Nano-Sized Fucoidan Interpolyelectrolyte Complexes: Recent Advances in Design and Prospects for Biomedical Applications.

The marine polysaccharide fucoidan (FUC) is a promising polymer for pharmaceutical research and development of novel drug delivery systems with modified release and targeted delivery. The presence of a sulfate group in the polysaccharide makes FUC an excellent candidate for the formation of interpolyelectrolyte complexes (PECs) with various polycations. However, due to the structural diversity of FUC, the design of FUC-based nanoformulations is challenging. This review describes the main strategies for the use of FUC-based PECs to develop drug delivery systems with improved biopharmaceutical properties, including nanocarriers in the form of FUC-chitosan PECs for pH-sensitive oral delivery, targeted delivery systems, and polymeric nanoparticles for improved hydrophobic drug delivery (e.g., FUC-zein PECs, core-shell structures obtained by the layer-by-layer self-assembly method, and self-assembled hydrophobically modified FUC particles). The importance of a complex study of the FUC structure, and the formation process of PECs based on it for obtaining reproducible polymeric nanoformulations with the desired properties, is also discussed.

Colloidal nanoparticles of sodium polygalacturonate prepared by nanoprecipitation.

Polygalacturonic acid (PGA), being the backbone of pectins, governs their aggregation that is widely applied in industry. The PGA aggregation was studied by dynamic and static light scattering within a limited space of sodium polygalacturonate nanoparticles obtained by nanoprecipitation (drop-wise addition of alkaline solution of PGA to an ethanol bath). With increasing buffer's pH from 4.0 to 9.1, the colloids changed their form from elongated to spherical one, as indicated by decreasing the structure-sensitive ratio Rg/Rh from 1.7 to 1.1. Molecular mass-per-unit-length determined in Holtzer coordinates decreased from 5000 to 1600 Da nm-1 with increasing pH, suggesting partial disintegration of helical bundles due to electrostatic repulsion. Kratky plots also pointed out partial disintegration of the PGA junctions with increasing pH. Nonmonotonic dependence of the colloidal radius of gyration Rg on [NaCl] characterized the osmotic regime characteristic of annealed polyelectrolytes and thus confirmed the star-like structure of junctions.

Hyaluronan-colistin conjugates: Synthesis, characterization, and prospects for medical applications.

The development of nanotechnology-based antibiotic delivery systems (nanoantibiotics) is an important challenge in the effort to combat microbial multidrug resistance. These systems have improved biopharmaceutical characteristics by increasing local bioavailability and reducing systemic toxicity and the number and frequency of drug side effects. Conjugation of low -molecular -weight antibacterial agents with natural polysaccharides is an effective strategy for developing optimal targeted delivery systems with programmed release and reduced cytotoxicity. This study describes the synthesis of conjugates of colistin (CT) and hyaluronic acid (HA) using carbodiimide chemistry to conjugate the amino groups of CT with the carboxyl groups of HA. The obtained polysaccharide carriers had a degree of substitution (DS) with CT molecules of 3-10 %, and the CT content was 129-377 µg/mg. The size of the fabricated particles was 300-600 nm; in addition, there were conjugates in the form of single macromolecules (30-50 nm). The ζ-potential of developed systems was about -20 mV. In vitro release studies at pH 7.4 and pH 5.2 showed slow hydrolysis of amide bonds, with a CT release of 1-5 % after 24 h. The conjugates retained antimicrobial activity depending on the DS: at DS 8 %, the minimum inhibitory concentration (MIC) of the conjugate corresponded to the MIC of free CT. The resulting systems also reduced CT nephrotoxicity by 20-50 %. These new conjugates of CT with HA are promising for the development of nanodrugs for safe and effective antimicrobial therapy.

Diethylaminoethyl chitosan-hyaluronic acid polyelectrolyte complexes.

Polysaccharide-based polyelectrolyte complexes (PECs) are of great interest for the development of drug delivery systems, as they are easily prepared and exhibit a wide range of colloidal properties. The water-soluble diethylaminoethyl chitosan (DEAE-CS) was synthesized with various degrees of substitution (DS), ranging from 26 to 113%. Analysis of the substitution pattern of DEAE-CS by different NMR techniques revealed N- and O-substitution, as well as quaternization of the tertiary amino group of the DEAE substituent; the fraction of quaternary amino groups increased with the DS. Unlike the tertiary amino groups, the quaternary amino groups did not support increases in the ζ-potential of DEAE-CS with the DS and the complexation with hyaluronic acid (HA). The influence of the PEC composition, DS of DEAE-CS, and mixing order on the size and polydispersity of PEC nanoparticles was investigated by dynamic and static light scattering. Internal disordered heterogeneous PEC nanoparticles were formed by the aggregates of several primary PECs. Disordered and structurally heterogeneous spherical complexes were formed (Rg/Rh = 1.0 ± 0.3). The obtained PECs were metastable and their properties were influenced by mixing order. The high molecular weight component (HA), being a minor component, was more exposed on the surface than was the low molecular weight DEAE-CS.

Smart colloids containing ensembles of gold nanoparticles conjugated with κ-carrageenan.

We study colloids of nanobiocomposites (NBC) containing Au nanoparticles (NP) obtained by reduction of gold precursor with functional groups of κCAR. The AuNPs content was changed from 2.0 to 5.6 w/w %. Hydrolysis of κCAR during reduction of gold ions produced carboxylate groups supporting nanobioconjugation (FT-IR data) and electrostatic stabilization through increased negative ζ-potential. The self-assembly of AuNPs took place after storing NBC, as shown by UV/vis. extinction and transmission electron microscopy. Analysis of the structure-sensitive Rg/Rh ratios obtained by dynamic and static light scattering showed that the colloids have core-shell structure. The macromolecules in the shell exhibited polyelectrolyte expansion at [NaCl] and [KCl] < 0.02 M. Above 0.02 M, the difference between non-specific sodium and specific potassium ions on the shell thickness was registered. The temperature hysteresis of the hydrodynamic radius Rh was similar to that of the pristine κCAR observed previously by optical rotation. Monitoring the equilibration of light scattering intensity at each mini-quenching step of the cooling run allowed further insight into the hysteresis origin. These colloids are interesting for sensing applications because of enhanced scattering of plasmonically coupled AuNPE. Their thermo- and ion-sensitivity can be useful in drug delivery.

Association of κ-carrageenan subjected to deep alkaline hydrolysis.

κ-carrageenan is a linear sulfated anionic gelling polysaccharide obtained from red seaweed algae by an alkaline hydrolysis. We applied static and dynamic light scattering (DLS), capillary viscometry, FT-IR, and electrophoretic DLS to gain insight into the effect of deep alkaline hydrolysis (95 °C, pH = 10 during Th = 60, 75, and 90 min) on κ-carrageenan macromolecules in a coil conformation. As DLS of coil-like κ-carrageenans is usually complicated by spurious permanent aggregates, the alkaline hydrolysis of κ-carrageenans has not been studied by DLS. By applying a double-dialysis procedure (first against water, then against 0.1 M NaCl), we succeeded in obtaining dilute solutions of coil-like κ-carrageenans with unimodal DLS distributions. Association that started with increasing concentration was attributed to attractive dipole-dipole interactions between ion-pairs formed by condensed counter-ions in the vicinity of carboxyl groups of the reducing ends. The second type of stickers resulted from the compositional heterogeneity of κ-carrageenan, namely, from the traces of ι-carrageenan blocks which amount increased with hydrolysis. With increasing Th we observed both the progressive decrease of molecular mass and the growth of association. Lowering the temperature and increasing concentration during lyophilization strengthened the intermolecular junctions, leading to the formation of permanent aggregates.

Preparation of N-succinyl-chitin nanoparticles and their applications in otoneurological pathology.

Succinyl-chitin (SCH) nanoparticles were obtained by acylation of partially deacetylated chitin (DCH) nanofibers. Introduction of the succinyl moiety induced a partial amorphization of DCH, as viewed by X-ray diffraction, and increased the fractal dimension of the colloids from df = 1.2 (DCH) to 1.5-1.7 (SCH), as revealed by light scattering. The spherically symmetric form of the colloids remained almost unchanged, as indicated by the range of structure-sensitive ratios 1.0 < Rg/Rh < 1.2; the hydrodynamic diameter ranged from 200 to 300 nm. The cytoprotective activity of the SCH nanoparticles was evaluated in vivo in an acute hearing pathology model (220-250 g male Wistar rats, n = 90) following prophylactic and therapeutic administrations. Ototropic action was estimated using the amplitude of otoacoustic emissions at the frequency of the distortion product otoacoustic emissions in the range of 4-6.4 kHz before acoustic stimulation, as well as at 1 h, 24 h, and 7 days after acoustic stimulation. A dispersion of 0.3% SCH nanoparticles demonstrated prolonged ototropic action and earlier regeneration of hearing functions when compared to a meglumine sodium succinate solution. Thus, intravenous administration of the SCH nanoparticles increases the cycling time of exogenous succinate and improves biodistribution in tissues possessing a hemato-labyrinth barrier.

Chiroplasmonic magnetic gold nanocomposites produced by one-step aqueous method using κ-carrageenan.

Novel water-soluble chiroplasmonic nanobiocomposites with directly varied gold content were synthesized by a one-step redox method in water using a biocompatible polysaccharide κ-carrageenan (industrial product from algae) as both reducing and stabilizing matrix. The influence of the reactants ratio, temperature, and pH on the reaction was studied and the optimal reaction parameters were found. The structure and the properties of composite nanomaterials were examined in solid state and aqueous solutions by using complementary physical-chemical methods X-ray diffraction analysis, transmission electron microscopy, spectroscopy of electron paramagnetic resonance, atomic absorption and optical spectroscopy, polarimetry including optical rotatory dispersion with registration of interphase-crossbred Cotton effect of a chiral polysaccharide matrix on plasmonic chromophore of gold nanoparticles, dynamic and static light scattering. The new perspective multi-purpose nanocomposites demonstrate a complex of chiroplasmonic and magnetic properties, imparted by both nanoparticles and radicals enriched chiral polysaccharide matrix.

Development of drug delivery systems for taxanes using ionic gelation of carboxyacyl derivatives of chitosan.

Nanoparticles of two chitosan derivatives - N-succinyl-chitosan (SC) and N-glutaryl-chitosan (GC) - were developed as passive transport systems for taxanes (paclitaxel and docetaxel) using an ionic gelation technique with sodium tripolyphosphate. These nanoparticles had an apparent hydrodynamic diameter of 300-350nm, a ζ-potential of 25-31mV, an encapsulation efficiency of 21-26%, and a drug loading efficiency of 6-13%. DLS and SLS analysis shows that the nanoparticles have a unimodal size distribution and spherical form. Drug release kinetics of the taxane-loaded nanoparticles demonstrates that more than 50% of the loaded taxane could be released upon the degradation of the nanoparticles after targeted delivery. The drug-loaded SC and GC nanoparticles exhibit high cytotoxicity towards AGS cancer cell lines and their antitumor activity is consequently enhanced when compared with free taxanes.

O,N-(2-sulfoethyl)chitosan: Synthesis and properties of solutions and films.

A series of water-soluble sulfoethylated chitosans (SEC) with degrees of substitution (DS) up to 130% were obtained using a heterogeneous reaction of chitosan with sodium 2-chloroethanesulfonate in 85% isopropanol in the presence of NaOH. NMR and FTIR spectroscopy confirmed that sulfoethylation of chitosan preferentially happens at hydroxyl groups and to some extent at amino groups, giving mixed substituted O,N-SEC. Chitosan shows positive birefringence, whereas SEC shows negative values, indicating self-organization in dilute solution. Dynamic light scattering studies revealed the presence of aggregates in dilute solutions of chitosan and SEC. The sizes of the SEC aggregates are sensitive to the DS and the nature of the solvent. X-ray diffraction of SEC films revealed that the introduction of sulfoethyl groups into chitosan leads to amorphization, which is more pronounced at higher DS. During the storage of SEC films, the samples loose solubility due to the formation of ionic crosslinks upon dehydration.

Colloidal aggregates of Pd nanoparticles supported by larch arabinogalactan.

Palladium nanoparticles (PdNPs) are used in catalysis, hydrogen storage, biomedicine, and so on. Arranging the self-assembly of PdNPs within colloidal aggregates is desirable for improving their consumer properties. Stable widely dispersed colloidal aggregates of larch arabinogalactan (LARB) containing nanosized (5-nm) PdNPs were obtained by reducing Pd ions in alkaline solutions of LARB. Centrifugation resulted in a set of LARB-PdNP colloids ranging from 60 to 240 nm. The colloids were studied by static light scattering (SLS) and dynamic light scattering (DLS). The SLS data presented as Kratki plots correspond to a particle scattering factor of linear rather than branched chains. The fractal dimension of the LARB-PdNP colloids was found by SLS to be d = 1.96, which is between the values for diffusion- and reaction-limited aggregation. This result is ascribed to the aggregate's internal motion, which is evident from the power-law exponent of the dependence of the DLS relaxation rate on the scattering vector, <Γ> ~ q(α) with α = 2.24. The structure-sensitive ratio of the radius of gyration to the hydrodynamic radius was found to vary within the interval of 0.8 ≤ R(g)/R(h) ≤ 1.2 corresponding, to the spherical form of LARB-PdNP colloids. A spiderweblike PdNP distribution pattern was observed by transmission electron microscopy. Insertion of PdNPs did not affect the fractal dimension, the power-law exponent α, or the architecture of the pristine LARB aggregates in water. The red shift of the surface plasmon extinction observed with increasing LARB-PdNP colloidal size indicates the collective optical response of the PdNP ensemble in the colloid.

Light scattering from aqueous solutions of colloid metal nanoparticles stabilized by natural polysaccharide arabinogalactan.

Colloids of metal nanoparticles (NPs) of Au, Ag, Pd, and Pt protected by natural polymer arabinogalactan (ARB) extracted from Larix sibirica were studied. The nanocomposites were prepared by reduction of metal salts in the water solutions of ARB. We carried out dynamic (DLS) and static light scattering resonantly enhanced by the NP plasmons. The translational diffusion was examined via DLS and a polarized interferometer. The virgin ARB was shown to form aggregates in dilute aqueous solutions. The introduction of NPs reduced the size of the virgin ARB aggregates. The aggregate forms as viewed by the scanning electron microscopy support the light scattering results.