Author: Kandeel, Mahmoud; Alâ€Taher, Abdulla; Park, Byoung Kwon; Kwon, Hyungâ€Joo; Alâ€Nazawi, Mohammed
Title: A pilot study of the antiviral activity of anionic and cationic polyamidoamine dendrimers against the Middle East respiratory syndrome coronavirus Cord-id: plrlpyk9 Document date: 2020_5_8
ID: plrlpyk9
Snippet: The Middle East respiratory syndrome coronavirus (MERSâ€CoV) is an emerging virus that causes infection with a potentially fatal outcome. Dendrimers are highly branched molecules that can be added to antiviral preparations to improve their delivery, as well as their intrinsic antiviral activity. Studies on identifying antiâ€MERSâ€CoV agents are few. Three types of polyanionic dendrimers comprising the terminal groups sodium carboxylate (generations 1.5, 2.5, 3.5, and 4.5), hydroxyl (generatio
Document: The Middle East respiratory syndrome coronavirus (MERSâ€CoV) is an emerging virus that causes infection with a potentially fatal outcome. Dendrimers are highly branched molecules that can be added to antiviral preparations to improve their delivery, as well as their intrinsic antiviral activity. Studies on identifying antiâ€MERSâ€CoV agents are few. Three types of polyanionic dendrimers comprising the terminal groups sodium carboxylate (generations 1.5, 2.5, 3.5, and 4.5), hydroxyl (generations 2, 3, 4, and 5), and succinamic acid (generations 2, 3, 4, and 5) and polycationic dendrimers containing primary amine (generations 2, 3, 4, and 5) were used to assess their antiviral activity with the MERSâ€CoV plaque inhibition assay. The hydroxyl polyanionic set showed a 17.36% to 29.75% decrease in MERSâ€CoV plaque formation. The most potent inhibition of MERSâ€CoV plaque formation was seen by G(1.5)â€16COONa (40.5% inhibition), followed by G(5)â€128SA (39.77% inhibition). In contrast, the cationic dendrimers were cytotoxic to Vero cells. Polyanionic dendrimers can be added to antiviral preparations to improve the delivery of antivirals, as well as the intrinsic antiviral activity.
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