Phototheranostic Zinc Porphyrin Nanoparticles Triggered by an 808 nm Laser: NIR-II Fluorescence/Photoacoustic Imaging-Guided Combined Photothermal/Photodynamic/NO Therapy

被引:0
作者
Chen, Hongyu [1 ,2 ]
Zhao, Xiaobo [1 ,2 ]
Halimov, Akbar [3 ,4 ]
Fu, Mingkai [4 ]
Tu, Jing [1 ,2 ]
Liu, Hui [1 ,2 ]
Xu, Huajun [5 ]
Liu, Jun [1 ,2 ]
机构
[1] North Sichuan Med Coll, Affiliated Hosp, Sch Pharm, Nanchong 637100, Sichuan, Peoples R China
[2] North Sichuan Med Coll, Affiliated Hosp, Inst Pharm, Med Imaging Key Lab Sichuan Prov Thyroid & Breast, Nanchong 637100, Sichuan, Peoples R China
[3] Uzbek Acad Sci, Phys Tech Inst, Tashkent 100084, Uzbekistan
[4] Chinese Acad Sci, Inst Elect Engn, Beijing 100190, Peoples R China
[5] Shandong Univ, Inst Frontier Chem, Sch Chem & Chem Engn, Shandong Prov Key Lab Sci Mat Creat & Energy Conve, Qingdao 266237, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOTODYNAMIC THERAPY; DESIGN;
D O I
10.1021/acs.bioconjchem.5c00086
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Single-wavelength lasers that trigger intelligently designed multifunctional theranostic nanoplatforms are urgently needed for early cancer diagnosis and imaging-guided therapy. In this study, a novel zinc porphyrin, Por-TR, was fabricated by incorporating thiophene as a donor and introducing electron acceptors on both sides to expand the conjugation. The presence of multiple flexible chains in the molecular structure of Por-TR inhibits pi-pi stacking, which allows it to form J nanoaggregates when coassembled with DSPE-PEG2000, demonstrating maximum absorption at approximately 808 nm. These Por-TR NPs provide NIR-II fluorescence/PA dual-modal signals for imaging and serve as a combined PTT/PDT therapeutic agent, making them a suitable multifunctional theranostic nanoplatform. To further improve their therapeutic effects, we embedded a thermosensitive NO donor, BNN6, in the Por-TR nanosystem to achieve combined PDT/PTT/NO therapy. Intravenous injection of Por-TR-NO NPs into 4T1 tumor-bearing mice enabled the accurate observation of tumor location via NIR-II fluorescence/PA dual-modal imaging. In vivo therapy results show that the Por-TR-NO NPs exhibited remarkable antitumor efficacy in combined PTT/PDT/NO therapy, which was triggered by an 808 nm laser. Overall, this nanoplatform offers a versatile approach to cancer diagnosis and treatment.
引用
收藏
页码:838 / 845
页数:8
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