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Hydroxyapatite-Collagen Composite Made from Coral and Chicken Claws for Bone Implant Application

机译:氨基磷灰石 - 胶原蛋白复合材料由珊瑚和鸡爪爪制成,用于骨植入物应用

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摘要

Synthesis of porous hydroxyapatite-collagen composites for bone implant applications has been carried out. Hydroxyapatite synthesized from coral by the precipitation method, while Collagen synthesized from chicken claws. Collagen formation was carried out by freeze-dry technique with variations in freezing time of 2, 4 and 6 hours at -80 ° C. The next process was by drying in a lyophilizer. Characterization of samples was carried out using Fourier Transform Infra Red (FTIR), Scanning Electron Microscopy (SEM), compressive strength test and cytotoxicity test with Microtetrazolium (MTT) assay. FTIR results proved that collagen uptake and hydroxyapatite combine chemically. This is indicated by the absorption of functional groups that did not coincide between collagen and hydroxyapatite functional groups with composites. SEM observations showed that the largest pore size was obtained at freezing for 2 hours which was 774 μm and the smallest in freezing for 6 hours was 640 μm. This pore size was an important parameter of the bone implant because it played a role in the osteoinductive process. The composite compressive strength test results for freezing 2 hours, 4 hours and 6 hours respectively was 737 KPa, 842 KPa and 707.7 KPa. The results of the cytotoxicity test with MTT showed the percentage of cell viability above 100%. This means that the Hydroxyapatite-collagen composite is non-toxic. So, the sample formed has qualified as a bone implant candidate.
机译:已经进行了多孔羟基磷灰石 - 胶原复合材料的骨植入物应用。羟基磷灰石通过沉淀法从珊瑚合成,而胶原蛋白由鸡爪合成。通过冷冻干燥技术进行胶原蛋白形成,在-80℃下的冷冻时间为2,4和6小时的变化进行。下一个方法是通过在冻干器中干燥。使用傅里叶变换红外线(FTIR),扫描电子显微镜(SEM),扫描强度试验和细胞毒性试验进行样品的表征,用微量四唑(MTT)测定。 FTIR结果证明胶原蛋白摄取和羟基磷灰石化学结合。这是通过用复合材料在胶原蛋白和羟基磷灰石官能团之间不一致的官能团的吸收来表示。 SEM观察结果表明,在冷冻2小时内获得最大的孔径,其为774μm,最小的冷冻6小时为640μm。这种孔径是骨植入的重要参数,因为它在骨诱导过程中发挥了作用。冻结2小时,4小时和6小时的复合抗压强度试验结果分别为737kPa,842kPa和707.7kPa。用MTT的细胞毒性试验结果显示出高于100%的细胞活力百分比。这意味着羟基磷灰石 - 胶原复合材料无毒。因此,所形成的样品具有符合骨植入候选者的资格。

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