Stimuli‐Responsive Reversible Switching of Intersystem Crossing in Pure Organic Material for Smart Photodynamic Therapy
Photosensitizers (PSs) with stimuli‐responsive reversible switching of intersystem crossing (ISC) are highly promising for smart photodynamic therapy (PDT), but achieving this goal remains a tremendous challenge. This study introduces a strategy to obtain such reversible switching of ISC in a new cl...
Gespeichert in:
Veröffentlicht in: | Angewandte Chemie 2019-08, Vol.131 (32), p.11222-11228 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Photosensitizers (PSs) with stimuli‐responsive reversible switching of intersystem crossing (ISC) are highly promising for smart photodynamic therapy (PDT), but achieving this goal remains a tremendous challenge. This study introduces a strategy to obtain such reversible switching of ISC in a new class of PSs, which exhibit stimuli‐initiated twisting of conjugated backbone. We present a multidisciplinary approach that includes femtosecond transient absorption spectroscopy and quantum chemical calculations. The organic structures reported show remarkably enhanced ISC efficiency (ΦISC), switching from nearly 0 to 90 %, through an increase in the degree of twisting, providing an innovative mechanism to promote ISC. This leads us to propose here and demonstrate the concept of smart PDT, where pH‐induced reversible twisting maximizes the ISC rate, and thus enables strong photodynamic action only under pathological stimulus (such as change in pH, hypoxia, or exposure to enzymes). The ISC process is turned off to deactivate PDT ability, when the PS is transferred or metabolized away from pathological region.
Sauer macht produktiv: Reversibles An/Aus‐Schalten des Intersystem Crossing (ISC) in einer neuen Klasse organischer niedermolekularer Photosensibilisatoren beruht auf der Stimuli‐induzierten Verdrillung ihres konjugierten Gerüstes. Diese Moleküle könnten sich für eine smarte photodynamische Therapie (PDT) eignen, da ihre Singulettsauerstoffbildung in der sauren Umgebung von Tumorzellen angeschaltet werden würde. |
---|---|
ISSN: | 0044-8249 1521-3757 |
DOI: | 10.1002/ange.201905129 |