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Preparation, characterization, and blood compatibility of polyurethanes derived from aliphatic diisocyanates and polycarbonate urethane

机译:脂肪族二异氰酸酯和聚碳酸酯氨基甲酸酯衍生的聚氨酯的制备,表征和血液相容性

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Introduction: In this study, to obtain biomedical polyurethane elastomers with good mechanical properties and biocompatibily ,a series of polycarbonate urethanes were synthesized via a two-step solution of polymerization method using the poly(1,6-hexanediol)carbonate diols (PCDL) as the soft segment, 4,4'-methylenebis(cyclohexyl isocyanate) (H_(12)MDI). 1,6-hexamethylene diisocyanate (HDI) and 1,4-butanediol (BDO) as the hard segment with dibutyltin dilaurate as the catalyst. In this article, we illustrated the physical behaviors were obviously influenced by synthetic routes. And their chemical and physical structures were investigated by GPC.DSC,FT-IR and mechanical properties tests .The surface wettability were studied by contact angle measurement (CA). A comparative analysis was made between the commercial medical polyurethane materials and the synthesized materials, showing the poly(carbonate-urethane) elastomers were better in mechanical properties . Finally, the results of the hemolysis and platelet adhesive tests were recorded by spectrophotometer and SEM, indicating the materials were in accordance with the standard for biomaterials. Materials and Methods: The polyurethane films can be easily synthesized via a two-step reaction using PCDL and diisocyanate coupled with a chain extender BDO.And all the reagents added to the reacting round-bottomed flask were dissolved in DMAc or DMF. After that, the mixture was cast into a beaker for precipitation, with ether-water solution in it. And then the polymer was placed in Soxhlet extrator using deionized water as extracing agent for removing small molecules for at least 24h. And then, after being dissolved in THF (7.5 wt%) with stirring at 800 r/min for 2 h, the polyurethane solution was placed in a vacuum oven at 45°C. Finally, in order to keep the surface of the polyurethane flat, the prepared polymer solution was put in homemade molds carefully for drying at room temperature. The tests on mechanical properties could be carried out after drying in the vacuum oven at 40 °C for at least 5 days. Results and Discussion: The polycarbonate polyurethane films have been successfully synthesized and the results of CA measurement indicated H12MDI-PUs were better in hydrophobic property. As for mechanical properties showed in, the series of polyurethane films were better than Pellethane 2363-80A did, especially for H_(12)MD11.5-PU. It displayed tensile strength of less than 10 MPa and showed the best properties in elongation getting about 850% at break. The results of the hemolytic tests indicated the materials were in accordance with the standard for biomaterials and the SEM pictures of platelet adhesion experiment in showed there were little platelet adhering to the polyurethane films. In order to get more advantages as a kind of short-term biomaterial, we'll concentrated on doing some researches to enhance the hydrophobicity and improve the biocompatibility without reducing the mechanical properties. Conclusion: In this article, the physical properties of our prepared polymers were even better in flexibility and elongation at break after the comparison with a commercial biomedical polyurethane. Our ongoing work have demonstrated that H_(12)MDM ,5-PU has great potential in biomedical field. In order to get better applications as a candidate for elastic biomedical material, some modifications are still should be made to improve their biocompatibility.
机译:简介:为了获得具有良好机械性能和生物相容性的生物医学聚氨酯弹性体,采用聚(1,6-己二醇)碳酸二醇(PCDL)为原料,通过两步聚合法合成了一系列聚碳酸酯聚氨酯。软链段4,4'-亚甲基双(环己基异氰酸酯)(H_(12)MDI)。 1,6-六亚甲基二异氰酸酯(HDI)和1,4-丁二醇(BDO)作为硬链段,以二月桂酸二丁基锡为催化剂。在本文中,我们说明了物理行为显然受到合成路线的影响。并通过GPC,DSC,FT-IR和力学性能测试研究了它们的化学和物理结构。通过接触角测量法(CA)研究了表面润湿性。对商用医用聚氨酯材料与合成材料进行了比较分析,结果表明聚碳酸酯-氨基甲酸酯弹性体的机械性能更好。最后,通过分光光度计和SEM记录了溶血和血小板粘附性测试的结果,表明材料符合生物材料标准。材料和方法:使用PCDL和二异氰酸酯与扩链剂BDO偶联,可通过两步反应轻松合成聚氨酯膜,并将添加到反应的圆底烧瓶中的所有试剂溶解在DMAc或DMF中。此后,将混合物倒入烧杯中进行沉淀,并在其中加入乙醚水溶液。然后使用去离子水作为萃取剂将聚合物放入索氏萃取器中至少24小时,以去除小分子。然后,在800r / min的搅拌下将其溶于THF(7.5wt%)中2小时后,将聚氨酯溶液置于45℃的真空烘箱中。最后,为了保持聚氨酯表面平坦,将制备的聚合物溶液小心地放入自制模具中,以在室温下干燥。机械性能测试可以在真空烘箱中于40°C干燥至少5天后进行。结果与讨论:成功地合成了聚碳酸酯聚氨酯薄膜,CA测量结果表明H12MDI-PUs的疏水性更好。至于所显示的机械性能,该系列聚氨酯膜优于Pellethane 2363-80A,特别是对于H_(12)MD11.5-PU。它显示出小于10 MPa的拉伸强度,并显示出最佳的伸长率特性,断裂时达到850%左右。溶血试验的结果表明该材料符合生物材料的标准,并且血小板粘附实验的SEM照片显示几乎没有血小板粘附到聚氨酯膜上。为了获得作为一种短期生物材料的更多优势,我们将集中精力进行一些研究,以增强疏水性并提高生物相容性而不降低机械性能。结论:在本文中,与市售生物医学聚氨酯相比,我们制备的聚合物的物理性能在柔韧性和断裂伸长率方面甚至更好。我们正在进行的工作表明,H_(12)MDM,5-PU在生物医学领域具有巨大的潜力。为了获得更好的应用作为弹性生物医学材料的候选者,仍应进行一些修改以提高其生物相容性。

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