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Heng Sun

Researcher at Zhejiang University

Publications -  10
Citations -  420

Heng Sun is an academic researcher from Zhejiang University. The author has contributed to research in topics: Cerium oxide & Nanoparticle. The author has an hindex of 4, co-authored 10 publications receiving 175 citations.

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Responsive Assembly of Upconversion Nanoparticles for pH-Activated and Near-Infrared-Triggered Photodynamic Therapy of Deep Tumors.

TL;DR: The development of tumor‐pH‐sensitive photodynamic nanoagents (PPNs) comprised of self‐assembled photosensitizers grafted pH‐responsive polymeric ligands and UCNPs demonstrates the attractive properties of both UCNP‐mediated deep‐tissue penetration of light and high therapeutic selectivity in vitro and in vivo.
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Catalytic activity tunable ceria nanoparticles prevent chemotherapy-induced acute kidney injury without interference with chemotherapeutics.

TL;DR: In this article, the authors reported catalytic activity tunable ceria nanoparticles (CNPs) as context-dependent reactive oxygen species scavengers, which can prevent chemotherapy-induced acute kidney injury without interfering with chemotherapeutic agents.
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Dual detoxification and inflammatory regulation by ceria nanozymes for drug-induced liver injury therapy

TL;DR: CeNZs can effectively scavenge ROS in impaired hepatocytes for detoxification and generate abundant oxygen based on their catalase (CAT)-mimic activity, thus further alleviating hypoxia and suggesting the future clinical use of CeNZs for DILI treatment, especially for the late stage DILi treatment.
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A Phosphatase-Mimetic Nano-Stabilizer of Mast Cells for Long-Term Prevention of Allergic Disease

TL;DR: In this paper, a ceria nanoparticle (CeNP-) based phosphatase-mimetic nano-stabilizer with a long-term therapeutic time window is developed for allergic disease prevention.
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A Tauopathy-Homing and Autophagy-Activating Nanoassembly for Specific Clearance of Pathogenic Tau in Alzheimer's Disease.

TL;DR: The THN can bind to hyperphosphorylated and/or aggregated tau and selectively accumulate in cells undergoing tauopathy and further promotes the clearance of pathogenic tau accumulation by stimulating autophagic flux, consequently rescuing neuron viability and cognitive functions in AD rats.