regenerative medicine applications. Membrane material properties, protein mass loss, and release kinetics of BMP-2, as well as biocompatibility and osteogenic potential in vitro and in vivo using a subcutaneous mouse model were assessed. Scanning electron microscopy and mechanical testing confirmed no loss of structural or mechanical integrity upon BMP-2 incorporation into the membranes. Slow and steady release of the growth factor was demonstrated with 17% of total loaded BMP-2 released over the course of 49 days. To test biocompatibility and osteogenic potential in vitro, human mesenchymal stem cells were cultured on collagen-HyA membranes and showed greater proliferation rates (for up to 28 days) on membranes without BMP-2, but a greater alkaline phosphatase activity and osteocalcin production on membranes releasing BMP-2. In vivo subcutaneous implantation of the membranes showed a minimal immune response with osteoblasts and mineral deposits present in the ectopic site for BMP-2-releasing membranes, further demonstrating the potential of the BMP-2-releasing membranes to induce osteogenic differentiation. This study presents a novel strategy to create self-assembled membranes using two biocompatible molecules that can deliver bioactive agents in a sustained manner to induce a local regenerative response.
我们在此报告了一种新型自组装胶原-透明质酸(HyA)膜在骨科应用中递送骨形态发生蛋白-2(BMP-2)的用途。先前的工作已经表明,胶原-HyA 膜最初是通过带相反电荷的胶原和 HyA 分子之间的静电相互作用形成的,并且膜的生长是由胶原和 HyA 溶液之间的渗透压不平衡驱动的。本研究的目的是研究在膜中掺入带电生长因子(如 BMP-2)用于再生医学应用的潜力。评估了膜材料性能、BMP-2 的蛋白质质量损失和释放动力学、体外和体内的生物相容性和成骨潜力,使用皮下小鼠模型。扫描电子显微镜和机械测试证实,BMP-2 掺入膜中不会导致结构或机械完整性丧失。研究表明,生长因子的释放是缓慢而稳定的,在 49 天的过程中,总加载 BMP-2 的 17%被释放。为了测试体外的生物相容性和成骨潜力,将人骨髓间充质干细胞培养在胶原-HyA 膜上,发现无 BMP-2 的膜上细胞增殖率更高(长达 28 天),但释放 BMP-2 的膜上碱性磷酸酶活性和骨钙素产量更高。体内皮下植入膜显示出最小的免疫反应,在 BMP-2 释放膜的异位部位存在成骨细胞和矿物质沉积,进一步证明了 BMP-2 释放膜诱导成骨分化的潜力。本研究提出了一种使用两种生物相容性分子创建自组装膜的新策略,该策略可以以持续的方式递送生物活性药物,以诱导局部再生反应。