| Literature DB >> 35299643 |
Xiao Sheng1, Ao Wang1, Zhonghan Wang1,2, He Liu1,2, Jincheng Wang1,2, Chen Li1,2.
Abstract
With the development of three-dimensional (3D) printed technology, 3D printed alloy implants, especially titanium alloy, play a critical role in biomedical fields such as orthopedics and dentistry. However, untreated titanium alloy implants always possess a bioinert surface that prevents the interface osseointegration, which is necessary to perform surface modification to enhance its biological functions. In this article, we discuss the principles and processes of chemical, physical, and biological surface modification technologies on 3D printed titanium alloy implants in detail. Furthermore, the challenges on antibacterial, osteogenesis, and mechanical properties of 3D-printed titanium alloy implants by surface modification are summarized. Future research studies, including the combination of multiple modification technologies or the coordination of the structure and composition of the composite coating are also present. This review provides leading-edge functionalization strategies of the 3D printed titanium alloy implants.Entities:
Keywords: 3D-printed; implant interface; surface functionalization; surface modication; titanium alloy
Year: 2022 PMID: 35299643 PMCID: PMC8921557 DOI: 10.3389/fbioe.2022.850110
Source DB: PubMed Journal: Front Bioeng Biotechnol ISSN: 2296-4185
FIGURE 13D-printing of titanium alloy process diagram (A) 3D-printed customized implant data acquisition process (Sing et al., 2016). (B) Process chain for preparing orthopedic implants by 3D-printed technology (Sing et al., 2016). (C) Schematic diagram of powder bed process (Wang et al., 2017). (D) Lens process schematic diagram (Antolak-Dudka et al., 2019).
Summary of different implant manufacturing technologies, manufacturing principle, cost and personalization.
| Implant manufacturing technology | Manufacturing principle | Cost | Personalization | References |
| Machining | Using turning, milling and grinding ect. to form base material with specific shape | High | Poor |
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| Multipoint forming | Creating a mould that can be adapted to the part to be produced and thus it is not necessary to produce a mould for each individual part | Low | Poor |
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| NC machining | Using the control system sends out instructions to make the cutting tool make various movements that meet the requirements, and represent the shape and size of the workpiece in the form of numbers and letters for machining | High | Great |
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| 3D-printed technology | Firstly, the 3D image is obtained by CT scanning, then the raw material powder is deposited layer by layer by computer-controlled 3D printer, and finally the molten material is cast into a pre-designed 3D shape | Low | Great |
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Summary of surface modification technology, advantages and disadvantages.
| Surface modification technology | Advantages | Disadvantages | References |
| MAO | Low cost, simple equipment, easy operation, high coating efficiency, strong adhesion with base material, adapt to complex structures, high biological activity, high wear resistance | Reducing the fatigue strength of the base material |
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| Anodizing | Low cost, simple equipment, easy operation, high biological activity, form TiO2 nanotube structures, reduce bacterial adhesion | Reducing the fatigue strength of the base material, the coating quality is poor than MAO |
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| EPD | High-quality coatings, adapt to complex structures, precise controllable coating thickness | High temperature sintering is required when depositing specific materials |
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| CVD | High-quality coatings, adapt to complex structures | High cost, high equipment demand, high temperature environment required |
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| ALD | Precise thickness control, nano-precision coating, exceptional large-area uniformity, strong bonding strength, low growth temperature, excellent reproducibility | High cost, low working voltage, and slower coating production speed |
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| Alkali heating | Low cost, simple equipment, easy operation, high biological activity | The coating state cannot be accurately controlled |
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| LSE | Accurately control the 3D shape of the coating | High temperature environment required |
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| AIP | Strong adhesion with base material, low deposition temperature | High equipment demand |
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| Shot peening | Increase fatigue resistance and wear resistance of implant | May have certain cytotoxicity |
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| UNSM | Improving the yield strength and wear resistance | High equipment demand |
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| LBL | Low cost, simple equipment, easy operation, precise coating control | Poor adhesion with base material |
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| Hydrogel | Low cost, simple equipment, easy operation adapt to complex structures, excellent drug carrier | Poor adhesion with base material |
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SCHEME 1Surface modification technologies and biological functionalization of 3D-printed titanium alloy implants.
FIGURE 2Schematic diagram of chemical, physical, and biological surface modification technologies. (A) Implant surface microstructure produced by electrophoretic deposition (Surmeneva et al., 2019). (B) Microstructure of implant surface produced by laser peening (Soyama and Takeo, 2020). (C) Surface microstructures of implants produced by hydrogel packaging (Mieszkowska et al., 2020).
Summary of surface modification technology, coating constructing methods, and functions.
| Implantmaterial | 3D-printed method | Surface modificationtechnology | Coating materials | Function | References | ||||
| Ti6Al4V | SLM | MAO | Ag+, Sr, CaP, BMP-2, Vancomycin | MAO can produce micro-nano structures that promote osteogenesis on the implant surface, and different substances can be deposited by changing the electrolyte |
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| Ti6Al4V | SLM | Anodizing | Ag+, HA, MBG, MTANi | Anodic oxidation can form TiO2 nanotube structure on the surface of implants, which can be used as a carrier for a variety of drugs. |
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| Ti6Al4V | EBM | EPD | CaP, AgNPs, Vancomycin | Electrophoretic deposition can deposit solid particles suspended in solution on the implant surface to form a uniform coating |
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| Ti6Al4V | EBM | CVD | Quercitrin | CVD deposited gaseous substances on the implant surface to form uniform coatings, and prepared coatings with different functions by depositing different substances |
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| Ti6Al4V | EBM | ALD | AlN | ALD can deposit materials on the implant surface in the form of monatomic films, and there is a correlation between each layer of atomic films. |
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| Ti6Al4V | SLM | Alkali heating | Sr, HA, Ga | Alkali heating can form micro-nano surfaces with osteogenic induction ability on the implant surface. |
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| Pure Ti, Ti6Al4V | SLA, LES, SLM Laser cladding | LSE | Si3N4, CaP, TiN-TiB, SiC | LSE can form a coating with 3D shape on the substrate by controlling the movement of high-energy laser source. |
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| Ti6Al4V | SLM | AIP | Mg, Ti-Cu/Ti-Cu-N | AIP forms a coating with strong adhesion on the implant surface by plasma bombarding gas substances. |
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| Ti6Al4V | DMLS | Shot peening | No | Shot peening can produce a strengthening layer with high residual stress on the implant surface to improve the fatigue strength of the implant. |
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| NiTi | SLM | UNSM | No | UNSM produces plastic deformation by impacting the implant surface with ultrasonic and shot peening to improve the wear resistance and tensile strength of the implant. |
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| Pure Ti | SLM | LBL | Gelatin, Chitosan, BMP-2, Vancomycin Rifampicin | LBL can alternatively deposit different substances on the implant surface by means of molecular interaction to form a coating with complete structure, stable performance, and specific function. |
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| Ti6Al4V | EBM | Hydrogel | HA, Phloroglucinol, Simvastatin | Hydrogels can encapsulate different drugs in hydrogels and control the release of drugs through the degradation of hydrogels. |
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FIGURE 3LBL vancomycin and BMP-2-coated implants (Amin Yavari et al., 2020). (A) Schematic illustration of the layer-by-layer coating process. (B) The biocompatibility of the scaffold was analyzed 8 weeks after implantation, the porous Ti structures did not induce an adverse tissue response in any of the groups, shown by the absence of acute inflammation or fibrous encapsulation at the material-tissue interface. In the case of any LBL remnants, no acute inflammatory response was seen around the polymer. At the same time, we observed a high density of blood vessel formation. (C) Representative images of planktonic and adherent bacteria on the surfaces of different experimental groups. In the experimental group containing vancomycin, the number of bacteria was significantly less. (D) In the live death staining experiment, the surface of the implant was completely covered by living cells, and the surface coating had no inhibitory effect on cell adhesion and proliferation.
FIGURE 4Ti6Al4V alloy/GelMA hybrid implant with dual bionic features (GMPT) for bone defect repair (Ma et al., 2021). (A) Schematic illustrations of the biomimetic GMPT with dual-bionic features. (B) In situ implantation of PT and GMPT implants, micro-CT 3D reconstruction of PT and GMPT in critical radius defects of rabbits. The implants in GMPT group had higher osteogenic activity than uncoated implants, and the osteogenic ability of the 10% GMPT group was the strongest. (C) The fabrication process and characterization of GMPT. (D) Histological analysis of implant samples after 4 and 12 weeks in rabbit radius defect sites. The GMPT group showed thicker and higher number of trabeculae than the PT group at both weeks 4 and 12 (yellow arrows indicate the PT implant, white arrows indicate new bone, and green arrows reveal new vessels). The 10% GMPT group showed the best osteogenesis and angiogenesis ability.
FIGURE 5Ag+ coating of nanotubes prepared by anodic oxidation (Amin Yavari et al., 2016). (A) Schematic diagram of 3D-printed titanium alloy surface covered with nanotubes and carrying Ag+ to inhibit bacterial growth. (B) The inhibitory effect of different concentrations of Ag+ loaded on the implant surface on cell proliferation and adhesion. (C) SEM images of anodized porous titanium with the following parameters: 20 V, 3 h; 30 V, 2 h; 40 V, 3 h. (D) Antibacterial performance of AsM, NT, NT-0.02 Ag+, NT-0.1 Ag+, and NT-0.5 Ag+ against Staphylococcus aureus after 7 days. The first row corresponds to planktonic bacteria and the second row to adherent bacteria; the group with higher Ag+concentration had obvious antibacterial ability than the group with lower Ag+ concentration.
FIGURE 6A 3D-printed titanium cage combined with a drug-releasing system for in situ drug release and bactericidal action (Li Y et al., 2020). (A) The schematic illustration of a 3D-printed titanium cage coated with PVA-vancomycin for preventing surgical site infections (Berbel, Banczek et al.) after spine surgery. (B) Antibacterial evaluation of Ti-VH@PVA cages in vitro. The obvious bacteriostatic circle was observed with regard to Staphylococcus aureus and Staphylococcus epidermidis. (C) Evaluation of Ti-VH@PVA cages for preventing SSIs in vivo. With the extension of time, the infiltration of inflammatory cells decreased significantly in Ti-VH@PVA cage. Furthermore, the thickness of the discontinuous fibrous capsule between the trabecular bone and the Ti-VH@PVA cage increased. This indicates that Ti-VH@PVA cage has a significant inhibitory effect on Staphylococcus aureus.
FIGURE 7Osteogenic exosomes induce osteogenic differentiation (Zhai et al., 2020). (A) The schematic illustration of cell-free bone tissue regeneration by the stem cell-derived exosomes. (B) The characterization of the stem cell-derived exosomes. a) AFM and b) TEM showing the size and morphology of the exosomes derived from hMSCs. Scale bar: 200 nm. c) The size and concentration of the hMSCs-derived exosomes by the NanosightNS300. The inset is an image showing the snapshot of video tracking. d) The western blot analysis of the exosome derived from the pre-differentiated hMSCs and hMSCs. (C) Osteogenic differentiation of hMSCs by the osteogenic exosomes a) Immunofluorescence staining of osteogenic markers (COL-1, OPN) in hMSCs induced by osteogenic exosomes. b) Immunofluorescence staining of osteogenic markers (COL-1, OPN) in hMSCs induced by osteogenic medium. There was no significant difference between osteogenic exosomes treatment and osteogenic medium treatment, which proved the osteogenic induction function of osteogenic exosomes.
FIGURE 8Effect of UNSM treatment on 3D-printed NiTi alloy surface (Ma et al., 2017). (A) Schematic of the UNSM processing showing its effect on surface finish, subsurface porosity, and surface hardening. (B) Wear scars of untreated (a and b) samples and UNSM-treated (c and d) samples at 6,000 (a and c) and 24,000 (b and d) cycles. (C) Porosity distribution on the untreated surface and UNSM-treated surface. (D) a) Appearance of the AM NiTi samples before and after UNSM treatment; b) and c) show the optical images of the non-treated sample. d) and e) show the optical images of the UNSM-treated sample. The treated samples have better wear resistance and lower porosity than untreated samples.