Increased oxidative stability of orthopedic implants can be achieved by adding an antioxidant, such as Vitamin E (VE) to UHMWPE[1]. The effect of shelf live and accelaterated aging in combination with shelf live on antioxidative effectiveness of VE needs to be investigated to better understand the long-time behavior of VE-blended UHMWPE in an oxidative environment. Currently, IR techniques provide detection limits as low as 0.05 %w/w[2], also it is known that thermo analytical techniques can push the limit of detection down to 10 ppm[3]. The goal of this study was to quantify VE in UHMWPE powder and compression molded UHMWPE with 11 different VE concentrations using FTIR and DSC techniques and to establish respective regression curves. GUR 1050 UHMWPE resin (Ticona, Germany) was blended with VE (DSM, Netherlands) to the following target concentrations (%w/w): 0.01, 0.02, 0.05, 0.1, 0.25, 0.35. Concentrations of 0.001, 0.002, 0.003, 0.004, 0.005 were obtained by mixing of the 0.1 powder with virgin GUR 1050 powder. VE-free GUR 1050 was used as reference. Samples of blended resin were compression molded in a low oxygen environment atmosphere at Zimmer Inc. (Warsaw, IN). Subsequently the blocks were microtomed, creating films with a thickness of 200µm for each concentration. The VE concentration was measured using infrared (IR) spectroscopy (BioRad FT6000). The ratios were calculated by normalizing the integrated ether C-O(R) signal (1232cm−1 to 1275cm−1) and the integrated hydroxyl C-O(H) signal (1190cm−1 to 1228cm−1) using the twisting CH bond (1980cm∗∗∗∗∗ to 2100cm−1) as reference peak area. Oxidative induction time (OIT) at 200°C was measured according to ASTM D 3895–98 using blended and mixed powder samples.Introduction
Methods & Materials
