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负载于HA/PLL水凝胶中的姜黄素/BMP-2对体内外成骨的双重作用

Dual Effect of Curcumin/BMP-2 Loaded in HA/PLL Hydrogels on Osteogenesis In Vitro and In Vivo.

作者信息

Kim Eun-Cheol, Yoon Sun Jung, Noh Kwantae, Lee Deok-Won

出版信息

J Nanosci Nanotechnol. 2017 Jan;17(1):143-52. doi: 10.1166/jnn.2017.12380.

DOI:10.1166/jnn.2017.12380
PMID:29617095
Abstract

In the present study, we evaluated the potential of poly-l-lysine/hyaluronic acid (HA/PLL) hydrogels containing curcumin (CUR) and bone morphogenetic protein-2 (BMP-2) as bone tissue regeneration scaffolds. Hydrogels HP-1˜2 were formed by amide bonds via the condensation reactions between 0.02 μmol HA and 0.06–0.12 μmol poly-l-lysine · hydrobromide (PLL · HBr). Physical, chemical, and thermal analyses revealed that the amount of PLL · HBr significantly influenced hydrogel properties. Based on an In Vitro MG-63 cell proliferation test, HP-1˜2 were cytocompatible, and all hydrogels containing different amounts of CUR and BMP-2, except for HA0.02/PLL0.06/CUR20/BMP-2100 (HPCB-4), resulted in cell proliferation above 80%. An In Vitro release test showed that CUR and BMP-2 were consistently released from HA0.02/PLL0.06/CUR15 (HPC), HA0.02/PLL0.06/BMP-2100 (HPB), HA0.02/PLL0.06/CUR15/BMP-210 , 50 , or 100 (HPCB-1˜3), and HA0.02/PLL0.06/CUR10 or 20/BMP-2100 (HPCB-4˜5) for 7 and 28 days, respectively. In Vitro ALP activity and calcium deposition and In Vivo micro-computed tomography (micro-CT) tests demonstrated the potential application of HPCB-3 as bone tissue regeneration scaffolds, suggesting that bone tissue regeneration can be optimized by controlling the amounts of CUR and BMP-2.

摘要

在本研究中,我们评估了含有姜黄素(CUR)和骨形态发生蛋白-2(BMP-2)的聚-L-赖氨酸/透明质酸(HA/PLL)水凝胶作为骨组织再生支架的潜力。水凝胶HP-1至2通过0.02 μmol HA与0.06 - 0.12 μmol聚-L-赖氨酸·氢溴酸盐(PLL·HBr)之间的缩合反应由酰胺键形成。物理、化学和热分析表明,PLL·HBr的量显著影响水凝胶性能。基于体外MG-63细胞增殖试验,HP-1至2具有细胞相容性,并且除了HA0.02/PLL0.06/CUR20/BMP-2100(HPCB-4)之外,所有含有不同量CUR和BMP-2的水凝胶导致细胞增殖高于80%。体外释放试验表明,CUR和BMP-2分别从HA0.02/PLL0.06/CUR15(HPC)、HA0.02/PLL0.06/BMP-2100(HPB)、HA0.02/PLL0.06/CUR15/BMP-210、50或100(HPCB-1至3)以及HA0.02/PLL0.06/CUR10或20/BMP-2100(HPCB-4至5)中持续释放7天和28天。体外碱性磷酸酶活性和钙沉积以及体内微型计算机断层扫描(micro-CT)试验证明了HPCB-3作为骨组织再生支架的潜在应用,表明通过控制CUR和BMP-2的量可以优化骨组织再生。

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