Schubert M A, Wiggins M J, Schaefer M P, Hiltner A, Anderson J M
Department of Macromolecular Science, Case Western Reserve University, Cleveland, Ohio 44106, USA.
J Biomed Mater Res. 1995 Mar;29(3):337-47. doi: 10.1002/jbm.820290309.
As part of ongoing studies in polyurethane biostability and biodegradation, we have investigated an in vitro system to test strained poly(etherurethane urea) (PEUU). Recently, we utilized this system to reproduce in vivo stress cracking in strained Pellethane. In this study, strained PEUU was tested to determine whether it degrades through a common mechanism with Pellethane and to further examine the steps involved in this degradation. Biaxially strained PEUU elastomers were treated with an alpha 2-macroglobulin (alpha 2-Mac) protein solution followed by an oxidative H2O2/CoCl2 treatment. Characterization of the strained PEUU specimens was performed with attenuated total reflectance-Fourier transform infrared spectroscopy, scanning electron microscopy (SEM), electron spectroscopy for chemical analysis, and contact angle analysis. The results from these characterization techniques provide conclusive evidence that biodegradation of PEUU and Pellethane occurs through a common mechanism. Chemical changes to the PEUU include cleavage of the polyether soft segments and urethane linkages, leaving the hard segment domains unaffected. SEM analysis shows that this chain cleavage leads to the development of severe pitting and cracking of the PEUU surface. In addition, the in vitro degradation accurately reproduces the in vivo degradation chemically and physically. This result verifies that the primary species responsible for biodegradation of PEUUs, in vivo, are hydroxyl and/or hydroperoxide radicals. alpha 2-Mac pretreatment increases the rate of degradation compared to direct treatment in H2O2/CoCl2. As the PEUU soft segment chains are cleaved, the degradation products are extracted into the treatment solution or environment. Finally, a new biodegradation mechanism of PEUUs is presented that involves crosslinking of the polyether soft segments.
作为正在进行的聚氨酯生物稳定性和生物降解研究的一部分,我们研究了一种体外系统来测试应变聚(醚聚氨酯脲)(PEUU)。最近,我们利用该系统在应变的百利威弹性体中重现体内应力开裂。在本研究中,对应变的PEUU进行测试,以确定其是否通过与百利威相同的机制降解,并进一步研究这种降解所涉及的步骤。将双轴应变的PEUU弹性体先用α2-巨球蛋白(α2-Mac)蛋白溶液处理,然后进行氧化H2O2/CoCl2处理。用衰减全反射傅里叶变换红外光谱、扫描电子显微镜(SEM)、化学分析电子能谱和接触角分析对应变的PEUU试样进行表征。这些表征技术的结果提供了确凿的证据,证明PEUU和百利威的生物降解是通过相同的机制发生的。PEUU的化学变化包括聚醚软段和脲键的断裂,而硬段域不受影响。SEM分析表明,这种链断裂导致PEUU表面出现严重的点蚀和开裂。此外,体外降解在化学和物理上准确地重现了体内降解。这一结果证实,在体内负责PEUUs生物降解的主要物质是羟基和/或氢过氧化物自由基。与直接在H2O2/CoCl2中处理相比,α2-Mac预处理提高了降解速率。随着PEUU软段链的断裂,降解产物被提取到处理溶液或环境中。最后,提出了一种新的PEUUs生物降解机制,该机制涉及聚醚软段的交联。