Table 3.
Techniques for changing surface roughness.
Techniques for porous surface preparation | Modification strategy | Experimental category | Evidence of improved anti-inflammation | Reference |
---|---|---|---|---|
Sulfonation | Concentrated sulfuric acid treatment | in vivo | Decreased TNF-α concentration, increased IL-10 concentration, and promoted M2 macrophage polarization | [144] |
Concentrated sulfuric acid treatment followed by immersion in ASP solution and grafting of BFP onto sulfonated PEEK surface | in vitro | Down-regulated COX-2 and IL-6 expression | [146] | |
Acid etching | HNO3 treatment | in vitro | Enhanced cell adhesion | [147] |
HF and HNO3 treatment | in vitro | Down-regulated the expression of proinflammatory cytokines, promoted M2 macrophage polarization | [148] | |
3D printing technology prepared porous PEEK | 3D printed PEEK etched with sulfuric acid | in vivo | Reduced fibrous tissue formation, decreased the expression of IL-1β and TNF-α | [149] |
in vitro | Promoted M2 macrophage polarization and enhanced secretion of anti-inflammatory cytokines IL-4 and IL-10 | [150] | ||
Extrusion under heat and pressure | Sodium chloride powder and PEEK powder were extruded under high temperature and high pressure and dissolved in sodium chloride in water after cooling | in vivo | Reduced fibrous tissue formation | [141] |
LBL self-assembly | Alternate dipping in PAA/PAH solution, then rinsing in acid solution | in vitro | Reduced the level of proinflammatory factors, down-regulated the TNF-α and JAK-STAT signaling pathways, and promoted M2 macrophage polarization | [151] |
Argon PIII | Argon PIII and subsequent hydrogen peroxide treatment | in vitro | Reduced fibrous tissue formation around the implant | [152] |