Cyclodextrin-Activated Porphyrin Photosensitization for Boosting Self-Cleavable Drug Release
By:
Tang, M (Tang, Mian) [1] ;
Song, YQ (Song, Yanqiu) [2] ;
Lu, YL (Lu, Yi-Lin) [1] ;
Zhang, YM (Zhang, Ying-Ming) [1] ;
Yu, ZL (Yu, Zhilin) [2] ;
Xu, XF (Xu, Xiufang) [1] ;
Liu, Y (Liu, Yu) [1]
DOI
10.1021/acs.jmedchem.2c00105
Abstract
Supramolecular prodrugs that combine the merits of stimuli-responsiveness and targeting ability in a controllable manner have shown appealing prospects in disease diagnostics and therapeutics. Herein, we report that a new theranostic agent with the host-guest-binding-activated photosensitization has been fabricated by a binary supramolecular assembly consisting of the permethyl-beta-cyclodextrin-grafted hyaluronic acid and a combretastatin A-4-appended porphyrin derivative. Illuminated by a red-light source, the production efficiency of singlet oxygen (O-1(2)) pronouncedly increases by similar to 60-fold once the porphyrin core is encapsulated by cyclodextrins. Consequently, the cell-selective fluorescence emission is dramatically enhanced, the microtubule-targeted drug is rapidly and completely released, and the O-1(2)-involved combinational treatment is simultaneously achieved both in vitro and in vivo. To be envisaged, this complexation-boosted light-activatable photosensitizing prodrug delivery system with improved photophysical performance and remarkable phototheranostic outcomes will make a significant contribution to the creation of more advanced stimulus-based biomaterials.