摘要
This study aimed to add two functional components—antibacterial 45S5BGs particles and AIE nanoparticles (TPE-NIM+) with bioprobe characteristics—to the guided tissue regeneration (GTR) membrane, to optimize the performance. The PLGA/BG/TPE-NIM+membrane was synthesized. The static water contact angle, morphologies, and surface element analysis of the membrane were then characterized. In vitro biocompatibility was tested with MC3T3-E1 cells using CCK-8 assay, and antibacterial property was evaluated withStreptococcus mutansandPorphyromonas gingivalisby the LIVE/DEAD bacterial staining and dilution plating procedure. The fluorescence staining of bacteria was observed by Laser Scanning Confocal Microscope. The results showed that the average water contact angle was 46°. In the cytotoxicity test, except for the positive control group, there was no significant difference among the groups (p> 0.05). The antibacterial effect in the PLGA/BG/TPE-NIM+group was significantly (p< 0.01), while the sterilization rate was 99.99%, better than that in the PLGA/BG group (98.62%) (p< 0.01). Confocal images showed that the membrane efficiently distinguished G+bacteria from G−bacteria. This study demonstrated that the PLGA/BG/TPE-NIM+membrane showed good biocompatibility, efficient sterilization performance, and surface mineralization ability and could be used to detect pathogens in a simple, fast, and wash-free protocol.Keywords:aggregation-induced emission nanoparticles;antibacterial;antibacterial differentiation;bioactive glass;bioprobe;guided tissue regeneration (GTR)
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