Wabers H D, McCoy T J, Okkema A T, Hergenrother R W, Wolf M F, Cooper S L
Department of Chemical Engineering, University of Wisconsin, Madison 53706.
J Biomater Sci Polym Ed. 1992;4(2):107-33.
Sulfonate-containing polyurethanes were evaluated for in vivo biodegradation using subcutaneously implanted tensile bars. In addition, these anionically charged polyurethanes were evaluated for in vivo activation of human complement C3a and ex vivo platelet deposition in arteriovenously-shunted canines. The sulfonate derivatized polymers included laboratory synthesized polyurethane and Biomer. Other polymers used for references included Intramedic polyethylene, Silastic and a poly(ethylene oxide) based polyurethane. The biodegradation results indicated that Biomer and the laboratory sulfonated Biomer (both manufactured with stabilizers), remained mechanically stable, retaining both tensile strength and elasticity after 4 weeks of subcutaneous implantation. The unstabilized polyurethanes (with or without sulfonation), however, showed marked cracking and a loss of mechanical properties after the same period of subcutaneous implantation. Sulfonated polyurethanes depressed human complement C3a activation in plasma, as indicated by decreased levels of anaphylatoxin production. The results of canine ex vivo blood contacting experiments were conducted in both an acute and chronic model and demonstrated decreased platelet deposition and activation for the sulfonated polyurethanes.
使用皮下植入的拉伸棒对含磺酸盐的聚氨酯进行体内生物降解评估。此外,对这些带负电荷的聚氨酯进行了人体补体C3a体内激活和动静脉分流犬体内血小板沉积的体外评估。磺酸盐衍生化聚合物包括实验室合成的聚氨酯和Biomer。用于参考的其他聚合物包括医用级聚乙烯、硅橡胶和聚环氧乙烷基聚氨酯。生物降解结果表明,Biomer和实验室磺化Biomer(均添加稳定剂制造)在皮下植入4周后仍保持机械稳定性,同时保留拉伸强度和弹性。然而,未添加稳定剂的聚氨酯(无论有无磺化)在相同皮下植入期后均出现明显开裂并丧失机械性能。磺化聚氨酯可降低血浆中人体补体C3a的激活,表现为过敏毒素产生水平降低。犬体内血液接触实验的结果在急性和慢性模型中均进行了研究,结果表明磺化聚氨酯可减少血小板沉积和激活。