A multifunctional nanoplatform for lysosome targeted delivery of nitric oxide and photothermal therapy under 808 nm near-infrared light

被引:51
作者
Xiang, Hui-Jing [1 ,2 ]
Guo, Min [1 ,2 ]
An, Lu [3 ,4 ]
Yang, Shi-Ping [3 ,4 ]
Zhang, Qian-Ling [5 ]
Liu, Jin-Gang [1 ,2 ]
机构
[1] East China Univ Sci & Technol, Key Lab Adv Mat MOE, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Dept Chem, Shanghai 200237, Peoples R China
[3] Shanghai Normal Univ, Key Lab Resource Chem MOE, Shanghai 200234, Peoples R China
[4] Shanghai Normal Univ, Shanghai Key Lab Rare Earth Funct Mat, Shanghai 200234, Peoples R China
[5] Shenzhen Univ, Coll Chem & Environm Engn, Shenzhen Key Lab Funct Polymer, Shenzhen 518060, Peoples R China
关键词
CANCER-THERAPY; RUTHENIUM NITROSYLS; PHOTODYNAMIC THERAPY; FLUORESCENT-PROBE; LIVING CELLS; CARBON DOTS; NO DONORS; IN-VITRO; NANOPARTICLES; COMPLEXES;
D O I
10.1039/c6tb00730a
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
Nitric oxide (NO) plays important roles in various physiological and pathological processes. The development of multifunctional nanoplatforms that enable site-specific delivery of NO is expected to provide new insights toward the realization of NO-mediated therapy. We report herein a novel nanoplatform {Lyso-Ru-NO@ FA@CDs}, (1), where a lysosome-targeting NO donor, Lyso-Ru-NO, and a folic-acid (FA)-directing group were incorporated into carbon dots (CDs). Nanoplatform 1 exhibited immediate NO release and a rapid temperature increase when irradiated using an 808 nm laser. This nanoplatform was capable of targeting folate-receptor-positive cancer cell lines and specifically accumulated in the subcellular lysosomal organelle. The dual-targeted nanoplatform 1 exhibited high cytotoxicity toward cancer cells under irradiation with 808 nm light, demonstrating substantially enhanced efficacy compared with its nontargeted counterparts. NIR-light-controlled spatiotemporal delivery of NO to targeted sites accompanied by photothermal therapy offers new possibilities for NO-involved multimodal cancer treatment.
引用
收藏
页码:4667 / 4674
页数:8
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