Magnesium-Alloy for Orthopedic Application: Long Term Evaluation on Bone Compatibility and Degradation Under In Vivo Environment
Introduction
Bone resorption around stress-shielded area in bone fixation treatments is an important consideration within clinical sectors. To reduce the effect, a secondary surgery is usually required to remove the fixation devices after healing has completed Li [1]. This procedure may create additional surgical risks to the patient Beaupre et al. [2,3]. A biodegradable fixation device is a possible solution to counter this situation Li [1]. Among all the degradable biomaterials, magnesium alloy with its unique mechanical properties of metal has an advantage in fixation operation. Li [1,4- 7] Magnesium and its alloys possess similar elastic modulus (41–45 GPa) and density (1.72–1.84 g cm-3) to that of bones (15–25 GPa; 1.8–2.1 g cm-3) Staiger et al. [8], making them more bone friendly than other metal-based alloys with higher density. Magnesium ion, the major degradation product, is tolerable by human body in considerable amount Trumbo et al. [9], with no toxic byproduct formed during the degradation process Li et al. [1,4,5]. Furthermore, magnesium implants have shown to stimulate new bone formation when used as bone fixture Witte et al. [10]. In this study, two magnesium-alloys with low and high zinc composition, namely LZnMg and HZnMg, were put under in-vivo evaluation inside the femur of S.D rats. Degradation rate and bone compatibility of the alloys were monitored online with micro CT within an 24 weeks duration [11-15].
Results
Degradation Behavior
The degradation process of the implant is visualized by 3D reconstruction images, as shown in Figure 1. The differences in the remaining volume and the degradation behaviors were already distinguishable at early stage (1 month) of the experiment. By week 4 there was an obvious volume loss in pure Mg implants [16-20]. The average volume was reduced by an average of 45% from its original volume [21,22]. In comparison, an average loss of only 4% is recorded in LZnMg implants while the structure remained almost unchanged except the formation of small and shallow pits on the surface [23-25]. For the H, Zn, Mg implants, over half of the implant volume was lost within 4 weeks and there was obvious change in implant dimensions. A sharp reduction in implant volume in week 16 was found in Mg group, while fragmentation of implant begins at week 6 in the H, Zn, Mg group. On the contrary, little dimension change could be detected inside LZnMg groups throughout the 24 weeks period. Degradation of LZnMg remained slow throughout the 24 weeks period. There was increasing amounts of small and shallow surface pits with an overall intact structure [26-30]. Overall, the degradation process in pure Mg implants was relatively uniform compared to H, Zn, Mg until the shape decreases in volume after week 12. For H, Zn, Mg, the implants generally disintegrate into small pieces by week 12 and completely degraded within 16 weeks.
Surrounding Tissue Response
Newly grown cortical bone could be found in all samples, as seen in Figure 2. Soft bone callus was found above the pure Mg and H, Zn, Mg implants. For the pure Mg group, bone callus appeared between week 3 and week 4, and a gap was observed between the cortical bone and the drill hole. These gaps, together with the drill holes, were eventually filled by the new cortical bone at later stage of healing (Figure 3). In the H, Zn, Mg group, bone callus was found between week 3 and week 8 [31-35]. The rate of new bone formation was not fast enough to cover the loss of implant volume. After complete degradation, the drill holes could still be observed until week 20. At the end of the experiment, there was an increase in thickness of the cortical bone. A small pit could sometimes be found on the surface of the femur. No callus formation could be observed with LZnMg implantation. Thin layers of new cortical bones were found around the implant instead.
Calcified tissue could be found proliferating around the implant at around week 5 of the experiment, which was considerably earlier than other experimental groups [36,37]. Nevertheless, the degradation process was not completed, and the implants could still be found occupying the drill hole at week 24. New bone growth is indicated by the light shallow area around the operation area. Gas capsule is seen around the implant indicated by the dark empty space. Histological staining indicated that there were close contact between bone and pure magnesium implant residues. New bones could grow around the implant material, as shown in Figure 3. Similar observation was found in samples with LZnMg implants, where new bones could grow around and make close contact with the implanted material. The drill hole was still occupied by the implant in this experimental group due to the much slower degradation rate [38-40].
In the experimental group implanted with H, Zn, Mg, the implant completely degraded after 24 weeks. In both experimental groups with magnesium alloy implants, dark particles are found near the implant site under histological sections (Figure 3). The implant or the drill hole can still be seen clearly on the femurs of most samples. Toluidine Blue O staining of the cross-sections (side view: b, e, h; top view: c, f, i) of the implants and bones harvested at week 24. Black circles in (b) indicate the filled gaps and drill holes by new cortical bone. Red circles in (f, i) indicate particles/debris located near the operation area in experimental groups implanted with magnesium-alloys [40-43].
Conclusion
Degradation process and bone compatibility of magnesium can be modified with Zn/Mn alloying. The LZnMg alloy in this presented study can provide good structural integrity throughout a 24 weeks implantation in the femur of rat models. The alloy can also allow the formation of a close bone-implant interface, with new bone formation next to and around the implant. All these findings demonstrated the LZnMg alloy’s potential as the basial material of an new orthopaedics fixation device. Evaluation on toxicity measurement and biomechanical properties during the degradation is suggested for further investigation.
Acknowledgement
The work described in this paper was partially supported by the Research Committee of the Hong Kong Polytechnic University (Project No. G-YBRL) and the Small Project Funding of the University of Hong Kong (Project No. 201309176011).
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