Andriano K P, Daniels A U
Orthopedic Bioengineering Laboratory, Division of Orthopedic Surgery, University of Utah School of Medicine, Salt Lake City.
J Appl Biomater. 1992 Fall;3(3):191-5. doi: 10.1002/jab.770030305.
Preliminary experiments suggest pretreatment of absorbable crystalline, calcium-sodium-metaphosphate (CSM) microfibers with trimethoxy-based silane coupling agents yields a polysiloxane film barrier which protects the fiber surface from early dissolution due to water. Compared to thermoplastic poly(L-lactic acid) (PLLA) composites reinforced with untreated fibers, PLLA composites reinforced with a variety of silane pretreated microfibers showed increased mechanical properties, suggesting improved adhesion was achieved at the fiber/matrix interface. Unfortunately, the silane pretreated CSM/PLLA composite showed no increase in wet strength retention after short-term in vitro exposure. This may be due to plasticization from water entering the composite at areas of incomplete fiber wetting by the highly viscous molten PLLA. However, when a nonabsorbable, low viscosity unsaturated polyester thermoset resin was reinforced with methacryloxy-silane pretreated CSM microfibers, there was no decrease in flexural strength and less than a 10% decrease in flexural modulus after 7 days exposure to 7.4 pH Tris-buffered saline at 37 degrees C.
初步实验表明,用三甲氧基硅烷偶联剂对可吸收的结晶性偏磷酸钙钠(CSM)微纤维进行预处理,可产生一种聚硅氧烷薄膜屏障,该屏障可保护纤维表面免受因水导致的早期溶解。与用未处理纤维增强的热塑性聚(L-乳酸)(PLLA)复合材料相比,用各种硅烷预处理的微纤维增强的PLLA复合材料显示出机械性能提高,这表明在纤维/基体界面处实现了更好的粘附。不幸的是,硅烷预处理的CSM/PLLA复合材料在短期体外暴露后湿强度保持率没有增加。这可能是由于水在高粘性熔融PLLA不完全润湿纤维的区域进入复合材料导致的增塑作用。然而,当用甲基丙烯酰氧基硅烷预处理的CSM微纤维增强一种不可吸收的低粘度不饱和聚酯热固性树脂时,在37℃下暴露于pH值为7.4的Tris缓冲盐水中7天后,弯曲强度没有降低,弯曲模量降低不到10%。