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Di-Wei Zheng

Researcher at Wuhan University

Publications -  68
Citations -  3981

Di-Wei Zheng is an academic researcher from Wuhan University. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 25, co-authored 53 publications receiving 2387 citations. Previous affiliations of Di-Wei Zheng include Hubei University.

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Carbon-Dot-Decorated Carbon Nitride Nanoparticles for Enhanced Photodynamic Therapy against Hypoxic Tumor via Water Splitting.

TL;DR: In vitro study showed that PCCN could increase the intracellular O2 concentration and improve the reactive oxygen species generation in both hypoxic and normoxic environments upon light irradiation, and in vivo experiments indicated that P CCN had superior ability to overcome tumor hypoxia.
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Preferential Cancer Cell Self-Recognition and Tumor Self-Targeting by Coating Nanoparticles with Homotypic Cancer Cell Membranes.

TL;DR: MNP@DOX@CCCM nanovehicle showed strong potency for tumor treatment in vivo and the MR imaging and shows great potential for precise therapy/diagnosis of various tumors merely by adjusting the cell membrane source accordingly on the nanoparticle surface.
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Switching Apoptosis to Ferroptosis: Metal–Organic Network for High-Efficiency Anticancer Therapy

TL;DR: MON encapsulated with p53 plasmid (MON-p53) was designed to eradicate cancer cells via ferroptosis/apoptosis hybrid pathway by harnessing the recently discovered oxidative stress regulation ability of p53 and the Fenton reaction inducing capability of metal-organic network.
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Enhanced Immunotherapy Based on Photodynamic Therapy for Both Primary and Lung Metastasis Tumor Eradication

TL;DR: A chimeric peptide, PpIX-1MT, is synthesized, which integrates photosensitizer Ppix with immune checkpoint inhibitor 1MT via a caspase-responsive peptide sequence, Asp-Glu-Val-Asp (DEVD), to realize a cascaded synergistic effect that could inhibit both primary and lung metastasis tumor effectively.
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Phage-guided modulation of the gut microbiota of mouse models of colorectal cancer augments their responses to chemotherapy.

TL;DR: Dextran nanoparticles loaded with a chemotherapeutic agent and bound to phages that eliminate a pro-tumoural gut bacterium and promote the growth of anticancer-compound-producing bacteria boost chemotherapy responses in mouse models of colorectal cancer.