Journal: |
Colloids and Surfaces B: Biointerfaces
Elsevier
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Volume: |
113703
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Abstract: |
The management of coronavirus necessitates that medicines are available, reasonably priced, and easy to
administer. The work aimed at formulating and characterizing remdesivir and licorice extract nanoemulsions and
comparing their efficacy against coronavirus for further subcutaneous injection. First, the solubility of remdesivir
was determined in different oils, surfactants, and co-surfactants to choose the optimal nanoemulsion components. Nanoemulsions were optimized concerning surfactant: co-surfactant ratio (5:1, 4:1, 3:1, 2:1, and 1:1) and
oil to surfactant: co-surfactant ratio (1:9, 1:8, 1:7, 1:6, 1:5, 1:4, 1:3, 1:2, and 1:1). The formulations were
evaluated concerning % transmittance, emulsification time, pH, viscosity, droplet size, polydispersity index, zeta
potential, drug content, transmission electron microscopy, in-vitro drug release, stability (of the optimal formulas), and antiviral effect against coronavirus. The optimal nanoemulsion formula was F7, exhibiting an
acceptable pH level, a rapid emulsification rate, a viscosity of 20 cP, and 100% drug content. The formulation
droplet size was 16 and 17 nm, the polydispersity index was 0.18 and 0.26, and the zeta potential was − 6.29 and
− 10.34 mV for licorice extract and remdesivir nanoemulsions, respectively. However, licorice extract nanoemulsion exhibited better release and physical stability. Licorice extract nanoemulsion may be a potential
subcutaneous injection for combating mild to moderate coronavirus.
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