Stability and narrow size distribution are among the main requirements that apply to drug formulations based on polymeric nanoparticles. In this study, we obtained a series of particles based on biodegradable poly(D,L-lactide)-b-poly(ethylene glycol) (P(D,L)LA_n-b-PEG₁₁₃) copolymers with varied hydrophobic P(D,L)LA block length n from 50 to 1230 monomer units stabilized by poly(vinyl alcohol) (PVA) by a simple “oil-in-water” emulsion method. We found that nanoparticles of P(D,L)LA_n-b-PEG₁₁₃ copolymers with relatively short P(D,L)LA block (n ≤ 180) are prone to aggregate in water. P(D,L)LA_n-b-PEG₁₁₃ copolymers with n ≥ 680 can form spherical unimodal particles with values of hydrodynamic diameter less than 250 nm and polydispersity less than 0.2. The aggregation behavior of P(D,L)LA_n-b-PEG₁₁₃ particles was elucidated in terms of tethering density and conformation of PEG chains at the P(D,L)LA core. Docetaxel (DTX) loaded nanoparticles based on P(D,L)LA₆₈₀-b-PEG₁₁₃ and P(D,L)LA₁₂₃₀-b-PEG₁₁₃ copolymers were formulated and studied. It was observed that DTX-loaded P(D,L)LA_n-b-PEG₁₁₃ (n = 680, 1230) particles are characterized by high thermodynamic and kinetic stability in aqueous medium. The cumulative release of DTX from the P(D,L)LA_n-b-PEG₁₁₃ (n = 680, 1230) particles is sustained. An increase in P(D,L)LA block length results in a decrease in DTX release rate. The in vitro antiproliferative activity and selectivity studies revealed that DTX-loaded P(D,L)LA₁₂₃₀-b-PEG₁₁₃ nanoparticles demonstrate better anticancer performance than free DTX. Favorable freeze-drying conditions for DTX nanoformulation based on P(D,L)LA₁₂₃₀-b-PEG₁₁₃ particles were also established. Full article

Owing to the remarkable antimicrobial potential of these materials, research into the possible use of nanomaterials as alternatives to fungicides in sustainable agriculture is increasingly progressing. Here, we investigated the potential antifungal properties of chitosan-decorated copper oxide nanocomposite (CH@CuO NPs) to control gray mold diseases of tomato caused by Botrytis cinerea throughout in vitro and in vivo trials. The nanocomposite CH@CuO NPs were chemically prepared, and size and shape were determined using Transmission Electron Microscope (TEM). The chemical functional groups responsible for the interaction of the CH NPs with the CuO NPs were detected using the Fourier Transform Infrared (FTIR) spectrophotometry. The TEM images confirmed that CH NPs have a thin and semitransparent network shape, while CuO NPs were spherically shaped. Furthermore, the nanocomposite CH@CuO NPs ex-habited an irregular shape. The size of CH NPs, CuO NPs and CH@CuO NPs as measured through TEM, were approximately 18.28 ± 2.4 nm, 19.34 ± 2.1 nm, and 32.74 ± 2.3 nm, respectively. The antifungal activity of CH@CuO NPs was tested at three concentrations of 50, 100 and 250 mg/L and the fungicide Teldor 50% SC was applied at recommended dose 1.5 mL/L. In vitro experiments revealed that CH@CuO NPs at different concentrations significantly inhibited the reproductive growth process of B. cinerea by suppressing the development of hyphae, spore germination and formation of sclerotia. Interestingly, a significant control efficacy of CH@CuO NPs against tomato gray mold was observed particularly at concentrations 100 and 250 mg/L on both detached leaves (100%) as well as the whole tomato plants (100%) when compared to the conventional chemical fungicide Teldor 50% SC (97%). In addition, the tested concentration 100 mg/L improved to be sufficient to guarantee a complete reduction in the disease’s severity (100%) to tomato fruits from gray mold without any morphological toxicity. In comparison, tomato plants treated with the recommended dose 1.5 mL/L of Teldor 50% SC ensured disease reduction up to 80%. Conclusively, this research enhances the concept of agro-nanotechnology by presenting how a nano materials-based fungicide could be used to protect tomato plants from gray mold under greenhouse conditions and during the postharvest stage. Full article

Construction of superhydrophobic woods with high abrasion resistance is still a major challenge, and micro analysis for abrasion resistance is scarce. To improve these issues, cellulose nanocrystals (CNC)@SiO₂@phosphorylated lignin (PL) rods were prepared by SiO₂ in situ generated on CNC, and then the modified lignin attached to the CNC@SiO₂ rods surface. Subsequently, the superhydrophobic coating was constructed using hydrophobic modified CNC@SiO₂@PL rods as the main structural substance by simple spraying or rolling them onto wood surfaces, and both polydimethylsiloxane (PDMS) and epoxy resin were used as the adhesives. The resulting coating had excellent superhydrophobic properties with a water contact angle (WCA) of 157.4° and a slide angle (SA) of 6°. The introduced PL could enhance ultraviolet (UV) resistance of the coating due to the presence of these groups that absorbed UV light in lignin. In the abrasion resistance test, compared with the SiO₂/PL coating, the abrasion resistance of the one with CNC was much higher, suggesting that CNC could improve the abrasion resistance of the coating due to its high crystallinity and excellent mechanical strength. The coating with PDMS performed better than the one with epoxy resin because the soft surface could offset part of the external impact by deformation in the abrasion process. This was also consistent with the results of the nanoindentation (NI) tests. In view of the simple preparation and good performance, this superhydrophobic wood will have broad application potential. Full article

Gold nanoparticles (AuNPs) stabilized with poly(1-vinyl-1,2,4-triazole) (PVT) have been synthesized via a one-pot manner in irradiated solutions of 1-vinyl-1,2,4-triazole (VT) and Au(III) ions. The transmission electron microscopy examinations have shown that the sizes of nanoparticles formed range from 1 to 11 nm and are affected by the ratio of VT to gold ions. To study the kinetics peculiarities of the VT polymerization and assembling of AuNPs, UV-Vis spectroscopy was used. The analysis of the data obtained reveals that an inhibition period, influenced by Au(III) concentration, is followed by the polymerization of a monomer. Importantly, the absorbed doses, corresponding to the onset of rapid polymerization, correlate with the doses at which the accelerated formation of AuNPs begins. The kinetics aspects, which could lead to such an effect, are discussed. Full article

A straight-forward method was exploited to construct a multifunctional hybrid photoinitiator by supporting 2-hydroxy-2-methylpropiophenone (HMPP) onto a nano-silica surface through a chemical reaction between silica and HMPP by using (3-isocyanatopropyl)-triethoxysilane (IPTS) as a bridge, and this was noted as silica-s-HMPP. The novel hybrid-photoinitiator can not only initiate the photopolymerization but also prominently improve the dispersion of nanoparticles in the polyurethane acrylate matrix and enhance the filler-elastomer interfacial interaction, which results in excellent mechanical properties of UV-cured nanocomposites. Furthermore, the amount of extractable residual photoinitiators in the UV-cured system of silica-s-HPMM shows a significant decrease compared with the original HPMM system. Since endowing the silica nanoparticle with photo-initiated performance and fairly lower mobility, it may lead to a reduction in environmental contamination compared to traditional photoinitators. In addition, the hybrid-photoinitiator gives rise to an accurate resolution object with a complex construction and favorable surface morphology, indicating that multifunctional nanosilica particles can be applied in stereolithographic 3D printing. Full article

Waterborne silicone coatings are prepared in this paper by using silicone emulsion as a film-forming material, γ-methacryloxypropyltrimethoxysilane, and dibutyltin dilaurate as a curing agent and a catalyst, respectively. The corresponding coatings are obtained by controlling different microwave times to accelerate the coating curing. The surface morphology, roughness, surface properties, mechanical properties, and antifouling properties of the coating are studied by laser confocal microscope, contact angle measurement, tensile test, marine bacterial attachment test, and benthic diatom adhesion test. Additionally, the action mechanism of microwaves in the curing process of the coatings is also discussed. The results show that the microwave can greatly reduce the curing time of waterborne silicone coating. It can improve the painting efficiency, the surface roughness of the coating, and the mechanical properties of the coatings. The change in roughness increases the contact angle of the coating, reduces the apparent surface energy, and then improves the antifouling performance. For the coating cured by microwave, with the increase in microwave curing time, the water and diiodomethane contact angles of the coating gradually increase, and the surface energy gradually decreases from about 20 mJ/m² to 10.8 mJ/m². With the increase in microwave time, the attachment amount of Navicular Tenera gradually decreases, the removal rate gradually increases, and the removal rate of Navicular Tenera in the coating increases from 15.36% to 31.78%. The bacterial removal rate of the coating can be increases from 11.05% to 22.28% after microwave curing. Microwave-assisted curing is helpful in improving the antifouling and self-cleaning performance of waterborne silicone coatings, showing promising potential applications. Full article

Cyclodextrins (CDs) are promising drug carriers that are used in medicine. We chose CDs with different substituents (polar/apolar, charged/neutral) to obtain polymers (CDpols) with different properties. CDpols are urethanes with average Mw of ~120 kDa; they form nanoparticles 100–150 nm in diameter with variable ζ-potential. We studied the interaction of CD and CDpols with model (liposomal) and bacterial membranes. Both types of CD carriers cause an increase in the liposomal membrane permeability, and for polymers, this effect was almost two times stronger. The formation of CD/CDpols complexes with levofloxacin (LV) enhances LV’s antibacterial action 2-fold in vitro on five bacterial strains. The most pronounced effect was determined for LV-CD complexes. LV-CDs and LV-CDpols adsorb on bacteria, and cell morphology influences this process dramatically. According to TEM studies, the rough surface and proteinaceous fimbria of Gram-negative E. coli facilitate the adsorption of CD particles, whereas the smooth surface of Gram-positive bacteria impedes it. In comparison with LV-CDs, LV-CDpols are adsorbed 15% more effectively by E. coli, 2.3-fold better by lactobacilli and 5-fold better in the case of B. subtilis. CDs and CDpols are not toxic for bacterial cells, but may cause mild defects that, in addition to LV-CD carrier adsorption, improve LV’s antibacterial properties. Full article

The functional polyethers of N-(2,3-epoxypropyl)-4,5,6,7-tetrahydroindole (in up to 61% yield, M_w = 8.7–11.7 kDa) and copolymers with ethylene glycol methylglycidyl ether (M_w = 5.6–14.2 kDa) and ethylene glycol vinylglycidyl ether (M_w = 6.4–12.3 kDa) have been synthesized via anionic ring-opening polymerization in the presence of KOH without solvent. The polymerization involves the opening of the epoxy ring to deliver the linear polyethers bearing free tetrahydroindole rings and oxyethylene or vinyloxy groups in the side chain. The polyethers are soluble in ethanol, benzene, chloroform, dioxane, DMF, and DMSO. The polyethers obtained exhibit the properties of high-resistance organic semiconductors: their electrical conductivity reaches 10⁻¹⁴ S/cm. Full article

Despite the fact that amphiphilic block copolymers have been studied in detail by various methods both in common solvents and aqueous dispersions, their hydrodynamic description is still incomplete. In this paper, we present a detailed hydrodynamic study of six commercial diblock copolymers featuring the same hydrophilic block (poly(ethylene glycol), PEG; degree of polymerization is ca. 110 ± 25) and the following hydrophobic blocks: polystyrene, PS₃₅-b-PEG₁₁₅; poly(methyl methacrylate), PMMA₅₅-b-PEG₉₅; poly(1,4-butadyene), PBd₉₀-b-PEG₁₃₀; polyethylene PE₄₀-b-PEG₈₅; poly(dimethylsiloxane), PDMS₁₅-b-PEG₁₁₅; and poly(ɛ-caprolactone), PCL₄₅-b-PEG₁₁₅. The hydrodynamic properties of block copolymers are investigated in both an organic solvent (tetrahydrofuran) and in water micellar dispersions by the combination of static/dynamic light scattering, viscometry, and analytical ultracentrifugation. All the micellar dispersions demonstrate bimodal particle distributions: small compact (hydrodynamic redii, R_h ≤ 17 nm) spherical particles ascribed to “conventional” core–shell polymer micelles and larger particles ascribed to micellar clusters. Hydrodynamic invariants are (2.4 ± 0.4) × 10⁻¹⁰ g cm² s⁻² K⁻¹ mol^−1/3 for all types of micelles used in the study. For aqueous micellar dispersions, in view of their potential biomedical applications, their critical micelle concentration values and cytotoxicities are also reported. The investigated micelles are stable towards precipitation, possess low critical micelle concentration values (with the exception of PDMS₁₅-b-PEG₁₁₅), and demonstrate low toxicity towards Chinese Hamster Ovarian (CHO-K1) cells. Full article

A facile technique for the preparation of mixed polylactide micelles from amorphous poly-D,L-lactide-block-polyethyleneglycol and crystalline amino-terminated poly-L-lactide is described. In comparison to the classical routine solvent substitution method, the ultrasonication assisted formation of polymer micelles allows shortening of the preparation time from several days to 15–20 min. The structure and morphology of mixed micelles were analyzed with the assistance of electron microscopy, dynamic and static light scattering and differential scanning calorimetery. The resulting polymer micelles have a hydrodynamic radius of about 150 nm and a narrow size distribution. The average molecular weight of micelles was found to be 2.1 × 10⁷ and the aggregation number was calculated to be 6000. The obtained biocompatible particles were shown to possess low cytotoxicity, high colloid stability and high stability towards enzymatic hydrolysis. The possible application of mixed polylactide micelles as drug delivery vehicles was studied for the antitumor hydrophobic drug paclitaxel. The lethal concentration (LC50) of paclitaxel encapsulated in polylactide micelles was found to be 42 ± 4 µg/mL—a value equal to the LC50 of paclitaxel in the commercial drug Paclitaxel-Teva. Full article

Polymer blends, obtained by polymerization of methyl methacrylate in the presence of poly(propylene glycol), are investigated. Poly(propylene glycol) acts as a plasticizer, significantly lowering poly(methyl methacrylate)’s glass transition temperature and decreasing its elasticity modulus and yield stress. The mixture of methyl methacrylate with poly(propylene glycol) is more stable than its mixture with currently used poly(ethylene glycol), which leads to more uniform distribution and higher possible content of the plasticizer. Unlike low molecular weight plasticizers, poly(propylene glycol) is less prone to migration and exudation during manufacturing process and in use, and has low toxicity. Dynamic mechanical thermal analysis, compression testing and X-ray diffraction were used to investigate how the properties of the material depend on the content and molecular weight of the poly(propylene glycol) in the polymer blend. It was shown that the dependence of the glass transition temperature of methyl methacrylate polymerized in the presence of poly(propylene glycol) on the molar fraction of propylene glycol units is linear, and poly(propylene glycol) with lower molecular weight affects properties of the material stronger than poly(propylene glycol) with higher molecular weight. Therefore, the addition of poly(propylene glycol) allows to control the properties of poly(methyl methacrylate) easily and within wide range. Full article

Narrow dispersed poly(1-vinyl-1,2,4-triazole) (PVT) was synthesized by reversible addition–fragmentation chain transfer (RAFT) polymerization of 1-vinyl-1,2,4-triazole (VT). AIBN as the initiator and dithiocarbamates, xanthates, and trithiocarbonates as the chain transfer agents (CTA) were used. Dithiocarbamates proved to be the most efficient in VT polymerization. Gel permeation chromatography was used to determine the molecular weight distribution and polydispersity of the synthesized polymers. The presence of the CTA stabilizing and leaving groups in the PVT was confirmed by ¹H and ¹³C NMR spectroscopy. The linear dependence of the degree of polymerization on time confirms the conduct of radical polymerization in a controlled mode. The VT conversion was over 98% and the PVT number average molecular weight ranged from 11 to 61 kDa. The polydispersity of the synthesized polymers reached 1.16. The occurrence of the controlled radical polymerization was confirmed by monitoring the degree of polymerization over time. Full article

Polymer coatings based on polycations represent a perspective class of protective antimicrobial coatings. Polydiallyldimethylammonium chloride (PDADMAC) and its water-soluble complexes with sodium polystyrenesulfonate (PSS) were studied by means of dynamic light-scattering, laser microelectrophoresis and turbidimetry. It was shown that addition of six mol.% of polyanion to polycation results in formation of interpolyelectrolyte complex (IPEC) that was stable towards phase separation in water-salt media with a concentration of salts (NaCl, CaCl₂, Na₂SO₄, MgSO₄) up to 0.5 M. Most of the polyelectrolyte coatings are made by layer-by-layer deposition. The utilization of water-soluble IPEC for the direct deposition on the surface was studied. The coatings from the PDADMAC and the PSS/PDADMAC complex were formed on the surfaces of hydrophilic glass and hydrophobic polyvinylchloride. It was found that formation IPEC allows one to increase the stability of the coating towards wash-off with water in comparison to individual PDADMAC coating on both types of substrates. The visualization of the coatings was performed by atomic force microscopy and scanning electron microscopy. Full article

Reversible addition-fragmentation chain transfer polymerization was successfully applied to the synthesis of the gradient copolymer of acrylic acid and vinyl acetate in the selective solvent. The gradient degree of the copolymer was varied by the monomer feed. The monomer conversion was found to affect the ability of the copolymer to self-assemble in aqueous solutions in narrowly dispersed micelles with an average hydrodynamic radius of about 250 nm. Furthermore, the synthesized copolymers also tended to self-assemble throughout copolymerization in the selective solvent. Full article

Metal–polymer nanocomposite polyvinyltriazole–silver nanoparticles were obtained using one-pot synthesis in irradiated aqueous solutions of 1-vinyl-1,2,4-triazole (VT) and silver ions. Gel permeation chromatography data show that upon radiation initiation, the molecular weight of poly(1-vinyl-1,2,4-triazole) increases with increasing monomer concentration. To study the kinetics of polymerization and the features of the radiation–chemical formation of nanoparticles, UV-Vis spectroscopy was used. TEM images show a relatively small average size of the forming nanoparticles (2–3 nm) and a narrow size distribution, which shows the effective stabilization of nanoparticles by triazole substituents at a molar ratio of VT and silver ions of 25/1. The addition of ethyl alcohol was used to increase the efficiency of synthesis and suppress the crosslinking of macromolecules in solution. The results of the work show that aqueous–alcoholic solutions of 1 wt.% VT can be used to obtain soluble nanocomposite materials. 10 wt.% monomer solutions have prospects for use in the preparation of polymer gels filled with nanoparticles. Full article