Simmons Anne, Hyvarinen Jari, Odell Ross A, Martin Darren J, Gunatillake Pathiraja A, Noble Kathryn R, Poole-Warren Laura A
Graduate School of Biomedical Engineering, University of New South Wales, Sydney NSW 2052, Australia.
Biomaterials. 2004 Sep;25(20):4887-900. doi: 10.1016/j.biomaterials.2004.01.004.
The long-term biostability of a novel thermoplastic polyurethane elastomer (Elast-Eon 2 80A) synthesized using poly(hexamethylene oxide) (PHMO) and poly(dimethylsiloxane) (PDMS) macrodiols has been studied using an in vivo ovine model. The material's biostability was compared with that of three commercially available control materials, Pellethane 2363-80A, Pellethane 2363-55D and Bionate 55D, after subcutaneous implantation of strained compression moulded flat sheet dumbbells in sheep for periods ranging from 3 to 24 months. Scanning electron microscopy, attenuated total reflectance-Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy were used to assess changes in the surface chemical structure and morphology of the materials. Gel permeation chromatography, differential scanning calorimetry and tensile testing were used to examine changes in bulk characteristics of the materials. The results showed that the biostability of the soft flexible PDMS-based test polyurethane was significantly better than the control material of similar softness, Pellethane 80A, and as good as or better than both of the harder commercially available negative control polyurethanes, Pellethane 55D and Bionate 55D. Changes observed in the surface of the Pellethane materials were consistent with oxidation of the aliphatic polyether soft segment and hydrolysis of the urethane bonds joining hard to soft segment with degradation in Pellethane 80A significantly more severe than that observed in Pellethane 55D. Very minor changes were seen on the surfaces of the Elast-Eon 2 80A and Bionate 55D materials. There was a general trend of molecular weight decreasing with time across all polymers and the molecular weights of all materials decreased at a similar relative rate. The polydispersity ratio, Mw/Mn, increased with time for all materials. Tensile tests indicated that UTS increased in Elast-Eon 2 80A and Bionate 55D following implantation under strained conditions. However, ultimate strain decreased and elastic modulus increased in the explanted specimens of all three materials when compared with their unimplanted unstrained counterparts. The results indicate that a soft, flexible PDMS-based polyurethane synthesized using 20% PHMO and 80% PDMS macrodiols has excellent long-term biostability compared with commercially available polyurethanes.
使用体内绵羊模型研究了一种使用聚(氧化六亚甲基)(PHMO)和聚(二甲基硅氧烷)(PDMS)大分子二醇合成的新型热塑性聚氨酯弹性体(Elast-Eon 2 80A)的长期生物稳定性。在将应变压缩模塑平板哑铃皮下植入绵羊体内3至24个月后,将该材料的生物稳定性与三种市售对照材料Pellethane 2363-80A、Pellethane 2363-55D和Bionate 55D的生物稳定性进行了比较。使用扫描电子显微镜、衰减全反射傅里叶变换红外光谱和X射线光电子能谱来评估材料表面化学结构和形态的变化。使用凝胶渗透色谱、差示扫描量热法和拉伸试验来检查材料整体特性的变化。结果表明,基于柔软灵活的PDMS的测试聚氨酯的生物稳定性明显优于类似柔软度的对照材料Pellethane 80A,并且与两种较硬的市售阴性对照聚氨酯Pellethane 55D和Bionate 55D一样好或更好。在Pellethane材料表面观察到的变化与脂肪族聚醚软段的氧化以及连接硬段和软段的聚氨酯键的水解一致,Pellethane 80A中的降解明显比Pellethane 55D中观察到的更严重。在Elast-Eon 2 80A和Bionate 55D材料的表面上观察到非常微小的变化。所有聚合物的分子量都有随时间降低的总体趋势,并且所有材料的分子量以相似的相对速率降低。所有材料的多分散比Mw/Mn随时间增加。拉伸试验表明,在应变条件下植入后,Elast-Eon 2 80A和Bionate 55D中的拉伸强度增加。然而,与未植入未应变的对应物相比,所有三种材料的外植标本中的极限应变降低,弹性模量增加。结果表明,与市售聚氨酯相比,使用2