Search Results (251)

This study aimed to evaluate the effect of adding extracts obtained from by-products on the physicochemical and functional properties of cleansing gels. Micellar extraction (2% decyl glucoside solution in water) was performed on secondary raw materials: banana peel (BP), pomegranate peel (PP), tomato pomace (TP), and grape pomace (GP). The extracts were analyzed for soluble substances and active compounds (polyphenols, carotenoids, and vitamin C). Cleansing gels containing plant extracts were also prepared and evaluated for their color and physicochemical and functional properties. The extracts contained natural polyphenols (10.99–16.54 mg·100 mL⁻¹), carotenoids (1.391–2.402 mg·mL⁻¹), and vitamin C (0.651–1.529 mg·100 mL⁻¹). The extract-enriched gels showed altered color (lower brightness, greater redness and yellowness), enhanced foaming properties, and modified viscosity (402.9–416.8 mPA for BP and GP; lower for PP and TP). The pH of the gels ranged from 5.391 to 5.917, which is within the physiological range of human skin. Dissolution times were reduced by up to 60% compared to the control, with PP extract producing the shortest time of 15.7 min. These results indicate that plant by-product extracts can improve both the functional performance and skin compatibility of cleaning gels. Full article

Hot-melt extrusion produces a solid dispersion (SD) containing a poorly water-soluble drug (k) and matrix polymer surfactant (PS), thereby enhancing k’s solubility. When dissolving the SD, the PS is first dissolved, forming micelles. The amorphous form of the solid phase k remains and is further dissolved by micellar solubilization. The goal here is to rigorously derive, on the basis of thermodynamics, a new expression for the change in the standard Gibbs free energy (${∆G}_{\Sigma }^0$). This change serves as a measure for increasing the degree of spontaneity in the dissolution of amorphous k from an SD with a polymeric surfactant relative to the dissolution of the crystalline-form k in an aqueous solution without surfactants (reference state). In the micelle-pseudophase model, it was found that ${∆G}_{\Sigma }^0$ depends on the natural logarithm of the ratio of mole fraction k in the aqueous phase to mole fraction k in the micellar pseudophase. In a simpler model, ${∆G}_{\Sigma }^0$ can be expressed as ln of the solubility ratio of the crystalline and SD forms, assuming that the activity coefficient depends on the process of incorporating k into the micellar particles and that the total amount of surfactants is many times smaller than the water amount, which is acceptable for polymeric surfactants with low values of the critical micellar concentration. Full article

Τhe self-assembly behavior of a series of amphiphilic diblock copolymers, each consisting of a hydrophilic poly(N-vinyl pyrrolidone) (PNVP) block and a hydrophobic block derived from n-alkyl vinyl esters, namely poly(vinyl butyrate) (PVBu), poly(vinyl decanoate) (PVDc), and poly(vinyl stearate) (PVSt), in aqueous solutions was investigated. Dynamic and static light scattering (DLS and SLS) techniques were employed to monitor the micellization behavior. In addition, the self-assembled structures were observed with Transmission Electron Microscopy (TEM). The effect of the nature of the hydrophobic block, the copolymer composition and the copolymer molecular weight on the self-assembly properties was thoroughly examined. The encapsulation of curcumin and indomethacin within the dry cores of the micellar structures was conducted in aqueous solutions for all block copolymers at various curcumin/indomethacin-to-polymer mass ratios. UV-Vis spectroscopy was used to evaluate the drug-loading capacity and efficiency (%DLC and %DLE). In several cases, the encapsulation of both hydrophobic drugs was found to be nearly quantitative. Combined with the observed stability of the micellar structures, these findings suggest that the block copolymers demonstrate significant potential as carriers for drug delivery applications. Full article

The association behavior of amphiphilic block copolymers of N-vinyl pyrrolidone (NVP) and several vinyl esters (Ves) (PNVP-b-PVEs), as exemplified by vinyl butyrate (VBu), vinyl decanoate (VDc), and vinyl stearate (VSt), was studied in tetrahydrofuran (THF), which serves as the selective solvent for the PVE blocks. Static (SLS) and dynamic light scattering (DLS) techniques were adopted as the tools to investigate micellar properties and acquire information regarding the degree of association, the hydrodynamic radii, and the shape of the aggregates. In addition, CONTIN analysis provided insights concerning the association equilibria in THF solutions. The effect of the chemical structure of the corona-forming PVE block on the association process was investigated. Finally, the experimental results were compared with those obtained in previous studies describing the micellization properties of block copolymers consisting of PNVP and polymethacrylate blocks in the same selective solvent. Full article

Aqueous singlet oxygen (¹O₂) sensitization is of high interest due to its wide application in bio-imaging and photodynamic therapy. For organic photosensitizers like porphyrin derivatives, surfactant-assisted micelles have been intensively explored for dispersing hydrophobic sensitizers in aqueous phase; however, they can suffer from poor long-term stability. In this work, palladium octaethylporphyrin (PdOEP)-embedded silica particles were prepared with assistance from Tween micelles, and their corresponding application in aqueous ¹O₂ sensitization was explored. With assistance from Tween 80 at a >3 mg/mL concentration, superior (>95%) solubilization of PdOEP was observed in aqueous solution, leading to a high ¹O₂ quantum yield (Φ_Δ ≈ 93%). By optimizing the synthesis conditions, >95% of micellar PdOEP was embedded into silica particles, exhibiting comparable Φ_Δ (up to 70%) to micellar systems by effectively suppressing PdOEP aggregation in particles. The PdOEP-embedded silica particles exhibited dramatically enhanced long-term stability (more than one year) compared to corresponding micelles with a half-life of ~38 days. In addition, aqueous ¹O₂ sensitization by PdOEP-embedded silica particles was demonstrated upon two-photon excitation in a near-infrared regime (λ_ex = 1030 nm), highlighting the great potential of this method for future biological applications. Full article

Surfactant flooding has shown potential in enhanced oil recovery (EOR), but conventional surfactants often underperform in heterogeneous reservoirs. This study investigates the impact of a surfactant mixture, combining anionic sodium dodecyl sulfate (SDS) and zwitterionic oleylamidopropyl betaine (OAB-30), on two-phase flow behavior and its EOR potential. Six surfactant solutions with varying concentrations were first screened using an idealized dead-end shaped microchannel in combination with interfacial properties and rheological tests. The results showed that 0.2% SDS and 0.6% OAB-30 produced the highest oil recovery in the dead-end structure. Interfacial tension was reduced to 0.374 mN/m and strong viscoelastic behavior was observed using the optimized surfactant mixture. Wettability of the surface tended to be more hydrophilic after the application of the surfactant mixture as well. Subsequently, the microscale oil displacement process was examined using the optimized surfactant mixture via microfluidic devices with an idealized pore–throat network with permeability contrast and realistic pore–throat structure. The application of the optimal surfactant formula resulted in 28.46% and 49.96% improvement over conventional water flooding in a realistic pore–throat structure and idealized pore–throat network. The critical micelle concentration measurements of the mixture suggested favorable micelle formation, contributing to gel-like properties that improved sweep efficiency by lowering the mobility ratio. In heterogenous pore–throat networks, the emulsification, micellar solubilization, wettability alteration, and viscoelastic properties of the surfactant mixture favored the oil recovery process. This work provides experimental evidence and mechanistic insights for the application of viscoelastic surfactants in EOR in heterogeneous reservoirs. Full article

A novel centrifuge-less cloud point extraction (CL-CPE) method was developed for the spectrophotometric determination of copper(II) using 4-nitrocatechol (4NC) as the chelating agent. The extraction system utilizes a mixed micellar phase composed of the nonionic surfactant Triton X-114 and the ionic liquid (IL) Aliquat^® 336 (A336). The extracted ternary ion-association complex, identified as (A336⁺)₂[Cu(4NC)₂], exhibits a maximum absorbance at 451 nm, with a molar absorption coefficient of 8.9 × 10⁴ M⁻¹ cm⁻¹ and a Sandell’s sensitivity of 0.71 ng cm⁻². The method demonstrates a linear response in the copper(II) concentration range of 32–763 ng mL⁻¹ and a limit of detection of 9.7 ng mL⁻¹. The logarithmic extraction constant (log K_ex) was determined to be 7.9, indicating efficient extraction. Method performance, evaluated by the Blue Applicability Grade Index (BAGI) and the Click Analytical Chemistry Index (CACI), confirmed its feasibility, practicality, simplicity, convenience, cost-effectiveness, environmental friendliness, and analytical competitiveness. The proposed IL-CL-CPE method was successfully applied to the analysis of a dietary supplement, a solution for infusion, and synthetic mixtures simulating various copper alloys. Full article

The covalent cross-linking of caseins by the enzyme transglutaminase (Tgase) stabilizes the structure of casein micelles. In our study, the effects of a pretreatment of skim milk (SM) by Tgase on milk protein fractionation by microfiltration were tested. Tgase was found to induce amount-dependent modifications of all milk proteins in SM and a reduction in deposit resistance for laboratory dead-end filtrations of up to 20%. This improvement in process performance could partially be confirmed in pilot-scale cross-flow filtrations of Tgase-pretreated SM and micellar casein solutions (MCC). These comparative trials with untreated retentates under a variation of ΔpTM (0.5–2 bar) at 10 and 50° revealed distinct differences in deposit behavior and achieved the reduction in deposit resistance in a range of 0–20%. The possibility of pre-fouling with enzymatically pretreated MCC prior to SM filtration was also investigated. Under different pre-fouling conditions, practical modes of retentate change, and pre-foulant compositions, a switch to untreated SM consistently resulted in an immediate and major increase in deposit resistance by 50–150%. This was partially related to the change in the ionic environment and the protein fraction. Nevertheless, our results underline the potential of Tgase pretreatment and pre-fouling approaches to alter filtration performance for different applications. Full article

The specific features of the phase diagrams of aqueous Pluronic systems, and particularly those of reverse Pluronics, are critically important for their broad range of applications, notably as nanocarriers for anticancer molecules. This work aims to investigate the effect of increasing hydrophobicity, achieved by varying the PPO/PEO ratio and the molecular weight, on the phase behavior of three reverse Pluronics: 10R5 [(PPO)₈–(PEO)₂₂–(PPO)₈], 17R4 [(PPO)₁₄–(PEO)₂₄–(PPO)₁₄] and 31R1 [(PPO)₂₆–(PEO)₇–(PPO)₂₆]. A broad set of physical measurements, including density, sound velocity, viscosity, and surface tension, was used to characterize the physical properties of the solutions. These data were complemented by additional techniques such as direct observation, dynamic light scattering, and rheological measurements. Based on the primary measurements, molar volume, apparent adiabatic compressibility, and hydration profiles were subsequently derived. Phase diagrams were constructed for each system over concentration ranges of 0.1–90 wt.% and temperatures between 6 and 70 °C, identifying distinct regions corresponding to random networks, flower-like micelles, and micellar networks. Notably, the 31R1/water system does not form flower-like micelles, whereas both the 17R4/water and 10R5/water systems display such structures, albeit in a narrow interval, that shift toward higher concentrations and temperatures with increasing PPO/PEO ratio. Altogether, the present study provides new insights into the physicochemical behavior of reverse Pluronic systems, offering a foundation for their rational design as hydrophobic nanocarriers, either as standalone entities or in conjunction with other copolymers. Full article

This work presents a solving method for problems of Ambrosetti-Prodi type involving p-Laplacian and p-pseudo-Laplacian operators by using adequate variational methods. A variant of the mountain pass theorem, together with a kind of Palais-Smale condition, is involved in order to obtain and characterize solutions for some mathematical physics issues. Applications of these results for solving some physical chemical problems evolved from the need to model real phenomena are displayed. Solutions for Dirichlet problems containing these two operators applied for modeling critical micellar concentration, as well as the volume fraction of liquid mixtures, have been drawn. Full article

In this study, a methacrylic derivative of xylan (XYLMA) was synthesized through transesterification reactions, with the aim of evaluating its physicochemical behavior and its interaction with kaolinite particles. Structural characterization by FT-IR and NMR spectroscopy confirmed the incorporation of methacrylic groups into the xylan (XYL) structure, with a degree of substitution of 0.67. Thermal analyses (TGA and DSC) showed a decrease in melting temperature and enthalpy in XYLMA compared to XYL, attributed to a loss of structural rigidity. Thermal analyses (TGA and DSC) revealed a decrease in the melting temperature and enthalpy of XYLMA compared to XYL, which is attributed to a loss of structural rigidity and a reduction in the crystalline order of the biopolymer. Aggregation tests in solution revealed that XYLMA exhibits amphiphilic behavior, forming micellar structures at a critical aggregation concentration (CAC) of 62 mg L⁻¹. In adsorption studies on kaolinite, XYL showed greater affinity than XYLMA, especially at acidic pH, due to reduced electrostatic forces and a greater number of hydroxyl groups capable of forming hydrogen bonds with the mineral surface. In contrast, modification with methacrylic groups in XYLMA reduced its adsorption capacity, probably due to the formation of supramolecular aggregates. These results suggest that interactions between xylan and kaolinite clay are key to understanding the role that hemicelluloses play in increasing copper recovery when added to flotation cells during the processing of copper sulfide ores with high clay content. Full article

Delivering of hydrophobic drugs by polymeric nanoparticles is an intensively investigated research and development field worldwide due to the insufficient solubility of many existing and potential new drugs in aqueous media. Among polymeric nanoparticles, micelles of biocompatible amphiphilic block copolymers are among the most promising candidates for solubilization, encapsulation, and delivery of hydrophobic drugs to improve the water solubility and thus the bioavailability of such drugs. In this study, amphiphilic ABA triblock copolymers containing biocompatible hydrophilic hyperbranched (dendritic) polyglycerol (HbPG) outer and hydrophobic poly(tetrahydrofuran) (PTHF) inner segments were synthesized using amine-telechelic PTHF as a macroinitiator for glycidol polymerization. These hyperbranched–linear–hyperbranched block copolymers form nanosized micelles with 15–20 nm diameter above the critical micelle concentration. Coagulation experiments proved high colloidal stability of the aqueous micellar solutions of these block copolymers against temperature changes. The applicability of block copolymers as drug delivery systems was investigated using curcumin, a highly hydrophobic, water-insoluble, natural anti-cancer agent. High and efficient drug solubilization up to more than 3 orders of magnitude to that of the water solubility of curcumin (>1500-fold) is achieved with the HbPG-PTHF-HbPG block copolymer nanomicelles, locating the drug in amorphous form in the inner PTHF core. Outstanding stability of and sustained curcumin release from the drug-loaded block copolymer micelles were observed. The in vitro bioactivity of the curcumin-loaded nanomicelles was investigated on U-87 glioblastoma cell line, and an optimal triblock copolymer composition was found, which showed highly effective cellular uptake and no toxicity. These findings indicate that the HbPG-PTHF-HbPG triblock copolymers are promising candidates for advanced drug solubilization and delivery systems. Full article

The unregulated consumption of corticosteroids causes significant adverse effects on human health. Therefore, it is important to develop methodologies that allow their analysis in pharmaceutical matrices with competitive analysis times and costs. The determination of corticosteroids by micellar electrokinetic chromatography (MEKC) using a background electrolyte (BGE) composed of phosphate buffer and a micellar pseudo-stationary phase constituted by a mixture of surfactants is proposed as an alternative quantification technique. The variables involved in the BGE: phosphate concentration, surfactant (sodium dodecyl sulfate (SDS) or sodium lauryl ether sulfate (SLES)), sodium taurocholate (STC) and the pH value were optimized using a Taguchi L₉ (3⁴) experimental design. Employing the optimal BGE, the separation of the three corticosteroids is possible in a linear range of 1.05–10.0 mg L⁻¹, with limits of detection (LOD) of 0.28–0.35 mg L⁻¹. The relative standard deviation (RSD) values obtained for the repeatability (n = 3) and intermediate precision (n = 9) were less than 5.0%. Pharmaceutical formulations (ointments, injectable solution and ophthalmic solution) were analyzed using the proposed methodology (MEKC) and the official methodology (high-performance liquid chromatography, HPLC), and no significant differences were found between the corticosteroid contents obtained from both methods. Full article

Poloxamer-based drug delivery systems are widely used in the pharmaceutical sector. The structural characterization of these systems is crucial for the development of new drug delivery systems and for the optimization of their properties. In this study, we utilized small-angle neutron scattering (SANS) to investigate the structures of poloxamer-based drug delivery systems. The samples were measured using the SANS technique on the VSANS-V16 instrument at Helmholtz-Zentrum Berlin (HZB), Germany. The samples contained 20% poloxamer (P407) and 0.2% of a drug (ibuprofen, ketoprofen, diclofenac) in deuterated water (D₂O) for SANS. The samples varied in terms of temperature analysis (25 °C, common storage temperature; 37 °C, human body temperature; 40 °C, fever temperature). The data analysis involved modeling the data using a Python-based routine. The model used consisted of an isotropic solution of polydisperse spherical micelles. The intensity as a function of the scattering vector was modeled as the product of the form factor and the interparticle structure factor, with the latter described within the local monodisperse approximation regime. Additionally, a scattering contribution was observed, which was associated with the presence of crystalline superstructures formed by micelles that organized into a cubic structure. The data analysis provided important information about the system, such as the average radius, the size distribution, and the thickness of the layer surrounding the micellar core. The results will contribute to the development and optimization of new drug delivery systems that are more effective and safer for medical applications. Full article

Reversible addition–fragmentation chain-transfer (RAFT) polymerization was used to synthesize novel thermoresponsive cationic molecular brushes with high yields—namely of copolymers of methoxyoligo(ethylene glycol) methacrylate, alkoxyoligo(ethylene glycol) methacrylate, and N-methacryloylaminopropyl-N,N-dimethyl-N-propylammonium bromide. Controlled polymerization yielded polymers with a molecular weight dispersity of ≤1.3 and conversions exceeding 80%. The influence of the cationic molecular brushes’ composition on their solubility in water and organic solvents, interfacial tension at the water–oil interface, and aggregation behavior in aqueous solutions was investigated. For the first time, we report the design of thermoresponsive cationic molecular brushes combining an antibacterial potential and tunable hydrophilic–hydrophobic properties, enabling highly precise control over their LCST behavior (17–68 °C) through composition tuning. The solubilization capacity of the hydrophobic compounds of brush micelles in water increased with the hydrophobic comonomer content. These polymers exhibited interfacial activity, significantly reducing the water–oil interfacial tension, with critical micelle concentrations (CMCs) of 3–10 mg/L. It was shown that the amphiphilic properties of the copolymers in aqueous solutions can be easily tuned in a desired direction by varying the content of the comonomer units. The obtained data indicate the potential of the polymers as micellar nanocarriers for controlled drug delivery. Full article