Investigation of the Aggregation of Aß Peptide (1-40) in the Presence of κ-Carrageenan-Stabilised Liposomes Loaded with Homotaurine.

The kinetics of amyloid aggregation was studied indirectly by monitoring the changes in the polydispersity of mixed dispersion of amyloid ß peptide (1-40) and composite liposomes. The liposomes were prepared from the 1,2-dioleoyl-sn-glicero-3-phoshocholine (DOPC) phospholipid and stabilised by the electrostatic adsorption of κ-carrageenan. The produced homotaurine-loaded and unloaded liposomes had a highly negative electrokinetic potential and remarkable stability in phosphate buffer (pH 4 and 7.4). For the first time, the appearance and evolution of the aggregation of Aß were presented through the variation in the standard percentile readings (D10, D50, and D90) obtained from the particle size distribution analysis. The kinetic experiments indicated the appearance of the first aggregates almost 30 min after mixing the liposomes and peptide solution. It was observed that by adding unloaded liposomes, the size of 90% of the particles in the dispersion (D90) increased. In contrast, the addition of homotaurine-loaded liposomes had almost minimal impact on the size of the fractions of larger particles during the kinetic experiments. Despite the specific bioactivity of homotaurine in the presence of natural cell membranes, this study reported an additional inhibitory effect of the compound on the amyloid peptide aggregation due to the charge effects and 'molecular crowding'.

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.

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.

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.

Electro-optics of colloid-polyelectrolyte complexes: counterion condensation on free and adsorbed sodium carboxymethyl cellulose.

Electrical properties of sodium carboxymethyl cellulose (NaCMC) in aqueous solution and after addition to a dilute suspension of beta-ferric hydrous oxide particles (beta-FeOOH) are studied by means of electric birefringence method. We established extended conformation of the NaCMC chains in a solution at concentration 10(-2) g dm(-3), which is found high enough to assure overcharging of the particle surface. The frequency behavior of the electric birefringence of NaCMC solution with concentration 10(-2) gdm(-3) is found similar to the behavior of the suspension of beta-FeOOH particles containing same amount of polyelectrolyte. The observed decrease in the relaxation frequency of the electro-optical effect in both systems is attributed to polarization of condensed counterions near to the polyion surface. These results are in line with our previous estimation, showing that the condensed counterions are not released from NaCMC because of its adsorption onto weakly charged particle surface. They also reveal that, at overcompensation of the particle charge, the electrical properties of the adsorbed polyion dominate the electro-optical behavior of the weakly charged particle.

Polypeptide multilayer films on colloidal particles: an in situ electro-optical study.

The buildup of poly(L-glutamic acid) (PGA) and poly(L-lysine) (PLL) multilayers on beta-FeOOH colloidal particles was investigated by means of electro-optics and electrophoresis. The films were built at different (acidic) pH in the absence of salt. We found that the thickness of the film grows linearly when the fully charged PLL (at pH 5.5) is combined with almost fully charged PGA (at pH 6.5), with a thickness of about 2 nm per single layer. When the fully charged PLL is combined with weakly charged PGA (at pH 4.5), the film thickness increases exponentially with the number of deposited layers. The thickness of the exponentially growing film increases to 300 nm after deposition of 16 layers. The exponential film growth is attributed to the ability of the PLL to diffuse "in" and "out" of the film bulk at each deposition step. The variation in the electrical polarizability of the film-coated particles was also monitored as a function of the number of adsorbed layers. The result reveals that the PLL chains, which can diffuse into the film bulk, have no measurable contribution to the electro-optical effect of the films terminated with PLL. It is only due to the polarization of counterions of the PLL adsorbed on the film surface.

Formation of polyelectrolyte multilayers from polysaccharides at low ionic strength.

Layer-by-layer deposition of sodium carboxymethylcellulose (NaCMC) and chitosan (CHI) was used to create polyelectrolyte multilayers on ellipsoidal beta-FeOOH particles at low ionic strength. Using electro-optics, we investigated the formation of films in dependence on the polyelectrolyte charge density by controlling pH of the dipping solutions. We found out a linear growth of the CMC/CHI films when they are constructed from highly charged CHI (at pH 4.0) and weakly charged NaCMC (at pH 4.0 and 5.5). The hydrodynamic thickness of the film constructed at pH 4.0/4.0 is unusually large for a linearly growing film (ca. 220 nm after deposition of 8 bilayers), but it strongly decreases (ca. 4 times) with increasing ionization of NaCMC (at pH 5.5). In both cases, the multilayer buildup proceeded through a series of adsorption-desorption steps. This was explained by a partial loss of CHI from the film surface on exposure to the solution of longer NaCMC molecules. The irregular film growth correlated quite well with the variations in the electrical polarizability of the polymer-coated particles. This correlation enabled us to conclude that the adsorption of both polymers occurs only on the film surface, with no diffusion in and out of the film bulk during deposition of each CMC/CHI bilayer.

Electro-optics of colloid-polyelectrolyte complexes: counterion release from adsorbed macromolecules.

Complexation between sodium carboxymethylcellulose (NaCMC) and ellipsoidal particles of oppositely charged beta-FeOOH is studied using electric light scattering and electrophoresis. We focus on the complex behavior for overcharging of the particle surface. In this case, the fraction of condensed counterions on NaCMC is found to remain unchanged during polymer adsorption onto a weakly charged particle surface. Using the theory of Sens and Joanny, we evaluate the fraction of condensed counterions and compare it with results for nonadsorbed NaCMC. The polarization of condensed counterions along the chain of the adsorbed macromolecule is proved to create the electro-optical effect in suspensions stabilized by NaCMC adsorption.