F,N-Doped carbon dots as efficient Type I photosensitizers for photodynamic therapy

被引:64
作者
Wu, Xiaoyan [1 ]
Xu, Mingsheng [1 ]
Wang, Shuna [1 ]
Abbas, Khurram [1 ]
Huang, Xin [2 ]
Zhang, Renquan [2 ]
Tedesco, Antonio Claudio [1 ,3 ]
Bi, Hong [1 ,4 ]
机构
[1] Anhui Univ, Sch Chem & Chem Engn, Hefei 230601, Peoples R China
[2] Anhui Med Univ, Affiliated Hosp 1, Dept Thorac Surg, Hefei 230032, Peoples R China
[3] Univ Sao Paulo, Fac Philosophy Sci & Letters Ribeirao Preto, Photobiol & Photomed Res Grp, Dept Chem,Ctr Nanotechnol & Tissue Engn, BR-14040901 Ribeirao Preto, SP, Brazil
[4] Anhui Univ, Sch Mat Sci & Engn, Hefei 230601, Peoples R China
基金
中国国家自然科学基金;
关键词
GRAPHENE QUANTUM DOTS; TUMOR; NANOPARTICLES; LUMINESCENCE; CANCER;
D O I
10.1039/d1dt03788a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Photodynamic therapy (PDT) is a promising and emerging method for the treatment of cancer. Usually, Type II PDT is used in the clinic, and mainly involves three key elements: a photosensitizer, molecular oxygen and laser light. However, it is known that tumor tissue is deficient in oxygen molecules which is why Type I PDT is mostly preferred in the therapy of tumors in which the hypoxic tissue plays a major role. Fluorescent carbon dots (CDs) have shown great potential in cancer theranostics, acting as bioimaging agents and photosensitizers. Herein, we have synthesized novel kinds of fluorine and nitrogen co-doped carbon dots (F,NCDs) that emit bright green fluorescence under ultra-violet light. The F,NCDs have excellent water solubility and low cytotoxicity. They can generate hydroxyl radicals (OH) and superoxide anions (O-2(-)) under LED light (400-500 nm, 15 mW cm(-2)) irradiation, making them ideal photosensitizers for Type I PDT. Furthermore, upon using the HepG2 cell line as an in vitro model, the F,NCDs exhibit a better cell imaging effect and higher PDT efficiency than the control sample of CDs without F and N doping. This work has illustrated that the F,NCDs are promising in achieving the image-guided PDT of cancers, usually in a hypoxia tumor microenvironment.
引用
收藏
页码:2296 / 2303
页数:8
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