Anthracene-Bridged Photosensitizers for Effective and Safe Photodynamic Therapy

被引:24
作者
Gao, Jucai [1 ]
Yang, Hui [1 ]
Lu, Yaru [2 ]
Shi, Qiankun [1 ]
Xu, Shidang [3 ]
Wu, Wenbo [2 ]
Hu, Fang [1 ]
Liu, Bin [3 ]
机构
[1] Southern Med Univ, Biomat Res Ctr, Sch Biomed Engn, Guangzhou 510515, Peoples R China
[2] Tianjin Univ, Inst Mol Aggregat Sci, Tianjin 300072, Peoples R China
[3] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 117585, Singapore
基金
中国国家自然科学基金;
关键词
AGGREGATION-INDUCED EMISSION; CANCER-CELLS; PRINCIPLES; MECHANISMS;
D O I
10.1021/acs.chemmater.2c03274
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photodynamic therapy (PDT) is a minimally invasive therapeutic modality. However, the residual photosensitizers (PSs) after PDT can still produce toxic singlet oxygen (1O2) under sunlight to damage normal tissues. The PS that can be switched off after PDT is desirable but rare. Herein, we propose a general strategy to design effective and self degradable PSs by embedding an anthracene bridge into donor-acceptor (D-A) structures. First, the steric anthracene can regulate the orbital distribution for enhancing the 1O2 production capacity. More importantly, the anthracene is responsive to the self-produced 1O2 for self-degradation. Besides, the degradation rate can be fine-tuned by the hydrophilicity of PSs. In this way, the PSs can realize a balance between treatment and suicide to ensure PDT and post-treatment safety. This work provides new insights into the design of degradable PSs with a clear mechanism, aiming to improve the post-safety of PDT.
引用
收藏
页码:1229 / 1237
页数:9
相关论文
共 30 条
[1]   Photodynamic Therapy (PDT): PDT Mechanisms [J].
Allison, Ron R. ;
Moghissi, Keyvan .
CLINICAL ENDOSCOPY, 2013, 46 (01) :24-29
[2]   In vivo wireless photonic photodynamic therapy [J].
Bansal, Akshaya ;
Yang, Fengyuan ;
Xi, Tian ;
Zhang, Yong ;
Ho, John S. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (07) :1469-1474
[3]   Excellent cosmetic result of daylight photodynamic therapy for facial flat warts in a child [J].
Borgia, Francesco ;
Coppola, Marialorena ;
Giuffrida, Roberta ;
Cannavo, Serafinella P. .
PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2019, 26 :27-28
[4]   Photodynamic therapy and anti-tumour immunity [J].
Castano, Ana P. ;
Mroz, Pawel ;
Hamblin, Michael R. .
NATURE REVIEWS CANCER, 2006, 6 (07) :535-545
[5]   Mechanisms in photodynamic therapy: Part three- Photosensitizer pharmacokinetics, biodistribution, tumor localization and modes of tumor destruction [J].
Castano, Ana P. ;
Demidova, Tatiana N. ;
Hamblin, Michael R. .
PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2005, 2 (02) :91-106
[6]   A Feasible Strategy of Fabricating Type I Photosensitizer for Photodynamic Therapy in Cancer Cells and Pathogens [J].
Chen, Kongqi ;
He, Ping ;
Wang, Zhiming ;
Tang, Ben Zhong .
ACS NANO, 2021, 15 (04) :7735-7743
[7]   Thiocarbonyl photosensitizer, a feasible way to eliminate the photosensitizer residues in photodynamic therapy [J].
Chen, Tian-Ge ;
Zhang, Xiao-Qing ;
Ge, Jian-Feng ;
Xu, Yu-Jie ;
Sun, Ru .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2022, 270
[8]  
DABESTANI R, 1995, J PHOTOCH PHOTOBIO A, V86, P231
[9]   Photodynamic therapy for cancer [J].
Dolmans, DEJGJ ;
Fukumura, D ;
Jain, RK .
NATURE REVIEWS CANCER, 2003, 3 (05) :380-387
[10]   Photosensitizers with Aggregation-Induced Emission: Materials and Biomedical Applications [J].
Hu, Fang ;
Xu, Shidang ;
Liu, Bin .
ADVANCED MATERIALS, 2018, 30 (45)