AgNPs |
Inhibit the virus binding with the cells in the initial stage of virus life cycles |
Inactivate replication and minimize virucidal activity |
[106] |
Restrict structural change due to viral invasion in the entry cell |
Stop replication and act as an antiviral agent |
[107] |
It blocked to form CD4+ T cells through CD4 binding with present gp120 on the surface envelope glycoprotein |
Replication of virus entry into the target cell |
[108] |
Control viral culture |
Prevents non–envelope viruses entry |
[109] |
Produce electrospun coating to stop interaction with the viral surface |
Reduce virus reproduction during entry into the cell |
[110] |
Ricinus Communis AgNPs |
Viral fusion between envelope protein and host cell |
Anti-enterovirus agent |
[111] |
Fungi-AgNPs |
Minimize virus infection and stop interaction of the virus with the host cell |
Antimicrobial agent |
[112] |
Cinnamon-AgNPs |
Inhibit virus propagation and blocked hemagglutinin function |
Restrict virus penetration inside the cell |
[113] |
Coffee and green tea-AgNPs |
Destroy the viral genome organism morphology and restrict hemagglutinin function |
Viral replication and functioning as a viricidal agent |
[114] |
AgNps immobilized onto textile fabrics |
Stop virus surface passivation |
Act as a virucidal agent |
[115] |
TiO2 ~ DNA nanocomposites |
Produce nucleic acid precipitation |
Inhibit virus reproduction in cell culture |
[116] |
TiO2 NPs |
Affect and control transport into the subsurface of virus |
Inactivate the virus entry |
[117] |
Silica-NPs |
Enable to detect antigen and enhance blood safety by minimizing antibody |
Infection detection and adopted to obtain detection range antigen of viruses |
[118] |
β-cyclodextrin-graphene oxidecomposite |
Initially stop the function of virus and blocked its attachment with the host cell |
Protect and enhanced healing ability against the virus |
[119] |
Carbon dots |
It prevents to make any linkage between virus and histo-blood group antigen, mostly with saliva secretor of the host cell |
Control the degradation of capsid proteins of the virus and slightly blocked to bind with the antibody |
[120] |
Protein NPs |
Maintained hemagglutinin function |
It leads to activate an enhanced immune response against the virus |
[121] |
Polypeptide NPs |
Reduction of cell protected by CD4+ T cells and transfusion provide immune serum |
Lifetime immune response |
[122] |
Polystyrene NPs |
Mannose-specific lectin |
Mucosal vaccine |
[123] |
PVP-stearic acid-polyethylene glycol -NPs |
Enhanced endocytosis pathways |
Anti-viral agents |
[124] |
Magnetic NPs |
Virus detected through different quantification methods |
Treatments and diagnosis of the infected cells |
[125] |
POD-NLCs |
Controlled cell proliferation |
Anti-viral agents |
[126] |
Dendrimer-RNA NPs |
Enhanced CD4+ T cells on the surface of envelope glycoprotein to work against IgG responses |
Detection of antigen and vaccine preparation |
[127] |
G2-dendrimer-citric acid-polyethylene glycol |
Antibody neutralization and boost immune response |
Vaccine technology |
[128] |
AuNPs |
Inhibit hemagglutinin function and produce antibody-protein antigens |
Enhanced immunity response and cell protection against virus |
[129] |
Useful to generate an antibody that can be bind with the membrane matrix protein of the infected cells |
Preparation of vaccine and as viricidal agents |
[130] |
Detection of virus pathogen by incorporating a specific antibody |
Applied as an immunosensor |
[131] |