Bismuth Sulfide Nanorods with Retractable Zinc Protoporphyrin Molecules for Suppressing Innate Antioxidant Defense System and Strengthening Phototherapeutic Effects

被引:125
作者
Cheng, Yan [1 ]
Chang, Yun [1 ,2 ]
Feng, Yanlin [1 ,3 ]
Jian, Hui [1 ]
Wu, Xiaqing [1 ,3 ]
Zheng, Runxiao [1 ,3 ]
Xu, Keqiang [1 ,3 ]
Zhang, Haiyuan [1 ,3 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Lab Chem Biol, Changchun 130022, Jilin, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
[3] Univ Sci & Technol China, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
bismuth sulfide; heme oxygenase-1; near-infrared; photodynamic therapy; zinc protoporphyrin IX; HEME OXYGENASE-1; PHOTOTHERMAL THERAPY; INHIBITION; TARGET; AGENT; OXIDE;
D O I
10.1002/adma.201806808
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bismuth (Bi)-based nanomaterials (NMs) are widely used for computed tomography (CT) imaging guided photothermal therapy, however, the photodynamic property is hardly exhibited by these NMs due to the fast electron-hole recombination within their narrow bandgap. Herein, a sophisticated nanosystem is designed to endow bismuth sulfide (Bi2S3) nanorods (NRs) with potent photodynamic property. Zinc protoporphyrin IX (ZP) is linked to Bi2S3 NRs through a thermoresponsive polymer to form BPZP nanosystems. The stretching ZP could prebind to the active site of heme oxygenase-1 overexpressed in cancer cells, suppressing the cellular antioxidant defense capability. Upon NIR laser irradiation, the heat released from Bi2S3 NRs could retract the polymer and drive ZP to the proximity of Bi2S3 NRs, facilitating an efficient electron-hole separation in ZP and Bi2S3 NRs, and leading to reactive oxygen species generation. In vitro and in vivo studies demonstrate the promising photodynamic property of BPZP, together with their photothermal and CT imaging performance.
引用
收藏
页数:8
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