An acid-triggered BODIPY-based photosensitizer for enhanced photodynamic antibacterial efficacy

被引:16
作者
Liang, Xuning [1 ]
Xia, Lei [1 ]
Zhu, Yucheng [1 ]
Zhang, Chen [1 ]
Gong, Feirong [1 ]
Zhang, Weian [1 ]
机构
[1] East China Univ Sci & Technol, Shanghai Key Lab Funct Mat Chem, Meilong Rd 130, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
NANOPARTICLES; FLUORESCENCE; RESISTANCE;
D O I
10.1039/d2bm00780k
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Photodynamic inactivation of bacteria has emerged as a promising antibacterial strategy due to its high antibacterial activity and low bacterial resistance. Herein, an acid-triggered photodynamic antibacterial nanoplatform (IBPAAs) was constructed by co-assembly of an acid-triggered photosensitizer BODIPY (I-NBDP) and the POEGMA-b-PDEAEMA block copolymer for enhancing the antibacterial efficacy and biofilm-dissipation capability. IBPAAs could have great biocompatibility and stability by the formation of self-assemblies, and it could be cleaved to release the I-NBDP photosensitizer under a dual-step acidic response due to the protonation of the diethylamino groups on both I-NBDP and the POEGMA-b-PDEAEMA block copolymer. On the one hand, the photoinduced electron transfer (PET) of I-NBDP in IBPAAs under neutral conditions could be attenuated, resulting in an increase of its( 1)O(2) yield, effectively improving its photodynamic antibacterial efficacy. On the other hand, the protonation of IBPAAs made it easier to target negatively charged bacterial surfaces, further enhancing its photodynamic antibacterial activity. The antibacterial experiments in vitro showed that the IBPAAs assemblies had great photodynamic antibacterial efficacy and biofilm dissipation capability, and it could effectively relieve bacterial infection of wounds and accelerate wound healing in vivo. Therefore, this acid-triggered strategy is expected to provide a new path for enhanced photodynamic antibacterial therapy.
引用
收藏
页码:4235 / 4242
页数:8
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