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Foscarnet-Type Inorganic-Organic Hybrid Nanoparticles for Effective Antiviral Therapy

[Image: see text] [ZrO](2+)[(FCN)(0.4)(OH)(0.8)](2–) and Gd(3+)[FCN](3–) inorganic-organic hybrid nanoparticles (IOH-NPs) are novel saline antiviral nanocarriers with foscarnet (FCN) as a drug anion. FCN as a pyrophosphate analogue serves as a prototype of a viral DNA polymerase inhibitor. FCN is us...

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Detalles Bibliográficos
Autores principales: Khorenko, Mikhail, Rand, Ulfert, Cicin-Sain, Luka, Feldmann, Claus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007112/
https://www.ncbi.nlm.nih.gov/pubmed/35344659
http://dx.doi.org/10.1021/acsbiomaterials.2c00074
Descripción
Sumario:[Image: see text] [ZrO](2+)[(FCN)(0.4)(OH)(0.8)](2–) and Gd(3+)[FCN](3–) inorganic-organic hybrid nanoparticles (IOH-NPs) are novel saline antiviral nanocarriers with foscarnet (FCN) as a drug anion. FCN as a pyrophosphate analogue serves as a prototype of a viral DNA polymerase inhibitor. FCN is used for the treatment of herpesvirus infections, including the drug-resistant cytomegalovirus (CMV) and herpes simplex viruses, HSV-1 and HSV-2. The novel [ZrO](2+)[(FCN)(0.4)(OH)(0.8)](2–) and Gd(3+)[FCN](3–) IOH-NPs are characterized by aqueous synthesis, small size (20–30 nm), low material complexity, high biocompatibility, and high drug load (up to 44 wt % FCN per nanoparticle). The antiviral activity of the FCN-type IOH-NPs is probed for the human cytomegalovirus (HCMV). Moreover, the uptake of FCN-type IOH-NPs into vesicles, cytoplasm, and nuclei of nonphagocytic lung epithelial cells is evaluated. As a result, a promising antiviral activity of the FCN-type IOH-NPs that significantly outperforms freely dissolved FCN at the level of clinical formulations is observed, encouraging a future use of FCN-type IOH-NPs for the delivery of antivirals against respiratory viruses.