The removal of mature biofilm from the surface of implant has been a formidable challenge in treating implant-associated infection. Prevention of biofilm formation rather than removal of existing biofilm is a more effective approach. Immobilization of biofilm-dispersing enzymes on material surfaces is regarded as one of the most promising strategies. Deoxyribonuclease I (DNase I) can degrade extracellular DNA (eDNA) and then destabilize biofilm. In this study, DNase I was immobilized on a titanium (Ti) surface by using dopamine as an intermediate. The water contact angle, SEM, EDS and XPS confirmed that DNase I was successfully coated to the bare Ti and the final coating was highly hydrophilic. The DNase I coating showed significant effects in preventing Streptococcus mutans (S. mutans) and Staphylococcus aureus (S. aureus) adhesion and biofilm formation over a time span of 24h. The favorable biocompatibility was demonstrated by cell study in vitro. In addition, cell adhesion results suggested that DNase I coating had the potential to facilitate MC3T3-E1 cell attachment. DNase I coating with anti-infection ability and biocompatibility has great potential for increasing success rates of implant applications.
Keywords: Anti-infection ability; Biocompatibility; Biofilm; DNase I coating; Polydopamine coating; Titanium biomaterials.
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