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Wei Zhao
Researcher at Qingdao University of Science and Technology
Publications - 7
Citations - 338
Wei Zhao is an academic researcher from Qingdao University of Science and Technology. The author has contributed to research in topics: Drug delivery & Superhydrophobic coating. The author has an hindex of 5, co-authored 7 publications receiving 198 citations. Previous affiliations of Wei Zhao include University of Queensland.
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Remote Light-Responsive Nanocarriers for Controlled Drug Delivery: Advances and Perspectives.
TL;DR: Recent advances of light-responsive nanoplatforms for controlled drug release are reviewed, covering the mechanism of light responsive small molecules and polymers, UV and Vis light responsive nanocarriers, and NIR light responsive nmaterials.
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Polymerization-Induced Self-Assembly (PISA) - Control over the Morphology of 19F-Containing Polymeric Nano-objects for Cell Uptake and Tracking
TL;DR: It was found that the extent of cell uptake strongly depends on the morphology of the nano-objects, with preferable uptake for worm-like particles compared to spherical nanoparticles and vesicles.
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Salinomycin-Loaded Gold Nanoparticles for Treating Cancer Stem Cells by Ferroptosis-Induced Cell Death
TL;DR: Analysis of the mechanism of action of Sal-AuNPs indicated ferroptosis, an iron-dependent cell death, was achieved as a result of iron accumulation and inhibition of antioxidant properties, which led to the induction of oxidative stress, mitochondrial dysfunction, and lipid oxidation.
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A novel nanoparticle drug delivery system based on PEGylated hemoglobin for cancer therapy.
TL;DR: It is found that PEG-Hb-PTX NPs possess a better in vivo antitumor effect than the commercially available Taxol® formulation and has great potential as an efficient drug delivery system for further clinic study.
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Functional magnetic porous silica for T 1-T 2 dual-modal magnetic resonance imaging and pH-responsive drug delivery of basic drugs.
TL;DR: Abundant hydroxyl groups and a large surface area enabled the γ-Fe2O3@p-silica particles to be readily loaded with a large payload of the basic model drug rhodamine B (RB) and demonstrate an excellent pH-triggered drug release.