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Collagen as Coating Material for 45S5 Bioactive Glass-Based Scaffolds for Bone Tissue Engineering

机译:胶原蛋白作为骨组织工程用45S5生物活性玻璃基支架的涂层材料

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摘要

Highly porous 45S5 bioactive glass-based scaffolds were fabricated by the foam replica technique and coated with collagen by a novel method. After an initial cleaning step of the bioactive glass surface to expose reactive –OH groups, samples were surface functionalized by (3-aminopropyl)triethoxysilane (APTS). Functionalized scaffolds were immersed in a collagen solution, left for gelling at 37 °C, and dried at room temperature. The collagen coating was further stabilized by crosslinking with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) and N-hydroxysuccinimide (NHS). Applying this coating method, a layer thickness of a few micrometers was obtained without affecting the overall scaffold macroporosity. In addition, values of compressive strength were enhanced by a factor of five, increasing from 0.04 ± 0.02 MPa for uncoated scaffolds to 0.18 ± 0.03 MPa for crosslinked collagen-coated scaffolds. The composite material developed in this study exhibited positive cell (MG-63) viability as well as suitable cell attachment and proliferation on the surface. The combination of bioactivity, mechanical competence, and cellular response makes this novel scaffold system attractive for bone tissue engineering.
机译:通过泡沫仿制技术制造高度多孔的45S5生物活性玻璃基支架,并通过一种新方法涂覆胶原蛋白。在对生物活性玻璃表面进行初步清洁步骤以暴露反应性-OH基团后,将样品通过(3-氨丙基)三乙氧基硅烷(APTS)表面官能化。将功能化的支架浸入胶原溶液中,在37°C放置胶凝,并在室温下干燥。通过与1-乙基-3-(3-二甲基氨基丙基)碳二亚胺(EDC)和N-羟基琥珀酰亚胺(NHS)交联进一步稳定胶原蛋白涂层。应用这种涂覆方法,可获得几微米的层厚度,而不会影响整个支架的大孔隙率。另外,抗压强度值提高了五倍,从未涂覆的支架的0.04±0.02 MPa增加到交联的胶原涂覆的支架的0.18±0.03 MPa。在这项研究中开发的复合材料显示出阳性细胞(MG-63)的活力以及合适的细胞附着和表面增殖。生物活性,机械能力和细胞反应的结合使这种新型支架系统对骨组织工程具有吸引力。

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