One-photon red light-triggered disassembly of small-molecule nanoparticles for drug delivery

Background: Photoresponsive drug delivery can achieve spatiotemporal control of drug accumulation at desired sites. Long-wavelength light is preferable owing to its deep tissue penetration and low toxicity. One-photon upconversion-like photolysis via triplet-triplet energy transfer (TTET) between ph...

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Veröffentlicht in:Journal of nanobiotechnology 2021-11, Vol.19 (1), p.357-14, Article 357
Hauptverfasser: Long, Kaiqi, Han, Han, Kang, Weirong, Lv, Wen, Wang, Lang, Wang, Yufeng, Ge, Liang, Wang, Weiping
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Sprache:eng
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Zusammenfassung:Background: Photoresponsive drug delivery can achieve spatiotemporal control of drug accumulation at desired sites. Long-wavelength light is preferable owing to its deep tissue penetration and low toxicity. One-photon upconversion-like photolysis via triplet-triplet energy transfer (TTET) between photosensitizer and photoresponsive group enables the use of long-wavelength light to activate short-wavelength light-responsive groups. However, such process requires oxygen-free environment to achieve efficient photolysis due to the oxygen quenching of triplet excited states. Results: Herein, we report a strategy that uses red light to trigger disassembly of small-molecule nanoparticles by one-photon upconversion-like photolysis for cancer therapy. A photocleavable trigonal molecule, BTAEA, self-assembled into nanoparticles and enclosed photosensitizer, PtTPBP. Such nanoparticles protected TTET-based photolysis from oxygen quenching in normoxia aqueous solutions, resulting in efficient red light-triggered BTAEA cleavage, dissociation of nanoparticles and subsequent cargo release. With paclitaxel as the model drug, the red light-triggered drug release system demonstrated promising anti-tumor efficacy both in vitro and in vivo. Conclusions: This study provides a practical reference for constructing photoresponsive nanocarriers based on the one-photon upconversion-like photolysis.
ISSN:1477-3155
1477-3155
DOI:10.1186/s12951-021-01103-z