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壳聚糖凝胶联合明胶微球序贯递送 BMP-2 和 IGF-1 促进早期成骨细胞分化。

Sequential delivery of BMP-2 and IGF-1 using a chitosan gel with gelatin microspheres enhances early osteoblastic differentiation.

机构信息

Department of Orthopedic Surgery, Stanford University, Stanford, CA, USA.

出版信息

Acta Biomater. 2012 May;8(5):1768-77. doi: 10.1016/j.actbio.2012.01.009. Epub 2012 Jan 18.

Abstract

The purpose of this study was to develop and characterize a chitosan gel/gelatin microsphere (MSs) dual delivery system for sequential release of bone morphogenetic protein-2 (BMP-2) and insulin-like growth factor-1 (IGF-1) to enhance osteoblast differentiation in vitro. We made and characterized the delivery system based on its degree of cross-linking, degradation, and release kinetics. We also evaluated the cytotoxicity of the delivery system and the effect of growth factors on cell response using pre-osteoblast W-20-17 mouse bone marrow stromal cells. IGF-1 was first loaded into MSs, and then the IGF-1-containing MSs were encapsulated into the chitosan gel which contained BMP-2. Cross-linking of gelatin with glyoxal via Schiff bases significantly increased thermal stability and decreased the solubility of the MSs, leading to a significant decrease in the initial release of IGF-1. Encapsulation of the MSs into the chitosan gel generated polyelectrolyte complexes by intermolecular interactions, which further affected the release kinetics of IGF-1. This combinational delivery system provided an initial release of BMP-2 followed by a slow and sustained release of IGF-1. Significantly greater alkaline phosphatase activity was found in W-20-17 cells treated with the sequential delivery system compared with other treatments (P<0.05) after a week of culture.

摘要

本研究旨在开发和表征壳聚糖凝胶/明胶微球(MSs)双重递药系统,以顺序释放骨形态发生蛋白-2(BMP-2)和胰岛素样生长因子-1(IGF-1),从而增强体外成骨细胞分化。我们根据其交联度、降解和释放动力学来制备和表征递药系统。我们还使用前成骨细胞 W-20-17 小鼠骨髓基质细胞来评估递药系统的细胞毒性以及生长因子对细胞反应的影响。首先将 IGF-1 载入 MSs 中,然后将含有 IGF-1 的 MSs 包封到含有 BMP-2 的壳聚糖凝胶中。通过席夫碱将明胶与乙二醛交联可显著提高其热稳定性并降低 MSs 的溶解度,从而导致 IGF-1 的初始释放显著减少。MSs 包封到壳聚糖凝胶中通过分子间相互作用生成聚电解质复合物,这进一步影响了 IGF-1 的释放动力学。这种组合递药系统提供了 BMP-2 的初始释放,随后是 IGF-1 的缓慢和持续释放。与其他处理方式相比,培养一周后,用序贯递药系统处理的 W-20-17 细胞的碱性磷酸酶活性明显更高(P<0.05)。

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