玻璃增强羟基磷灰石复合材料的显微结构和体外表征

U. Batra, S. Kapoor
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引用次数: 1

摘要

摘要:通过添加2、5、10 wt %的28.5%CaO-28.5%P2O5-38%Na2 o5 - caf2基玻璃增强商用羟基磷灰石(HA),然后烧结。虽然透明质酸与人体具有良好的生物相容性,但由于其力学性能较差,其应用仅限于非承重区域和涂料。这些机械性能可以通过烧结添加玻璃陶瓷得到大幅度改善。在本研究中,量化了上述指定的磷酸盐玻璃添加量对羟基磷灰石烧结的影响。每种成分都是在一定温度范围内烧结的。利用扫描电子显微镜和x射线衍射对复合材料的微观组织和物相进行表征。分别采用阿基米德原理、维氏显微硬度计(0.98 N)和Instron万能试验机(横移速度0.5 mm/min)测定密度、显微硬度和抗压强度。这些结果用于表明哪种组合物为硬组织替代提供了合适的材料。添加10 wt %玻璃的复合材料形成致密的HA/TCP(磷酸三钙)复合材料,具有比HA更好的抗压强度和硬度。体外生物活性是通过评价这些复合材料在sbf模拟体液中浸泡两周后pH和ca2 +离子浓度的变化来评估的。
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Microstructural and In-Vitro Characterization of Glass-Reinforced Hydroxyapatite Composites
1 Abstract—Commercial hydroxyapatite (HA) was reinforced by adding 2, 5, and 10 wt % of 28.5%CaO-28.5%P2O5-38%Na2 O5%CaF2 based glass and then sintered. Although HA shows good biocompatibility with the human body, its applications are limited to non load-bearing areas and coatings due to its poor mechanical properties. These mechanical properties can be improved substantially with addition of glass ceramics by sintering. In this study, the effects of sintering hydroxyapatite with above specified phosphate glass additions are quantified. Each composition was sintered over a range of temperatures. Scanning electron microscopy and x-ray diffraction were used to characterize the microstructure and phases of the composites. The density, microhardness, and compressive strength were measured using Archimedes Principle, Vickers Microhardness Tester (at 0.98 N), and Instron Universal Testing Machine (cross speed of 0.5 mm/min) respectively. These results were used to indicate which composition provided suitable material for use in hard tissue replacement. Composites containing 10 wt % glass additions formed dense HA/TCP (tricalcium phosphate) composite materials possessing good compressive strength and hardness than HA. In-vitro bioactivity was assessed by evaluating changes in pH and Ca 2+ ion concentration of SBF-simulated body fluid on immersion of these composites in it for two weeks.
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