Abstract
Given that type I photosensitizers (PSs) possess a good hypoxic tolerance, developing an innovative tactic to construct type I PSs is crucially important, but remains a challenge. Herein, we present a smart molecular design strategy based on the Förster resonance energy transfer (FRET) mechanism to develop a type I photodynamic therapy (PDT) agent with an encouraging amplification effect for accurate hypoxic tumor therapy. Of note, benefiting from the FRET effect, the obtained nanostructured type I PDT agent (NanoPcSZ) with boosted light-harvesting ability not only amplifies superoxide radical (O2•-) production but also promotes heat generation upon near-infrared light irradiation. These features facilitate NanoPcSZ to realize excellent phototherapeutic response under both normal and hypoxic environments. As a result, both in vitro and in vivo experiments achieved a remarkable improvement in therapeutic efficacy via the combined effect of photothermal action and type I photoreaction. Notably, NanoPcSZ can be eliminated from organs (including the liver, lung, spleen, and kidney) apart from the tumor site and excreted through urine within 24 h of its systemic administration. In this way, the potential biotoxicity of drug accumulation can be avoided and the biosafety can be further enhanced.
| Original language | English |
|---|---|
| Article number | e202411514 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 63 |
| Issue number | 44 |
| DOIs | |
| State | Published - 24 Oct 2024 |
Bibliographical note
Publisher Copyright:© 2024 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH.
Keywords
- Förster resonance energy transfer
- nanostructure
- photodynamic therapy
- renal clearable
- type I photoreaction
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