Activatable and multifunctional supramolecular photosensitizers via macrocycle-based host–guest interactions: Enabling safe and efficient photodynamic therapy
Abstract
Photodynamic therapy (PDT) has emerged as a novel therapeutic approach to treat tumors, bacterial infection and various other diseases. To further improve the safety and efficacy of PDT, diverse photosensitizers (PSs) have been designed to improve reactive oxygen species (ROS) generation, promote targeted accumulation and activation, reduce off-target toxicity and dark toxicity, and enable synergistic multimodal therapy. Among these advances, supramolecular PSs constructed via host–guest inclusion with macrocycles (e.g., cyclodextrins, calixarenes, cucurbiturils, pillararenes) offer unique advantages, such as enhanced solubility, inhibited aggregation, controlled nano-assembly, as well as versatile functionalization and intelligentization. Recent progress has demonstrated that host–guest interactions can be harnessed to reduce oxygen dependence, accelerate post-PDT degradation, construct activatable PSs responsive to competitive binding at lesion sites, and modularly integrate targeting, imaging, or therapeutic elements into nano-PSs in a “Lego-like” manner. This feature article reviews these emerging strategies, highlighting how macrocycle-based host–guest chemistry provides a universal platform for the rational construction of safe and efficient PSs to advance the clinical potential of PDT.
- This article is part of the themed collection: Photodynamic Therapy (PDT)