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Anion-exchange membranes (AEMs) are the key components of AEM-based water electrolysis (AEMWE) for green hydrogen production. Unfortunately, many AEMs have unsatisfactory ion conductivity, and the factors governing their ion transport remain unclear. To address these limitations, herein, a new pyrrolidinium-containing diallylammonium-cyclopolymerized (PDT) AEM is proposed. Cyclopolymerization between diallyldimethylammonium chloride and tetraallylammonium bromide (TAAB, crosslinker) monomers in a porous polytetrafluoroethylene support yielded a pore-filled crosslinked PDT membrane, whose structure is controlled by adjusting its TAAB content. The OH conductivity of the PDT membrane is more strongly correlated with its OH diffusivity (determined by its internal water content) than its OH partitioning (determined by its internal charge content). The optimized PDT membrane exhibited low gas crossover and high thermomechanical stability. Importantly, it displayed excellent AEMWE performance in both pure water (0.71 A cm at 1.8 V) and 1 m KOH (5.25 A cm at 1.8 V) at 80 °C with half-platinum-group metal electrodes, outperforming many previously reported and commercial AEMs, owing to its significantly high OH conductivity. The PDT membrane also demonstrated stable AEMWE performance in 1 m KOH at 60 °C for 300 h. This study offers an effective means to fabricate high-performance AEMs and sheds light on their ion-transport mechanisms.
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http://dx.doi.org/10.1002/smll.202507437 | DOI Listing |
Biomater Sci
September 2025
Britton Chance Center for Biomedical Photonics at Wuhan National Laboratory for Optoelectronics Hubei Bioinformatics & Molecular Imaging Key Laboratory, Department of Biomedical Engineering, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, 430074, Hubei,
Cuproptosis is a copper-dependent programmed cell death triggered by mitochondrial dysfunction, which offers significant anti-tumor potential but requires tumor-specific copper delivery to avoid systemic toxicity. Here, we developed a synergistic nanoplatform (CuO@SiO-Ce6, CSC) integrating cuproptosis induction with photodynamic therapy (PDT). A cuprous oxide (CuO) core was encapsulated in silicon dioxide and covalently linked to the photosensitizer Ce6.
View Article and Find Full Text PDFAdv Healthc Mater
September 2025
Brain Center, Department of Neurosurgery, Zhongnan Hospital of Wuhan University, Ministry of Education Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, School of Pharmaceutical Sciences, Wuhan University, Wuhan, Hubei, 430071, China.
Glioblastoma multiforme (GBM) continues to pose a significant challenge in the field of neuro-oncology primarily because of the limited penetration of therapeutics across the blood-brain barrier (BBB) and the presence of immunosuppressive tumor microenvironments. To address these challenges, a HD-PEG@BM biomimetic nanoplatform (hereinafter referred to as HD-P@BM) is developed that cloaks the near-infrared II photosensitizer HD-PEG (HD-P) inside microglial membranes to enable enhanced BBB penetration and tumor-targeted delivery. In this study, it is found that the microglia-derived membranes enhanced the uptake of nanoparticles by both the glioma cells and tumor-associated microglia.
View Article and Find Full Text PDFMater Today Bio
October 2025
Department of Thoracic Surgery, The Shengjing Hospital of China Medical University, Shenyang, Liaoning, 110004, PR China.
In addition to early diagnosis and on-time treatment, the adoption of new therapeutic strategies is of great significance for improving the clinical outcomes of patients with esophageal cancer. Although emerging therapies such as photothermal and photodynamic therapy (PDT) can precisely eliminate cancer cells and are alternative strategies to conventional treatments, hypoxia status of solid tumors have hindered their application. In recent years, nanoplatforms have been developed to address these limitations and improve the efficacy and safety of treatments.
View Article and Find Full Text PDFAnal Chem
September 2025
State Key Laboratory of Antiviral Drugs, Henan Joint International Research Laboratory of Environmental Pollution Control Materials, College of Chemistry and Molecular Sciences, Henan University, Kaifeng 475004, China.
Observing the dynamic changes of important organelles during photodynamic therapy (PDT) can more intuitively elucidate the mechanism of action, but organelle-targeted fluorescent probes capable of accomplishing this task face challenges. Herein, we designed a dual organelle-targeted near-infrared fluorescent probe () with a D-π-A structure to investigate PDT-induced dynamic nuclear changes and tumor ablation mechanisms. exhibited precise nuclear and lysosomal targeting capabilities, which enabled the tracing of nuclear changes during the cell division cycle.
View Article and Find Full Text PDFPharmaceuticals (Basel)
August 2025
Department of Biochemistry and Molecular Biology, School of Basic Medicine, Guangdong Medical University, Zhanjiang 524023, China.
: Hepatocellular carcinoma (HCC) remains a global health challenge with limited therapeutic efficacy. Photodynamic therapy (PDT) using 5,10,15-triethoxycarbonyl P(V) corrole () shows promise, but its molecular mechanisms and regulatory factors, particularly the role of SIRT1, are poorly understood. : The effects of combined with red light irradiation (625 nm) on HCC cells (HepG2, PLC/PRF5, MHCC97H) were evaluated via MTT, clonogenic assays, flow cytometry (apoptosis, mitochondrial membrane potential, ROS), and Western blotting (p53, Bax, Bcl-2, cleaved caspase-3, SIRT1).
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