Remdesivir-Loaded Nanoliposomes Stabilized by Chitosan/Hyaluronic Acid Film with a Potential Application in the Treatment of Coronavirus Infection.

An object of the present study was the development of liposomes loaded with the medicine Veklury® (remdesivir) stabilized by electrostatic adsorption of polysaccharide film formed from chitosans with different physicochemical characteristics and hyaluronic acid. The functionalization of the structures was achieved through the inclusion of an aptamer (oligonucleotide sequence) with specific affinity to the spike protein of the human coronavirus HCoV-OC43. The hydrodynamic size, electrokinetic potential and stability of the structures were evaluated at each step in the procedure. The encapsulation efficiency and loaded amount of remdesivir (99% and 299 µg/mL) were estimated by UV-vis spectroscopy. Our investigations showed manifestation of promising tendencies for prolonged periods of the drug release and increased effectiveness of its antiviral action. Among all studied versions of the delivery system, the most distinguished and suitable in a model coronavirus therapy are the liposomes formed from chitosan oligosaccharides. The cytotoxicity of the liposomes was determined against the HCT-8 cell line. A cytopathic effect inhibition test was used for the assessment of the antiviral activity of the compounds. The virucidal activity and the effect on the viral adsorption of the samples were reported by the end-point dilution method, and the alteration in viral titer was determined as Δlgs compared to untreated controls. The redox-modulating properties of the nanoparticles were studied in vitro in certain/several/a few chemical model systems. Our investigations showed a manifestation of promising tendencies for a prolonged effect of the drug release and increased effectiveness of its antiviral action.

Polysaccharide/Carbon Quantum Dots Composite Film on Model Colloidal Particles-An Electro-Optical Study.

Negatively charged carbon dots (Cdots) were successfully impregnated into chitosan/alginate film formed on model colloidal particles as a result of the attractive interactions with the chitosan molecules. The electrical properties of the produced films were studied by electrokinetic spectroscopy. In this study, the electric light scattering method was applied for first the time for the investigation of suspensions of carbon-based structures. The electro-optical behavior for the suspension of polymer-coated particles showed that the electric polarizability of the particle-covered layer from alginate was significantly higher compared to that of the layer from chitosan due to the higher charge density of alginate. The presence of a low concentration of Cdots in the film results in partial charge screening. It was confirmed that the polarizability of counterions with lower mobility along the adsorbed polyion chains was responsible for the registered electro-optical effect from the suspension of polymer-coated particles and that the participation of diffuse H+ counterions of Cdots in the creation of the electro-optical effect was negligible. The observed oscillation behavior in the evolution of the film thickness was interpreted through the participation of compensatory effects due to the additional adsorption/desorption of polyelectrolyte complexes from the film surface. The concentration of Cdots in the film was determined, and the loaded amount was ca. 6.6 µg/mL per layer.

Comparative Electrokinetic Study of Alginate-Coated Colloidal Particles.

Alginates are a family of natural polysaccharides with promising potential in biomedical applications and tissue regeneration. The design of versatile alginate-based structures or hydrogels and their stability and functionality depend on the polymer's physicochemical characteristics. The main features of alginate chains that determine their bioactive properties are the molar ratio of mannuronic and glucuronic residues (M/G ratio) and their distribution along the polymer chain (MM-, GG-, and MG blocks). The present study is focused on investigating the influence of the physicochemical characteristics of alginate (sodium salt) on the electrical properties and stability of the dispersion of polymer-coated colloidal particles. Ultrapure and well-characterized biomedical-grade alginate samples were used in the investigation. The dynamics of counterion charge near the vicinity of adsorbed polyion is studied via electrokinetic spectroscopy. The results show that the experimental values of the frequency of relaxation of the electro-optical effect are higher compared to the theoretical ones. Therefore, it was supposed that polarization of the condensed Na+ counterions occurs at specific distances according to the molecular structure (G-, M-, or MG-blocks). In the presence of Ca2+, the electro-optical behavior of the particles with adsorbed alginate molecules almost does not depend on the polymer characteristics but was affected by the presence of divalent ions in the polymer layer.

Bulgarian Medicinal Extracts as Natural Inhibitors with Antiviral and Antibacterial Activity.

BACKGROUND: Bulgaria is a country with a wide range of medicinal plants, with uses in traditional medicine dating back for centuries. METHODS: Disc diffusion assay was used to evaluate the antimicrobial activity of the plant extracts. A cytopathic effect inhibition test was used for the assessment of the antiviral activity of the extracts. The virucidal activity of the extracts, their influence on the stage of viral adsorption, and their protective effect on uninfected cells were reported using the end-point dilution method, and Δlgs was determined as compared to the untreated controls. RESULTS: The results of the study reveal that the antibacterial potential of G. glabra and H. perforatum extracts in Gram-positive bacteria is more effective than in Gram-negative bacteria. When applied during the replication of HSV-1 and HCov-OC-43, only some of the extracts showed weak activity, with SI between 2 to 8.5. Almost all tested extracts inhibited the extracellular virions of the studied enveloped viruses (HSV-1 and HCov-OC-43) to a greater extent than of the non-enveloped viruses (PV-1 and HAdV-5). They inhibited the stage of viral adsorption (HSV-1) in the host cell (MDBK) to varying degrees and showed a protective effect on healthy cells (MDBK) before they were subjected to viral invasion (HSV-1). CONCLUSION: The antipathogenic potential of extracts of H. perforatum and G. glabra suggests their effectiveness as antimicrobial agents. All 13 extracts of the Bulgarian medicinal plants studied can be used to reduce viral yield in a wide range of viral infections.

Electrosteric stabilization of oil/water emulsions by adsorption of chitosan oligosaccharides-An electrokinetic study.

The present study was focused on investigation of electrokinetic behaviour of lecithin-stabilized oil/water emulsions in the presence of chitosan oligosaccharides (COS). The oligosaccharides give unique opportunity for precisely characterization of the properties of chitosan as a function of the degree of acetylation (DA) and degree of polymerization (DP) of the polymer. For the study were chosen well characterized ultra pure COS molecules with completely acetylated monomers and mixture of COS molecules with acetylated and deacetylated monomers. The obtained results confirmed experimentally for the first time, the suggestion for the predominant contribution of hydrophobic (at high DA) and electrostatic (at low DA) interactions between chitosan monomers and the lecithin-covered droplet surface.

Nanocolloids of indomethacin prepared using sonication and subsequent encapsulation with polysaccharide films.

A new procedure was applied for preparation of indomethacin (IMC) nano-particles (ca. 200nm), which includes ultrasonication of micron range IMC crystals in water, followed by short centrifugation to remove the larger drug particles. In order to stabilize the suspension against aggregation and to reduce the release time of the drug, water insoluble IMC particles were coated with chitosan/pectin (CHI/PEC) multilayer film at pH 4. Charge balance in the multilayer film and increase in the film thickness with the number of adsorbed layers was studied by means of electro-optics. The release time of IMC molecules from the encapsulated particles was measured at physiological pH 7, when the solubility of IMC in water increases several times. Addition of small amount of CaCl2 after deposition of PEC layers was applied to compact the multilayer films on the IMC particles.

Complexation of ferric oxide particles with pectins of ordered and random distribution of charged units.

Complexation between ferric oxide particles and pectins with degree of methylation 50% but having ordered or random arrangement of free carboxyl groups is investigated by electric light scattering and electrophoresis. The influence of charge distribution in pectin chain on the electrical properties of oppositely charged oxide particles and stability of their suspensions is examined as a function of pectin concentration. Although the difference in charge density of pectin samples is ~5%, we found small but measurable difference in the behavior of both oxide/pectin complexes. This is attributed to condensation of counterions near the chains of pectin with ordered distribution of charges, leading to a decrease in the effective charge density and to a corresponding decrease in the contour length of the adsorbing pectin chains. Two parameters are sensitive to the conformation of the adsorbed chains in suspensions, stabilized by pectin adsorption (at particle charge reversal). The electro-optical effect is higher for the complex with less charged pectin, which is explained with larger amount of chains, adsorbed in more coiled conformation than the chains of pectin with random distribution of free carboxyl groups. The addition of small amounts of CaCl(2) has no significant influence on the thickness of the layer from the less charged pectin, in agreement with a more compact conformation of the chains in this adsorbed layer. In contrast, the thickness of the layer from pectin with random distribution of charged groups decreases with increasing concentration of CaCl(2), indicating a more loose structure of this layer.

Dynamics and heterogeneity of Pb(II) binding by SiO2 nanoparticles in an aqueous dispersion.

Pb(II) binding by SiO(2) nanoparticles in an aqueous dispersion was investigated under conditions where the concentrations of Pb(2+) ions and nanoparticles are of similar magnitude. Conditional stability constants (log K) obtained at different values of pH and ionic strength varied from 4.4 at pH 5.5 and I = 0.1 M to 6.4 at pH 6.5 and I = 0.0015 M. In the range of metal to nanoparticle ratios from 1.6 to 0.3, log K strongly increases, which is shown to be due to heterogeneity in Pb(II) binding. For an ionic strength of 0.1 M the Pb(2+)/SiO(2) nanoparticle system is labile, whereas for lower ionic strengths there is loss of lability with increasing pH and decreasing ionic strength. Theoretical calculations on the basis of Eigen-type complex formation kinetics seem to support the loss of lability. This is related to the nanoparticulate nature of the system, where complexation rate constants become increasingly diffusion controlled. The ion binding heterogeneity and chemodynamics of oxidic nanoparticles clearly need further detailed research.

Electrical properties of polyelectrolyte layers adsorbed on colloidal particles at different ionic strength.

The investigation presents results on the low-frequency electrical polarization of ß-FeOOH particles with adsorbed layers from sodium salts of poly(4-styrene sulfonate), poly(acrylic acid), and carboxymethyl cellulose, obtained by electric light scattering. The adsorption is realized in aqueous NaCl solutions of different concentration, and the suspensions of the coated particles are then rinsed to low conductivity. Several electro-optical parameters are sensitive to the conformation of the adsorbed polyelectrolyte layer. The particle electrical polarizability increases drastically with the concentration of NaCl (correlating with significant increase of the adsorbed amount of polyelectrolyte), while their electrophoretic mobility remains practically unchanged. Two time scales are involved in the stepwise relaxation of the electrical polarizability. The faster process is attributed to movement of ions in the polymer layer, restricted by the coiled conformation to smaller distances. The contribution of the Debye atmosphere outside the polymer layer remains almost unchanged, which correlates with the low sensitivity of the electrophoretic mobility to the increasing amount of adsorbed polyelectrolyte. Abrupt increase in a narrow interval of salt concentrations is observed both for the low-frequency component of the particle polarization and for the hydrodynamic layer thickness, indicating changes in the surface electric state, most probably due to swelling of the adsorbed polymer layer.

Complexation of ferric oxide particles with pectins of different charge density.

The effect of polyelectrolyte charge density on the electrical properties and stability of suspensions of oppositely charged oxide particles is followed by means of electro-optics and electrophoresis. Variations in the electro-optical effect and the electrophoretic mobility are examined at conditions where fully ionized pectins of different charge density adsorb onto particles with ionizable surfaces. The charge neutralization point coincides with the maximum of particle aggregation in all suspensions. We find that the concentration of polyelectrolyte, needed to neutralize the particle charge, decreases with increasing charge density of the pectin. The most highly charged pectin presents an exception to this order, which is explained with a reduction of the effective charge density of this pectin due to condensation of counterions. The presence of condensed counterions, remaining bound to the pectin during its adsorption on the particle surface, is proved by investigation of the frequency behavior of the electro-optical effect at charge reversal of the particle surface.

Effect of pectin charge density on formation of multilayer films with chitosan.

The effect of pectin charge density on the formation of multilayer films with chitosan (PEC/CHI) is studied by means of electro-optics. Pectins of low (21%) and high (71%) degrees of esterification, which are inversely proportional to the pectin charge density, are used to form films on colloidal beta-FeOOH particles at pH 4.0 when the CHI is fully ionized. We find that, after deposition of the first 3-4 layers, the film thickness increases linearly with the number of adsorbed layers. However, the increase in the film thickness is larger when the film is terminated with CHI. Irregular increase of the film thickness is more marked for the PEC with higher density of charge. Oscillation in the electrical polarizability of the film-coated particles with the number of deposited layers is also registered in the PEC/CHI films. The charge balance of the multilayers, calculated from electrical polarizability of the film-coated particles, is positive, with larger excess of positive charge within the film constructed from CHI and less charged PEC. This is attributed to the ability of CHI to diffuse into the film at each deposition step. Despite the CHI diffusion, the film thickness increases linearly due to the dissolution of unstable PEC/CHI complexes from the film surface.

Effect of chain length and charge density on the construction of polyelectrolyte multilayers on colloidal particles.

Two combinations of sodium poly(4-styrene sulfonate) (PSS) and poly(allylamine hydrochloride) (PAH) of different chain length and charge density are employed to construct multilayer films. The polyelectrolytes are assembled layer-by-layer on colloidal particles in the absence of salt. We have investigated the formation and electrical characteristics of the films by using electric light scattering technique. The results show that the film thickness is independent of the chain length when fully charged PAH (at pH 4.6) is combined with fully charged PSS. When the films are prepared with less charged PAH (at pH 6.7) and fully charged PSS, lower thickness is found for the film with shorter polymer chains. In all cases, the thickness increment realized on addition of the polymer with lower molar concentration is partially lost on exposure to the solution with higher concentration of the oppositely charged partner. When the film growth is regular (at equal molar concentrations of the fully charged polyelectrolytes), the ratio of PSS to PAH charge, estimated from the electro-optical effect values, exceeds 1. The electro-optical effect is also higher for the films ending with PSS when fully charged PSS is combined with less charged PAH (at pH 6.7). This reveals the key role of the charge in the last-adsorbed layer for the electro-optical behavior of the whole film.

Counterion release from adsorbed highly charged polyelectrolyte: an electrooptical study.

The adsorption of sodium poly(4-styrene sulfonate) on oppositely charged beta-FeOOH particles is studied by electrooptics. The focus of this paper is on the release of condensed counterions from adsorbed polyelectrolyte upon surface charge overcompensation. The fraction of condensed Na+ counterions on the adsorbed polyion surface is estimated according to the theory of Sens and Joanny and it is compared with the fraction of condensed counterions on nonadsorbed polyelectrolyte. The relaxation frequency of the electrooptical effect from the polymer-coated particle is found to depend on the polyelectrolyte molecular weight. This is attributed to polarization of the layer from condensed counterions on the polyion surface, being responsible for creation of the effect from particles covered with highly charged polyelectrolyte. The number of the adsorbed chains is calculated also assuming counterion condensation on the adsorbed polyelectrolyte and semiquantative agreement is found with the result obtained from the condensed counterion polarizability of the polymer-coated particle. Our findings are in line with theoretical predictions that the fraction of condensed counterions remains unchanged due to the adsorption of highly charged polyelectrolyte onto weakly charged substrate.

Electrical properties of multilayers from low- and high-molecular-weight polyelectrolytes.

The formation of stable multilayer films by using as constituents sodium poly(4-styrene sulfonate) (PSS) and poly(4-vinyl pyridine) (PVP) was studied by electrooptics. A strong increase in basicity of the pyridine rings in the electrical field of the oppositely charged PSS chains was suggested to be the driving force for multilayer film formation. A linear increase in the film thickness was registered after deposition of the first three layers, with no dependence on the polyelectrolyte molecular weight. The electrooptical effect was found to increase with increasing area of each next layer, but depended on the molecular weights of both polymers. Polarization of "condensed" counterions along the chains of the last-adsorbed layer was suggested to explain this dependence. Following the counterion dynamics, we come to the conclusion that the electrical properties of the top layer govern the electrooptical behavior of the PSS/PVP film.

Electro-optics of colloids coated with multilayers from strong polyelectrolytes:surface charge relaxation.

The electrical properties and structure of polyelectrolyte multilayers prepared by layer-by-layer deposition of poly(sodium 4-styrenesulfonate) (PSS) and poly(diallyldimethylammonium chloride) (PDADMAC) on ellipsoidal beta-ferric hydrous oxide particles are examined in situ using the electric light scattering method. In the initial nonlinear growth regime, the electro-optical effect is found to increase almost in the same manner as the thickness of the multilayer film. This reveals an increase in the multilayer surface charge due to the nonlinear increase in polyelectrolyte adsorption. Above five deposition cycles, the electro-optical effect reaches a plateau and the thickness increment per layer becomes constant, indicating regular film growth. Evidence is given that the concentration of small residual ions incorporated into the PSS/PDADMAC film is negligible. Polarization of counterions, bound near to the surface of the last-adsorbed polyion, is assumed to explain the relaxation of the electro-optical effect in the frequency range 10(3)-10(5) Hz.