Synthetic carbon-based lanthanide upconversion nanoparticles for enhanced photothermal therapy.

Publication date: Jul 09, 2025

Photothermal therapy (PTT), a vanguard strategy in cancer/ocular neovascularization treatment, has attracted considerable attention owing to its precision, controllability, high efficacy, and minimal side effects. Nevertheless, its inherent limitations necessitate innovative solutions. One promising strategy is to develop reagents with enhanced photothermal conversion efficiency under long-wavelength laser irradiation. Carbon nanomaterials, known for their broad absorption spectra, are currently hindered by single-wavelength lasers in clinical treatments. In this study, we address this limitation by coating mesoporous carbon nanomaterials (MCNs) with a lanthanide oxysulfide up-conversion material (YOS:Yb,Er), converting 980 nm light into visible light. This advancement enhances the photothermal conversion efficiency of the produced MCNs/Ln/GD/FR nanocomposites from 59. 48% to 82. 86%. Furthermore, the incorporation of gambogic acid and doxorubicin intensifies the synergistic photothermal therapy effect. A dual stimuli-responsive hydrogel (PNIPAM) is employed to ensure controlled drug release and safe delivery to tumors. Evaluations demonstrate that the MCNs/Ln/GD/FR nanocomposites exhibit exceptional tumor targeting and evident photothermal synergistic therapy effects on both subcutaneous and ocular in situ melanoma tumors by activating tumor-suppressive signaling pathways while inhibiting proliferation and differentiation-related pathways. These findings might pave the way for the development of photothermal reagent and offer valuable insights for advancing therapeutic strategies.

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Concepts Keywords
Advancingtherapeutic Animals
Cancer Carbon
Controllability Carbon
Hydrogel Cell Line, Tumor
Lasers Doxorubicin
Doxorubicin
Humans
Hydrogels
Hydrogels
Lanthanoid Series Elements
Lanthanoid Series Elements
Mice
Nanocomposites
Nanoparticles
Photothermal Therapy

Semantics

Type Source Name
drug DRUGBANK Activated charcoal
disease MESH cancer
drug DRUGBANK Doxorubicin
pathway REACTOME Release
disease MESH melanoma
pathway KEGG Melanoma
drug DRUGBANK Troleandomycin
disease MESH pathological neovascularization
disease MESH residual tumor
drug DRUGBANK Albendazole
disease MESH shock
drug DRUGBANK Folic Acid
drug DRUGBANK Trestolone
drug DRUGBANK Poloxamer 188
drug DRUGBANK Water
drug DRUGBANK Carbonate ion
disease MESH weight loss
drug DRUGBANK Tretamine
drug DRUGBANK Coenzyme M
drug DRUGBANK Nitrate
drug DRUGBANK Glutathione
disease MESH Necrosis
drug DRUGBANK Podofilox
drug DRUGBANK Glutamic Acid
drug DRUGBANK Creatinine
drug DRUGBANK Urea
drug DRUGBANK Uric Acid
disease MESH ARC
drug DRUGBANK 3 7 11 15-Tetramethyl-Hexadecan-1-Ol
pathway REACTOME Apoptosis
disease MESH metastasis
drug DRUGBANK Myricetin
drug DRUGBANK Trastuzumab
disease MESH oxidative stress
drug DRUGBANK Tropicamide
drug DRUGBANK Phenol
drug DRUGBANK Formaldehyde
drug DRUGBANK Sodium lauryl sulfate
drug DRUGBANK Trypsin
drug DRUGBANK Edetic Acid
drug DRUGBANK Dextrose unspecified form
drug DRUGBANK Dimethyl sulfoxide
drug DRUGBANK Ethanol
drug DRUGBANK Medical air
drug DRUGBANK Tricyclazole
pathway REACTOME Digestion
drug DRUGBANK Tromethamine
drug DRUGBANK Proparacaine
drug DRUGBANK L-Phenylalanine
disease MESH dehydration
disease MESH Hemolysis
drug DRUGBANK Chromium
drug DRUGBANK Pidolic Acid
drug DRUGBANK Pentaerythritol tetranitrate

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