A versatile strategy for improving phototherapeutic efficacy on deep-sited tumor by tissue optical clearing technique

被引:25
作者
Zhao, Hao [1 ,2 ]
Xu, Jiabao [1 ]
Wan, Jiangshan [1 ]
Huang, Wenjing [1 ]
Zhao, Yanbing [1 ,2 ]
Yang, Xiangliang [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Coll Life Sci & Technol, Natl Engn Res Ctr Nanomed, Wuhan 430074, Peoples R China
[2] Huazhong Univ Sci & Technol, Hubei Key Lab Bioinorgan Chem & Mat Med, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
Tissue optical clearing; Tissue penetration; Deep-sited tumor; Targeted delivery; Photothermal;
D O I
10.1016/j.nantod.2020.101058
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Phototherapies are almost entirely ineffective against deep-sited tumors, due to the poor tissue-penetration ability of light, including ultraviolet light, visible light and infrared light. Although tissue optical clearing (TOC) technique, based on refractive index matching between scatterers and media, has been used to improve in vivo optical imaging quality, it is the first time that TOC technique was employed to realize efficient phototherapeutic effect on deep-sited tumor in the present work. A hybrid TOC agent consisting of glycerol, polyethylene glycol 400 and butylbenisothiazolene (TGP), were optimized for achieving the synergistic antitumor efficacy of photothermal therapy (PTT) and chemotherapy on a simulated deep-sited tumor model (with the coverage of pigskin). Temperature-sensitive gold nanocages (PGNCs) was used to load doxorubicin (DOX@PGNCs) as a nano-platform model of PTT and chemotherapy, for a proof of concept to prove the TOC effect of TGP on the phototherapeutic efficacy against deep-sited tumor. As the pigskin was treated by TGP for 30 min, the Delta T of DOX@PGNCs increased to 12.1 degrees C under NIR irradiation, while it only increased to ca. 2.0 degrees C with the coverage of untreated-pigskin. Moreover, PTT-triggered release of DOX increased from 6.3% with the coverage of untreated pigskin up to 22.8% with the coverage of TGP-treated pigskin under three times of NIR irradiation, indicating enhanced photothermal conversion efficiency. Meanwhile, the TOC effect of TGP enhanced cellular uptakes of DOX@PGNCs and boosted delivery efficiency of DOX@PGNCs into the tumor by photothermal-induced hydrophilicity-hydrophobicity transition. Owing to the improvement on the tissue-penetration depth of NIR light, DOX@PGNCs accomplished a robustly synergistic antitumor efficacy of PTT-chemotherapy on a deep-sited H22 tumor model. It is promising to be developed as a versatile strategy for improving PTT efficacy on deep-sited tumors and showed great potential in the improvement of clinical application of various phototherapies. (c) 2020 Elsevier Ltd. All rights reserved.
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页数:12
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