Designing nanoparticle carriers for enhanced drug efficacy in photodynamic therapy

被引:24
作者
Chu, Zhiqin [1 ]
Zhang, Silu [1 ]
Yin, Chun [2 ]
Lin, Ge [2 ]
Li, Quan [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Phys, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Fac Med, Sch Biomed Sci, Shatin, Hong Kong, Peoples R China
关键词
MESOPOROUS SILICA NANOPARTICLES; METHYLENE-BLUE; SINGLET OXYGEN; FREE-RADICALS; APOPTOSIS; CANCER; DEATH; CELLS; DELIVERY; NECROSIS;
D O I
10.1039/c4bm00024b
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
082905 [生物质能源与材料]; 100103 [病原生物学];
摘要
Although nanoparticles (NPs) have been proposed as carriers for photosensitizers (PS) in photodynamic therapy (PDT), how the design parameters of nanocarriers affect the final drug efficacy remains unclear. By designing SiO2-PS NPs with specific features (such as enabling easy release of PS from the nanocarriers, or introducing plasmonic Au NPs in the vicinity of the PS), and comparing the respective efficacy of PS to that of the conventional dense SiO2-PS NPs (PS were tightly confined into the silica matrix), we identified that both PS trapping-in/releasing from the silica nanocarriers and the Au plasmonic effect were responsible for the PS efficacy variation. The mechanistic study also disclosed that the different NP configurations would affect the cellular death pathway. These findings provide a general guideline for the design of NP-based PDT applications.
引用
收藏
页码:827 / 832
页数:6
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