NIR Light‐Driving Barrier‐Free Group Rotation in Nanoparticles with an 88.3% Photothermal Conversion Efficiency for Photothermal Therapy
Traditional photothermal therapy requires high‐intensity laser excitation for cancer treatments due to the low photothermal conversion efficiency (PCE) of photothermal agents (PTAs). PTAs with ultra‐high PCEs can decrease the required excited light intensity, which allows safe and efficient therapy...
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Veröffentlicht in: | Advanced materials (Weinheim) 2020-03, Vol.32 (11), p.e1907855-n/a |
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Sprache: | eng |
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Zusammenfassung: | Traditional photothermal therapy requires high‐intensity laser excitation for cancer treatments due to the low photothermal conversion efficiency (PCE) of photothermal agents (PTAs). PTAs with ultra‐high PCEs can decrease the required excited light intensity, which allows safe and efficient therapy in deep tissues. In this work, a PTA is synthesized with high PCE of 88.3% based on a BODIPY scaffold, by introducing a CF3 “barrier‐free” rotor on the meso‐position (tfm‐BDP). In both the ground and excited state, the CF3 moiety in tfm‐BDP has no energy barrier to rotation, allowing it to efficiently dissipate absorbed (NIR) photons as heat. Importantly, the barrier‐free rotation of CF3 can be maintained after encapsulating tfm‐BDP into polymeric nanoparticles (NPs). Thus, laser irradiation with safe intensity (0.3 W cm−2, 808 nm) can lead to complete tumor ablation in tumor‐bearing mice after intravenous injection of tfm‐BDP NPs. This strategy of “barrier‐free rotation” provides a new platform for future design of PTT agents for clinical cancer treatment.
A photothermal agent (PTA) with a “barrier‐free” group rotor based on BODIPY is synthesized, which demonstrates an ultrahigh photothermal conversion efficiency of 88.3%. The PTA is encapsulated into biocompatible polymer nanoparticles, which can accumulate at tumor sites in a mouse model. Low‐intensity near‐infrared light activates the nanoparticles to efficiently generate heat, resulting in complete ablation of the tumor. |
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ISSN: | 0935-9648 1521-4095 |
DOI: | 10.1002/adma.201907855 |