Carbon Dots @ Platinum Porphyrin Composite as Theranostic Nanoagent for Efficient Photodynamic Cancer Therapy

被引:74
作者
Wu, Fengshou [1 ]
Yue, Liangliang [1 ]
Su, Huifang [2 ]
Wang, Kai [1 ]
Yang, Lixia [1 ]
Zhu, Xunjin [3 ]
机构
[1] Wuhan Inst Technol, Sch Chem Engn & Pharm, Key Lab Green Chem Proc, Minist Educ, Wuhan 430205, Hubei, Peoples R China
[2] Zhengzhou Univ, Dept Orthopaed, Affiliated Hosp 1, Zhengzhou 450052, Henan, Peoples R China
[3] Hong Kong Baptist Univ, Dept Chem, Waterloo Rd, Hong Kong, Hong Kong, Peoples R China
来源
NANOSCALE RESEARCH LETTERS | 2018年 / 13卷
基金
中国国家自然科学基金;
关键词
Carbon dots; Porphyrin; Photodynamic therapy; Energy transfer; Photoluminescence; GRAPHENE QUANTUM DOTS; SINGLET OXYGEN GENERATION; IN-VITRO; SUBCELLULAR-LOCALIZATION; FACILE SYNTHESIS; NANODOTS; PHOTOCYTOTOXICITY; PHOTOSENSITIZER; NANOPARTICLES; NANOCAPSULES;
D O I
10.1186/s11671-018-2761-5
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Photosensitizers are light-sensitive molecules that are highly hydrophobic, which poses a challenge to their use for photodynamic therapy. Hence, considerable efforts have been made to develop carriers for the delivery of PSs. Herein, we synthesized a new theranostic nanoagent (CQDs@PtPor) through the electrostatic interaction between the tetraplatinated porphyrin complex (PtPor) and the negatively charged CQDs. The size and morphology of as-prepared CQDs and CQDs@PtPor were characterized by a series of methods, such as XRD, TEM, XPS, and FTIR spectroscopy. The CQDs@PtPor composite integrates the optical properties of CQDs and the anticancer function of porphyrin into a single unit. The spectral results suggested the effective resonance energy transfer from CQDs to PtPor in the CQDs@PtPor composite. Impressively, the CQDs@PtPor composite showed the stronger PDT effect than that of organic molecular PtPor, suggesting that CQDs@PtPor is advantageous over the conventional formulation, attributable to the enhanced efficiency of O-1(2) production of PtPor by CQDs. Thus, this CQDs-based drug nanocarrier exhibited enhanced tumor-inhibition efficacy as well as low side effects in vitro, showing significant application potential in the cancer therapy.
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页数:10
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