Table 6.
Surface modification method | Substrate | Techniques and modified layer | Main layer structure | Layer thickness | Efficiency of the coating | Ref. |
---|---|---|---|---|---|---|
Organic coating | Pure Zn (99.9%) | Immersing in MPS for 30 min followed by dip-coating in PLLA solution at room temperature. | PLLA | 1–12 μm | Increased corrosion resistance in vitro and in vivo. Decreased cytocompatibility with signs of toxicity and active neointima. |
[222] |
Pure Zn foil (99.9%) | Immersing in the 2 mg/ml dopamine solution for 12 h. | Polydopamine | Improved cell viability of human dermal fibroblasts, human aortic smooth muscle cells and human aortic endothelial cells. | [221] | ||
Pure Zn foil (99.9%) | Zn foils were incubated in the 2 mg/ml dopamine solution for 12 h. A 100 μm-thickness section of gelatin was produced, and affixed to the dopamine-coated Zn foil by bringing them into contact. Gelatin-covered foils were then immersed in 10 mM EDC in 90% ethanol for 20 min to cross-link the gelatin. | Polydopamine/gelatin | Improved cell viability of human dermal fibroblasts, human aortic smooth muscle cells and human aortic endothelial cells. | [221] | ||
Zn–1Mg | Zn–1Mg plates were immersed in 1 mol/L NaOH solution for 0.5 h at 60 °C. Then, they were immersed in 2 mL silane hydrolysate solution for 12 h at 37 °C. Next, the samples were immersed in 2 mL of 1 mol/L glutaraldehyde for 12 h at 37 °C. Finally, they were immersed in 2 mg/ml phosphorylcholine chitosan copolymer solution for 12 h. | APTES/phosphorylcholine chitosan copolymer | Increased corrosion resistance. Excellent hemocompatibility with hemolysis rate below 0.2%. Improved cell attachment and proliferation of human umbilical vein endothelial cells. |
[225] | ||
Air oxidation | Pure Zn wire (>99.99%) | 350 °C for 1 and 2 h in a regular furnace in air. | ZnO | 0.3–1.4 μm | [223] | |
Electropolishing | Pure Zn wire (>99.99%) | 0.25 A/cm2, 10 V, 2 min, electrolyte: 885 ml ethanol, 100 ml butanol, 109 g AlCl3·6H2O, 250 g ZnCl2, 120 ml H2O. | 0.06–0.08 (+0.05–0.15) μm | [223] | ||
Pure Zn (99.99%) | 0.45 A, ~90s, electrolyte: 885 m L C2H5OH, 100 mL C4H9OH, 109 g AlCl3·6H2O , 250 g ZnCl2. |
A 22% failure rate in vivo (2 out of 9 samples), with 44% of the observations meeting the full biocompatibility benchmarks. | [226] | |||
Anodization | Pure Zn wire (>99.99%) | I. Electropolishing: 0.25 A/cm2, 10 V, 2 min, electrolyte: 885 ml ethanol, 100 ml butanol, 109 g AlCl3·6H2O, 250 g ZnCl2, 120 ml H2O. II. Anodization ~4 A, 10 V, 1 min, electrolyte: 1 L oxalic acid (0.1, 0.3 or 0.5 M) solution. |
ZnO | 5–10 μm | [223] | |
Pure Zn (99.99%) | I. Electropolishing: 0.45 A, ~90s, electrolyte: 885 m L C2H5OH, 100 mL C4H9OH, 109 g AlCl3·6H2O, 250 g ZnCl2. II. Anodization: ~4 A, 1min, electrolyte: 0.5 M (COOH)2. |
100% of the treated samples (9 out of 9) met the full biocompatibility benchmarks in vivo, leading to a failure rate of 0% (0 out of 9). |
[226] | |||
Microarc oxidation | Zn-0.1Mg | 300 V, 120 s, electrolyte: 14 g/L Na2SiO3, 2 g/L KOH, 15 ml/L glycol and 10 ml/L glycerol. | ZnO and Zn2SiO4 | 28.6 ± 2 μm | Improved blood compatibility with decreased hemolysis rate, lower lytic activity against red blood cells and lower platelet adhesion. Improved adhesion and viability of human umbilical vein endothelial cells. |
[224] |