Landes Constantin, Ballon Alexander, Ghanaati Shahram, Ebel Daniel, Ulrich Dieter, Spohn Uwe, Heunemann Ute, Sader Robert, Jaeger Raimund
Oral, Craniomaxillofacial and Plastic Facial Surgery, The Center of Surgery, Goethe University Medical Centre, Frankfurt, Theodor-Stern-Kai 7, 60596 Frankfurt am Main, Germany.
Fraunhofer Institute for Mechanics of Materials IWM, Wöhlerstraße 11, 79108 Freiburg, Germany.
Open Biomed Eng J. 2013 Nov 29;7:133-46. doi: 10.2174/1874120701307010133. eCollection 2013.
The fatigue performance of explanted in-situ degraded osteofixations/osteosyntheses, fabricated from poly (70L-lactide-co-24DL-lactide-6-trimethylane-carbonate or PLDLLA-TMC) copolymer was compared to that of virgin products. The fatigue test was performed on 21 explants retrieved from 12 women and 6 men; 16-46 years by a custom-designed three-point bend apparatus using a staircase method and a specified failure criterion (an increase of the deflection of the specimen > 1 mm) with run-out designated as "no failure" after 150,000 loading cycles. While all the virgin products showed run-out at 38N, all of the specimens fabricated from explants failed at this load level. For the explant specimens, although there was a trend of decreased failure load with increased in-situ time, this decrease was pronounced after 4 months in-situ, however, not yet statistically significant, while a 6-month in-situ explant had significantly less failure load. Three and four month in-situ explants had highly significant differences in failure load between measurements close and distant to the osteotomy line: p=0.0017 (the region of maximum load in-situ). In the virgin products, there were only traces of melt joining and cooling, left from a stage in the manufacturing process. For the implants retrieved after 4.5 months in-situ, the fracture surfaces showed signs of degradation of the implants, possibly caused by hydrolysis, and for those retrieved after 9 months in-situ, there were cracks and pores. Thus, the morphological results are consistent with those obtained in the fatigue test. The present results suggest that resorbable osteofixations fabricated from PLDLLA-TMC are stable enough to allow loading of the healing bone and degrade reliably.
将由聚(70L-丙交酯-co-24DL-丙交酯-6-三甲基碳酸酯或PLDLLA-TMC)共聚物制成的取出的原位降解骨固定物/骨合成物的疲劳性能与原始产品进行了比较。对从12名女性和6名男性(年龄16 - 46岁)身上取出的21个植入物进行了疲劳测试;使用定制的三点弯曲装置,采用阶梯法和指定的失效标准(试样挠度增加>1mm),在150,000次加载循环后,将未失效指定为“无失效”。虽然所有原始产品在38N时均未失效,但所有由取出的植入物制成的试样在此载荷水平下均失效。对于取出的植入物试样,尽管存在随着原位时间增加失效载荷降低的趋势,但这种降低在原位4个月后才明显,不过尚未具有统计学意义,而原位6个月的取出植入物的失效载荷明显更低。原位3个月和4个月的取出植入物在靠近和远离截骨线处的测量失效载荷存在高度显著差异:p = 0.0017(原位最大载荷区域)。在原始产品中,仅留有制造过程中一个阶段的微量熔体连接和冷却痕迹。对于原位4.5个月后取出的植入物,断裂表面显示出植入物降解的迹象,可能是由水解引起的,而对于原位9个月后取出的植入物,则存在裂缝和孔隙。因此,形态学结果与疲劳测试中获得的结果一致。目前的结果表明,由PLDLLA-TMC制成的可吸收骨固定物足够稳定,能够承受愈合骨骼的负荷并可靠地降解。