Table 2.
Examples of drug-containing surface modification of Ti and Ti alloys.
Drugs | Methodology | Incorporating Structure | Results | Refs. |
---|---|---|---|---|
Gentamicin | Multilayers of gentamicin and polyacrylic acid obtained by LBL method on Ti64 treated by alkali-heating | Homogeneous cross-link multilayers’ deposition, gentamicin and polyacrylic acid coated layer-by-layer | Antibacterial rates compared to Ti64: 99.86% for S. aureus and 99.93% for E. coli | [153] |
Vancomycin | Electrodeposition to coat HA/collagen/ vancomycin on Ti | Many small vancomycin crystals that aggregate and form larger islands | 5 h antibacterial ratio (S. Aureus): ~97% 30 h drug release: ~85% |
[154] |
Tobramycin | Alkali-treated Ti screws with anodized surfaces soaked in Dulbecco’s PBS were soaked in tobramycin solution at 70 °C. | Tobramycin is deposited on a thin leaf-like HA coating that adheres tightly to the substrate. | Screws injected with S. aureus suspension were implanted into rabbits. The drug-laden group showed significantly lower signs of infection. | [155] |
Rifampicin | Electrospinning process: the poly-caprolactone nanofibers loaded with HA nanoparticles and rifampicin were coated on acid-etched annealed Ti. | Regular and smooth fibers without beads or coagulations | Mechanical properties of nanocomposite scaffolds: increased threefold. Antibacterial: log reduction in the bacterial growth Drug release: 1 h: ~27%; 1 d: ~41%; 32 d: ~61% |
[156] |
Clindamycin | Hydrogel 3D bioprinting: hydrogels containing clindamycin were extruded on acid-etched Ti64 | Rough surface by nanofibrillated cellulose filaments with furrows and without drug clusters | 10-day degradation: ~57.8% (hydrogels without drug: 7-day: 100%) Drug release: 1 h: ~25%; 1 d: ~80%; 3 d: 100% |
[157] |