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用于协同骨再生的双药物递送涂层的自组装

Self-assembly of dual drug-delivery coating for synergistic bone regeneration.

作者信息

Qu Xue, He Fan, Tan Haoqi, Yu Yuanman, Axrap Akbar, Wang Meng, Dai Kai, Zhang Zheng, Yang Fei, Wang Shenguo, Kohn Joachim, Liu Changsheng

机构信息

The State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China.

出版信息

J Mater Chem B. 2016 Jul 28;4(28):4901-4912. doi: 10.1039/c6tb01262k. Epub 2016 Jul 4.

Abstract

Bone regeneration for the treatment of bone diseases represents a major clinical need. Introducing recombinant human bone morphogenetic protein-2 (rhBMP-2) into biomaterials is an extensively used approach to induce osteogenic differentiation and accelerate bone regeneration. However, serious adverse events can occur in the event of an overdose of rhBMP-2. Dexamethasone (DEX) is a synthetic hydrophobic glucocorticoid, which can enhance rhBMP-2-induced osteogenic differentiation by binding to a glucocorticoid receptor intracellularly. In this study, we have developed a multilayered composite coating made of poly(l-lactide-co-glycolide) (PLGA) nanoparticles, heparin and chitosan to deliver DEX and rhBMP-2 dually. The coating can reserve DEX and rhBMP-2 using the building blocks of the PLGA nanoparticles and heparin. Sustained release of DEX and rhBMP-2 by this coating was achieved. Moreover, a flow cytometry assay suggests that the PLGA nanoparticles could be transported across the cell membrane and presumably could improve the intracellular delivery of DEX via cell internalization. The in vitro osteogenesis studies reveal that the dual drug-loaded coating has a synergistic osteogenic differentiation effect on C2C12 myoblasts, as indicated by the upregulation of the alkaline phosphatise activity and osteo-related gene expression. In addition, μCT and histological analysis of the in vivo experiments demonstrate that the dual drug-loaded coating induced more ectopic bone formation than the individual drug-loaded coating. Therefore, this study demonstrates that our coating system can reserve these two drugs and deliver them locally to cells with the ability to induce rapid osteogenic differentiation and bone regeneration synergistically. Compared to other reported DEX/rhBMP-2 delivery systems, our coating system represents a simple, safe and effective dual drug delivery alternative. Moreover, since a layer-by-layer strategy is easily applied onto varying substrates, our coating system can be combined with many commercially available or existing biomaterials to improve their osteogenetic performance.

摘要

骨再生用于治疗骨疾病是一项重大的临床需求。将重组人骨形态发生蛋白-2(rhBMP-2)引入生物材料是一种广泛使用的诱导成骨分化和加速骨再生的方法。然而,rhBMP-2过量时会发生严重不良事件。地塞米松(DEX)是一种合成的疏水性糖皮质激素,它可以通过在细胞内与糖皮质激素受体结合来增强rhBMP-2诱导的成骨分化。在本研究中,我们开发了一种由聚(L-丙交酯-共-乙交酯)(PLGA)纳米颗粒、肝素和壳聚糖制成的多层复合涂层,用于双重递送DEX和rhBMP-2。该涂层可以利用PLGA纳米颗粒和肝素的构建块来保留DEX和rhBMP-2。通过该涂层实现了DEX和rhBMP-2的持续释放。此外,流式细胞术分析表明,PLGA纳米颗粒可以穿过细胞膜,并且可能通过细胞内化改善DEX的细胞内递送。体外成骨研究表明,双载药涂层对C2C12成肌细胞具有协同的成骨分化作用,碱性磷酸酶活性和骨相关基因表达上调表明了这一点。此外,体内实验的μCT和组织学分析表明,双载药涂层比单载药涂层诱导更多的异位骨形成。因此,本研究表明我们的涂层系统可以保留这两种药物并将它们局部递送至细胞,具有协同诱导快速成骨分化和骨再生的能力。与其他报道过的DEX/rhBMP-2递送系统相比,我们的涂层系统是一种简单、安全且有效的双药递送替代方案。此外,由于层层策略易于应用于各种基材上,我们的涂层系统可以与许多市售或现有的生物材料结合,以改善它们的成骨性能。

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