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      In vitro and in vivo degradation behavior of Mg–2Sr–Ca and Mg–2Sr–Zn alloys

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          Abstract

          Magnesium alloys with integration of degradability and good mechanical performance are desired for orthopedic implants. In this paper, Mg–2Sr–Ca and Mg–2Sr–Zn alloys were prepared and the degradation as well as the bone response were investigated. Compared with the binary Mg–2Sr alloys, the addition of Ca and Zn improved the in vitro and in vivo corrosion resistance. Mg–2Sr–Ca and Mg–2Sr–Zn alloys exhibited more uniform corrosion and maintained the configuration of the implants 4 weeks post-implantation. The in vivo corrosion rates were 0.85 mm/yr for Mg–2Sr–Zn and 1.10 mm/yr for Mg–2Sr–Ca in comparison with 1.37 mm/yr for Mg–2Sr. The in vitro cell tests indicated that Mg–2Sr–Ca and Mg–2Sr–Zn alloys exhibited higher MG63 cell viability than Mg–2Sr alloy. Furthermore, these two alloys can promote the mineralization and new bone formation without inducing any significant adverse effects and this sound osteogenic properties suggest its attractive clinical potential.

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          Highlights

          • The in vitro and in vivo corrosion of Mg–2Sr–Ca and Mg–2Sr–Zn alloys were improved than that of Mg–2Sr alloys.

          • The Mg–2Sr–Ca and Mg–2Sr–Zn alloys showed promoted MG63 cell viability and high alkaline phosphatase activity.

          • The Mg–2Sr–Ca and Mg–2Sr–Zn alloys promoted new bone formation and show good osteogenic performance.

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          Most cited references45

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          Biodegradable metals

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            The development of binary Mg-Ca alloys for use as biodegradable materials within bone.

            Binary Mg-Ca alloys with various Ca contents were fabricated under different working conditions. X-ray diffraction (XRD) analysis and optical microscopy observations showed that Mg-xCa (x=1-3 wt%) alloys were composed of two phases, alpha (Mg) and Mg2Ca. The results of tensile tests and in vitro corrosion tests indicated that the mechanical properties could be adjusted by controlling the Ca content and processing treatment. The yield strength (YS), ultimate tensile strength (UTS) and elongation decreased with increasing Ca content. The UTS and elongation of as-cast Mg-1Ca alloy (71.38+/-3.01 MPa and 1.87+/-0.14%) were largely improved after hot rolling (166.7+/-3.01 MPa and 3+/-0.78%) and hot extrusion (239.63+/-7.21 MPa and 10.63+/-0.64%). The in vitro corrosion test in simulated body fluid (SBF) indicated that the microstructure and working history of Mg-xCa alloys strongly affected their corrosion behaviors. An increasing content of Mg2Ca phase led to a higher corrosion rate whereas hot rolling and hot extrusion could reduce it. The cytotoxicity evaluation using L-929 cells revealed that Mg-1Ca alloy did not induce toxicity to cells, and the viability of cells for Mg-1Ca alloy extraction medium was better than that of control. Moreover, Mg-1Ca alloy pins, with commercial pure Ti pins as control, were implanted into the left and right rabbit femoral shafts, respectively, and observed for 1, 2 and 3 months. High activity of osteoblast and osteocytes were observed around the Mg-1Ca alloy pins as shown by hematoxylin and eosin stained tissue sections. Radiographic examination revealed that the Mg-1Ca alloy pins gradually degraded in vivo within 90 days and the newly formed bone was clearly seen at month 3. Both the in vitro and in vivo corrosion suggested that a mixture of Mg(OH)2 and hydroxyapatite formed on the surface of Mg-1Ca alloy with the extension of immersion/implantation time. In addition, no significant difference (p>0.05) of serum magnesium was detected at different degradation stages. All these results revealed that Mg-1Ca alloy had the acceptable biocompatibility as a new kind of biodegradable implant material. Based on the above results, a solid alloy/liquid solution interface model was also proposed to interpret the biocorrosion process and the associated hydroxyapatite mineralization.
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              Fundamentals and advances in magnesium alloy corrosion

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                Author and article information

                Contributors
                Journal
                Bioact Mater
                Bioact Mater
                Bioactive Materials
                KeAi Publishing
                2452-199X
                25 February 2020
                June 2020
                25 February 2020
                : 5
                : 2
                : 275-285
                Affiliations
                [a ]Key Laboratory for Biomechanics and Mechanobiology of Ministry of Education, School of Biological Science and Medical Engineering, Beihang University, Beijing, 100083, China
                [b ]Beijing Advanced Innovation Centre for Biomedical Engineering, Beihang University, Beijing, 100083, China
                [c ]The Department of Orthopedics, ZhongDa Hospital, School of Medicine, Southeast University, Nanjing, 210009, China
                [d ]Department of Orthopaedics and Traumatology, The Chinese University of Hong Kong, Hong Kong National Research Center for Rehabilitation Technical Aids, Beijing, 100176, China
                [e ]Department of Materials Science and Engineering, College of Engineering, Peking University, Beijing, 100871, China
                [f ]National Research Center for Rehabilitation Technical Aids, Beijing, 100176, China
                Author notes
                []Corresponding author. School of Biological Science and Medical Engineering, Beihang University, Beijing, 100083, China. xngu@ 123456buaa.edu.cn
                [∗∗ ]Corresponding author. School of Biological Science and Medical Engineering, Beihang University, Beijing, 100083, China. yubofan@ 123456buaa.edu.cn
                [1]

                The authors contribute equally to this work.

                Article
                S2452-199X(20)30037-2
                10.1016/j.bioactmat.2020.02.014
                7044521
                32128466
                77f2c51b-9166-47e3-8ebd-c3bc0b1ad528
                © 2020 Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 15 January 2020
                : 19 February 2020
                : 19 February 2020
                Categories
                Article

                magnesium alloys,degradation,in vivo test,biocompatibility,orthopedic implants

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