» Articles » PMID: 37447594

Synergistic Effect of Zinc-Chitosan Nanoparticles and Hydroxychloroquine to Inhibit Buffalo Coronavirus

Overview
Publisher MDPI
Date 2023 Jul 14
PMID 37447594
Authors
Affiliations
Soon will be listed here.
Abstract

Zinc ions can hinder the synthesis of proteins required for accomplishing several stages of the viral life cycle. The intracellular zinc concentration can be increased by using zinc ionophores which transport zinc ions into the cells and hinder viral replication. (Hydroxy)chloroquine is an example of a zinc ionophore, but both zinc and (hydroxy)chloroquine can be toxic to the host organism. The nanocarriers may serve as camouflage to evade the adverse effects of drugs, chemicals, and nanoparticles on the host. We formulated ZnO nanoparticles with flower-like morphology (ZnONFs). It was further decorated with chitosan along with hydroxychloroquine (as a zinc ionophore) (CHCZnO NPs). We have chosen the cationic polymer chitosan since it is biocompatible, biodegradable and binds easily with the cells, and enhances the transport of drugs across cell membranes. The formulation was investigated for size, shape, surface charge, and interaction of chemicals used. We evaluated the formulations for cytotoxicity, and biocompatibility in embryonated chicks and their efficacy against bovine coronavirus (BCoV) isolated from a buffalo calf, and pneumo-enteric coronaviruses isolated from a buffalo calf with promising results in comparison to ZnONFs/hydroxychloroquine alone. Furthermore, we elucidate the mechanism underlying the lysosomotropic effect of various formulations on Vero cells infected with the buffalo coronavirus.

Citing Articles

Chitosan-Zinc-Ligated Hydroxychloroquine: Molecular Docking, Synthesis, Characterization, and Trypanocidal Activity against .

Manuja A, Rani R, Devi N, Sihag M, Rani S, Prasad M Polymers (Basel). 2024; 16(19).

PMID: 39408487 PMC: 11478425. DOI: 10.3390/polym16192777.


Antiviral and Cytoprotective Effect of Zinc (Yasad Bhasma) Based Nanoformulations Against Bovine Coronavirus.

Manuja A, Kumar B, Chhabra D, Brar B, Riyesh T, Pal Y Indian J Microbiol. 2024; 64(3):1123-1131.

PMID: 39282188 PMC: 11399353. DOI: 10.1007/s12088-024-01255-0.

References
1.
Raguvaran R, Manuja A, Manuja B, Riyesh T, Singh S, Kesavan M . Sodium alginate and gum acacia hydrogels of zinc oxide nanoparticles reduce hemolytic and oxidative stress inflicted by zinc oxide nanoparticles on mammalian cells. Int J Biol Macromol. 2017; 101:967-972. DOI: 10.1016/j.ijbiomac.2017.03.180. View

2.
Ooi E, Chew J, Loh J, Chua R . In vitro inhibition of human influenza A virus replication by chloroquine. Virol J. 2006; 3:39. PMC: 1481635. DOI: 10.1186/1743-422X-3-39. View

3.
Arndt A, Larson B, Hogue B . A conserved domain in the coronavirus membrane protein tail is important for virus assembly. J Virol. 2010; 84(21):11418-28. PMC: 2953170. DOI: 10.1128/JVI.01131-10. View

4.
Manuja A, Chhabra D, Kumar B . Chloroquine chaos and COVID-19: Smart delivery perspectives through pH sensitive polymers/micelles and ZnO nanoparticles. Arab J Chem. 2022; 16(2):104468. PMC: 9710101. DOI: 10.1016/j.arabjc.2022.104468. View

5.
Gao J, Tian Z, Yang X . Breakthrough: Chloroquine phosphate has shown apparent efficacy in treatment of COVID-19 associated pneumonia in clinical studies. Biosci Trends. 2020; 14(1):72-73. DOI: 10.5582/bst.2020.01047. View