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首页> 外文期刊>Journal of Materials Science. Materials in Medicine >Screening biomaterials with a new in vitro method for potential calcification: Porcine aortic valves and bovine pericardium
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Screening biomaterials with a new in vitro method for potential calcification: Porcine aortic valves and bovine pericardium

机译:使用新型体外钙化方法筛选生物材料:猪主动脉瓣和牛心包膜

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Calcification is still a major cause of failure of implantable biomaterials. A fast and reliable in vitro model could contribute to the study of its mechanisms and to testing different anticalcification techniques. In this work, we attempted to investigate the potential calcification of biomaterials using an in vitro model. We purposed to test the ability of this model to screening possible anticalcification efficacy of different biomaterials. Porcine heart valve (PAV) and bovine pericardial (BP) tissues, fixed with glutaraldehyde were immersed into biological mimicking solution, where the pH and the initial concentrations of calcium and phosphoric ions were kept stable by the addition of precipitated ions during calcification. Kinetics of calcification was continuously monitored. The evaluation of biomaterials was carried out by comparing the kinetic rates of formation of calcific deposits. After 24 h, the calcific deposits on PAVs were found to be developed at significant higher rates (ranged from 0.81 x 10~(-4)-2.18x 10~(-4)mol/min m~2) than on BP (0.19 x 10~(-4)-0.52 x 10~(-4)mol/min m~2) (one-way ANOVA, p < 0.05) depending on the experimental conditions (supersaturation of the solution). Parallel tests for similar biomaterials implanted subcutaneously in animal (rat) model showed after 49 days that significant higher amounts of total minerals deposited on PAV (236.73 + -139.12, 9 animals mg minerals/g dry net tissue) (mean +- standard deviation) compared with that formed on BP (104.36 +- 79.21, #9 mg minerals/g dry net tissue) (ANOVA, p < 0.05). There is evidence that in vitro calcification was correlated well with that of animal model and clinical data.
机译:钙化仍然是植入式生物材料失败的主要原因。快速而可靠的体外模型可能有助于研究其机理并测试不同的抗钙化技术。在这项工作中,我们尝试使用体外模型研究生物材料的潜在钙化。我们旨在测试该模型筛选不同生物材料可能的抗钙化功效的能力。将用戊二醛固定的猪心脏瓣膜(PAV)和牛心包(BP)组织浸入生物模拟溶液中,在钙化过程中通过添加沉淀离子使pH值以及钙和磷离子的初始浓度保持稳定。持续监测钙化动力学。通过比较钙化沉积物形成的动力学速率来进行生物材料的评估。 24小时后,发现PAV上的钙质沉积物以比BP(0.19)高得多的速率(范围为0.81 x 10〜(-4)-2.18x 10〜(-4)mol / min m〜2)形成。 x 10〜(-4)-0.52 x 10〜(-4)mol / min m〜2)(单向ANOVA,p <0.05)取决于实验条件(溶液过饱和)。皮下植入动物(大鼠)模型中的相似生物材料的平行测试显示,在49天后,沉积在PAV上的总矿物质含量明显更高(236.73 + -139.12,9动物mg矿物质/ g干净组织)(平均值+-标准差)与BP形成的相比(104.36 +-79.21,#9 mg矿物质/ g干净组织)(ANOVA,p <0.05)。有证据表明,体外钙化与动物模型和临床数据具有很好的相关性。

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