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Electrical energy enables tumor therapy by generating reactive oxygen species (ROS); however, its clinical translation remains hindered by the reliance on external electrodes and the biocompatibility challenges of inorganic sensitizers. Here, covalent organic frameworks (COFs)-based energy-conversion platform termed as Py-ttTII@PEG, is engineered for non-invasive photo-triggered electrocatalysis augmented immunotherapy. The donor-acceptor-donor (D-A-D) building block, composed of electron-rich thienoisoindigo, electron-deficient thienothiophene, and tetradentate counterpart, pyrene tetraaniline (Py(NH)), is used to construct Py-ttTII@PEG. Under NIR-II laser irradiation, Py-ttTII@PEG NPs (nanoparticles) produce heat to ablate tumors, and multiple reactive oxygen species via triggered electrocatalysis to damage heat shock proteins and augment the therapeutic effect. Significantly, the cascade effects activate robust immunogenic cell death. In vivo studies reveal its potent anti-tumor effectiveness and the stimulation of an effective immune response under NIR-II laser irradiation, which suppresses the progression of distant tumors and lung metastasis. Additionally, RNA sequencing analysis indicate that Py-ttTII@PEG NPs induce the activation of immune-related pathways and the enrichment of regulatory genes in cell death- and immune-related pathways under NIR-II laser exposure. Thus, this work provides a feasible strategy by tightly coupling energy conversion to establishes an in vivo pyroelectricity generator for improving the therapeutic efficacy of immunotherapy against tumor metastasis.
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http://dx.doi.org/10.1002/smll.202504883 | DOI Listing |
Adv Sci (Weinh)
September 2025
State Key Laboratory of Luminescent Materials and Devices, Institute of Polymer Optoelectronic Materials and Devices, School of Materials Science and Engineering, South China University of Technology, Guangzhou, Guangdong, 510640, P. R. China.
Inspired by the electron-withdrawing ability of nitroxide radicals, a novel open-shell material, EDOT-TPAO is reported, synthesized via one-step demethylation and oxidation of its closed-shell precursor, EDOT-TPAOMe. Time-dependent density functional theory calculations confirm an acceptor-donor-acceptor configuration of EDOT-TPAO where radical termini act as electron acceptors. This structural transformation narrows the optical bandgap from 2.
View Article and Find Full Text PDFInorg Chem
August 2025
Beijing Key Laboratory for Optical Materials and Photonic Devices, Department of Chemistry, Capital Normal University, Beijing 100048, China.
Crystalline coordination polymers (CCPs) have emerged as promising platforms for photothermal conversion due to their structural tunability. However, the development of high-performance CCPs is often limited by the high cost of photoactive ligands. In this study, we report a low-cost, scalable approach to synthesize three CCPs─-, -, and -─via a solvothermal method using the inexpensive industrial precursor tetrafluoroterephthalonitrile, which is converted in situ into a tetraoxolene ligand.
View Article and Find Full Text PDFNat Commun
August 2025
National & Local Joint Engineering Research Center of High-throughput Drug Screening Technology, Hubei University, Wuhan, China.
The second near-infrared (NIR-II) dyes provide advantages for in vivo imaging, but challenges persist. A primary issue is the lack of practicable strategies to balance emission wavelength and molecular weight, particularly for low-molecular-weight (<500 Da) NIR-II (λ > 1000 nm) dyes. Here, we propose a strategy that tunes NIR-II emissions by reducing Coulomb attraction interaction, contrasting with traditional approaches that redshift absorption wavelengths through energy gap reduction.
View Article and Find Full Text PDFChemistry
August 2025
Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, School of Chemistry, IGCME, Guangdong Basic Research Center of Excellence for Functional Molecular Engineering, Sun Yat-Sen University, Guangzhou, 510275, P. R. China.
The synthesis of multifunctional materials that exhibit two or more distinct physicochemical properties is critical for the development of advanced smart materials. To date, the research regarding the near-infrared II (NIR-II) photothermal properties of spin crossover (SCO) materials remains scarce. Here, we synthesized an inverse-Hofmann-type cationic framework, [Fe{Ag(CN)}(TTF(py))] (1, TTF(py) = tetra(4-pyridyl)tetrathiafulvalene), which exhibits hysteretic SCO behavior.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
Department of Cardiovascular Surgery, Zhongnan Hospital of Wuhan University, School of Pharmaceutical Sciences, Wuhan University, Wuhan, 430071, P. R. China.
Infected diabetic wound management confronts significant challenges, including bacterial resistance, oxidative stress, and impaired vascular repair, resulting in substantial unmet clinical needs. To address these issues, a multifunctional therapeutic nanoplatform, mCu-SAE@BNN6@PEG-Van (CBPV), is developed by sequentially functionalizing mesoporous copper single-atom nanozymes (mCu-SAE) loaded with the nitric oxide (NO) donor BNN6 and vancomycin-conjugated polyethylene glycol (PEG-Van). CBPV integrates three synergistic therapeutic modalities: 1) pathogen-specific targeting via Van-mediated bacterial recognition; 2) NIR-II photothermally enhanced catalytic therapy via Cu-N centers in mCu-SAE, generating reactive oxygen species; 3) photoactivated NO release from BNN6, enabling peroxynitrite (ONOO) formation through radical coupling.
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