Abstract
Activatable photosensitizers (PSs) have been widely used for the simultaneous fluorescence imaging and photodynamic ablation of cancer cells. However, the ready aggregation of traditional PSs in aqueous media can lead to fluorescence quenching as well as reduced phototoxicity even in the activated form. We have developed a series of PSs that show aggregation-enhanced emission and phototoxicity and thus the exact opposite behavior to that of previously reported PSs. We further developed a dual-targeted enzyme-activatable bioprobe based on the optimized photosensitizer and describe simultaneous light-up fluorescence imaging and activated photodynamic therapy for specific cancer cells. The design of smart probes should thus open new opportunities for targeted and image-guided photodynamic therapy.
| Original language | English |
|---|---|
| Pages (from-to) | 1780-1786 |
| Number of pages | 7 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 54 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 9 Feb 2015 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Aggregation-induced emission (aie)
- Cancer
- Fluorescence imaging
- Image-guided therapy
- Photodynamic therapy
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