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International Journal of Bioprinting         The biological properties of WE43 scaffolds via the oxidative heat strategy



            very important to find a more suitable bone substitute.   oxide to the metal consumed to create the metal oxide. A
            Some artificial bone materials, such as calcium phosphate   PBR less than 1 indicates that the metal oxide has weak
            and  calcium  sulfate  bone  cements,  can  fill  bone  defects   passivation, while a PBR larger than 2 indicates that the
            but lack biological activities, e.g., osteoinduction and   oxide is easily peeled off and that the passivation is poor.
            durable mechanical support . External fixator distraction   When the PBR is greater than 1 and less than 2, the metal
                                  [3]
            osteogenesis  can repair  defects  of  the  diaphysis  of the   oxide has a significant passivation effect and may create a
            extremities, but the repair may take a long time and it   protective layer to prevent corrosion of the matrix metal.
            is difficult to repair the metaphysis due to anatomical   The oxidation of magnesium can generate MgO with a PBR
            mismatch . In recent years, 3D printing technology has   of 0.81, which cannot slow its degradation rate , while the
                    [4]
                                                                                                   [16]
            been used to prepare medical implants and biological   PBR values of Nd O , Y O  and Gd O  are 1.0584, 1.1923,
                                                                                           2
                                                                                    3
                                                                               3
                                                                                  2
                                                                             2
                                                                                             3
            organs , which can make prostheses personalized to the   and 1.29, respectively [17,18] . Moreover, Y, Nd, and Gd are
                 [5]
            patient, achieve good anatomical shape matching, and   more reactive than Mg, so they preferentially react with
            control the elastic modulus by adjusting the printing   oxygen at high temperatures, forming a thin oxide layer on
            parameters (structures, porosity, etc.) to repair large-  the surface. At present, microarc oxidation and phosphate
            segment bone defects and achieve the desired clinical   coating  of  magnesium  alloys  have  been  widely  studied,
            effect [6,7] . However, currently, 3D printing still uses Ti6Al4V   which can indeed significantly slow down the degradation
            as the main component. Due to its nonabsorbability, the   rate of magnesium alloys [19,20] . However, the complicated
            relative stability between bone and prosthesis and the long-  process requires the use of specific instruments. For porous
            term effects of stress conduction are uncertain and remain   structures, it is not easy to use microarc oxidation to
            to be observed [8,9] . A bone defect filling material with overall   uniformly modify the surface of prostheses. In our previous
            strong support, osteoinductive ability, and biodegradability   studies , oxidation heat treatment is a very cost-effective
                                                                    [21]
            over time is urgently needed in the treatment of bone   and simple passivation method. Under a high-temperature
            defects in limbs with 3D-printed prostheses.       oxidizing atmosphere, the degradable magnesium alloy
               Among biodegradable bioactive metals, magnesium   undergoes a controllable oxidation reaction, and on the
            and  magnesium  alloys  have  broad application  prospects   surface, a thick layer of passivation will eventually develop,
            in orthopedic repair and reconstruction. The compression   which effectively isolates magnesium alloy and body fluid
            screw MAGNEZIX® developed by Syntellix AG, with    and slows the degradation rate of magnesium alloy medical
                                                                                               [22]
            the magnesium alloy WE43 as the main component, has   implants in  a body fluid environment . However, no
            been successfully applied in clinical practice, e.g., fracture   literature has investigated the effects of thermal oxidation
            fixation, and it presents biodegradable and osteogenic   treatment on the biocompatibility, and osteogenic
            properties . Magnesium is an element that is required for   properties of magnesium alloys. Therefore, in this work,
                    [10]
            the proper functioning of the human body and is involved   thermal oxidation-treated WE43 magnesium alloy and
            in a large variety of different biological processes. The   as-printed WE43 were used to explore the differences in
            beneficial role of magnesium ions in the development of   biocompatibility and osteogenic properties.
            bone has been proven in a number of in vivo and in vitro
            studies, and it has been found that magnesium alloys can   2. Materials and methods
            increase the expression of alkaline phosphatase (ALP)   2.1. Scaffold manufacturing and oxidation
            in osteoblasts [11-13] . For example, Li et al. showed that the   heat treatment
            number of osteoblasts around magnesium alloy implants   The scaffold was facilitated with laser powder bed fusion
            was significantly increased compared to the number   (L-PBF) using a compact L-PBF machine (BLT S210,
            around titanium implants . He  et al. used different   China). The WE43 powder was prepared using centrifugal
                                  [14]
            concentration gradients (0–3 mM) of magnesium ions   atomization (Tangshan Weihao, China). The powder was
            to culture human osteoblasts in vitro and found that the   composed of 3.87% Y, 2.24% Nd, 1.16% Gd, 0.39% Zr, and
            proliferative and osteogenic effects of magnesium ions on   residual Mg (in mass). The scaffolds were created with a
            osteoblasts increased with increasing concentration .  pore size of 800 μm and a porosity of 60.0% as per design.
                                                     [15]
               However, the rapid degradation rate of WE43     The scaffold manufacturing protocol has been reported
                                                                       [23]
            magnesium alloy is a hindrance to its clinical application.   previously . The scaffolds used in our experiments were
            Whether the oxide generated by metal oxidation can   cylindrical with the sheet gyroid structure and the strut
            reduce the pace of WE43 magnesium alloy deterioration   size is 600 μm. The size was Ф10 mm × 10 mm. A 1-h
            depends on the Pilling–Bedworth’s ratio (PBR). PBR is   preheating at 200°C was performed on the WE43 powder
            used to quantify the passivation impact of metal oxides,   bed before the melting process. The processing chamber for
            which is defined as the volumetric ratio of the surface   the L-PBF process was filled with argon that had a purity


            Volume 9 Issue 3 (2023)                         95                         https://doi.org/10.18063/ijb.686
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