| Literature DB >> 27513690 |
Xiao-Qiang Wang1, Qi Lei1, Jing-Yi Zhu1, Wen-Jing Wang1, Qian Cheng1, Fan Gao1, Yun-Xia Sun1, Xian-Zheng Zhang1.
Abstract
Activatable photosensitizers (aPSs) have emerged as promising photodynamic therapy (PDT) agents for simultaneous imaging and selective ablation of cancer. However, traditional synthetic aPSs are limited by complex design and tedious synthesis. Here, aPS regulated by cucurbit[8]uril (CB[8]) for targeted cancer imaging and PDT is reported. This system is based on the host-guest interaction between biotinylated toluidine blue (TB-B) and CB[8] to form 2TB-B@CB[8]. Moreover, a facile strategy to turn off/on the fluorescence and photodynamic activity of TB-B is developed through the reversible assembly/disassembly of 2TB-B@CB[8]. This established system can achieve selective accumulation in tumor, light-up cancer imaging, and enhanced anticancer behavior. Therefore, this work provides a novel and promising strategy for the aPS build via simple and facile regulation of supramolecular chemistry.Entities:
Keywords: activatable photosensitizer; anticancer; photodynamic therapy; singlet oxygen; supramolecular chemistry
Mesh:
Substances:
Year: 2016 PMID: 27513690 DOI: 10.1021/acsami.6b07507
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229