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Research citation

Enhanced FGF21 Delivery via Neutrophil-Membrane-Coated Nanoparticles Improves Therapeutic Efficacy for Myocardial Ischemia-Reperfusion Injury.

Animal StudyLow Moderate evidence

This record provides bibliographic details and links to the original research. An editorial study breakdown is not available.

What the researchers found

Neutrophil-membrane-coated nanoparticles loaded with FGF21 reduced heart damage after ischemia-reperfusion in mice by targeting inflamed cardiac tissue.

Why it matters

FGF21 is a metabolic regulator (like GLP-1 drugs) that protects the heart. Wrapping it in neutrophil membranes helps it reach damaged heart tissue more effectively.

The numbers in context

Neutrophil-membrane coated liposomal NPs with FGF21; tested in mouse ischemia-reperfusion model; improved cardiac outcomes vs uncoated NPs.

How the study worked

Nanoparticle fabrication, neutrophil membrane coating, characterization, and in vivo testing in mouse I/R injury model.

Who was studied

Mice with ischemia-reperfusion cardiac injury

What this study cannot tell us

Mouse model. Complex manufacturing process. Long-term safety of neutrophil-coated particles unknown. FGF21 may have off-target effects.

Read the original research

Enhanced FGF21 Delivery via Neutrophil-Membrane-Coated Nanoparticles Improves Therapeutic Efficacy for Myocardial Ischemia-Reperfusion Injury.

Nanomaterials (Basel, Switzerland), 15(5)

Citation

Rao, Zhiheng; Tang, Yuli; Zhu, Jiamei; Lu, Zhenzhen; Chen, Zhichao; Wang, Jiaojiao; Bao, Yuxuan; Mukondiwa, Alan Vengai; Wang, Cong; Wang, Xiaojie; Luo, Yongde; Li, Xiaokun. (2025). Enhanced FGF21 Delivery via Neutrophil-Membrane-Coated Nanoparticles Improves Therapeutic Efficacy for Myocardial Ischemia-Reperfusion Injury.. Nanomaterials (Basel, Switzerland), 15(5). https://doi.org/10.3390/nano15050346