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Copper, silver and gold nanoparticles were obtained by reduction of metal ions under X-ray irradiation of "layer-by-layer" (LbL) coatings in a water-alcohol medium. The precursors for metal polymer composites (metallopolymer complexes) were prepared by sorption of metal ions in polyethyleneimine - poly (styrenesulfonic acid) and polyethyleneimine - poly (acrylic acid) coatings deposited on cotton fibers. EPR spectroscopy was use to characterize the complexation of metal ions in coatings with different chemical structure and variable number of polyanion-polycation layers. The effect of coating structure and thickness on the size and stability of nanoparticles was studied using TEM and microdiffraction measurements. Antibacterial activity was found for composites containing silver nanoparticles. • Radiation-induced reduction of metal ions in the ultrathin polymer coatings. • Obtaining of nanocomposite antibacterial coatings on the textile fabrics. • The effect of the number of layers of polyelectrolyte on the ions sorption capacity. • Advantages of PEI-PAA as a matrix for metal nanocomposite preparation. [ABSTRACT FROM AUTHOR]

The bimetallic nanostructures are of considerable interest for various prospective applications. This paper reports a generation of the Cu/Ag and Cu/Au nanoparticles in the interpolyelectrolyte films irradiated in aqueous media. It was shown that the radiation-induced reduction of (Cu/Ag) or (Cu/Au) ions in the matrix of poly(acrylic acid)-polyethylenimine complexes led to formation of the nanoparticles with narrow size distribution. The core-shell structure of nanoparticles was demonstrated by the TEM results. According to the X-ray diffraction data, the nanoparticle cores (Ag or Au) are formed at early stage of irradiation, while increase of the absorbed dose results in the growth of copper shell. It was demonstrated that the radiation-induced reduction could be applied for effective preparation of bimetallic nanoparticles directly in the polymer matrix. [ABSTRACT FROM AUTHOR]

Structural organization, morphology and thermomechanical properties of nanocomposites based on pectin, polyethyleneimine and Cu nanoparticles, formed by the thermal reduction method from interpolyelectrolyte–metal complexes (IMC) pectin–Cu 2+ –polyethyleneimine have been investigated using WAXS (wide-angle X-ray scattering), SAXS (small-angle X-ray scattering) methods as well as TEM (transmission electron microscopy) and thermomechanical analysis. It is defined that thermal reduction of Cu 2+ ions in IMC bulk (while films are heated to the temperature around 170 °C and higher temperatures) results in nanocomposites based on interpolyelectrolyte complexes “pectin–polyethyleneimine” and Cu nanoparticles being formed. In its turn, thermal reduction of copper ions is found out to take place owing to polyethyleneimine (namely, on account of electrons transfer from the amino groups’ nitrogen atoms of polyethyleneimine to Cu 2+ ions). It has been shown by thermomechanical analysis that the optimal time for complete thermal reduction of Cu 2+ ions to metallic copper at T = 170 °C is 30 min. The antimicrobial investigations of the elaborated nanocomposites revealed they possess a high antimicrobial activity against S. aureus and E. coli strains. [ABSTRACT FROM AUTHOR]

Solutions of the series of polymers (sodium polystyrene sulfonate, polyethyleneimine, and poly-N-vinylpyrrolidone) and certain mixtures thereof were studied by NMR relaxation and ESR spectroscopy using manganese(II) and gadolinium(III) ions as paramagnetic probes. The growth of the NMR-relaxation efficiency (relaxivity, R 1,2 ) is observed in solutions of the anionic polymer, as well as the decrease of R 1,2 - in the case of the cationic polymer. For mixtures of polymers, the dependent on the solution composition non-monotonic changes of R 1,2 are caused either by a formation of metal-interpolymer complexes or by a competitive cation/polymer substitution. For both ions, the changes in the ESR spectra of their polyelectrolyte solutions were analyzed. In case of sodium polystyrene sulfonate and blends thereof, the ESR spectra parameters are only slightly broadened compared to the pure metal aqua ion's, whereas for the polyethyleneimine solution the ESR spectra lines broaden greatly at pH > 7 up to their disappearance. All these effects were explained by the distinction of ion probes' binding mode to polyelectrolytes of different nature. Addition of NaCl to manganese(II) solutions containing polystyrene sulfonate, or mixtures thereof with PVP or PEI, lead to recovery of R 1,2 values, close to the probes' aqua ions relaxivities due to the release of the latter from the polymer/medium interface into the bulk water, while no changes were detected for PEI solutions. [ABSTRACT FROM AUTHOR]

Interpolyelectrolyte complexes (IPEC) have been used in different fields, ranging from biomedicine to oil exploration. Particle dimension is a key parameter for the use of an IPEC for a particular application. In this work, dynamic and static scattering (in the form of optical DLS and SAXS, respectively) were used to follow particle growth as a function of anionic/cationic polyelectrolyte mass ratio, w A C , coupled to turbidimetry, conductometry, viscometry, and zeta potential measurements. Turbidimetry, conductometry, and viscometry showed that at w A C ≅ 2 the IPEC dispersions presented changes that were associated to a massive production of IPEC particles. At the same w A C value, zeta potential measurements indicated an apparent isoelectric point, showing that this w A C must be related to a stoichiometric point for IPEC formation. Double KWW equation was adjusted to data from DLS intensity correlation functions, and parameters related to the distribution of relaxation rates presented characteristic changes at the same value of w A C . SAXS was used to follow particle growth until massive IPEC production. It showed that particles firstly were in the form of small, globular particles, tending to unfolded chain geometry, which can be related to the occurrence of flocculation, just at the point of massive IPEC production. [ABSTRACT FROM AUTHOR]

[Display omitted] • New interpolyelectrolyte non-toxic complexes based on the self-assembly of water-soluble pillar[5]arenes were obtained. • Spherical aggregates with an average diameter of 10 nm are found. • Interpolyelectrolyte complex more efficiently binds quercetin (pK a 5.13) compared with individual macrocycles. • The influence of the pH media on the ability of quercetin to be released from the IPEC was shown. The using of pH-sensitive delivery systems is a promising strategy to significantly improve the pharmacological properties of water-insoluble drugs. Herein, we propose and develop an approach to synthesis of interpolyelectrolyte complexes based on combination of two water-soluble decasubstituted non-toxic pillar[5]arenes for encapsulation poor-soluble quercetin and its subsequent release depending on the pH. Interpolyelectrolytes were obtained by mixing aqueous solutions one of which contained a polycationic (ammonium) and the other - a polyanionic (carboxylate) components. The shape and size evolution of interpolyelectrolytes were studied by dynamic light scattering and transmission electron microscopy. Spherical aggregates with an average diameter of 10 nm are found. The ability to form complexes and associates with quercetin by polycationic and polyanionic macrocycle, as well as an interpolyelectrolyte complex based on them, was studied by electron UV–vis and fluorescence spectroscopy, dynamic light scattering. Interpolyelectrolyte complex more efficiently binds quercetin (pK a 5.13) compared with individual macrocycles due to the greater stability of the associates formed by IPEC. The release of quercetin from the interpolyelectrolyte complex was studied in acidic (pH = 4.00), weakly acidic (pH = 5.00–5.50), neutral (pH = 7.44) and weakly alkaline (pH = 8.15) solutions. It was found the full release of the quercetin without oxidation of flavonoid is observed in the neutral solution. This work provides important guidance for the design of successful delivery systems via optimizing the structure and composition of nanocapsules. [ABSTRACT FROM AUTHOR]

The morphology, structural, thermomechanical and electric properties of nanocomposites prepared from interpolyelectrolyte–metal complex being formed involving anionic polyelectrolyte – pectin, CuSO 4 and cationic polyelectrolyte – polyethyleneimine have been investigated using the methods of wide-angle X-ray scattering, transmission electronic microscopy, thermomechanical analysis and dielectric spectroscopy. Such type of nanocomposites with Cu/Cu 2 O core–shell nanoparticles incorporated into polymer matrix is obtained due to the chemical reduction of Cu 2+ cations by NaBH 4 in the interpolyelectrolyte complex, and appearance of the copper’s metallic phase is observed in full extent while BH 4 − :Cu 2+ molar ratio is equal to 6.0. Applying thermomechanical analysis and dielectric spectroscopy, it was observed that transformation of interpolyelectrolyte–metal complexes into nanocomposites results in decreasing of their glass-transition temperature and increasing of the electric conductivity. [ABSTRACT FROM AUTHOR]

The article is devoted to the design, development and application of a new generation of binders for various dispersed systems, including soil, ground, sand, waste rock and others. The binders are formed by interaction of oppositely charged polyelectrolytes, both chemically stable and (bio)degradable. The fundamental aspects of interpolyelectrolyte reactions are discussed; the IPC structure and properties of the resulting interpolyelectrolyte complexes (IPCs) allow considering them as unique and universal binders. Numerous results of laboratory experiments and field trials of the IPC formulations are presented. In particular, large-scale tests have been done in the Chernobyl accident zone where the IPC binders were shown to be effective means to suppress water and wind erosion thereby preventing a spread of radioactive particles (radionuclides) from contaminated sites. Ecologically friendly IPC compositions are described, including those based on commercially available polymers; prospects for improving their efficiency and extending the range of their possible use are discussed. [ABSTRACT FROM AUTHOR]

The interpolyelectrolyte complexes (IPECs) are widely used for various applications, ranging from agriculture and medicine to advanced technological processes. In many cases, they are subjected to the action of ionizing radiation or hard UV light, either intentionally (e.g., for fabrication of nanocomposites) or in the course of routine treatment (sterilization or weathering), or unexpected accidents. In this communication, we report the first preliminary results on the effect of ionizing radiation on the poly(acrylic acid) (PAA) – polyethyleneimine (PEI) complexes and their components as revealed by EPR spectroscopic studies. The obtained results clearly reveal that the yield of primary radicals trapped after irradiation is comparable in all the studied systems and the main processes are decarboxylation in the PAA moiety and proton loss in the PEI moiety. There are no evidences for main-chain scission, which might lead to the degradation of material properties (at least, at moderate doses), instead of this, the radiation-induced crosslinking looks plausible. Generally, it provides a positive forecast for the radiation resistance of such complexes. • Effect of ionizing radiation on interpolyelectrolyte complexes (IPECs) was studied by EPR. • The radicals produced in the polyacrylic acid – polyethyleneimine IPECs were identified. • No evidence for the radiation-induced destruction of the IPECs was found. • A plausible mechanism of the radiation-induced processes was proposed. [ABSTRACT FROM AUTHOR]

Abstract: Interpolymer interactions between the countercharged methacrylate copolymers Eudragit® RL 30D (polycation) and Eudragit® FS 30D (polyanion), were investigated in conditions mimicking the gastrointestinal environment. The formation of inter-macromolecular ionic bonds between Eudragit® RL 30D and Eudragit® FS 30D was investigated using FT-IR spectroscopy and modulated DSC. The FT-IR spectra of the tested polymeric matrices are characterized by visible changes in the observed IR region indicating the interaction between chains of two oppositely charged copolymers. A new band at 1570cm−1 appeared which was assigned to the absorption of the carboxylate groups that form the ionic bonds with the quaternary ammonium groups. Moreover, while increasing the pH values from pH 5.8 to 7.4, a decrease of the intensity of the band at 960cm−1 (quaternary ammonium group vibration) was observed. All binary mixtures were characterized by the presence of only one and narrow Tg, pointing to sample homogeneity, because of the compatibility of components. As a result of electrostatic interaction between the copolymer chains during swelling, the resulting Tg is decreased significantly and was dependent on the quantity of copolymers present in the structure of polycomplexes formed. Overall, the interaction between countercharged copolymers during passage in gastrointestinal tract can strongly modify the release profile of the model drug diclofenac sodium. [Copyright &y& Elsevier]

Abstract: We have studied the interpolyelectrolyte complexation in chloroform between polystyrene-block-poly(cetyltrimethylammonium acrylate), (PA− CTA+), and poly(2-(methacryloyloxy)ethyldimethylethyl-ammonium dodecyl sulfate) (quaternized poly(2-(dimethylamino)ethyl methacrylate) complexed with sodium dodecyl sulfate), (PDMAEMAQ+ DS−). Turbidimetry, dynamic/static light scattering, and transmission electron microscopy show the formation of large aggregated interpolyelectrolyte complex species, which are colloidally stable in chloroform or even chloroform-soluble if the certain conditions are met. We suggest such co-assemblies to be micellar species with a core assembled from electrostatically coupled fragments of the polymeric components. The corona is built up either from a mixture of polystyrene blocks and excessive fragments of (PDMAEMAQ+ DS−) chains or from a mixture of polystyrene blocks and excessive fragments of (PA− CTA+) blocks, depending on which polymeric component was taken in excess for the interpolyelectrolyte complexation. However, their real structures may deviate from such idealized consideration because of the non-equilibrium character of interpolyelectrolyte complexation in organic media of low polarity. [Copyright &y& Elsevier]

Abstract: Aim of this paper was that to prepare biocompatible, polyaspartamide based copolymers containing spermine or spermine/hydrophobic side chains able to condense nucleic acids and to transfect mammalian cells. Copolymers were prepared starting from α,β-poly-(N-2-hydroxyethyl)-d,l-aspartamide (PHEA) and exploiting the reactive hydroxyl groups in the polymeric side chains by subsequent activation reactions to obtain PHEA-Spermine (PHEA-Spm) and PHEA-Spermine-Butyramide (PHEA-Spm-C4). Molecular, physico-chemical and biological characterization of copolymers and interpolyelectrolyte complexes with plasmid DNA was performed. Experimental results evidenced that these copolymers are able to form complexes with plasmid DNA already at low polycation/DNA weight ratio ranging from 0.75/1 to 2/1. Interpolyelectrolyte complexes with decreased size were obtained when increasing the polycation/DNA weight ratio, until nanosized dimensions were reached. Copolymers as well as complexes were not haemolytic and non toxic in vitro. In vitro cell transfection with PHEA derivatives showed good biocompatibility and high transfection efficiency (luciferase) in cancer cells in comparison with commercially available, but toxic transfection agents. [Copyright &y& Elsevier]

Abstract: The formation of a novel interpolyelectrolyte complex (IPEC) between basic butylated methacrylate copolymer and kappa-carrageenan was investigated and the product formed was characterized. Turbidity measurements and elemental analyses pointed to a 1:1 interaction of the repeating units. These results and FT-IR confirmed IPEC formation. Electronic microscopy images, particle size determination by image analysis and N2 (77K) adsorption measurements were consistent with a porous material. This IPEC formed presented very good flowability and compactibility. Two maxima were observed in the swelling behaviour as a function of pH. The performance of the IPEC as a matrix for controlled release of drugs was evaluated, using ibuprofen as a model drug. Release profiles were properly represented by a mathematical model, which indicates that the system releases ibuprofen in a zero-order manner. These profiles could be controlled by conveniently modifying the proportion of the IPEC in the tablets. [Copyright &y& Elsevier]

Abstract: Static/structural characteristics of non-covalent complexes, formed by terminally charged hyperbranched polymers and oppositely charged neutralizing linear polyelectrolytes, are examined by means of Brownian dynamics computer simulations. Excluded-volume, electrostatic and hydrodynamic interactions are taken into account in implicit solvent. Three pairs of complexes consisting of linear chains and hyperbranched molecules each bearing different molecular weight and distinctly diverse topologies are examined under conditions of varying electrostatic interactions. The findings from the present work demonstrate that through an appropriate modification of internal structure and external stimuli, key attributes of such complexes like size, shape and local density distribution, can be tuned at desired levels, rendering them promising candidates for a wide range of pertinent nanoscale applications. [Copyright &y& Elsevier]

Abstract: Controlled/‘living’ radical polymerization methods, including the versatile reversible addition–fragmentation chain transfer (RAFT) polymerization process, are rapidly moving to the forefront in construction of drug and gene delivery vehicles. The RAFT technique allows an unprecedented latitude in the synthesis of water soluble or amphiphilic architectures with precise dimensions and appropriate functionality for attachment and targeted delivery of diagnostic and therapeutic agents. This review focuses on the chemistry of the RAFT process and its potential for preparing well-defined block copolymers and conjugates capable of stimuli-responsive assembly and release of bioactive agents in the physiological environment. Recent examples of block copolymers with designed structures and segmental compositions responsive to changes in pH or temperature are reviewed and hurdles facing further development of these novel systems are discussed. [Copyright &y& Elsevier]

The micellization of ionic amphiphilic diblock copolymers, polyisobutylene-block-poly(methacrylic acid) (PIB-b-PMAA), with a constant degree of polymerization of the non-ionic block (DPn=20) and various degrees of polymerization of the polyelectrolyte block (DPn=100–425) was examined in aqueous media by means of fluorescence spectroscopy using pyrene as a polarity probe. The molar values of the critical micellization concentration (cmc) were found to be around 2×10−6 mol/l, being nearly independent of the length of the polyelectrolyte block as well as pH (in the range 6–9) and ionic strength (≤0.5 M NaCl) while the specific cmc values varied from 20 to 100 mg/l. Small-angle neutron scattering (SANS) and dynamic light scattering (DLS) experiments provided evidence that aggregation numbers and hydrodynamic radii of the formed copolymer micelles are sensitive to variations of pH and ionic strength, indicating that these micelles might be ‘dynamic’ rather than ‘frozen’ ones. It was also shown by means of a combination of turbidimetry, analytical ultracentrifugation, fluorescence spectroscopy, SANS, and DLS that the formed copolymer micelles mixed with a strong cationic polyelectrolyte, poly(N-ethyl-4-vinylpyridinium bromide) at charge ratio Z=[+]/[−] not exceeding a certain critical value ZM<1, generate peculiar water-soluble micellar complex onion-like species, each containing a two-phase hydrophobic nucleus and a hydrophilic corona. The nucleus consists of a PIB core and a shell assembled from the fragments of water-insoluble interpolyelectrolyte complex. The corona is formed by the excess fragments of poly(sodium methacrylate) blocks not involved in complexation with poly(N-ethyl-4-vinylpyridinium bromide). [Copyright &y& Elsevier]

Interactions of a major whey protein, β-lactoglobulin (BLG), with an anionic polysaccharide, dextran sulfate (DS), were investigated by nephelometric titration and high-sensitivity differential scanning calorimetry at pH 2.5–7.0 and NaCl concentrations of 0–500 mM. The pH-dependences of the light scattering of the BLG−DS system revealed a maximum. Its position was dependent on the polysaccharide/protein ratio and salt concentration. Thermodynamic parameters of the denaturation of BLG in mixtures with DS were determined at different pH and salt concentrations. Conformational stability of BLG in the BLG–DS complexes was shown to either increase or decrease depending on the solution conditions and complex composition. The binding curves of BLG to DS were calculated from the light scattering and calorimetric data and analyzed using various binding models including the Langmuir and McGhee–von Hippel models as well as a stoichiometric interpolyelectrolyte reaction. Mechanisms responsible for changes in the BLG oligomer structure and conformational stability induced by the complex formation with the polysaccharide were proposed. [Display omitted] • BLG–DS complexes form at pH 3.0–pI BLG and NaCl concentration up to 0.5 M. • The complex formation can result in the dissociation of BLG dimer. • Stability of BLG is defined by charge-charge or charge-dipole interactions with DS. • Stoichiometric BLG–DS complexes are formed at high ionic strength. [ABSTRACT FROM AUTHOR]

• Benznidazole-loaded multiparticulate drug delivery systems (BZ-MDDS) were in vivo studied. • BZ-MDDS showed trypanocidal efficacy at conventional or low doses of BZ. • BZ-MDDS reduced heart and liver injury, increasing Chagas disease treatment safety. • BZ-MDDS exhibited an improved preclinical performance for Chagas disease treatment. Benznidazole (BZ) is a first-line drug for the treatment of Chagas disease; however, it presents several disadvantages that could hamper its therapeutic success. Multiparticulate drug delivery systems (MDDS) are promising carriers to improve the performance of drugs. We developed BZ-loaded MDDS intended for improving Chagas disease therapy. To assess their efficacy and safety, Trypanosoma (T) cruzi infected BALB/c mice were orally treated with free BZ or BZ-MDDS at different regimens (doses of 50 and 100 mg/kg/day, administered daily or at 2- or 5-days intervals) and compared with infected non-treated (INT) mice. At 100 mg/kg/day, independent of the administration regimen, both treatments were able to override the parasitemia, and at 50 mg/kg/day significantly reduced it compared to INT mice. BZ-MDDS at a dose of 100 mg/kg/day administered every 5 days (BZ-MDDS 100–13d) induced the lowest cardiac parasite load, indicating an improved efficacy with lower total dose of BZ when loaded to the MDDS. Reactive oxygen species produced by leukocytes were higher in INT and mice treated with BZ at 50 mg/kg/day compared to 100 mg/kg/day, likely because of persistent infection. BZ-MDDS treatments markedly reduced heart and liver injury markers compared to INT mice and those receiving the standard treatment. Therefore, BZ-MDDS exhibited enhanced activity against T. cruzi infection even at lower doses and reduced administration frequency compared to free BZ while increasing the treatment safety. They likely avoid undesired side effects of BZ by keeping a sustained concentration, avoiding plasmatic drug peaks. BZ-MDDS evidenced significant improvements in experimental Chagas disease treatment and can be considered as a potential improved therapeutic alternative against this illness. [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] In this study, volatile perfume was encapsulated in microcapsules (MCs) via interpolyelectrolyte complexes (IPECs) of oppositely charged polymers, with high encapsulation efficiency, to be delivered in a sustained manner. Positively charged chitosan (CTS) and negatively charged Eudragit® S100 (ES100) were used as eco-friendly biopolymers. Limonene (LMN) was selected as the model perfume. First, the solution of LMN in ethyl acetate and poloxamer 407 (POX407) in acidic solution was emulsified using ultrasonication. CTS and ES100 were added in that particular order to form o/w emulsion. LMN-loaded microcapsules (LMN-MCs) were prepared by adjusting the pH and freeze-drying for solidification. The electrostatic interactions of CTS and ES100 to form IPECs were highly dependent on pH, changing in the microscopic images of emulsion droplets and zeta potential. The NH 3 + group of CTS and the COO– group of ES100 caused the electrostatic interactions at a specific pH. The formation mechanism of LMN-MCs was successfully validated using instrumental analysis, charge density, and energy dispersive X-ray spectrometer (EDS) mapping. Encapsulation efficiency, loading content, and release rates of LMN-MCs varied according to the ratios of CTS and ES100, demonstrating optimal performance at a 1:1 ratio. The current LMN-MCs could provide a simple manufacturing process with high performance in terms of encapsulation efficiency (>94%), drug loading, yield and sustained release of volatile perfume for 120 h. [ABSTRACT FROM AUTHOR]

Magnetic compounds, based on magnetite nanoparticles and interpolyelectrolyte complexes (IPEC) were prepared from chitosan (CS) and poly(sodium 4-styrenesulfate) (NaPSS). Two types of composite were obtained: one with positive surface charge and another one with negatively charged surface. The composites were used to adsorb a cationic drug (tetracycline hydrochloride, HTCCl) and an anionic one (sodium cromoglycate, NaCG). Sorption occurred in the form of multiple layers, tending to a saturation value (following Sips isotherm), with saturation sorption concentrations of ca. 0.2 mmol of drug per gram of composite for HTCCl on both positively and negatively charged composites, probably due to the protonation of chitosan by HTCCl. In the case of the anionic drug, it was adsorbed with the same intensity on the composite of opposite charge, while for the composite with negative charge saturation occurred at a value of ca. 0.05 mol per gram of composite. Gibbs free energy of adsorption for dilute solution conditions was estimated, ranging from ‒17 to −3 kJ/mol, and the analysis of thermal degradation kinetics of composites, using the isoconversional approach, indicated that magnetite decreased apparent energy of activation (with values reaching 400 kJ/mol) for the degradation of the organic phase. [ABSTRACT FROM AUTHOR]

• An anionic cross-linked copolymer forms microgel particles after swelling in water. • Reaction of microgel with a linear polycation results in stable aqueous formulation. • Being applied to soil, the formulations give mechanically stable polymer-soil crusts. • Soil, associated with microgels, demonstrates a high water retention capacity. • Microgels are promising for preparing anti-erosion and water-saving formulations. In this article we describe the use of novel aqueous polymer formulations for stabilization of sand and soil against wind erosion and retention of water in polymer-treated sand/soil samples. Two series of formulations were prepared. The first consisted of polyacrylic acid (PAA) and two electrostatic complexes of PAA with cationic poly(diallyldimethylammonium chloride): negatively and positively charge; the second included PAA-based cross-linked copolymer (PAA#) which forms microgel particles upon swelling and two its electrostatic complexes with the polycation: negatively and positively charged. 1 mass% formulations showed the stability against aggregation for 3 months excepting the negative complex with PAA which aggregated within half an hour after preparation. The viscosity of 1 mass% formulations, which lies within a (1.6÷320)×10−6 m2/s interval, allowed their deposition over fine-grained sand and loamy sand soil using a conventional spray machine followed by formation of polymer-sand(soil) crusts. Both for sand and soil, the PAA#-based crusts demonstrated a higher resistance to mxechanical loads in comparison with the crusts formed by linear PAA: up to a 42.5 MPa mechanical strength for sand/PAA# crust against a 12.5 MPa strength for sand/PAA crust. Additionally, the PAA#-based crusts was not impacted by airstream, up to a 190 km per hour air speed, while PAA-based crust was destroyed within a minute. Finally, PAA# alone and its negative complex were characterized by a high swelling (degree of swelling up to 195) that allowed them to maintain a high water retention capacity, being bound to sand and soil. The results are promising for preparing anti-erosion and water-saving formulations, especially in areas with insufficient moisture content, and design of sand-based composite materials. [ABSTRACT FROM AUTHOR]

• Nanocomposites were obtained by thermochemical reduction of Ag+ at 150 °C for 30 min. • The least average size of silver nanoparticles is 4.7 nm for pectin––Ag–chitosan+. • The greatest average size of silver nanoparticles is 9 nm for starch––Ag–starch+. • The greatest antimicrobial activity is the pectin––Ag–chitosan+, and the least starch––Ag–starch+. The effect of the chemical structure of interpolyelectrolyte complexes (IPEC) based on polymers of natural origin (pectin––chitosan+, pectin––cationic starch (starch+), carboxymethylcellulose (CMC–)–cationic β-cyclodextrin (β-CD+), anionic starch (starch–)–cationic starch (starch+) on the structure, morphology, thermomechanical and antimicrobial properties of silver-containing nanocomposites obtained by thermochemical reduction of Ag+ ions in interpolyelectrolyte-metal complexes (IMC) was studied. Thermochemical reduction of Ag+ ions in the IMC bulk for 30 min at 150 °C led to formation of silver-containing nanocomposites and this fact was confirmed by wide-angle X-ray scattering method. Transmission electron microscopy showed that different sized of silver nanoparticles were formed depending on the chemical structure of IPEC. The average size of silver nanoparticles was found to be 4.7 nm for pectin––Ag–chitosan+; 5.3 nm for pectin––Ag–starch+; 6.3 for CMC––Ag–β-CD+ and 9 nm for starch––Ag–starch+, correspondingly. The nanocomposites having smaller average nanoparticle size exhibited higher antimicrobial activity against S. aureus and E. coli strains. Pectin––Ag–chitosan+ nanocomposites formed by thermochemical reduction of Ag+ ions showed that the diameter of the inhibition zone against S. aureus and E. coli strains was 19.7 and 32.6 mm, respectively, whereas these values were 15.6 and 14 mm, respectively, for the same nanocomposites obtained by chemical reduction using ascorbic acid. [ABSTRACT FROM AUTHOR]

The radiation-chemical synthesis of metal nanoparticles embedded into polymer matrices is an effective tool for preparation of the composite materials with very useful functional properties. This paper presents a review of an original approach to a single-step production of such materials via the radiation-induced reduction of the interpolyelectrolyte complex (IPEC) films containing metal ions under heterogeneous conditions, including the most recent results, and analysis of the prospects of this approach and its implications. First, the properties of IPECs as precursors for nanocomposites are briefly considered. Particular impact is given to the mechanistic aspects and principles of control of the nanoparticle formation and assembling at different stages. A common procedure of the radiation-chemical synthesis of metal polymer nanocomposites in the IPEC matrices implies irradiation of swollen films in an aqueous – organic environment. The kinetics of ion reduction and formation of nanoparticles was monitored by EPR and optical spectroscopy, whereas the obtained nanocomposites were characterized by TEM and diffraction methods. Using IPEC matrices allows us to reveal different stages of formation of metal nanostructures over a wide range of absorbed doses. Furthermore, it is possible to manipulate the processes of nucleation and growth of nanoparticles using both physical and chemical factors. Different kinds of radiation (e-beams, γ- and X-rays) were used in the experiments. It was shown that the penetration depth, dose rate and total absorbed dose had strong effect on the effect on nanoparticle size and their spatial distribution. The most striking feature were found for the processes induced by X-ray radiation. Detailed studies of this particular case revealed a very interesting effect described as radiation-chemical contrast, which is manifested by local intensification of the radiation-induced processes in the vicinity of existing nanoparticles. In addition to metal nanoparticles of different transition and noble metals, it was possible to obtain the bimetallic nanostructures within the IPEC matrix. Such nanocomposites may be potentially used as optical and magnetic materials, sensors, bactericide and fungicide products. The possibility of variation of nanoparticle size and specific properties of the IPEC films is crucially important for particular applications. [ABSTRACT FROM AUTHOR]