研究目的
Investigating the performance and mechanism of Staphylococcus epidermidis biofilm control and eradication on the surface of graphitic carbon nitride (g-C3N4) under visible light irradiation.
研究成果
g-C3N4 not only inhibited S. epidermidis biofilm development but also eradicated pre-established biofilms under visible light irradiation. Biofilm eradication was observed from the outside-to-inside inactivation of bacterial cells, and 1O2 is speculated to play a key role for biofilm removal. The inactivation of bacterial cells and the destruction of an integral and cohesive structure of biofilms via EPS removal contribute to successful biofilm eradication in photocatalysis.
研究不足
The presence of nutrients challenges biofilm removal in photocatalysis under weak visible light exposure; and the enhancement of photoactivity of g-C3N4 is needed for effective biofilm control.
1:Experimental Design and Method Selection:
The study involved the synthesis of g-C3N4 powder and coupons, bacterial strains and biofilm development in the dark and under visible light exposure, and various characterization techniques including OCT, CLSM, SEM, and AFM.
2:Sample Selection and Data Sources:
S. epidermidis biofilms were cultured on the surface of MCB
3:07 coupons under continuous white LED light irradiation and in the dark for comparison. List of Experimental Equipment and Materials:
Equipment included a hydraulic press, white LED lamp, OCT system, CLSM, SEM, AFM, and HPLC. Materials included melamine, cyanuric acid, barbituric acid, and various chemicals for bacterial culture and staining.
4:Experimental Procedures and Operational Workflow:
Biofilms were cultured, exposed to light, and characterized using various microscopy techniques. ROS were quantified using radical probes.
5:Data Analysis Methods:
Data from microscopy and ROS quantification were analyzed to understand biofilm inhibition and eradication mechanisms.
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