Despite
its promising potential in cancer treatment, synergistic
photothermal/chemodynamic therapy remains underdeveloped with regard
to the utilization of metal–organic materials under second
near-infrared (NIR-II) laser excitation. Herein, we report a three-dimensional
network constructed via the metal coordination between catechol-functionalized
aza-boron dipyrromethenes and iron ions (ABFe), which
was further encapsulated by F127 to obtain ABFe nanoparticles
(NPs) for combined photothermal/chemodynamic therapy. ABFe NPs exhibited intense absorption in the NIR-II range and negligible
fluorescence. Upon 1064 nm laser irradiation, ABFe NPs
showed high photothermal conversion efficiency (PCE = 55.0%) and excellent
photothermal stability. The results of electron spin resonance spectra
and o-phenylenediamine chromaticity spectrophotometry
proved that ABFe NPs were capable of generating harmful
reactive oxygen species from hydrogen peroxide for chemodynamic therapy,
which was promoted by photothermal performance. Notably, in
vitro and in vivo experiments demonstrated
the great potential of ABFe NPs in photoacoustic imaging
and photothermal-enhanced chemodynamic therapy under NIR-II laser
irradiation. Therefore, the current work presents a prospective NIR-II
excitation therapeutic nanomedicine for combination therapy, offering
a novel strategy for simultaneously achieving extended NIR absorption
of aza-BODIPY and enhanced chemodynamic therapy with metal–organic
materials.
The design of effcient photosensitisers for cancer theranostics is of great importance, especially for multimodal-imaging-guided synergistic therapy. The key to achieving accurate imaging-guided phototherapy is to balance the energy distribution...
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