Oral Ebru, Wannomae Keith K, Hawkins Nathaniel, Harris W H William H, Muratoglu O K Orhun K
Orthopaedic Biomechanics and Biomaterials Laboratory, Department of Orthopaedic Surgery, Massachusetts General Hospital, 55 Fruit Street, GRJ 1206, Boston, MA 02114, USA.
Biomaterials. 2004 Nov;25(24):5515-22. doi: 10.1016/j.biomaterials.2003.12.048.
Longevity of total joints has been compromised by wear and fatigue of ultrahigh molecular weight polyethylene (UHMWPE) components. Crosslinking reduces UHMWPE wear, but combined with postirradiation melting, also reduces its fatigue strength, therefore limiting its use in high-stress applications. We hypothesized that a lipophilic antioxidant (alpha-tocopherol, alpha-T) can protect UHMWPE against oxidation eliminating the need for postirradiation melting of crosslinked UHMWPE and improve its fatigue strength. To test these hypotheses, 65- and 100-kGy irradiated, alpha-T-doped and subsequently gamma-sterilized UHMWPE were used. (I) alpha-T-doped irradiated UHMWPEs showed significantly lower oxidation levels (0.48+/-0.25 and 0.44+/-0.06) compared to 100-kGy irradiated UHMWPE (3.74+/-0.16) after 5 weeks of accelerated aging at 80 degrees C in air. (II) Wear rate of alpha-T-doped irradiated UHMWPE (1.9+/-0.5, and 0.9+/-0.1mg/million cycles (MC) for 65- and 100-kGy irradiated UHMWPE, respectively) were comparable to that of 100-kGy irradiated/melted UHMWPE (1.1+/-0.7mg/million cycles). (III) The stress intensity factor at crack inception ( DeltaKi) of 100-kGy irradiated UHMWPE increased significantly upon doping with alpha-T from 0.74 to 0.87MPam(1/2) ( p<0.01 ). The DeltaKi for the 100-kGy irradiated and melted UHMWPE, currently in clinical use, was 0.55MPam(1/2). Doping with alpha-T eliminated the need for postirradiation melting to protect irradiated UHMWPE against long-term oxidation. The fatigue strength was improved by 58% for alpha-T-doped 100-kGy irradiated UHMWPE compared to irradiated and melted UHMWPE. The increase in oxidative stability of alpha-T-doped UHMWPE is attributed to the ability of alpha-T to react with peroxy free radicals on lipid chains and arrest the oxidation reactions. The improved fatigue strength is attributed to the increase in plasticity of UHMWPE due to the lipophilic nature of alpha-T.
超高分子量聚乙烯(UHMWPE)部件的磨损和疲劳降低了全关节的使用寿命。交联可减少UHMWPE的磨损,但与辐照后熔融相结合时,也会降低其疲劳强度,因此限制了其在高应力应用中的使用。我们假设一种亲脂性抗氧化剂(α-生育酚,α-T)可以保护UHMWPE免受氧化,从而无需对交联的UHMWPE进行辐照后熔融,并提高其疲劳强度。为了验证这些假设,使用了经65 kGy和100 kGy辐照、掺杂α-T并随后进行γ灭菌的UHMWPE。(I)在80℃空气中加速老化5周后,与100 kGy辐照的UHMWPE(3.74±0.16)相比,掺杂α-T的辐照UHMWPE的氧化水平显著更低(分别为0.48±0.25和0.44±0.06)。(II)掺杂α-T的辐照UHMWPE的磨损率(65 kGy和100 kGy辐照的UHMWPE分别为1.9±0.5和0.9±0.1mg/百万次循环(MC))与100 kGy辐照/熔融的UHMWPE(1.1±0.7mg/百万次循环)相当。(III)100 kGy辐照的UHMWPE在掺杂α-T后,裂纹萌生时的应力强度因子(ΔKi)从0.74显著增加至0.87MPam(1/2)(p<0.01)。目前临床使用的100 kGy辐照并熔融的UHMWPE的ΔKi为0.55MPam(1/2)。掺杂α-T无需进行辐照后熔融即可保护辐照后的UHMWPE免受长期氧化。与辐照并熔融的UHMWPE相比,掺杂α-T的100 kGy辐照的UHMWPE的疲劳强度提高了58%。掺杂α-T的UHMWPE氧化稳定性的提高归因于α-T与脂质链上的过氧自由基反应并阻止氧化反应的能力。疲劳强度的提高归因于α-T的亲脂性使UHMWPE的可塑性增加。