Daniels A U, Andriano K P, Smutz W P, Chang M K, Heller J
Orthopedic Bioengineering Laboratory, University of Utah School of Medicine, Salt Lake City.
J Appl Biomater. 1994 Spring;5(1):51-64. doi: 10.1002/jab.770050108.
Recent reports describe an unfavorable noninfective inflammatory response to acidic degradation products in clinical applications of bone fixation devices fabricated from bulk hydrolyzing polyglycolides and polylactides (PGA and PLA). The work described here suggests that poly(ortho esters) (POEs) offer an alternative. By comparison, hydrophobic POEs degrade predominately via surface hydrolysis, yielding first a combination of nonacidic degradation products, followed by alcoholic and acidic products gradually over time. POE specimens proved acutely nontoxic in United States Pharmacopeia tests of cellular, intracutaneous, systemic, and intramuscular implant toxicity. Hot-molded specimens degraded slowly in saline, retaining 92% initial stiffness (1.6 GPa flexion) and retaining 80% initial strength (66 MPa flexion) in 12 weeks. Degradation was almost unaffected by decreasing saline pH from 7.4 to 5.0. This demonstrated the relative hydrophobicity of POEs, since incorporation of small amounts of acid within the polymer markedly increases the degradation rate. Degradation rates were increased substantially by dynamic mechanical loading in saline. This may be true for other degradable polymers also, but no data could be found in the literature. Presumably, tensile loading opens microcracks, allowing water to enter. Solvent cast POE films were strong in tension (30 + MPa tensile yield) and reasonably tough (12-15% elongation to yield). Higher molecular weight films (41-67 kDa) showed no degradation in mechanical properties after 31 days in physiological buffer at body temperature. A 27-kDa film offered similar initial strength and stiffness but began showing mechanical degradation at 31 days. The films showed a decrease in weight with exposure time but no change in either molecular weight or water absorption at 31 days, further supporting the observation that POE degrades by surface hydrolysis rather than by bulk hydrolysis.
最近的报告描述了在由大量水解聚乙交酯和聚丙交酯(PGA和PLA)制成的骨固定装置的临床应用中,对酸性降解产物产生的不良非感染性炎症反应。此处所述的研究表明聚原酸酯(POE)提供了一种替代方案。相比之下,疏水性POE主要通过表面水解降解,首先产生非酸性降解产物的组合,随后随着时间的推移逐渐产生醇类和酸性产物。在美国药典的细胞、皮内、全身和肌肉植入毒性测试中,POE标本被证明具有急性无毒性。热成型标本在盐水中降解缓慢,在12周内保持92%的初始刚度(1.6 GPa弯曲)和80%的初始强度(66 MPa弯曲)。将盐水pH值从7.4降至5.0时,降解几乎不受影响。这证明了POE的相对疏水性,因为在聚合物中加入少量酸会显著提高降解速率。在盐水中进行动态机械加载可大幅提高降解速率。这可能对其他可降解聚合物也适用,但文献中未找到相关数据。据推测,拉伸加载会打开微裂纹,使水得以进入。溶剂浇铸的POE薄膜具有较高的拉伸强度(30 + MPa拉伸屈服强度)和一定的韧性(12 - 15%伸长率至屈服)。较高分子量的薄膜(41 - 67 kDa)在体温下于生理缓冲液中放置31天后,机械性能未出现降解。一种27 kDa的薄膜具有相似的初始强度和刚度,但在31天时开始出现机械降解。这些薄膜的重量随暴露时间减少,但在31天时分子量和吸水率均无变化,进一步支持了POE通过表面水解而非本体水解进行降解的观察结果。