Search Results (128)

We present the creation of an alignment layer for liquid crystal molecules based on DNA from fish waste and a selected cationic surfactant. The implemented biodegradable DNA-based surface offers excellent optical and physical properties, cost-effectiveness, and environmental benefits compared to conventional polymers. Our findings demonstrate that the biopolymer DNA-DODA effectively induces homeotropic alignment of nematic liquid crystals, which was confirmed by topography visualization using atomic force microscopy, macroscopy, and polarizing optical microscopy observations. Anchoring energy and response time studies in the well-known electro-optical effect show that DNA-DODA exhibits molecular interaction strengths comparable to those of commercial polyimide. The successful implementation of DNA-DODA as an alignment layer highlights its promise for next-generation technologies, including flexible, sustainable, and biocompatible optical devices. Full article

Thermosensitive hydrogel, as a smart polymer material, showed great potential for application in the field of wound repair due to its unique external temperature responsiveness and excellent biocompatibility. Chitosan, a natural macromolecular polysaccharide derived from the deacetylation of chitin, possessed not only strong interactions with biomolecules such as DNA, proteins, and lipids, but also unique biocompatibility and degradability. Chitosan-based thermosensitive hydrogels, prepared by compounding chitosan with surfactants, underwent sol–gel phase transitions at varying external temperatures, which provided an ideal healing environment for wounds. This comprehensive review was initiated by elucidating the sol–gel phase transformation mechanism underlying thermosensitive hydrogels and the intricate process of wound repair. In addition, this review provided a detailed overview of the prevalent types of chitosan-based thermosensitive hydrogels, highlighting their unique characteristics and applications in different types of wound repair. Finally, the challenges and development directions of chitosan-based thermosensitive hydrogels in wound repair were discussed, aiming to provide theoretical support and practical guidance for their future applications in wound healing. Full article

Most novel active pharmaceutical ingredients have low water solubility; therefore, solubility-enhancing methods are applied. The aim of the present investigation is to study the impact of nine commonly used pharmaceutical excipients (fillers, surfactants, cyclodextrins, polymers) on solubility, permeability and their relationship. This is crucial for ensuring optimal bioavailability. Carbamazepine, naproxen and pimobendan were chosen as model compounds due to their different acid–base properties. Equilibrium solubility was measured by the traditional shake flask method. Effective permeability was determined by the PAMPA model. Measurements of ionizable compounds were carried out at three pH values. The pH-dependent change in the investigated parameters is maintained even in the presence of excipients. Fillers resulted in a slight or no effect, while the impact of other excipients showed a significant concentration dependence. The impact of excipients was influenced by the structure and ionization state of the molecules. The dominance of the ionized form moderates the impact of excipients. The changes in solubility were more pronounced than in the case of permeability. By examining the effect of the ionization state and interactions with excipients, this work supports the development of formulations that enhance solubility with minimal impacts on permeability. Additionally, it can serve as good basis for preformulation studies and design optimization. Full article

The incorporation of essential oils into the oil phase of oil-in-water microemulsions is an emerging strategy for the development of stable water-based topical formulations. The introduction of a suitable polymer to formulate film-forming microemulsions may improve topical administration; however, the effect of formulation variables on film quality attributes has not been studied. In this study, thermodynamically stable microemulsion concentrates consisting of surfactant (Kolliphor^® RH40), alone or in combination with cosurfactant Transcutol^® at surfactant-to-cosurfactant mass ratio 7:3, cosolvent (propylene glycol), and synthetic oils (medium-chain triglycerides or isopropyl myristate) with tea tree, cinnamon, or thyme essential oil were formulated and diluted with hypromellose solution in a water/isopropanol mixture (1:1 w/w) to produce film-forming microemulsions. The type and concentration of synthetic and essential oils and cosurfactant influenced the dynamics of structural transformations upon dilution as well as the rheological behavior, viscosity, and pH of film-forming microemulsions. Films obtained by casting film-forming microemulsions were opalescent, smooth, flexible, and swellable in artificial sweat and water. The weight and yield of films increase with the synthetic oils present and without cosurfactant added. Optimizing the ratio of essential oil/synthetic oil, the type of synthetic oil, and the inclusion/exclusion of cosurfactant allows for achieving the targeted film attributes for cosmetic and pharmaceutical applications, including wound treatment. Full article

Enhanced oil recovery (EOR) methods traditionally rely on polymer solutions to improve viscosity and elasticity; however, their effectiveness is limited under high-temperature, high-salinity, and high-shear conditions, leading to elevated operational costs. Anionic/cationic formulations have been studied in terms of interfacial tension reduction for EOR applications. This study presents a novel approach to EOR by enhancing the rheological properties of an anionic internal olefin sulfonate surfactant through interactions with cationic surfactants, eliminating the need for polymer molecules. This research demonstrates that cationic surfactants can induce micellization changes, resulting in substantial viscosity enhancement and viscoelasticity development. The effect is found to depend on the hydrocarbon chain length and concentration of the cationic surfactants, with longer chains yielding higher viscosity and more pronounced non-Newtonian behavior. Additionally, this study reveals that the addition of NaCl alters micellar organization, with the order of component additions playing a critical role in rheological performance. This kinetic-dependent micellization behavior, rarely explored in EOR applications, highlights the potential of counterion surfactants as viscosity enhancers in surfactant-based flooding processes. Oscillatory rheology confirms that cationic/anionic surfactant systems in this study exhibit stable viscoelastic behavior, making them potentially more suitable for harsh reservoir environments than polymer-based EOR fluids. These findings open new avenues for the development of cost-effective and tailored surfactant formulations, offering an alternative to polymer solutions under challenging reservoir conditions. Full article

Understanding the interactions between polymers and surfactants is critical for designing advanced fluid systems used in applications such as enhanced oil recovery, drilling, and chemical processing. This study examines the effects of five surfactants: two anionic (Stepanol WA-100 and Stepwet DF-95), one cationic (HTAB), one zwitterionic (Amphosol CG), and one non-ionic (Alfonic 1412-3 Ethoxylate), on the steady shear rheology and surface activity of two polymers, namely cationic hydroxyethyl cellulose based polymer (LR-400) and anionic polyacrylamide based polymer (Praestol 2540TR). The polymer-surfactant solutions behave as shear-thinning fluids and follow the power-law model. Anionic surfactants exhibit a strong effect on the rheology of cationic polymer LR-400 solution. The consistency index rises sharply with the increase in surfactant concentration. Also, the solutions become highly shear-thinning with the increase in surfactant concentration. The effects of other surfactants on the rheology of cationic polymer solution are small to modest. None of the surfactants investigated exhibit a strong influence on the rheology of anionic polymer Praestol 2540TR. Only weak to modest effects of surfactants are observed on the rheology of anionic polymers. The surface tension of the polymer-surfactant solution decreases with the increase in surfactant concentration. Zwitterionic surfactant Amphosol CG is found to be most effective in reducing the surface tension at a given concentration in ppm. This surfactant also raises the electrical conductivity of the solution to the largest extent. From the changes in slope of surface tension versus surfactant concentration plots, the approximate values of critical aggregation concentration (CAC) and polymer saturation point (PSP) are estimated. Full article

Background/Objectives: This study investigates for the first time the use of the prilling technique in combination with solvent evaporation to produce nano- and submicrometric PLGA particles to deliver properly an active pharmaceutical ingredient. Curcumin (CCM), a hydrophobic compound classified under BCS (Biopharmaceutics Classification System) class IV, was selected as the model drug. Methods: Key process parameters, including polymer concentration, solvent type, nozzle size, and surfactant levels, were optimized to obtain stable particles with a narrow size distribution determined by DLS analysis. Results: Particles mean diameter (d₅₀) 316 and 452 nm, depending on drug-loaded cargo as Curcumin-loaded PLGA nanoparticles demonstrated high encapsulation efficiency, assessed via HPLC analysis, stability, and controlled release profiles. In vitro studies revealed a faster release for lower drug loadings (90% release in 6 h) compared to sustained release over 7 days for higher-loaded nanoparticles, attributed to polymer degradation and drug-polymer interactions on the surface of the particles, as confirmed by FTIR analyses. Conclusions: These findings underline the potential of this scalable technique for biomedical applications, offering a versatile platform for designing drug delivery systems with tailored release characteristics. Full article

Pore-scale remediation investigation of oil-contaminated soil is important in several environmental and industrial applications, such as quick responses to sudden accidents. This work aims to investigate the oil pollutant removal process and optimize the oil-contaminated soil remediation performance at the pore scale to find the underlying mechanisms for oil removal from soil. The conservative forms of the phase-field model and the non-Newtonian power-law fluid model are employed to track the moving interface between two immiscible phases, and oil pollutant flushing removal process from soil pores is investigated. The effects of viscosity, interfacial tension, wettability, and flushing velocity on pore-scale oil pollutant removal regularity are explored. Then, the oil pollutant removal effects of two flushing agents (surfactant system and surfactant–polymer system) are compared using an oil content prediction curve based on UV-Visible transmittance. The results show that the optimal removal efficiency is obtained for a weak water-wetting system with a contact angle of 60° due to the stronger two-phase fluid interaction, deeper penetration, and more effective entrainment flow. On the basis of the dimensionless analysis, a relatively larger flushing velocity, resulting in a higher capillary number (Ca) in a certain range, can achieve rapid and efficient oil removal. In addition, an appropriately low interfacial tension, rather than ultra-low interfacial intension, contributes to strengthening the oil removal behavior. A reasonably high viscosity ratio (M) with a weak water-wetting state plays synergetic roles in the process of oil removal from the contaminated soil. In addition, the flushing agent combined with a surfactant and polymer can remarkably enhance the oil removal efficiency compared to the sole use of the surfactant, achieving a 2.5-fold increase in oil removal efficiency. This work provides new insights into the often-overlooked roles of the pore scale in fluid dynamics behind the remediation of oil-contaminated soil via flushing agent injection, which is of fundamental importance to the development of effective response strategies for soil contamination. Full article

Polydiacetylenes (PDAs) are conjugated polymers that are well known for their colorimetric transition from blue to red with the application of energetic stimulus. Sensing platforms based on polymerized diacetylene surfactant vesicles and other structures have been widely demonstrated for various colorimetric biosensing applications. Although less studied and utilized, the transition also results in a change from a non-fluorescent to a highly fluorescent state, making polydiacetylenes useful for both colorimetric and fluorogenic sensing applications. Here, we focus on the characterization and optimization of polydiacetylene vesicles to tune their sensitivity for fluorogenic sensing applications. Particularly, we look at how the structure of the diacetylene (DA) hydrocarbon tail and headgroup affect the self-assembled vesicle size and stability, polymerization kinetics, and the fluorogenic, blue to red phase transition. Longer DA acyl tails generally resulted in smaller and more stable vesicles. The polymerization kinetics and the blue to red transition were a function of both the DA acyl tail length and structure of the headgroup. Decreasing the acyl tail length generally led to vesicles that were more sensitive to energetic stimuli. Headgroup modifications had different effects depending on the structure of the headgroup. Ethanolamine headgroups resulted in vesicles with potentially increased stimuli responsivity. The lower energy stimulus to induce the chromatic transition was attributed to an increase in headgroup hydrogen bonding and polymer backbone strain. Boronic-acid headgroup functionalization led to vesicles that were generally unstable, only weakly polymerized, and unable to fully transform to the red phase due to strong polar, aromatic headgroup interactions. This work presents the design of PDA vesicles in the context of biosensing platforms and includes a discussion of the past, present, and future of PDA biosensing. Full article

The synthesis of poly(N-isopropyl acrylamide) (pNIPA)-based polymers via the surfactant-free precipitation polymerization (SFPP) method produced thermosensitive nanospheres with a range of distinctive physicochemical properties. Nano- and microparticles were generated using various initiators, significantly influencing particle characteristics, including the hydrodynamic diameter (D_H), which varied from 87.7 nm to 1618.1 nm. Initiators, such as potassium persulfate and 2,2′-azobis(2-methylpropionamidine) dihydrochloride, conferred anionic and cationic functionalities, respectively, impacting the electrokinetic potential (EP) of the particles. Notably, certain particles with cationic initiators exhibited negative EP values at 18 °C, attributed to residual initiator components that affected the surface charge distribution. The presence of hydrophilic N-(2-hydroxyethyl)acrylamide (HEAA) segments also influenced solubility and phase transition behaviors, with critical dependencies on the HEAA/NIPA (N-isopropyl acrylamide) molar ratios. EP measurements taken at 18 °C and 42 °C revealed substantial differences, primarily governed by the initiator type and polymer composition. Observed variations in particle stability and size were associated with the choice of crosslinking agents and comonomer content, which affected both D_H and EP in distinct ways. This study provides insights into key factors influencing colloidal stability and electrostatic interactions within thermosensitive polymer systems, underscoring their potential applications in biomedical and industrial fields. Full article

In recent years, many studies have focused on improving the bioconversion of cellulose by adding non-ionic surfactants. In our study, the effect of the addition of a polymer, polyethylene glycol (PEG 4000), on the bioconversion of different cellulose materials was evaluated, focusing on the hydrolysis efficiency and structural changes in pure cellulose after the enzymatic hydrolysis process. The obtained results showed that the addition of non-ionic surfactant significantly improved the digestibility of cellulosic materials. The highest hydrolysis efficiency was observed for Sigmacel 101 (Cel-S101) cellulose, which consists mainly of amorphous regions. In the case of Avicel cellulose (Cel-A), PEG had a lesser effect on the bioconversion’s efficiency due to limited access to the crystal structure and limited substrate–cellulase interactions. The consistency of the obtained results is confirmed by qualitative and quantitative analyses (XRD, FTIR, and HPLC). Our findings may be helpful in further understanding the mechanism of the action of surfactants and improving the enzymatic hydrolysis process. Full article

Background/Objectives: Drug–polymer interactions and miscibility promote the formation and performance of amorphous solid dispersions (ASDs) of poorly soluble drugs for improved oral bioavailability. The objective of this study was to employ drug–polymer interaction calculations and small-scale experimental characterization to screen polymers for potential ASDs of ritonavir. Methods: Seven polymers across four polymer types were screened as follows: an enteric one (EudragitS100), amphiphilic ones (HPMCAS-L, HPMCAS-H, and their 1:1 combination), hydrophilic ones (PEG-6000, PVP-VA), and a surfactant (Soluplus), including PVP-VA as a positive control, as the commercial ASD employs PVP-VA. Drug–polymer interaction calculations were performed for Hansen solubility parameter, Flory–Huggins parameter, and glass transition temperature. ASDs were prepared via film casting. Experimental characterizations included drug solubility in polymer solutions, polymer inhibition of drug precipitation, polarized light microscopy, differential scanning calorimetry, solubilization capacity, and dissolution studies. Results: HPMCAS-L, HPMCAS L:H, and Soluplus, along with the positive control PVP-VA, were identified as polymers for potential ASDs of ritonavir, with HPMCAS-L and PVP-VA being preferable. HPMCAS-L and the positive control PVP-VA were always viable for both 20% and 40% drug loads across all tests. Films with each of these four polymers showed improved dissolution compared to amorphous ritonavir without polymer. Drug–polymer interaction calculations anticipated the unfavorable small-scale experimental results for PEG-6000 and EudragitS100. Conclusion: Overall, the results contribute towards a resource-sparing approach to identify polymers for ASDs. Full article

This study investigated the enhancing effects of the temperature-resistant polymer Poly(ethylene-co-N-methylbutenoyl carboxylate-co-styrenesulfonate-co-pyrrolidone) (hereinafter referred to as Z364) on the performance of cocamidopropyl hydroxy sulfobetaine (CHSB) foam under high-temperature and high-salinity conditions. The potential of this enhanced foam system for mobility control during heavy oil thermal recovery processes was also evaluated. Through a series of experiments, including foam stability tests, surface tension measurements, rheological assessments, and parallel core flooding experiments, we systematically analyzed the interaction between the Z364 polymer and CHSB surfactant on foam performance. The results indicated that the addition of Z364 significantly improved the strength, thermal resistance, and salt tolerance of CHSB foam. Furthermore, the adsorption of CHSB on the polymer chains enhanced the salt resistance of the polymer itself, particularly demonstrating stronger blocking effects in high-permeability cores. The experimental findings showed that Z364 increased the viscosity of the liquid film, slowed down liquid drainage, and reduced gas diffusion, effectively extending the half-life of CHSB foam and improving its stability under high-temperature conditions. Additionally, in parallel core flooding experiments, the polymer-enhanced foam exhibited significant flow diversion effects in both high-permeability and low-permeability cores, effectively directing more fluid into low-permeability channels and improving fluid distribution in heterogeneous reservoirs. Overall, Z364 polymer-enhanced CHSB foam demonstrated superior mobility control during heavy oil thermal recovery, offering new technical insights for improving the development efficiency of high-temperature, high-salinity reservoirs. Full article

Biofumigation was proposed as an alternative to synthetic pesticides for the disinfection of agricultural soils, in view of the biocidal effect of isothiocyanates (ITCs) released by some vegetal species, like Brassicaceae. However, biofumigation also presents limitations; thus, a novel and viable alternative could be the direct introduction of ITCs into agricultural soils as components loaded into biodegradable hydrogels. Thus, in this work, ITCs-based microemulsions were developed, which can be loaded into porous polymer-based hydrogel beads based on sodium alginate (ALG) or sodium carboxymethyl cellulose (CMC). Three ITCs (ethyl, phenyl, and allyl isothiocyanate) and three different surfactants (sodium dodecylsulfate, Brij 35, and Tween 80) were considered. The optimal system was characterized with attenuated ATR-FTIR spectroscopy and differential scanning calorimetry to study how the microemulsion/gels interaction affects the gel properties, such as the equilibrium water content or free water index. Finally, loading and release profiles were studied by means of UV–Vis spectrophotometry. It was found that CMC hydrogel beads showed a slightly more efficient profile of micelles’ release in water with respect to ALG beads. For this reason, and due to the enhanced contribution of Fe(III) to their biocidal properties, CMC-based hydrogels are the most promising in view of the application on real agricultural soils. Full article

In advanced powder metallurgy technologies such as metal injection molding (MIM) and material extrusion technology (MEX), the intricate synergy between binder components and metallic powders within feedstocks is predominant, dictating the technological boundaries of metal’s complexity, size, and thickness. This work suggests unique binder constituents (polymers, surfactants and melamine), aiming to boost the debinding efficacy and solid loading while ensuring processability. The interactions and role of melamine by thermal and rheological studies are detailed, spotlighting how, unlike traditional binder systems, the pioneering feedstock introduces beneficial modifications to storage modulus (G′) and loss tangent (tan δ), alongside a lubricating effect on metallic mixtures. This study highlights the potential of melamine to facilitate a more efficient debinding process, with superior formaldehyde management and environmental control. Through this material-centric lens, we offer new pathways to navigate the complexities of MIM and MEX, advancing towards technological enhancement and environmental protection. Full article