pH responsive superporogen combined with PDT based on poly Ce6 ionic liquid grafted on SiO(2) for combating MRSA biofilm infection

基于接枝在SiO₂上的聚Ce₆离子液体的pH响应型超致孔剂与光动力疗法相结合,用于对抗耐甲氧西林金黄色葡萄球菌(MRSA)生物膜感染。

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Abstract

Background: Biofilm infection caused by multidrug-resistant bacteria is difficult to eradicate by conventional therapies. Photodynamic therapy (PDT) is an effective antibacterial method for fighting against biofilm infection. However, the blocked photosensitizers outside of biofilm greatly limit the efficacy of PDT. Methods: Herein, a novel acid-responsive superporogen and photosensitizer (SiO(2)-P(Ce6-IL)) was developed. Because of the protonation of the photosensitizer and the high binding energy of the polyionic liquid, SiO(2)-P(Ce6-IL) changed to positive SiO(2)-P(IL)(+) in an acidic microenvironment of biofilm infection. SiO(2)-P(IL)(+) could combine with negatively charged extracellular polymeric substances (EPS) and create holes to remove the biofilm barrier. To strengthen the interaction between SiO(2)-P(IL)(+) and EPS, SiO(2)-P(IL)(+) of high charge density was prepared by grafting the high-density initiation site of ATRP onto the surface of the SiO(2) base. Results: Due to the rapid protonation rate of COO(-) and the strong binding energy of SiO(2)-P(IL)(+) with EPS, SiO(2)-P(Ce6-IL) could release 90% of Ce6 in 10 s. With the stronger electrostatic and hydrophobic interaction of SiO(2)-P(IL)(+) with EPS, the surface potential, hydrophobicity, adhesion and mechanical strength of biofilm were changed, and holes in the biofilm were created in 10 min. Combining with the release of photosensitizers and the porous structure of the biofilm, Ce6 was efficiently concentrated in the biofilm. The in vitro and in vivo antibacterial experiments proved that SiO(2)-P(Ce6-IL) dramatically improved the PDT efficacy against MRSA biofilm infection. Conclusion: These findings suggest that SiO(2)-P(Ce6-IL) could rapidly increase the concentration of photosensitizer in biofilm and it is an effective therapy for combating biofilm infection.

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