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Zn-based physiometacomposite nanoparticles: distribution, tolerance, imaging, and antiviral and anticancer activity
Robert K DeLong1,2, Ryan Swanson1,2, Megan C Niederwerder3
1Department of Anatomy & Physiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506, USA.
Nanomedicine (London, England)
|July 20, 2021
Summary
Zinc-based physiometacomposites (PMCs) show promising anticancer and antiviral potential. These nanoparticles distribute widely in mice without toxicity, supporting their preclinical development for treating cancer and infectious diseases.
Area of Science:
- Nanotechnology
- Materials Science
- Biomedical Engineering
Background:
- Physiometacomposites (PMCs) offer novel therapeutic platforms.
- Zinc-based materials are explored for biomedical applications.
- Targeted delivery of therapeutic agents is crucial for cancer and infectious diseases.
Purpose of the Study:
- To investigate the distribution, tolerance, and anticancer/antiviral activity of doped Zinc-based physiometacomposites (PMCs).
- To evaluate PMCs as imaging probes and for targeted drug delivery systems.
Main Methods:
- Synthesis of doped ZnO, ZnS, or ZnSe nanoparticles.
- Assessment of cell uptake, biodistribution in 3D cultures and mice using fluorescence, bioluminescence, and ICP-MS.
- Evaluation of anticancer and antiviral efficacy via viability, antitumor, and virus titer assays.
Main Results:
- Nanoparticle distribution in mice followed the order: liver > spleen > kidney > lung > brain, with no observed tissue or blood pathology.
- PMCs demonstrated high cell viability (≥98-99%) at 25 μg/ml for 48 hours.
- Significant 3-log inhibition of β-Galactosidase and porcine reproductive and respiratory syndrome virus infection was achieved.
Conclusions:
- Zinc-based PMCs exhibit favorable biodistribution and low toxicity in preclinical models.
- PMCs show potential for use as diagnostic imaging agents and therapeutic delivery vehicles.
- These findings support the preclinical advancement of PMCs for oncology and infectious disease applications.

