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International Journal of Bioprinting                      3D-printed biodegradable metals for bone regeneration




            3.3. Three-dimensional printing of BMs by          adhesives. 101,102  In addition, the wide selection of materials
            material extrusion                                 suitable for BJ enables the fabrication of components
            Material extrusion is also commonly known as 3D plotting   with appropriate mechanical strength by adjusting the
            or 3D gel printing. When applied to metals, the “ink”   materials used, such as magnesium–zinc alloy, magnesium
            made by mixing a metal powder with a binder is extruded   phosphate, and 316L stainless steel. 103-105  The microstructure
            through a nozzle during printing and stacked layer by layer   and mechanical properties of the components fabricated
            to obtain the initial finished product.  The preliminary   using BJs change with respect to the sintering temperature.
            product is then degreased and heat-treated to remove the   By using the appropriate heat treatment temperature and
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            binder, resulting in a metal component.  The most obvious   holding time, components with a density, compressive
            benefit of ME over other approaches is that products can   properties,  and an  elastic  modulus  similar to  those  of
            be processed and printed at room temperature; this not   human cortical bone and with appropriate porosity can be
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            only reduces vaporization, sputtering, and oxidation of the   obtained.  Physical properties similar to those of human
            metal but also allows the incorporation of materials that   bone tissue can provide support while minimizing stress
            are not resistant to high temperatures into the component.   shielding for bone regeneration. 106-108
            The equipment costs for ME are also lower than those for   3.5. Three-dimensional printing of BMs by
            other printing methods. The disadvantages of ME include   3D weaving
            the poor mechanical properties of the components,   In addition to traditional 3D printing methods, several
            rough surface of the products, possible distortion of the   new printing techniques have achieved excellent results.
            component structure during subsequent heat treatment,   For example, 3D weaving magnesium wires, in which
            possible presence of adhesive residues, and limited material   magnesium alloy filaments are woven in a fixed sequence
            selection. By choosing a lower extrusion temperature and   and structure supplemented by filler wires, can create
            layer thickness, it is possible to achieve a relatively smooth   magnesium implants with porous structures.   This
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            component surface and improve the precision. 97    method does not require heat treatment, and the mechanical
               Material extrusion can use high-purity magnesium   properties of the components are significantly improved
            powder as a raw material, while other printing methods,   after being covered with a polylactic acid (PLA) coating
            such as PBF and DED, cannot easily be applied to pure   with  appropriate  mechanical  strength.  The  structural
            magnesium due to vaporization during the printing   properties, including porosity, pore size, and connectivity,
            process.  The use of appropriate binders and methods   of the components fabricated using 3D braiding are
            such as short-term liquid-phase sintering can create   more  controllable  than  those  of  components  fabricated
            porous magnesium scaffolds with high porosity and high   by any other printing method, but this method has the
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            structural fidelity to support the regeneration of bone   disadvantages of difficult fabrication and high cost.  The
            tissue.  Furthermore, surface modification of porous   excellent connectivity of 3D woven components provides
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            magnesium scaffolds can reduce the degradation rate. 99,100    excellent support for cell attachment and spreading and
            A high porosity provides a pathway for bone growth into   provides pathways for neovascularization, which in turn
            the scaffold, and a reduced degradation rate provides time   promotes bone regeneration. 110
            for bone regeneration, while magnesium has properties
            such as osteogenic activity and pro-vascularization that   4. Selection of BM materials for 3D printing
            can enhance the effect of bone regeneration. 23,30,31  The main BM materials that can be used as implants are
                                                               magnesium, zinc, iron, and their alloys. Table 2 and Figure 3
            3.4. Three-dimensional printing of BMs by a        show the advantages, disadvantages, mainstream 3D
            binder jet                                         printing technologies, common alloys, implants, and
            The BJ manufacturing process is similar to that of PBF in   applications of these three BMs.
            that both use a powder bed for feeding; the difference is
            that PBF uses a laser or electron beam to sinter the metal   4.1. Magnesium and its alloys
            powder, whereas BJ binds the metal powder by directional   The Young’s modulus of magnesium-based alloys is
            spraying of a liquid binder or by relying on capillary forces.   similar to that of bone cancellous mass, and the density
            After the initial printing, the constructs are heat-treated   of magnesium and its alloys is also close to that of human
            to remove the adhesive and increase their mechanical   bone, which is favorable for eliminating the stress masking
            strength.  Binder jetting has the following advantages: (i)   of  magnesium  implants. 111,112   Moreover,  the  degradation
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            printing can be performed at room temperature, (ii) the   products of magnesium  in vivo, magnesium ions, are
            components are supported during the printing process,   biologically active and can directly induce osteoblast
            and (iii) the components can be printed without the use of   proliferation while promoting CGRP release from

            Volume 10 Issue 3 (2024)                        44                                doi: 10.36922/ijb.2460
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