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Drug delivery system based on PVA and clay for potential treatment of COVID-19

Tremendous efforts are being made around the world to develop efficient ways to prevent/treat the novel β-coronavirus disease (COVID-19) caused by SARS-CoV-2. There are currently many studies and clinical trials (either based on computational predictions or clinical experiences), in progress, focusi...

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Detalles Bibliográficos
Autores principales: Teodorescu, Mirela, Morariu, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8806360/
http://dx.doi.org/10.1007/s10965-022-02927-5
Descripción
Sumario:Tremendous efforts are being made around the world to develop efficient ways to prevent/treat the novel β-coronavirus disease (COVID-19) caused by SARS-CoV-2. There are currently many studies and clinical trials (either based on computational predictions or clinical experiences), in progress, focusing on finding relevant protein targets and medications anti-COVID-19. In the present study, we report a hydrogel drug delivery system based on Laponite® RD (Lap) entrapped in a poly(vinyl alcohol) (PVA) matrix obtained by freezing/thawing method. The PVA/Lap hydrogels were characterized in terms of their morphological, rheological, and swelling properties. Moreover, in vitro drug delivery investigations were performed with a promising drug, Rifampicin (Rif). Rif is an antitubercular drug and was selected for this study in order to demonstrate its efficacy as an anti-COVID-19 repurposed drug. In vitro studies were supplemented by in silico molecular docking simulations of Rif capacity of inhibition against SARS-CoV-2 target protein 3-chymotrypsin-like protease (3CL(pro)). The results obtained in this study are encouraging and we propose the Rif loaded PVA/Lap hydrogels as promising drug delivery systems for COVID-19 treatment, promoting a synergistic therapeutic effect by dual targeting of viral 3CL(pro) and S proteins. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10965-022-02927-5.