Search Results (211)

(1) Background: Carvedilol is a poorly water-soluble drug, which limits its therapeutic performance. Deep eutectic solvents (DES) and cyclodextrins (CD) are emerging solubilizing agents that can improve drug bioavailability. (2) Methods: Twenty-one DES were prepared using choline chloride and polyols or sugars (xylitol, sorbitol, glucose, and fructose) at different molar ratios with water. α and β cyclodextrins (CD) were added (0.5–2 mM) using two incorporation strategies: (Method 1) addition to the aqueous phase before DES formation; (Method 2) direct addition to the preformed DES. (3) Results: Carvedilol solubility markedly increased with DES–CD combinations. In Method 1, xylitol-based DES provided up to a 16-fold enhancement, especially with β-CD at low concentrations, while glucose and sorbitol systems showed modest effects. Fructose-based mixtures improved mainly at a 2:1:35 ratio without CDs. In Method 2, α-CD with xylitol or sorbitol yielded the highest increases (up to 38.9-fold). (4) Conclusions: The solubilization efficiency depends on DES composition, CD type, and concentration. α-CD combined with xylitol-based DES showed the best results, highlighting this approach as a promising strategy to enhance carvedilol solubility for pharmaceutical applications. Full article

Background/Objectives: Rebamipide is a gastroprotective agent with poor aqueous solubility and rapid gastrointestinal clearance, leading to reduced therapeutic efficiency. This study aimed to enhance the solubility, mucoadhesion, and sustained oral delivery of Rebamipide through the development of a deep eutectic mixture (DEM)-based bioadhesive controlled-release granule formulation. Methods: In silico hydrogen-bonding interactions between Rebamipide, malonic acid, and urea were analyzed using CCDC tools. A thermodynamically stable DEM (1:3:1) was prepared and incorporated into bioadhesive granules using chitosan and HPMC. Physicochemical characterization was conducted using FTIR, DSC, TGA, and PXRD. Solubility, in vitro dissolution, ex vivo mucoadhesion (sheep gastric mucosa), and in vivo gastric retention (BaSO₄-loaded granules in rats) were evaluated. Results: The optimized DEM significantly enhanced Rebamipide solubility (10.08 mg/mL vs. 0.045 mg/mL). Solid-state analyses confirmed hydrogen-bond formation and reduced crystallinity. DEM granules exhibited sustained drug release over 24 h (99.7 ± 0.8%) with improved dissolution efficiency compared to the marketed tablet (Mucosta®, 100 mg; T₅₀%: 5.03 h vs. 0.82 h). Kinetic modeling indicated non-Fickian anomalous transport (n = 0.47). The bioadhesive force of DEM granules (0.29 ± 0.02 N) was significantly higher than that of the pure drug and physical mixture. In vivo radiographic studies confirmed prolonged gastric retention. Conclusions: The DEM-based bioadhesive granule system effectively improves solubility, dissolution rate, mucoadhesion, and gastric retention of Rebamipide. This approach represents a promising platform for once-daily gastroretentive oral delivery, pending further pharmacokinetic evaluation. Full article

The selective removal of HCl from industrial HCl/SiF₄ mixtures was investigated using a series of alcohol-based and deep eutectic solvents (DESs). Among them, glycerol (GL) exhibited superior selectivity for HCl despite a moderate total capacity. Absorption at 60 °C ensured stable operation with minimal foaming. Desorption analysis revealed that both HCl and SiF₄ underwent partial irreversible absorption under N₂ stripping, while staged vacuum desorption enabled efficient and selective recovery—SiF₄ was fully removed at 70 °C and 6 kPa, followed by nearly complete HCl desorption at 90 °C. Cyclic tests confirmed excellent solvent stability and rapid regeneration, with complete desorption achieved within 10–15 min. A conceptual process was proposed based on these findings, demonstrating a practical and energy-efficient route for selective HCl recovery from acid–gas mixtures. Full article

Low extraction efficiency limits the availability and application of aescins, which exhibit various pharmacological activities. Here, we optimized parameters for ultrasound-assisted extraction of aescins from Aesculus chinensis seeds using deep eutectic solvent (DES)-water mixtures. Seven DES formulations were screened, and one providing the highest yield was selected for optimizing the molar ratio. The effects of four parameters were investigated using single-factor experiments combined with response surface methodology. The optimal extraction conditions were as follows: DES, a 1:1 mixture of 1,3-butanediol and lactic acid, with 42.5% water, used at a liquid-solid ratio of 25 mL/g; ultrasonic frequency, 40 kHz; extraction temperature, 70 °C; and extraction time, 27.5 min. The extraction yield under these conditions was significantly higher than that obtained via traditional methods. Aescin was purified from the DES extract using macroporous resin. AB-8 resin was most efficient in adsorbing aescin in static adsorption tests. Based on dynamic adsorption experiments, optimal separation, with a 100% recovery rate, was achieved by passing four bed volume (BV) of extract through AB-8 column, removing impurities with two BV of deionized water and four BV of 30% ethanol, and eluting with four BV of 60% ethanol at 5–10 mL/min. This green method should be suitable for large-scale applications. Full article

This paper reports initial experimental results related to the preparation of colored anodic titania thin layers using various deep eutectic solvent (DES)-based formulations. Electrolytes based on choline dihydrogen citrate–oxalic acid–ethylene glycol (1:1:1 molar ratio), choline chloride–oxalic acid (1:1 molar ratio) and choline chloride–lactic acid (1:2 molar ratio) eutectic mixtures were investigated. The anodization has been performed at constant voltage in a range of 10–100 V for various periods of time between 1 and 5 min at room temperature under mild stirring. A brief description of anodization procedures, as well as of some characteristics, from appearance and morphological viewpoints, is presented. A quantitative analysis of color characteristics in relation to the DES-based electrolyte and applied voltage using the CIELAB system is also discussed. The achieved chromatic scale follows this order of colors: golden—blue—light blue—light blue/green—pink—violet. This depends on the applied potential and the DES-based electrolyte. The films present a relatively high brightness and color saturation. The hue vs. anodization voltage diagrams suggest an almost linear dependence of the oxide growth measured against the applied voltage. The corrosion performance has been assessed through continuous immersion tests in (i) 0.5 M NaCl for 240 h and (ii) Hank’s biological solution for 96 h with intermediate visual examinations and recording corrosion potential, as well as potentiodynamic polarization curves and impedance spectra at open circuit potential. Different corrosion performances are discussed considering the aggressive medium involved and the used DES-based systems. Full article

Over the past few decades, ionic liquids (ILs) have gained attention as electrolytes, although concerns about their environmental persistence and toxicity challenge their status as green solvents. In this framework, choline chloride (ChCl) offers a more sustainable alternative due to its low toxicity, biodegradability, and cost-effectiveness. Although ChCl has a high melting point, its combination with hydrogen bond donor compounds (HBDs) can result in liquid mixtures at much lower temperatures, known as deep eutectic solvents (DESs). This study presents a comparative evaluation of three ChCl-based DESs, glyceline, ethaline, and reline (obtained from mixtures of ChCl and glycerol, ethylene glycol, and urea), with a focus specifically on their potential as electrolyte candidates for supercapacitors. Using differential scanning calorimetry (DSC), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and nuclear magnetic resonance (NMR), we assess their thermal, electrochemical, and structural properties. All DESs displayed amorphous behavior and a strong tendency to remain liquid even at very low temperatures. Among them, ethaline showed the most promising electrochemical performance, exhibiting the lowest resistivity and the highest capacity. Full article

Liquid is a fundamental requirement for life as we understand it, but whether that liquid has to be water is not known. We propose the hypothesis that ionic liquids (ILs) and deep eutectic solvents (DES) constitute a class of non-aqueous planetary liquids capable of persisting on a wide range of bodies where stable liquid water cannot exist. This hypothesis is motivated by key physical properties of ILs and DES. Many exhibit vapor pressures orders of magnitude lower than that of water and remain liquid across exceptionally wide temperature ranges, from cryogenic to well above terrestrial temperatures. These properties permit stable liquids to exist where liquid water would rapidly evaporate or freeze and outside of bulk phases as persistent microscale reservoirs—such as thin films and pore-filling droplets. In other words, ILs and DES can persist in environments without requiring oceans, thick atmospheres, or narrowly regulated climate conditions. We further hypothesize that ILs and DES could act as solvents for non-Earth-like life, based on their polar nature and the demonstrated stability and functionality of proteins and other biomolecules in ionic liquids. More speculatively, our hypothesis extends to the idea that ILs and DES could enable prebiotic chemistry by providing long-lived, protective liquid environments for complex organic molecules on bodies such as comets and asteroids, where liquid water is absent. Additionally, based on the occurrence of DES-like mixtures as protective intracellular liquids in desiccation-tolerant plants, we propose that ILs and DES might be solvents that life elsewhere purposefully evolves. We review protein and other biomolecule studies in ILs and DES and outline planetary environments in which ILs and DES might occur by discussing available anions and cations. We present strategies to advance the IL/DES solvent hypothesis using laboratory studies, computational chemistry, planetary missions, analysis of existing spectroscopic datasets, and modeling of liquid microniches and chemical survival on small bodies. Full article

Near-critical and supercritical carbon dioxide (SC-CO₂) is extensively utilized in high-pressure separation, extraction, polymer processing, and carbon capture and utilization (CCU) technologies owing to its tunable density, low viscosity, high diffusivity, and environmentally benign nature. Reliable phase equilibrium data are indispensable for process design and optimization, especially in the near-critical region characterized by pronounced non-idealities, high compressibility, and density fluctuations. This review synthesizes experimental phase behaviour studies for binary mixtures of CO₂ with diverse components, including hydrocarbons, alcohols, ethers, esters, ketones, water, monomers/polymers, ionic liquids (ILs), and deep eutectic solvents (DESs), compiling extensive vapour–liquid equilibrium (VLE), liquid–liquid equilibrium (LLE), and critical data across industrially relevant pressure (up to 40 MPa) and temperature (up to 400 K) ranges. It critically evaluates analytical (sampling and non-sampling) and synthetic methodologies, addressing challenges in CO₂-rich phase handling, depressurization artefacts, and near-critical phenomena, while assessing data consistency against established reliability criteria. Key trends emerge, such as enhanced solubility with increasing pressure and CO₂ density, chain-length dependencies in hydrocarbons and alcohols, and Lewis acid–base interactions driving solvation in polar systems. The review highlights gaps in multicomponent data and proposes integrating high-quality experiments with advanced thermodynamic modelling to enhance predictive accuracy. Future directions emphasize high-precision in situ techniques, expanded datasets for complex mixtures, and novel CO₂-philic solvents to advance sustainable SC-CO₂ applications. Full article

The development of deep eutectic solvents (DESs) is a key issue for the realization of green and efficient metal extraction processes. The present study aims to experimentally construct the phase diagram of the binary system consisting of tri-n-octylphosphine oxide (TOPO) and 4,4,4-trifluoro-1-phenyl-1,3-butanedione (HBTA) and, thus, determine its eutectic composition for the solvent extraction of Li⁺. Differential scanning calorimetry was used to characterize the phase transitions (melting temperatures and enthalpies) over the entire composition range of the binary mixture. Its eutectic composition was established at HBTA:TOPO mass ratio of 60:40. For further validation of the eutectic composition from the experimentally measured thermal effects for melting of different HBTA:TOPO mass ratios, a Tammann diagram was also constructed. Only mixtures with HBTA:TOPO mass ratios of 70:30, 60:40 (eutectic composition), and 50:50 were liquids at 30 °C, while at room temperature of 25 °C, the 70:30 mixture formed crystals. All three mixtures, which were liquids at 30 °C, were found to extract Li⁺ effectively. However, at a room temperature of 25 °C, only the eutectic mixture (60:40 mass ratio) extracted Li⁺ effectively, while the mixture with HBTA:TOPO mass ratio of 50:50 formed crystals when mechanically agitated and, therefore, was deemed as unsuitable for Li⁺ extraction. Full article

Deep eutectic solvents are a sustainable and chemically tunable class of solvents formed by strong hydrogen bonding between a hydrogen bond acceptor and a hydrogen bond donor. Their extreme versatility has established deep eutectic solvents in ten key applied areas, including the green extraction of bioactive compounds, CO₂ capture, electrochemistry, and the catalytic media. Research is shifting towards highly innovative frontier trends, such as the role of deep eutectic solvents in dynamic covalent chemistry and as templates for advanced photocatalytic nanomaterials. Other innovative directions include artificial organelles for bioremediation, thermoacoustic deep eutectic solvents for smart drug delivery, and their use as multifunctional interfaces for 2D materials. The future of deep eutectic solvents lies in process engineering and scale-up, supported by computational chemistry, confirming their position as a central pillar of the circular economy. This trajectory marks the transition of deep eutectic solvents from laboratory curiosities to a scalable industrial reality. Full article

Chemical recycling is one of the most prominent techniques that enables monomer recovery for plastics like polyethylene terephthalate (PET), which ultimately reduces the dependency on virgin material inputs. In this study, 40 deep eutectic solvents (DESs) were pre-screened using COSMO-RS to identify the best solvent for chemical recycling of PET. Quantitative evaluation was performed based on activity coefficients (γ) to assess solute–solvent interactions. Qualitatively, the sigma profile and sigma potential were analyzed to understand the polarity and affinity of each DES component. This study experimentally validated the two top-performing DESs based on COSMO-RS output. The DES formed by combining thymol with phenol (Thy/Phe (1:2)) achieved 100% PET degradation and 94.5% terephthalic acid (TPA) recovery from post-consumer PET in just 25 min. The rapid dissolution of PET into molten state accelerated the hydrolysis reaction, leading to efficient monomer recovery. The second DES, tetrabutylammonium bromide/sulfolane (TBABr/Sulf (1:7)), attained 93.7% PET degradation and 94% TPA recovery. The PET-to-solvent ratio used in this study was 0.75, while the PET-to-DES ratio in the mixture was only 0.15, the lowest reported for DES-assisted hydrolysis to date. Characterization of the recycled TPA confirmed a purity level comparable to its virgin grade, as verified by FT−IR analysis. This study presents two important outcomes. First, the use of COSMO-RS for DES selection provides a strong rationale for solvent choice in targeted reactions and processes. Second, the use of appropriate DES in this study helps reduce key parameters associated with depolymerisation process, including reaction time, temperature, and catalyst consumption. Full article

This study aimed to develop an efficient and environmentally sustainable method for extracting bioactive compounds from juçara palm (Euterpe edulis Mart.) fruit residues using deep eutectic solvents (DES) and conventional solvents, combined with ultrasound-assisted extraction (UAE). Seven DES formulations based on choline chloride (ChCl) and different hydrogen bond donors (glycerol, glucose, and organic acids) were prepared, and their performance was compared with water, ethanol, and ethanol/water mixtures. The phenolic composition, anthocyanins and antioxidant activity of the extracts were determined using spectrophotometric assays (Folin–Ciocalteu, DPPH, ABTS, and FRAP) and ESI–MS/MS analysis. The results showed that DES exhibited higher efficiency in recovering total phenolic compounds, anthocyanins and ABTS compared to conventional solvents, particularly in the ChCl–glycerol system. ESI–MS/MS analyses monitored around 40 phenolic compounds, including phenolic acids, flavanones, flavonoids, and anthocyanins. Acidic solvents favored anthocyanin extraction and stability, while ethanol- and glycerol-based systems provided broader compound profiles. The use of DES proved to be a green and selective alternative for obtaining extracts rich in bioactive compounds, enhancing the value of juçara residues and contributing to the sustainability of the species production chain. Full article

Deep eutectic solvents (DES) were selected for the extraction of anthocyanins from red grape skins as an efficient and environmentally friendly solvent alternative to traditional mixtures based on methanol. In silico studies (COSMO-RS) were employed as screening tools to identify the most suitable options, significantly reducing the chemical space of potential DES to be studied. A total of 30,132 DES combinations were assessed. The DESs selected were polyalcohols (ethyleneglycol, glycerol, 1,2-propanediol, and 1,6-hexanediol) and carboxylic acids (citric, oxalic, malic, and lactic acid) as hydrogen bond donors (HBD) and choline chloride, betaine, or salts (potassium carbonate, sodium acetate, and propionate), as hydrogen bond acceptors (HBA). Choline chloride:glycerol and choline chloride:oxaclic acic were selected as solvents to optimize time, temperature, and water content in ultrasound- and microwave-assisted extraction of anthocyanins. In both cases, around 20 wt% of water was found to be the optimum to maximize the extractions, whereas extraction time and temperature depended on the type of anthocyanin. The amount of malvidin-3-O-glucoside extracted by microwave-assisted extraction with choline chloride: oxalic acid was 172 ± 7 mg/kg and 119.5 ± 0.5 mg/kg by ultrasound-assisted extraction with choline chloride: glycerol, which means an increase in performance of, respectively, 64 and a 13% compared to the traditional method. Full article

Blackthorn (Prunus spinosa L.) is a wild, understudied plant rich in bioactive compounds such as polyphenols with designated antioxidant potential. The main objective of this research was to optimize ultrasound-assisted extraction of blackthorn pomace using natural deep eutectic solvents (NADES). To obtain the highest yield of polyphenols and improved in vitro antioxidant activity, response surface methodology (RSM) and central composite experimental design were used. The screening step of the study included ten different NADESs using a one-factor-at-a-time approach. Two NADES mixtures (N12, containing proline and lactic acid in a molar ratio of 1:2, and N14, containing choline chloride and glycerol in a molar ratio of 1:1) were chosen for the second step of the study, which aimed to select the most influential process parameters. A fractional factorial 2⁵⁻¹ design was used, varying five different parameters at two levels: extraction time (30 and 60 min), extraction temperature (40 and 50 °C), and liquid-to-solid ratio (10 and 20 mL/g), water content in NADES (15 and 20%), and NADES type (N12 and N14). After the second step, N12 containing 20% water was chosen as the most potent solvent for the optimization study. For the final step, the other three parameters were varied on three levels, and thus optimal conditions were obtained (extraction time 90 min, extraction temperature 65 °C, and liquid-to-solid ratio 22.65 mL/g). Blackthorn juice was also tested in the first step, as well as under optimal conditions established for pomace, in order to evaluate whether these conditions are suitable for juice and to determine the percentage of improvement in extraction efficiency. Full article

Reverse micelles (RMs) are versatile nanostructures traditionally formed in low-polarity organic solvents, but the need for greener alternatives has limited their broader applicability. Here, we demonstrate for the first time that a hydrophobic Natural Deep Eutectic Solvent (NADES), prepared from a simple 1:1 mixture of camphor and menthol (CM), can act as the continuous external phase for RM formation. Remarkably, CM dissolves the benchmark surfactant sodium dioctyl sulfosuccinate (AOT) at concentrations up to 0.5 M without co-surfactants and supports water solubilization up to W₀ = [H₂O]/[AOT] = 5, yielding thermodynamically stable systems. 1H and DOSY NMR analyses reveal clear structural rearrangements of the micellar interface, confirm the encapsulation of water in the polar core, and provide quantitative evidence of size modulation as a function of W₀. The resulting CM/AOT/water assemblies represent the first example of NADES-based reverse micelles, offering an easily prepared, sustainable, and biocompatible platform. This breakthrough opens new perspectives for the development of green self-assembled systems with promising applications in areas such as food technology, pharmaceuticals, and nanomedicine. Full article