Porous surfaces on orthopaedic implants have been shown to promote tissue ingrowth. This study evaluated biological fixation of novel additively manufactured porous implants with and without hydroxyapatite coatings in a canine transcortical model. Laser rapid manufacturing (LRM) Ti6Al4V cylindrical implants were built with a random interconnected architecture mimicking cancellous bone (5.2 mm diameter, 10mm length, 50–60% porous, mean pore size 450μm). Three groups were investigated in this study: as-built with no coating (LRM), as-built coated with solution precipitated hydroxyapatite (LRM-PA), and as-built coated with a plasma sprayed hydroxyapatite (LRM-PSHA). Implants were press-fit into a 5mm unicortical, perpendicular drill hole in the femoral diaphysis of the left and right femurs in 12 canines. Right femora were harvested for histology (SEM, bone ingrowth into implant within cortical region) and left femora for mechanical push-out testing (shear strength of bone-implant interface) at 4 and 12 weeks (N=6, un-paired Student's t-test, p=0.05). For mean bone ingrowth, there was no significant difference between groups at 4 weeks (LRM, LRM-PA, LRM-PSHA: 41.5+8.6%, 51+5.5% and 53.2+11%, respectively) or 12 weeks (LRM, LRM-PA, LRM-PSHA: 64.4+2.8%, 59.9+7.6%, 64.9+6.4%, respectively). LRM and LRM-PA implants had more bone ingrowth at 12 weeks than 4 weeks (p < 0 .05). Mean shear strength of all implants at 12 weeks (LRM, LRM-PA, LRM-PSHA: 39.9+3.6MPa, 33.7+4.6MPa, 36+4.1MPa respectively) were greater than at 4 weeks (LRM, LRM-PA, LRM-PSHA: 21.6+2.8MPa, 20.7+1.1MPa, 20.2+2.5MPa respectively) (p < 0 .05). No significant difference was observed between all groups at 4 or 12 weeks. Overall, this canine study confirmed the suitability of this novel additive manufacturing porous material for biological fixation by bone ingrowth. All implants exhibited high bone ingrowth and mechanical shear strength in this canine model. No difference was observed between uncoated and hydroxyapatite coated implants.
To characterize the intracellular penetration of osteoblasts and osteoclasts by methicillin-resistant Time-lapse confocal microscopy was used to analyze the interaction of MRSA strain USA300 with primary murine osteoblasts and osteoclasts. The effects of early and delayed antibiotic treatments on intracellular and extracellular bacterial colony formation and cell death were quantified. We tested the effects of cefazolin, gentamicin, vancomycin, tetracycline, rifampicin, and ampicillin, as well as agents used in surgical preparation and irrigation.Aims
Methods
The purpose of this study was to evaluate the biological fixation of a 3D printed porous implant, with and without different hydroxyapatite (HA) coatings, in a canine model. A canine transcortical model was used to evaluate the characteristics of bone ingrowth of Ti6Al4V cylindrical implants fabricated using laser rapid manufacturing (LRM). At four and 12 weeks post-implantation, we performed histological analysis and mechanical push-out testing on three groups of implants: a HA-free control (LRM), LRM with precipitated HA (LRM-PA), and LRM with plasma-sprayed HA (LRM-PSHA).Aims
Materials and Methods
Mechanical properties of irradiated Ultra High Molecular Weight Polyethylene (UHMWPE) after aging have been well documented. However there was no sufficient data for the dimensional change due to irradiation and aging. This change may have adverse effects to the implant modular locking mechanism. The purpose of this study was to characterize the dimensional change of UHMWPE after irradiation and aging. Total (30) ø15mm × 50mm virgin GUR 1050 UHMWPE rods were cleaned, dried, inspected, vacuum packaged and stored in 20°C environment for 2 days. Among them, (20) samples were measured along the 50mm length at 20°C +/-2°C before and after two conditions: 1, (10) were submerged in 40°C DI water for 2 hours and dried in 40°C to simulate the cleaning process and 2, (10) were soaked in 37°C saline for 14 days to simulate initial in-vivo environment. Remaining (10) samples were measured in the same way after irradiation of 30KGy dosage and then measured again after soaking in 37°C saline for 14 days to simulate the actual radiation sterilization and in-vivo soaking conditions. Same samples were measured once more after accelerated aging per ASTM-1980-07 for 80 days to simulate the 3 year in vivo life. The differences in measurements between virgin and end conditions were documented as the percentage dimensional change. After the measurements, in the groups of DI water, saline soaking and radiation + aging, (3) samples were randomly selected for DSC measurements. The results were compared with dimensional measurements. Statistical analysis was performed by the student t test to compare virgin condition and the conditions after each treatment. 95% significance level was assumed.Introduction
Materials and Method
Antioxidant containing UHMWPE particles induced similar levels of in vitro macrophage proliferation and in vivo inflammation in the mouse air pouch model as UHMWPE particles alone. Benefit of antioxidant in reducing wear particle induced inflammation requires further investigation. Wear particles derived from UHMWPE implants can provoke inflammatory reaction and cause osteolysis in the bone, leading to aseptic implant loosening. Antioxidants have been incorporated into UHMWPE implants to improve their long term oxidative stability. However it is unclear if the anti-inflammatory property of the antioxidant could reduce UHMWPE particle induced inflammation. This study evaluated the effect of cyanidin and vitamin E on UHMWPE induced macrophage activation and mouse air pouch inflammation.Summary Statement
Introduction
The solvent extraction step applied in conventional oxidation measurement protocols for UHMWPE retrievals resulted in an elevated oxidation index (OI) in remelted highly cross-linked UHMWPE (RM-HXLPE). The present study seeks to confirm the effect of solvent extraction on OI measurement and to understand the relationships among soak-aging, fluid uptake, and resulting OI from various test protocols. Two materials were tested, representing legacy gamma-in-air sterilized (GammaAir-PE, GUR4150, 30 kGy) and remelted highly cross-linked (RM-HXLPE, GUR1050, 100 kGy, 147°C/5h) UHMWPE. Concave discs approximately 19 millimeters (mm) in diameter and 3 mm in dome thickness were machined from both materials prior to soak-aging. Soak-aging consisted of a combination of: (1) ASTM F2003 accelerated aging (5 atm O2, 70 °C for 14 days), and (2) either static soaking (SS, for 11.57 days) or dynamic load-soaking (LS, 2280 N at 1 Hz for 1 million cycles) in bovine synovial fluid at 37 °C to simulate the combination of shelf and in-vivo aging, respectively. Unsoaked samples were used as control (C) group. Thin films (150 μm) were harvested from cross-sections of all groups and were subjected to two solvent extraction protocols using Sohxlet (Heptane for 6 h (HEP6) or Hexane for 16 h (HEX16)) prior to be analyzed by two OI analyses using Fourier transform infrared spectroscopy (FTIR). FTIR analyses (128 scans/spectra, 4 cm−1 resolution) were carried out using both peak height at and peak area centering 1714 cm−1 for OI and 1734 for fluid uptake index (FI); carbon-carbon vibration at 1368 cm−1 was used for normalization. All GammaAir-PE data was further normalized using prewash control while RM-HXLPE data used computed results. The paired t-test was used with a significance level of p < 0.05.Introduction:
Materials and Methods:
