| Literature DB >> 36091459 |
Rui Wang1, Shilei Ni2, Li Ma3, Meihua Li1.
Abstract
Titanium and titanium alloy implants are essential for bone tissue regeneration engineering. The current trend is toward the manufacture of implants from materials that mimic the structure, composition and elasticity of bones. Titanium and titanium alloy implants, the most common materials for implants, can be used as a bone conduction material but cannot promote osteogenesis. In clinical practice, there is a high demand for implant surfaces that stimulate bone formation and accelerate bone binding, thus shortening the implantation-to-loading time and enhancing implantation success. To avoid stress shielding, the elastic modulus of porous titanium and titanium alloy implants must match that of bone. Micro-arc oxidation technology has been utilized to increase the surface activity and build a somewhat hard coating on porous titanium and titanium alloy implants. More recently, a growing number of researchers have combined micro-arc oxidation with hydrothermal, ultrasonic, and laser treatments, coatings that inhibit bacterial growth, and acid etching with sand blasting methods to improve bonding to bone. This paper summarizes the reaction at the interface between bone and implant material, the porous design principle of scaffold material, MAO technology and the combination of MAO with other technologies in the field of porous titanium and titanium alloys to encourage their application in the development of medical implants.Entities:
Keywords: Micro-arc oxidation (MAO); Ti-based materials; implants; osteogenesis; porous; surface modification
Year: 2022 PMID: 36091459 PMCID: PMC9452912 DOI: 10.3389/fbioe.2022.973297
Source DB: PubMed Journal: Front Bioeng Biotechnol ISSN: 2296-4185
FIGURE 1Different coating morphologies were formed by micro-arc oxidation, (A) Micropores of unequal size, (B) Cortex-like structure, (C) Bioactive ions coatings developed.
Porosity and pore size of 3D printed titanium scaffold for bone regeneration (pore size is expressed as range or average pore size).
| Fabrication technique | Pore size range | Porosity | Type of study | Optimum pore size | References |
|---|---|---|---|---|---|
| SLM | 500–1200 μm |
| 500 μm |
| |
| SLM | 300 μm, 600 μm, 900 μm | 65% |
| 600 μm |
|
| SLM | 700 μm | orientated perpendicularly in all three spatial directions |
| 700 μm |
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| SLM | 400 μm, 700 μm, 900 μm | 70% |
| 600–700 μm |
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| 70%–90% | |||||
| EBM | 800 μm, 900 μm, 1000 μm | 86.30%–94.22% |
| 1000 μm |
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FIGURE 2Surface treatment methods of titanium substrate and factors affecting micro-arc oxidation.
MAO treatment of titanium and its alloys with different electrolyte compositions.
| Different electrolyte systems | Electrolyte composition | Substrate | Surface morphology | Results of XRD | Outcome | References |
|---|---|---|---|---|---|---|
| Silicate electrolyte system | Na2 (EDTA), CaO and Ca(H2PO4)2, H2O | Pure titanium | Porous microstructure, the pore size is around 1–5 μm | Anatase and rutile | Grows fast and corrodes fast in SBF solution |
|
| Na2SiO3·9H2O, (NaPO3)6, NaAlO2 | Ti6Al4V discs | Nano-scale TiO2 grains, of different size, ranging from several nm to tens nm | Rutile and a small amount of anatase TiO2 | The adhesion strength of coating interface is found to be about 70 MPa |
| |
| Sodium silicate (Na2SiO3·9H2O) and calcium glycerol phosphate (C3H7CaO6P) | Ti6Al4V alloys | Calcium phosphate electrolyte produces a thicker, more compact MAO layer than silicate | The silicate electrolyte consists of TiO2,SiO2, Ti3(PO4)4, TiP2O7, and the calcium phosphate electrolyte comprisingTiO2, CaO, CaTiO3, Ti3(PO4)4, TiP2O7 and Ca2P2O7 | The CaP apatites can integrate with human bone tissue and promote bone growth |
| |
| Phosphate electrolyte system | (NaPO3)6–NaF–NaAlO2 | Ti6Al4V alloy | As treatment duration increases, coating development slows and roughens | Anatase, rutile and AlPO4 phases | The adhesion strength of substrate/coating interface is about 40 MPa |
|
| β-glycerophosphate disodium salt pentahydrate and calcium acetate monohydrate | Pure titanium plates | Macro-porous, Ca- and P-containing titania-based films were formed on the titanium substrates | Rutile and anatase | Ca- and P-containing, micro-arc oxidized titanium implants have the capability to induce bone-like apatite |
| |
| CaCl2, KH2PO4 | Pure Ti | MAO micro-arcs decrease when CaCl2 concentration increases, while nanocrystals grow | XRD patterns didn’t show anatase or rutile titania (TiO2) production | First, a single MAO coating procedure was proposed to generate crystalline HAP coatings on Ti substrates |
| |
| Citric acid, ethylene diamine, and ammonium phosphate | Ti6Al4V alloy | An HA crystalline peak could not be detected by XRD | Coated with TiO2 film and hydroxyapatite | Improved bioactivity, cell adhesion, and viability while retaining film-substrate bonding |
| |
| H2SO4-H3PO4 | Pure titanium and Ti6Al4V | Ti6Al4V has a cortical morphology with irregular worm-like slots, unlike MAO/Ti | MAO films were successfully produced on pure Ti and Ti6Al4V materials at 180 V. MAO substantially improved the corrosion resistance of untreated materials |
| ||
| Na3PO4 and K3PO4 | Pure titanium | K3PO4 electrolyte’s oxide layer was rougher than Na3PO4’s | Anatase and rutile crystalline phases | Attachment and multiplication of osteoblast cells to K3PO4’s oxide layer were better than in Na3PO4 |
| |
| Aluminate electrolyte system | Aluminate solution | Ti6Al4V alloy | After MAO treatment, Ti6Al4V substrate microstructure is unaltered and no hardening zone is identified | TiO2 rutile and TiAl2O5 compounds | Nanohardness and elastic modulus rise from coating surface to inside |
|
| NaAlO2 electrolyte | Pure titanium | Increasing NaAlO2 lowers micropores, increases the quantity and size of sintered disks, and roughens the surface | Mainly composed of TiO2, rutile and anatase | The surface of the coating is rough, and the corrosion rate first decreases and then increases |
| |
| Sodium tetraborate electrolyte system | Na2B4O7·10H2O | Pure titanium slices | Cortex-like layers with pores and slots | Mostly rutile | Cortex-like coatings with interior pores and slots are more wettable than volcanic coatings |
|
| Li2B4O7,Na2B4O7 and K2B4O7 | Pure titanium disks | Novel “cortex-like” micro/nano dual-scale structured TiO2 coating | Rutile with a little anatase | Promotes stem cell adhesion, spreading, and differentiation, and leads to excellent osseointegration |
| |
| Phytic acid | Phytic acid, KOH, EDTA-Na2, Ca(CH3COO)2 | Ti6Al4V plates | Typically porous structure | Anatase- TiO2,rutile-TiO2 and perovskite-CaTiO3 phases | Porous TiO2 ceramic layer containing calcium and phosphate was prepared by MAO on Ti6Al4V alloy |
|
| EDTA-ZnNa2, KOH, and phytic acid | Ti6Al4V plates | Typical porous structure | Anatase and rutile | MAO coating combines Zn and P, and phytic acid concentration impacts Zn and P content, which is beneficial |
| |
| NaOH and Na12Phy | Ti6Al4V | Typical porous structure and the pore size is about 3 μm in diameter | Anatase TiO2 | MTT tests showed good biocompatibility |
| |
| Phytic acid | Ti6Al4V alloys | Porous structure with tiny micropores and great hydrophilicity | Rutile, anatase, TiP2O7 as well as some OH- groups | MC3T3-E1 Pre-osteoblasts had excellent cytocompatibility in viability, adhesion, proliferation and differentiation |
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FIGURE 3Combined application of MAO and other treatment methods.
Combined application of MAO and other treatment methods.
| MAO combined with other treatments | Substrate | Surface morphology | Outcome | References |
|---|---|---|---|---|
| Combined application of MAO and hydrothermal method | 3D-printed Ti6Al4V scaffolding | Micro-nano hybrid coating with moderate roughness | Enhance biocompatibility, osteogenesis, and osseointegration |
|
| 3D Printed Macroporous Ti6Al4V Implants | Nanofibers on microporous walls | Improve three-dimensional porous Ti64 scaffold apatite |
| |
| Combined application of MAO and ultrasound | Ti6Al4V alloy | Homogenized coating structure | Improve corrosion and wear resistance of coating |
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| Combined application of MAO and laser | Ti6Al4V titanium alloy plate | Microgrooves reduce liquid-solid contact angle and boost surface roughness | Significantly increase the proliferation and differentiation of MC3T3-E1 cells |
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| Ti6Al4V alloy | Pores are uniformly distributed, tiny, and thick | Higher hardness and better wear resistance |
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| MAO and bacteriostatic treatment | Grade 4 quality Cp-Ti discs | Adding calcium, phosphorus, and silver ions | Improve antibacterial efficiency while maintaining biological activity |
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| Ti6Al4V titanium discs | Hydroxyapatite (HA) and Ag+ | Good antibacterial activity |
| |
| Commercially pure titanium | Micro-porous with pore diameters of 1–4 μm | Reduce planktonic bacteria and |
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| Ti6Al4V | Surface becomes smoother as pores get smaller and more average | Ti-MAO-Cu2O group has the strongest antibacterial ability |
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| Ti6Al4V plate | Porous, uneven microstructure | Reduced planktonic and bacterial adherence |
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| Commercial Ti6Al4V plates | Double-layer structure, outer amorphous, inner polycrystalline | Good antibacterial activity is related to its strong electronic storage capacity |
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| Combined application of MAO with sand blasting and acid etching | Titanium discs | Irregular valleys, micropores, and roughness | Enhanced biocompatibility, favourable for osteoblast differentiation |
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| MAO combined with other bioactive factors | 3D-printed 600 μm pore Ti6Al4V plate | A numerous homogenously distributed pores | Promote osteogenesis and angiogenesis |
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