Table 3.
Polymer-based nanoformulation
Diseases | Antiviral drug | Type of nanodelivery system | Lipid/polymer used as carrier | Key findings | Ref |
---|---|---|---|---|---|
HIV | Efavirenz, darunavir, indinavir | Polymeric micelles | Poly(ethylene oxide)–poly(propylene oxide) block copolymer |
Protects against degradation Enhances solubility Improves palatability for pediatric formulations |
[77] |
HSV | Acyclovir | Polymeric micelles | Acyclovir–polycaprolactone (core)-methoxy PEG (shell) copolymer |
Nontoxic Efficient drug delivery |
[78] |
Hepatitis B | Lamivudine stearate (prodrug) | Polymeric micelles | Stearic acid–grafted chitosan oligosaccharide polymeric micelles | High drug loading, high cellular uptake in HBV-transfected human hepatoblastoma cells, more conspicuous inhibition of antigen expression and DNA replication | [79] |
HIV | Nevirapine | Polymeric nanoparticles | Cellulose acetate butyrate |
Increased therapeutic efficacy Decreased biocompatibility |
[80] |
HIV | Efavirenz (transferrin receptor-binding peptide) | Polymeric nanoparticles | PLGA |
Increased stability to interact with BBB Increased permeability |
[81] |
HIV | Nevirapine | Polymeric nanoparticles | PLGA nanoparticles conjugated with transferrin | Increased uptake in human brain microvascular endothelial cells | [82] |
HIV | Zidovudine | Polymeric nanoparticles | CRM 197–grafted zidovudine–loaded polybutylcyanoacrylate nanoparticles | Increased uptake in human brain microvascular endothelial cells | [83] |
HIV | Lamivudine | Polymeric nanoparticles | Chitosan cross-linked with glutaraldehyde nanoparticles | Brain targeting | [84] |
HIV | Combination antiretroviral drugs; efavirenz, lopinavir, ritonavir | Polymeric nanoparticles | Poly-(dl-lactide-co-glycolic acid), i.e., PLGA | > 79% drug entrapment efficiency for each of the three drugs, efficient uptake in nonimmune and immune cells, higher nuclear, cytoskeleton and membrane drug levels in HIV-1–infected H9 monocytic cells, inhibition of HIV infection and transduction with IC50 < 31 nM for each of the three drugs in TZM b1 cells | [85] |
Herpes infection | Lamivudine | Polymeric nanoparticles | PLGA |
Enhanced AUC High targeting |
[86] |
HIV | Elvitegravir | Polymeric nanoparticles | PLGA | Enhanced intracellular uptake | [87] |
VZV, HZV, HSV | Acyclovir | Mucoadhesive dendrimer | Cyanoacrylates, polyacrylic acid, Na carboxymethylcellulose, hyaluronic acid, hydroxypropylcellulose, polycarbophil, chitosan, and gellan | Improved mucoadhesion | [88] |
Chicken pox, HZV, HSV | Acyclovir | Nanoemulsion | Eudragit RLPO |
Low dose Minimizes side effects Improves oral bioavailability |
[89] |
VZV, HZV, HSV | Acyclovir | Nanoemulsion | Polylactic co-glycolic acid |
Prolonged circulation time Increased biodistribution and bioavailability |
[89] |
HIV | Nelfinavir mesylate, darunavir, atazanavir | Nanoemulsions | Poly-vinylpyrrolidone, HPMC, sodium carboxymethyl cellulose, and methyl cellulose |
Maximizes therapeutic efficacy Enhances solubility High drug-loading capacity |
[90] |
HIV | Efavirenz, saquinavir | Cyclodextrins-complexes | β-Cyclodextrin polymers |
Enhances solubility Enhances physicochemical properties |
[91] |
VZV, HZV, HSV | Acyclovir | Mucus-penetrating nanoparticles | Poly(lactide-co-glycolide), poly(anhydrides), polyethylenimine, chitosan, and polylysine | Improved mucoadhesion | [92] |
HIV | Nevirapine | Nanocrystals | Cellulose derivatives, PVA, PVP, polyoxyethylene sorbitan fatty acid esters, pluronics, poloxamers, copolymers—polyoxyethylene and polyoxypropylene |
Improved bioavailability Prolonged and increased availability of drug; less excretion of the drug Facilitates phagocytosis and targets the spleen |
[93] |
HIV | Efavirenz | Nanodispersion | PVP, PVA, HPMC, PEG |
Enhanced solubility Prolonged availability of drug |
[72] |
HSV | Acyclovir | Nanosponges |
Hyper cross-linked polystyrenes, methyl β-cyclodextrin, alkyloxycarbonyl cyclodextrins, 2-hydroxy, propyl β-cyclodextrins Copolymers like PVA, poly(valerolactone allylvalerolactone), poly(valerolactone-allylvalerolactoneoxepanedione), ethyl cellulose |
Increased solubility, stability, and formulation flexibility Modified release of drug |
[94] |
HSV | Acyclovir | Nanosponges | Cyclodextrins, ethylcellulose, PVA, poly(valero lactone allylvalero lactone), poly(valerolactone-allylvalerolactoneoxepanedione) | [95] | |
HIV | Zidovudine | Amide-functionalized alginate nanoparticles | Sodium alginate | Efficient cellular uptake | [96] |