Solubility Characteristics Research Articles

Effects of wheat gluten-soy protein ratios and moisture levels on high-moisture extruded meat analogues for burger patties.

In response to the growing demand for plant-based meat alternatives, this study explores the impact of incorporating wheat gluten (WG) into soy protein isolate (SPI) on both the proximate and functional properties of protein blends. The research also examines the effects of high moisture extrusion processing, varying feed moisture levels (60%, 65%, and 70%), and WG-SPI blends on extruder response, as well as the textural, rheological, and solubility characteristics of the resulting extruded meat analogues. Moreover, the prime objective was to gain insights into the impact of using HMMA made at different ratios and feed moisture levels on plant-based burgers. As the WG incorporation level increased in SPI, the RVA viscosity, water absorption, and oil absorption capacities, and foaming stability exhibited a decrease while foaming capacity increased. As feed moisture and WG incorporation levels in SPI increased, the system parameters, rheological, and textural parameters of high moisture extruded meat analogs decreased. WG25-SPI75 showed the highest degree of texturization or sulfide bonds, and its extruded meat analogues at 60% feed moisture level burger patties resemble a similar textural to a chicken burger patty. This study is pivotal in understanding how wheat gluten in SPIs and feeding moisture level influence the textural and rheology properties of HMMA.

A Study on the Stability of High Drug Solubility Characteristics of Hydroxyphenyl Adhesives under the Interference of CPEs.

Novel hydroxyphenyl adhesives (HP-PSAs) could significantly increase drug solubility and control drug release through a doubly ionic hydrogen bond (DIH bond) in the patch. However, chemical penetration enhancers (CPEs) always destroy the performance of most adhesives. As a result, this work investigated the stability of both the HP-PSA features and the DIH bond under the interference of the CPEs. Donepezil (DON) was chosen as the model drug, and CPEs with hydroxyl, carboxyl, amido, and ester groups were selected as model CPEs. Unlike the commonly used neutral H-bond, the DIH bond between DON and the HP-PSA was still stable under the interference of the CPEs, resulting in the 2-3-fold drug solubility in the HP-PSA, which was higher than that in the nonfunctional PSA, which reduced the drug crystallization risk and the difficulty of formulation design. FT-IR, 1H NMR, XPS, dynamic simulation, and molecular docking revealed the mechanism of the stability feature of both the DIH bond and the high drug solubility of the HP-PSA, which was that the formed neutral H-bond interaction caused by CPEs is weaker than that of the DIH bond between DON and the HP-PSA. Furthermore, the drug release, skin permeation, and CPE release study showed that the newly formed weak H-bond and strong ionic H-bond interaction promoted or controlled both DON and CPE release, respectively, thereby influencing drug skin permeation, which provided a theoretical basis for drug release regulation. To summarize, besides the reversible, strong features of the DIH bond in our previous study, the stability of the interaction made the HP-PSA's high drug solubility potential to be applied in the TDDS.

Exploring characteristic features for effective HCN1 channel inhibition using integrated analytical approaches: 3D QSAR, molecular docking, homology modelling, ADME and molecular dynamics.

Neuropathic pain (NP) is characterized by hyperalgesia, allodynia, and spontaneous pain. Hyperpolarization-activated cyclic nucleotide-gated (HCN) channel involved in neuronal hyperexcitability, has emerged as an important target for the drug development of NP. HCN channels exist in four different isoforms, where HCN1 is majorly expressed in dorsal root ganglion having an imperative role in NP pathophysiology. A specific HCN1 channel inhibitor will hold the better potential to treat NP without disturbing the physiological roles of other HCN isoforms. The main objective is to identify and analyze the chemical properties of scaffolds with higher HCN1 channel specificity. The 3D-QSAR studies highlight the hydrophobic & hydrogen bond donor groups enhance specificity towards the HCN1 channel. Further, the molecular interaction of the scaffolds with the HCN1 pore was studied by generating an open-pore model of the HCN1 channel using homology modelling and then docking the molecules with it. In addition, the important residues involved in the interaction between HCN1 pore and scaffolds were also identified. Moreover, ADME predictions revealed that compounds had good oral bioavailability and solubility characteristics. Subsequently, molecular dynamics simulation studies revealed the better stability of the lead molecules A7 and A9 during interactions and ascertained them as potential drug candidates. Cumulative studies provided the important structural features for enhancing HCN1 channel-specific inhibition, paving the way to design and develop novel specific HCN1 channel inhibitors.

Co/Er2O3/C ternary nanocomposites derived from cobalt/erbium Prussian blue analogs for efficient microwave absorption

This study presents the synthesis of Er[Co(CN)6], a Prussian blue analog (ErCo-PBA) with varied morphology, fabricated by modulating the solvent ratio between C2H6O and H2O. This approach leverages the solubility characteristics of K3[Co(CN)6] and the consequential influence of C2H6O on the crystal growth. When the solvent ratios are 1:8, 8:1, and 1:1, the resulting ErCo-PBA precursors nanorods, irregular particles, and spindle-shaped particles, respectively. After annealing, these precursors in an Ar environment allowed the Co/Er2O3/C derivatives to retain the morphology of the precursor well. Electromagnetic parameters testing revealed that Co/Er2O3/C-1 exhibits superior electromagnetic wave-absorbing (EMWA) performance among the synthesized derivatives with an effective absorption bandwidth of 5.1 GHz at 1.85 mm and a minimum reflection loss of −56.7 dB at 2.9 mm. The incorporation of Er2O3 is an effective method for adjusting and optimizing the electromagnetic parameters of materials, thereby enhancing the EMWA performance of Co/Er2O3/C composite. This study highlights the potential of rare-earth oxide/Co/C composites, synthesized through direct annealing rare-earth metal–organic frameworks, as an absorber and are promising candidate to achieve high-efficiency electromagnetic wave absorption.

Synthetic Protocols, Structural Activity Relationship, and Biological Activity of Piperazine and its Derivatives.

The versatile basic structure of piperazine allows for the development and production of newer bioactive molecules that can be used to treat a wide range of diseases. Piperazine derivatives are unique and can easily be modified for the desired pharmacological activity. The two opposing nitrogen atoms in a six-membered piperazine ring offer a large polar surface area, relative structural rigidity, and more acceptors and donors of hydrogen bonds. These properties frequently result in greater water solubility, oral bioavailability, and ADME characteristics, as well as improved target affinity and specificity. Various synthetic protocols have been reported for piperazine and its derivatives. In this review, we focused on recently published synthetic protocols for the synthesis of the piperazine and its derivatives. The structure-activity relationship concerning different biological activities of various piperazine-containing drugs was also highlighted to provide a good understanding to researchers for future research on piperazines.

Biological conversion of red garlic (Allium sativum L) protein to bioactive peptides: ACE- DPP-IV inhibitory, and Techno-functional features

This study explores the impact of enzymolysis on the free amino acid content, techno-functional properties, free-radical scavenging, ACE, DPP-IV inhibition, iron-ion chelation and TBARS production in O/W emulsion stabilized with red garlic protein (RGP) and hydrolysates (RGPHs). The research reveals that enzymolysis time and pH significantly influence the amino acid content (antioxidant, hydrophobic, and essential ones), functional and biological quality of RGP/RGPHs. The study demonstrates that enzymolysis positively correlates with solubility (up to 90 %), health-promoting and antioxidant characteristics like DPPH (74.2 %), ABTS (81.3 %), OH (63.4 %), Reducing power (1.1 Abs700), NO (59.5 %), TAA (1.4 Abs695), ACE (71.9 %), DPP-IV (51.5 %) inhibitory, Fe2+ chelating (46.8 %) activity, and leading to reduced water/oil holding capacities, TBARS (from 0.61 to 0.38) value and lipid oxidation. However, extensive enzymatic hydrolysis (over 90 min) reduced emulsion and foaming abilities. On the other hand, the techno-functional properties of RGP and RGPHs exhibited a significant decline near the isoelectric point. This enhancement suggests that RGP could be used as a natural antioxidant with potential health benefits (antihypertensive and antidiabetic) in food and pharmaceutical formulations.

Catalytic synthesis of DHHB using solid acids

Abstract DHHB (Diethylamino hydroxybenzoyl hexyl benzoate) is a widely regarded UV absorber with a high degree of safety, excellent efficiency and good solubility characteristics. In the conventional method of DHHB synthesis, H2SO4 is not effective as a catalyst. To address this drawback, we synthesized solid acid (sulfonic acid group-modified ion exchange resin) catalysts to replace H2SO4 by suspension polymerization modification and optimized the process. The experimental results showed that the yield of DHHB could reach 85% at 110 °C for 10 h, and the conversion of DHHB could be maintained above 90% after 10 cycles of the catalyst. SEM, FT-IR characterization and analysis of the solid acid catalysts before and after use revealed that the catalysts did not show any significant changes. The use of solid acid not only improves the yield of DHHB and reduces the energy consumption in the experimental process, but also the solid acid is simple to recover, recycled and has less waste acid. This experiment successfully explored a green and economic synthesis method for synthesizing DHHB.

Switchable Deep Eutectic Solvents for Sustainable Sulfonamide Synthesis.

A sustainable and scalable protocol for synthesizing variously functionalized sulfonamides, from amines and sulfonyl chlorides, has been developed using environmentally responsible and reusable choline chloride (ChCl)-based deep eutectic solvents (DESs). In ChCl/glycerol (1 : 2 mol mol-1) and ChCl/urea (1 : 2 mol mol-1), these reactions yield up to 97 % under aerobic conditions at ambient temperature within 2-12 h. The practicality of the method is exemplified by the sustainable synthesis of an FFA4 agonist and a key building block en route to anti-Alzheimer drug BMS-299897. A subtle interplay of electronic effects and the solubility characteristics of the starting materials in the aforementioned DESs seem to be responsible for driving the reaction successfully over the hydrolysis of sulfonyl chlorides. The procedure's eco-friendliness is validated by quantitative metrics like the E-factor and the EcoScale, with products isolated by extraction or filtration after decantation.

Investigation of the solubility behavior of emodin and aloe-emodin in water + ethanol mixtures at various temperatures ranging from 283.15 K to 323.15 K

A thermostated reactor and UV–visible spectrophotometer analysis were used to determine the solubility of emodin and aloe-emodin, two naturally occurring compounds with pharmacological activity. At a pressure of 0.1 MPa under atmospheric conditions, and temperatures from 283.15 to 323.15 K with intervals of 5 K, the solubility in different water–ethanol combinations was the primary focus of the investigation. Under constant solvent composition, a positive correlation was observed between the solubility of emodin/ or aleo-emodin and the experimental temperature in all examined mixed solvent systems. To better understand the relationships between solutes and solvents and the interactions between several solvents, the KAT-LSER model was used to conduct multiple linear regression analysis on systems containing either pure solvents or a combination of solvents. In addition, several thermodynamic models were used to establish a connection with the empirical solubility data. These models included the Jouyban-Acree, Apelblat-Jouyban-Acree, van’t Hoff-Jouyban-Acree, and Ma models. The correlation findings demonstrate that all four thermodynamic models accurately predicted emodin and aleo-solubility emodin’s behavior under different solvent and temperature settings. Furthermore, the thermodynamic characteristics of emodin solubility in binary solvent combinations were determined using the van’t Hoff model. According to the findings, two compounds were found to undergo endothermic and non-spontaneous dissolution.

Cyclodextrin Complexes for the Treatment of Chagas Disease: A Literature Review.

Cyclodextrins are ring-shaped sugars used as additives in medications to improve solubility, stability, and sensory characteristics. Despite being widespread, Chagas disease is neglected because of the limitations of available medications. This study aims to review the compounds used in the formation of inclusion complexes for the treatment of Chagas disease, analyzing the incorporated compounds and advancements in related studies. The databases consulted include Scielo, Scopus, ScienceDirect, PubMed, LILACS, and Embase. The keywords used were "cyclodextrin AND Chagas AND disease" and "cyclodextrin complex against Trypanosoma cruzi". Additionally, a statistical analysis of studies on Chagas disease over the last five years was conducted, highlighting the importance of research in this area. This review focused on articles that emphasize how cyclodextrins can improve the bioavailability, therapeutic action, toxicity, and solubility of medications. Initially, 380 articles were identified with the keyword "cyclodextrin AND Chagas disease"; 356 were excluded for not being directly related to the topic, using the keyword "cyclodextrin complex against Trypanosoma cruzi". Over the last five years, a total of 13,075 studies on Chagas disease treatment were found in our literature analysis. The studies also showed interest in molecules derived from natural products and vegetable oils. Research on cyclodextrins, particularly in the context of Chagas disease treatment, has advanced significantly, with studies highlighting the efficacy of molecules in cyclodextrin complexes and indicating promising advances in disease treatment.

Development of Enteric Diclofenac Sodium Microparticles Through a Spray-Drying Process Facilitated by Different Aqueous Dispersion Systems

The objective of this study was to prepare enteric diclofenac sodium microparticles using an aqueous dispersion system via spray-drying. Two aqueous-based solvent systems, phosphate buffer at pH 7.0 and ammonium hydrogen carbonate solution, were employed as the feed dispersion media in the spray-drying process based on the solubility characteristics of Eudragit® L100. At a drug-to-polymer ratio of 1:1, the optimal solids concentration in the feed dispersion was determined to be 2% w/v, as it enabled an approximately 5-30 µm smooth-surfaced spherical microparticle with a high production yield. Diclofenac sodium was efficiently encapsulated within the microparticles, existing as solid dispersion in a partially amorphous form. Notably, the spray-drying conditions utilized in this study obviated the need for further heating for microparticles prepared using ammonium hydrogen carbonate solution, as the residual ammonium could be completely eliminated during the spray-drying process. The two-stage biorelevant drug release profile of enteric microparticles demonstrated their ability to inhibit drug dissolution under acidic conditions while facilitating drug release under basic conditions. The phosphate buffer-based microparticles exhibited greater protection efficiency under acidic conditions compared to ammonium hydrogen carbonate-based systems, despite residual alkaline salt being present in the microparticles. These results validate the potential of the developed microparticles for use as an enteric drug delivery system.

Absolute purity determination of an organic fluorine pharmaceutical voriconazole via quantitative 19F NMR and method validation

The 19F NMR spectrum has a smaller number of signals than 1H NMR, therefore, quantitative 19F NMR (19F-qNMR) can replace quantitative 1H NMR (1H-qNMR) for the absolute quantitation of organic fluorine-bearing compounds. In this study, we determined the purity of voriconazole (VCZ), an organic fluorine pharmaceutical, using 19F-qNMR, validated the results in multiple laboratories, and compared them with those obtained using an established 1H-qNMR method. 3,5-Bis(trifluoromethyl)benzoic acid (3,5-BTFMBA) was selected as the reference standard for both 19F-qNMR and 1H-qNMR owing to its solubility characteristics and 19F-qNMR and 1H-qNMR chemical shifts.Since VCZ contains three fluorines, the 19F-qNMR spectrum of VCZ showed three major fluorine signals (FA, FB, and FC). 19F-qNMR measurements were performed under three conditions with each 19F signal of VCZ (FA, FB, and FC) and the 19F signal of RS as the center (offset) of each observation. The quantitative values of the three target signals FA, FB, and FC were calculated and were comparable; 99.40 %, 99.66 %, and 99.49 %, respectively.Owing to a difference of up to 8.8 % between the quantitative values of the two signals other than the targeted quantitative signal, the average FA, FB, and FC quantitative values were considered for purity (%). The purity of VCZ determined by 1H- and 19F-qNMR was comparable (99.65±0.29 % and 99.52±0.44 %, respectively), exhibiting variations within an acceptable range. Compared to conventional 1H-qNMR methods, the developed 19F-qNMR method has been proven efficient and highly promising for determining the accurate purity of organic fluorine pharmaceuticals.

SPHERICAL AGGLOMERATION OF TELMISARTAN - AN APPROACH TO IMPROVE PHYSICOCHEMICAL PROPERTIES

The study explains the preparation of spherical agglomerates (SA) of telmisartan (TLS), a BCS class II drug used to improve it’s physicochemical and bulk properties. Drugs of this class could potentially exhibit dissolution rate limited absorption. TLS spherical agglomerates were designed using hydrophilic polymer (PVP K-30), dimethyl formamide (DMF), water and ethyl acetate (bridging liquid) by solvent change method and evaluated for micromeritic properties. The SA were characterized by particle size determination, FTIR, PXRD and SEM. The results of micromeritic studies indicated that SA showed improved flow properties due to their spherical shape and bigger size. Absence of strong interaction at molecular level and alteration in the crystal structure of TLS with modification in crystallinity was confirmed by FTIR and PXRD respectively. TLS solubility characteristics were improved by this approach.

Comparison of plastic and glass cages on volatile compounds in protein extracted from Protaetia brevitarsis larvae

Edible insects, known for their high-protein production efficiency, are vital for enhancing food security. However, standardized breeding protocols are lacking, and research on the impact of cage materials on insect product composition is limited. This study investigated the volatile compounds and processing properties of protein from Protaetia brevitarsis larvae reared in plastic and glass cages. Protein extracts from larvae reared in plastic cages contained 14 types of hydrocarbons, 4 types of ketones, and 1 type of phenol. Those reared in glass cages contained two types of acids, seven types of alcohols, and five types of aldehydes. Notably, plastic-derived compounds, such as p-xylene (110.87 μg/mL) and o-xylene (37.98 μg/mL), were significantly higher in the extracts from plastic cages, indicating potential plastic exposure. Processing properties, including protein solubility, pH, color, foaming properties, and emulsion characteristics, showed no significant differences between the two rearing conditions (P > 0.05). Therefore, considering the detection and potential accumulation of plastic-derived volatile compounds, using glass cages may be more beneficial for rearing insects for protein production.

Oil in food waste to methane by anaerobic digestion: Co-effects of mixing intensity and long chain fatty acid loading

Oil in the food waste can contribute improved energy yield by anaerobic digestion, and also poses an inhibition risk from the intermediate long chain fatty acids (LCFAs). The digestion performance partly depends on the solubility of oil/LCFAs concerned recently, while mixing intensity control can disturb the solubility characteristics. Combined with oil loading such a fundamental control parameter, co-effects of mixing intensity and oil loading on methanogenic characteristics were illuminated. A series of mixing intensities 0–240 rpm and oil/inoculum (F/I) ratios 0.2–1.2 were set to conduct a batch experiment, and relevant affecting mechanisms were further disclosed as well. It turned out that variation of mixing intensity could have effects on methanogenesis from oil in food waste. Increasing mixing intensity prolonged lag phase. Mixing intensity at 120 rpm was proved as a starting point to disturb LCFA inhibition. Methanogenic rates climbed to the top at F/I 0.4, and further increase loading resulted in the rate decline. Methanogenic potential release was also reduced with both mixing intensity and loading at higher values. Hereinto, oleic acid (C18:1) as a key LCFA in oil played an important role in inhibition, while higher mixing intensity and loading could promote degradation and conversion of another critical LCFA palmitic acid (C16:0). The study favors achieving a cost-effective strategy controlled by mixing intensity to promote safe energy improvement.

Oral Administration of Berberine Hydrochloride Based on Chitosan/Carboxymethyl-β-Cyclodextrin Hydrogel.

In this study, a novel oral formulation of berberine hydrochloride (BBH) hydrogel was successfully synthesized through physical cross-linking using chitosan (CS) and carboxymethyl-β-cyclodextrin (CMCD). The characterization results confirmed the successful synthesis of the CS/CMCD hydrogel and the subsequent loading of BBH into this composite (CS/CMCD/BBH) was effectively accomplished. The BBH was used as a model drug and the resulting hydrogel demonstrated a sustained drug release profile. In addition to its improved solubility and sustained release characteristics, the hydrogel exhibited excellent antibacterial activity against common pathogens such as Escherichia coli (E. coli), Staphylococcus aureus (S. aureus), and Candida albicans (C. albicans). Additionally, in vitro studies indicated that the hydrogel was not cytotoxic to NIH3T3 and HaCaT cells, suggesting its safety for biomedical applications. This lack of cytotoxic effects, combined with the mechanical strength, solubility improvements, and antibacterial properties of the hydrogel, positions the CS/CMCD/BBH hydrogel as a promising candidate for the effective oral delivery of BBH. By addressing the solubility and delivery challenges of BBH, this hydrogel offers a viable solution for the oral administration of BBH, with potential applications in various biomedical fields.

PEGylation in Pharmaceutical Development: Current Status and Emerging Trends in Macromolecular and Immunotherapeutic Drugs.

The purpose of the research is to examine the advantages and difficulties of target-site drug delivery methods, with an emphasis on the application of polyethylene glycol (PEG) to enhance drug solubility, bioavailability, and immune response characteristics. It has been demonstrated that this method lowers immunogenicity, enhances pharmacokinetics, and helps drugs pass the blood-brain barrier while reducing reticuloendothelial system clearance. PEG and its derivatives are being used more and more to alter therapeutic substances, offering an escape from some of the drawbacks of conventional medication formulations. In the review, different PEGylation tactics are examined, including cutting-edge methods for reversing multi-drug resistance in nanocarriers. PEGylation has a number of benefits, but there are still drawbacks, including the immunogenic reaction to PEG, which is sometimes referred to as "anti-PEG antibodies," and stability problems that call for the creation of countermeasures. The study devotes a large amount of its space to listing FDA-approved PEGylated medications, emphasizing their therapeutic advantages and clinical uses in a range of medical specialties. The research also explores the regulatory environment that surrounds PEG, closely examining its effectiveness and safety in medication compositions. The review goes beyond PEGylation and includes lipid-based nanocarriers, including liposomes, nanostructured lipid carriers (NLCs), and solid lipid nanoparticles (SLNs). Because these nanocarriers can target specific tissues or cells, improve bioavailability, and encapsulate pharmaceuticals, they are becoming more and more significant in drug delivery systems. The Target Product Profile (TPP) and Quality by Design (QbD) principles serve as the foundation for the creation and characterization of these lipid-based systems. These tools direct the methodical assessment of material properties and risk assessments during the formulation phase. This method guarantees that the finished product satisfies the appropriate requirements for efficacy, safety, and quality. The regulatory status and safety profile of nano lipid carriers are covered in the paper's conclusion, which emphasizes the importance of careful examination and oversight in bringing these cutting-edge products to market. Overall, this thorough analysis highlights the revolutionary potential of lipid-based nanocarriers and PEGylation in improving drug delivery and therapeutic efficacy, but it also draws attention to the continued difficulties and legal issues that need to be resolved in order to fully reap the benefits of these technologies in biomedicine.

(Invited) Redox Flow Batteries – Exploring Electrolyte Additives and Hybrid Organic/Inorganic Redox Pairs

Renewable energy sources are intermittent and thus require provision to store the energy when available using energy storage devices. These energy storage devices should be safe, efficient, and have a long life cycle for use in grid-scale energy storage systems. Lead-acid, Li-ion, and Redox Flow Batteries (RFBs) are examples of such energy storage devices. Among these energy storage systems, RFBs have unique advantages that make them attractive for large-scale energy storage applications, like a high cycle life of about 10,000 cycles.[1] The current generation of commercial RFBs use vanadium solution in different oxidation states as electrolytes (anolyte and catholyte), carbon-based electrodes and Nafion as the ion-exchange membrane. High cost, risk of electrolyte crossover, low volumetric energy density, and pumping losses limit the vanadium redox flow batteries (VRFBs).[2] Also, the Nafion membrane accounts for about 40% of the system's total cost.[3] To ensure high cycle life, the electrolytes must be stable (active material must remain dissolved in the supporting electrolyte), and vanadium ions should not crossover the Nafion membrane. The VRFBs tend to lose vanadium from electrolyte solutions due to the precipitation of V2O5 during charging, resulting in a significant loss of energy density. Additives help in maintaining the long-term stability of vanadium electrolytes. In this work, we have monitored the solubility and electrochemical characteristics of vanadium electrolyte solutions with V2O5 in the presence of different additives, namely HCl and MSA (methanesulfonic acid), for over three months.[4] The findings of this study provide insight into using these additives for VRFBs. Further research in RFBs has recently shifted towards redox-active aqueous-organic-based electrolytes consisting of Earth-abundant elements (C, H, O, N, S), accommodating the need for green, safe, and low-cost energy storage. We have studied the feasibility of using quinone-based organic electrolytes for RFBs. A proof-of-concept membrane-free two-compartment cell with an auxiliary electrode in each compartment was also demonstrated. In the conventional design, the hydrogen ions move through the Nafion membrane to balance charges but in the auxiliary electrode-based membrane-free setup, the auxiliary electrode in each compartment undergoes redox reactions opposite to the primary electrodes to balance charges.[5]References[1] Y.E. Durmus, H. Zhang, F. Baakes, G. Desmaizieres, H. Hayun, L. Yang, M. Kolek, V. Küpers, J. Janek, D. Mandler, S. Passerini, Y. Ein‐Eli, Side by Side Battery Technologies with Lithium‐Ion Based Batteries, Adv. Energy Mater. 10 (2020). https://doi.org/10.1002/aenm.202000089.[2] B. Turker, S. Arroyo Klein, E.M. Hammer, B. Lenz, L. Komsiyska, Modeling a vanadium redox flow battery system for large scale applications, Energy Convers. Manag. 66 (2013) 26–32. https://doi.org/10.1016/j.enconman.2012.09.009.[3] J. Ye, D. Yuan, M. Ding, Y. Long, T. Long, L. Sun, C. Jia, A cost-effective nafion/lignin composite membrane with low vanadium ion permeation for high performance vanadium redox flow battery, J. Power Sources. 482 (2021) 229023. https://doi.org/10.1016/j.jpowsour.2020.229023.[4] O.H. Nguyen, P. Iyapazham Vaigunda Suba, M. Shoaib, V. Thangadurai, Investigating the Electro-Kinetics and Long-Term Solubility of Vanadium Electrolyte in the Presence of Inorganic Additives, J. Electrochem. Soc. 170 (2023) 110523. https://doi.org/10.1149/1945-7111/ad0a75.[5] S.V. Venkatesan, K. Karan, S.R. Larter, V. Thangadurai, An auxiliary electrode mediated membrane-free redox electrochemical cell for energy storage, Sustain. Energy Fuels. 4 (2020) 2149–2152. https://doi.org/10.1039/c9se00734b.

Exploring Salts of Memantine with Inorganic Anions: From Polymorphism and Solid-State Transitions to Potential for Drug Formulations.

This study examines pharmaceutically acceptable inorganic salts of memantine, specifically focusing on hydrogen sulfate, sulfate, and dihydrogen phosphate salts, with the aim of finding alternatives to the commonly used chloride salt in the treatment of Alzheimer's disease. Through comprehensive solid-state characterization, including powder X-ray diffraction, thermal analysis, and solubility testing, we unveil complex polymorphic behaviors, reversible solid-state transitions, and significant differences in solubility and stability among the salts. Notably, the hydrogen sulfate salt emerges as a promising candidate for drug formulations, offering improved solubility, nonhygroscopic nature, and favorable morphological characteristics compared to the existing chloride salt. This work establishes a foundation for further investigation into memantine salts as potential therapeutics with improved efficacy.

Esterified styrene-maleic acid copolymer modified silica as mixed-mode polymer-brush stationary phases for chromatographic separation

Styrene-maleic acid (SMA) copolymer has received much attention for its excellent solubilization characteristics. In this work, SMA copolymer brush-based chromatographic stationary phases were exploited and developed for the first time. First, SMA copolymer brush was in situ grown on the surface of spherical silica via living/controlled reversible addition-fragmentation chain transfer (RAFT) polymerization method. Subsequently, as a proof-of-concept demonstration, the copolymer was esterified by diethylene glycol mono-2-ethylhexyl ether (DGME) and 2-(2-ethylhexyloxy) ethanol (EHOE), respectively. The obtained Sil-SMA-DGME and Sil-SMA-EHOE copolymer-brush chromatographic stationary phases were characterized by transmission electron microscopy, Fourier transform infrared spectrometer, X-ray photoelectron spectroscopy, and thermogravimetric analysis, respectively. The chromatographic retention mechanism indicated that both the two packed columns exhibited hydrophilic/reverse mixed-mode retention modes. The maximum column efficiency was up to 71,000 N/m. The chromatographic separation performance evaluation indicated that the novel kind of stationary phases had excellent separation capabilities for hydrophilic, hydrophobic compounds and phospholipid standards. In addition, by combination with mass spectrometry identification, the Sil-SMA-DGME column was further exploited for separation and identification of phospholipids in human lung cancer cells. Totally, 9 classes including 186 phospholipid species were successfully identified. The results demonstrated the promising application prospects of the novel kind of SMA copolymer-brush chromatographic stationary phases.