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介孔生物活性玻璃对聚(DL-丙交酯-共-乙交酯)薄膜的物理化学、生物学及药物释放性能的影响

The effect of mesoporous bioactive glass on the physiochemical, biological and drug-release properties of poly(DL-lactide-co-glycolide) films.

作者信息

Wu Chengtie, Ramaswamy Yogambha, Zhu Yufang, Zheng Rongkun, Appleyard Richard, Howard Andrew, Zreiqat Hala

机构信息

Biomaterials and Tissue Engineering Research Unit, School of AMME, The University of Sydney, Sydney 2006, Australia.

出版信息

Biomaterials. 2009 Apr;30(12):2199-208. doi: 10.1016/j.biomaterials.2009.01.029. Epub 2009 Feb 8.

Abstract

Poly(lactide-co-glycolide) (PLGA) has been widely used for bone tissue regeneration. However, it lacks hydrophilicity, bioactivity and sufficient mechanical strength and its acidic degradation by-products can lead to pH decrease in the vicinity of the implants. Mesoporous bioactive glass (MBG) with highly ordered structure (pore size 2-50nm) possesses higher bioactivity than non-mesoporous bioactive glass (BG). The aim of this study is to investigate the effect of MBG on the mechanical strength, in vitro degradation, bioactivity, cellular response and drug release of PLGA films and optimize their physicochemical, biological and drug-delivery properties for bone tissue engineering application. The surface and inner microstructure, mechanical strength and surface hydrophilicity of MBG/PLGA and BG/PLGA films were tested. Results indicated that MBG or BG was uniformly dispersed in the PLGA films. The incorporation of MBG into PLGA films significantly improved their tensile strength, modulus and surface hydrophilicity. MBG/PLGA resulted in an enhanced mechanical strength, in vitro degradation (water absorbance, weight loss and ions release), apatite-formation ability and pH stability in simulated body fluids (SBF), compared to BG/PLGA. MBG/PLGA and BG/PLGA films enhanced human osteoblastic-like cells (HOBs) attachment, spreading and proliferation compared to PLGA. HOBs differentiation was significantly upregulated when cells were cultured on 30 MBG/PLGA for 14 days, compared to 30 BG/PLGA. MBG/PLGA enhanced the accumulative release of dexamethazone (DEX) at early stages (0-200h) compared to BG/PLGA, however, after 200h, DEX-release rates for MBG/PLGA was slower than that of BG/PLGA. The contents of MBG in PLGA films can control the amount of DEX released. Taken together, MBG/PLGA films possessed excellent physicochemical, biological and drug-release properties, indicating their potential application for bone tissue engineering by designing 3D scaffolds according to their corresponding compositions.

摘要

聚(丙交酯-乙交酯)(PLGA)已被广泛用于骨组织再生。然而,它缺乏亲水性、生物活性和足够的机械强度,并且其酸性降解副产物会导致植入物附近的pH值降低。具有高度有序结构(孔径2-50nm)的介孔生物活性玻璃(MBG)比非介孔生物活性玻璃(BG)具有更高的生物活性。本研究的目的是研究MBG对PLGA膜的机械强度、体外降解、生物活性、细胞反应和药物释放的影响,并优化其物理化学、生物学和药物递送性能以用于骨组织工程应用。测试了MBG/PLGA和BG/PLGA膜的表面和内部微观结构、机械强度和表面亲水性。结果表明,MBG或BG均匀分散在PLGA膜中。将MBG掺入PLGA膜中显著提高了其拉伸强度、模量和表面亲水性。与BG/PLGA相比,MBG/PLGA在模拟体液(SBF)中具有增强的机械强度、体外降解(吸水率、重量损失和离子释放)、磷灰石形成能力和pH稳定性。与PLGA相比,MBG/PLGA和BG/PLGA膜增强了人成骨样细胞(HOBs)的附着、铺展和增殖。与30 BG/PLGA相比,当细胞在30 MBG/PLGA上培养14天时,HOBs分化显著上调。与BG/PLGA相比,MBG/PLGA在早期阶段(0-200小时)增强了地塞米松(DEX)的累积释放,但在200小时后,MBG/PLGA的DEX释放速率比BG/PLGA慢。PLGA膜中MBG的含量可以控制DEX的释放量。综上所述,MBG/PLGA膜具有优异的物理化学、生物学和药物释放性能,表明通过根据其相应组成设计3D支架,它们在骨组织工程中具有潜在应用。

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