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Preparation of 3DP Hydroxyapatite Composite By Single And Double Pass Poly(e-caproiactone) Infiltration

机译:单次双通磷酸盐复合3DP羟基磷灰石复合(E-己基因酮)渗透

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Recently, porous hydroxyapatite was fabricated by three dimensional printing (3DP) in coupled with low temperature phosphorization to yield nanosized and low crystalline structure. However, brittleness was an intrinsic drawback for some foreseen applications. Polymer infiltration aiming to improve the toughness and mechanical integrity was thus carried out using biodegradable poly(s-caprolactone) (PCL) as an infiltrant since it has shown good biocompatibility together with a high elongation and energy to failure as compared to other medical polymers. Three routes of infiltration were performed including melt infiltration of low molecular weight PCL (Mw -10,000), solution infiltration by 10 % high molecular weight PCL (Mw - 80,000) and the combination of both melt and solution infiltration of low and high molecular weight PCL. The combination of low and high MW infiltration yielded the greatest increase in the mechanical properties and followed by the melt infiltration of low molecular weight PCL while the use of high MW infiltration yielded limited enhancement. After immersing in simulated body fluid (SBF), no significant changes in flexural properties were seen for both hydroxyapatite and high molecular weight infiltrated sample. However, flexural strength and strain at break of low molecular weight infiltrated sample largely dropped after 7 days of immersion to be closed to those of hydroxyapatite and high molecular weight infiltrated sample. The flexural properties of high-low infiltrated sample also decreased after immersion, but to a less degree and still maintained the greatest values amongst all samples. This could be associated to the difference in degradation of different molecular weight of PCL and the content of polymer infiltration induced by different infiltration routes. Calcium and phosphorus ions in the SBF were quantified and observed to be consumed continuously during immersion for all samples. Newly formed apatite crystals were observed to form on the surface of the infiltrated composites signifying that infiltration did not hinder the bioactivity of the composites.
机译:近来,通过三维印刷(3DP)制造多孔羟基磷灰石,其与低温磷化阳性结合,得到纳米化和低结晶结构。然而,脆性是一些预见的应用的内在缺点。因此,使用可生物降解的聚(S-己内酯)(PCL)作为渗透剂,以获得韧性和机械完整性的聚合物渗透,因为与其他医用聚合物相比,它与高伸长和能量一起显示出良好的生物相容性。进行三种渗透途径,包括低分子量PCL(MW -10,000)的熔体浸润,溶液浸润10%高分子量PCL(MW-80,000),熔体和溶液浸润的低和高分子量PCL的组合。低和高MW渗透的组合产生了机械性能的最大增加,然后在低分子量PCL的熔体渗透时,虽然使用高MW渗透产生有限的增强。在浸入模拟体液(SBF)后,对于羟基磷灰石和高分子量渗透样品,没有看到抗弯曲性能的显着变化。然而,低分子量渗透样品的抗弯曲强度和菌株在浸渍7天后在浸泡7天后滴到羟基磷灰石和高分子量渗透样品。高低渗透样品的弯曲性能也在浸入后降低,但较少程度,并且仍然保持所有样品中最大的值。这可能与PCL不同分子量的降解的差异和不同渗透途径诱导的聚合物浸润的含量有关。量化SBF中的钙和磷离子,并观察到浸入所有样品期间连续消耗。观察到新形成的磷灰石晶体在渗透复合材料的表面上形成,表示浸润没有阻碍复合材料的生物活性。

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