Porous organic polymer overcomes the post-treatment phototoxicity of photodynamic agents and maintains their antitumor efficiency

被引:6
|
作者
Liu, Yamin [1 ]
Wang, Ze-Kun [1 ]
Gao, Zhong-Zheng [1 ]
Zong, Yang [1 ]
Sun, Jian-Da [1 ]
Zhou, Wei [1 ]
Wang, Hui [1 ]
Ma, Da [1 ]
Li, Zhan-Ting [1 ]
Zhang, Dan -Wei [1 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200438, Peoples R China
关键词
Porous organic polymer; Phototoxicity reduction; Porphyrin photosensitizer; Photodynamic therapy; Safety improvement; PHOTOSENSITIZERS; FRAMEWORK; DELIVERY; THERAPY;
D O I
10.1016/j.actbio.2022.07.043
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Since 1995, photodynamic therapy (PDT) has been utilized as an effective method for cancer treatment. However, the residues of photosensitizers in the normal tissues after PDT can be activated by sunlight to cause severe skin phototoxicity, for which currently there are no clinical solutions. As a result, post-PDT patients need to remain out of sunlight for up to five weeks, which produces great living and mental burdens for patients. Herein, we report that a biocompatible porous organic polymer (POP) with aver-age 3.1 nm porosity is able to suppress the skin phototoxicity of clinically used porphyrin-based photo -dynamic agents (PDAs), including Photofrin, Talaporfin and Hiporfin, through an adsorption-elimination mechanism. Fluorescence titration and dialysis experiments show that POP can adsorb and retain the PDAs at a micromolar concentration. In vivo experiments demonstrate that POP can significantly suppress the skin phototoxicity caused by all the three PDAs without reducing their PDT efficacy.Statement of significance Up to now, no efficient clinical treatment for the inhibition of post-PDT phototoxicity of clinically used porphyrin-based PDAs is available. In the manuscript, a water-soluble cationic porous organic polymer has been revealed to include three clinically used PDAs. In vivo experiments show that this inclusion remarkably reduces the content of PDAs in mouse skins, leading to significant alleviation of their post -PDT phototoxicity without no negative effect on their PDT efficacy. Thus, this work provides a strategy for overcoming the drawback of clinically used photodynamic agents. (c) 2022 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:254 / 264
页数:11
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