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




            printing methods for magnesium and magnesium alloys   The remaining methods, such as atomic layer deposition
            mainly include PBF, ME, BJ, and 3D weaving. 3D-printed   (ALD), magnetron sputtering, or sandblasting, may delay
            regenerated magnesium phosphate implants can ensure   degradation while decreasing biocompatibility as well as
            the stability and recovery of hip joint dysplasia,  and   cracking and uneven degradation. 148,149
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            3D-printed polycaprolactone/magnesium porous scaffolds   The addition of other elements and the choice of
            can promote bone defect repair in the early stages and have   different manufacturing methods can also improve the
            good cell compatibility.  Porous 3D-printed Mg Nd Zn Zr   properties of alloys. For example, the addition of aluminum
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            (referred to as JDBM) implants possess good mechanical   to zinc-based alloys enhances the antimicrobial activity
            properties, are compatible with MC3T3-E1 and RAW267.4   of the components, but aluminum is also cytotoxic and
            cells, and prevent implant infections. 134         may  cause  inflammation. 150,151   The  addition  of titanium,

            4.2. Zinc and its alloys                           copper, magnesium, manganese, lithium, and other
            While pure zinc has a low tensile strength (20 MPa) and   metal elements to zinc can delay component corrosion.
            is usually not used in the manufacture of implants, zinc   Currently, the most studied zinc-based alloys are Zn–xMg
            alloys can achieve tensile strengths of 200–600 MPa, which   and Zn–xAl alloys, which, when prepared by appropriate
            satisfy the requirements for bone implants. 16,135,136  The main   fabrication methods, such as plasma sintering (MASPS)
            advantage of zinc alloys is that their biodegradation rate   to  control  the  porosity  of  the  components,  can  improve
                                                               the mechanical properties while reducing the degradation
            is between that of magnesium- and iron-based alloys and   rate. 152-154  Zn–Mg alloy scaffolds have great potential in
            is closest to the ideal biodegradation rate; this allows zinc   the treatment of load-bearing bone defects. On the one
            alloys to provide effective support for bone defect healing   hand, zinc and magnesium play important roles in bone
            before  complete degradation  and to  avoid  secondary   metabolism  and  are  conducive  to  cell  proliferation  and
            damage from stress interruption after healing. Second, zinc   bone tissue regeneration; on the other hand, Zn–Mg alloys
            ions are involved in bone formation and mineralization and   can avoid the production of hydrogen gas, severe pH
            can accelerate bone defect healing by activating Runx2 and   fluctuations, and rapid corrosion after injection. Moreover,
            Osterix  to  promote  osteoblast  differentiation,  inhibiting   Mg  is  added  to  the  Zn  matrix  to  provide  nucleation
            RANKL to reduce osteoclastogenesis, and promoting   sites and promote the production of secondary Mg2Z11
            citrate deposition. 137-139  Zinc also has a proangiogenic   phases, leading to grain refinement and strengthening.
            effect, which guarantees good blood circulation during   The synergistic effect of solid solution strengthening and
            bone regeneration. Moreover, zinc has strong antimicrobial   precipitation strengthening endows Zn–Mg alloys with
            activity with some anti-infective effects, providing a stable   unique advantages in the treatment of orthopedic diseases,
            immune microenvironment for bone regeneration. 140  helps avoid chronic inflammatory reactions caused by
               The disadvantages of zinc include its low biocompatibility   permanent implantation, and removes the need for
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            and high manufacturing  difficulty.  Excessive release of   additional surgeries.  At present, scholars have focused
            zinc ions during degradation results in cytotoxicity and   mainly on the mechanical properties, wear resistance,
            attenuates osteoblastic activity, decelerating the healing   fatigue resistance, corrosion resistance, degradation
            of bone defects. 141-144  Furthermore, zinc has a lower   behavior, microstructure, and other directions of Zn–
            melting point than magnesium, and although zinc does   Mg alloys. By introducing specific  metals or nonmetal
            not react with air, it is difficult to convert into porous   elements, improving preparation methods, programming
            structures due to vaporization and sputtering during   degradation behavior, etc., Zn–Mg alloys can be modified
            processing. 145,146  Retarding the corrosion of zinc-based   to improve their bone regeneration potential. 156,157
            alloys by surface modification, adding different elements   Magnesium–zinc alloys are the most biocompatible,
            or improving the alloy manufacturing process can improve   and the mechanical properties of these alloys can be
            the properties of these alloys. Surface modifications such   significantly improved by adjusting the Zn–Mg ratio. The
            as microarc oxidation (MAO) can regulate the oxidation   Mg–Zn alloy components molded by hot extrusion using
            of zinc and improve its biocompatibility, but there is still   a casting process have a low degradation rate and good
            a certain degree of cytotoxicity, and the degradation rate   mechanical strength.  However, whether the alloy phase
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            is far greater than that of pure zinc, deviating from the   of a component is uniformly distributed has an important
            ideal  biodegradation  rate.   Additionally,  biomimetic   impact on its mechanical properties and corrosion form,
                                  142
            deposition  can  improve  biocompatibility.  Immersing  the   and if a uniform distribution cannot be achieved during
            components in SBF solution for 14 days can result in the   the manufacturing process, the component may suffer
            formation of a protective layer of corrosion products, which   from  mechanical  strength  degradation,  localized  pitting
            can delay corrosion and improve cytocompatibility.    corrosion, and other problems. 159-162  However, how to
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            Volume 10 Issue 3 (2024)                        47                                doi: 10.36922/ijb.2460
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