Search Results (1,065)

This paper presents a method for the measurement of absolute molecular weight of cellulose using a multi-angle light scattering (MALS) detector in 99% dimethyl sulfoxide/1% 1-Ethyl-3-methylimidazolium acetate (DMSO/EmimOAc). The paper also delivers a suitable dn/dc value for cellulose in this solvent. It discusses the pros and cons of using absolute molecular weight measurements versus traditional column calibration in this solvent. The conclusion is that the dn/dc for cellulose in this solvent is 0.049 ± 0.003 mL/g. Absolute molecular weight measurements in this solvent are somewhat beneficial for celluloses with Mw > 250 kg/mol. However, for low-Mw celluloses (e.g., Avicel), it has severe limitations. Herein, it is confirmed that the DMSO/EmimOAc system can be used to replace the traditional DMAc/LiCl system for cellulose molecular weight analysis of some cellulose materials. However, the former is more costly and time-consuming than the latter. Full article

As a part of our research on the presence of conglomerates among the aryl benzyl sulfoxides, racemic-benzimidazolyl pentafluorobenzyl sulfoxide was synthesised, and its crystal structure was determined by a single crystal X-ray diffraction experiment. The main interactions building up the crystal structure were recognised and compared with those of similar compounds. Since the crystal structures of racemic and enantiopure benzimidazolyl pentafluorobenzyl sulfoxides are different, the presence of a conglomerate is excluded in the present case. Full article

Background/Objectives: Fungal keratitis remains a vision-threatening infection, and current amphotericin B (AmphB) eye drops suffer from low corneal residence time, poor aqueous solubility, and the need for frequent dosing. This study develops electrospun nanofiber-based ophthalmic inserts combining polyvinyl alcohol (PVA), gamma-cyclodextrin (γ-CD), and sodium taurocholate (STC) to enhance AmphB solubility and provide a non-invasive, rapidly dissolving ophthalmic dosage form. Methods: γ-CD and STC-enhanced AmphB-loaded PVA nanofiber-based ophthalmic inserts with varying γ-CD and STC concentrations were prepared by electrospinning and characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). Drug content, in vitro release (Weibull modeling), antifungal activity against Candida albicans, Fusarium solani, and Aspergillus fumigatus, ocular cytocompatibility using the Hen’s Egg Test on Chorioallantoic Membrane (HET-CAM), and accelerated stability (40 ± 2 °C, 75 ± 5% relative humidity, 4 weeks) were evaluated. Results: Bead-free nanofibers with mean diameters between 216 ± 33 nm and 310 ± 35 nm were obtained, and XRD confirmed complete amorphization of AmphB within the PVA nanofiber matrix, forming an amorphous solid dispersion. All formulations showed rapid and nearly complete AmphB release (≈100% within 60 min), with Weibull β values < 0.75, indicating Fickian diffusion-controlled release. AmphB-loaded PVA nanofiber-based ophthalmic inserts produced inhibition zones and broth susceptibility profiles comparable to AmphB in dimethyl sulfoxide (DMSO), demonstrating preserved antifungal activity. HET-CAM scores (0–0.9) classified the inserts as practically non-irritant, and SEM/FTIR after accelerated storage showed no relevant morphological or physicochemical changes. Conclusions: These γ-CD and STC-enhanced AmphB-loaded PVA nanofiber-based ophthalmic inserts provide a non-invasive, rapidly dissolving ophthalmic dosage form that combines amorphous AmphB, immediate drug availability, and good ocular tolerance, supporting their further development as a patient-friendly treatment option for fungal keratitis. Full article

Milk fat synthesis in dairy cows is a complex process affected by ruminal fermentation, systemic metabolism, and mammary gland activity. To explore the metabolic interplay across these systems, a multi-tissue metabolomics approach (rumen fluid, plasma, and milk) using ultra-high-performance liquid chromatography–mass spectrometry was used to identify metabolic differences between Chinese Holstein cows with high (H-MF, 5.82 ± 0.41%) and low (L-MF, 3.60 ± 0.12%) milk fat content under the same diet. The bovine mammary epithelial cells (BMECs) were also cultured to evaluate the impact of a key metabolite, malic acid (MA), on lipid metabolism. Our findings reveal distinct metabolic profiles across rumen fluid, plasma, and milk, with 96, 109, and 79 differential metabolites, respectively, between the L-MF and H-MF groups. In rumen fluid, H-MF cows showed higher levels of lauric acid and succinic acid, linked to fatty acid biosynthesis, while the L-MF cows had elevated citraconic and orotic acids, associated with amino acid metabolism and liver stress. Plasma from the H-MF cows contained higher β-hydroxybutyric acid, methionine sulfoxide, and phosphatidylcholine, supporting lipogenesis, whereas L-MF plasma showed increased 3-hydroxy-L-proline, indicating tissue catabolism. In milk, the L-MF cows had higher MA, while the H-MF cows exhibited elevated L-carnitine, linked to fatty acid β-oxidation. Metabolite trend analysis during rumen fluid–plasma–milk showed that 211 metabolites were classified into 8 profiles. Profile 1 had the largest number of metabolites whose levels were down-regulated from rumen to plasma and enriched in lipid metabolism. Profile 3 (mainly related to amino acid metabolism) and profile 4 (mainly related to energy metabolism) exhibited opposite trends from plasma to milk. In vitro, 200 μM of MA reduced the triglyceride content in BMECs and down-regulated lipogenic genes and their protein expression levels (fatty acid synthase, stearoyl-CoA desaturase and sterol regulatory element binding protein 1). These results highlight how rumen fluid, plasma, and milk metabolites collectively influence milk fat synthesis, with MA acting as a key regulator of lipid metabolism in mammary epithelial cells. Full article

The use of one-step products and their applications in sensory applications has gained much importance. Herein, Schiff’s base fluorescent turn-on sensor, namely FBTS, was synthesised via a condensation reaction between 6-fluorobenzo[d]thiazol-2-amine and 2-hydroxybenzaldehyde. The probe FBTS exhibits an intense “turn-on” blue fluorescence upon binding to Al³⁺ ions in a dimethyl sulfoxide–water (DMSO–H₂O (8:2, v/v)) medium. From photoluminescence (PL) titrations, the detection limit (LOD) for Al³⁺ is estimated to be 0.14 microM, and the Benesi–Hildebrand plot-based association constant (K_a) of 5.4 × 10⁴ M⁻¹ confirm a strong association between FBTS and Al³⁺. Negligible interference is observed in the presence of other metal ions. From the pH effect studies, the optimal pH range for Al³⁺ detection is 7–9. The recyclable reversibility of FBTS + Al³⁺ complex has been demonstrated via the sodium salt of ethylenediaminetetraacetic acid (Na₂-EDTA) chelation. A Job’s plot and interrogations, such as high-resolution mass spectrometry (HR-MS), ¹H-nuclear magnetic resonance (NMR) titration, and density functional theory (DFT), verified the 1:1 stoichiometry of binding between FBTS and Al³⁺. Based on multiple analyses, the binding mode and mechanism have been detailed. In addition, the practical application of FBTS for detecting Al³⁺ is demonstrated using the strip paper method, fish analysis, spiked real sample analysis, and cellular imaging. Full article

Botulinum toxin type A (BoNT/A) injection into the bladder wall is a milestone in the treatment of urinary incontinence in patients with neurogenic detrusor overactivity (NDOi) or overactive bladder syndrome (OABi) who are refractory to or unable to tolerate oral or transdermal therapies. However, the efficacy of BoNT/A is hampered by the low long-term adherence of patients to a treatment that requires repeated bladder injections under cystoscopy control. The discontinuation is particularly evident among incontinent patients with spontaneous voluntary voiding, regardless of whether the cause is NDOi or OABi, although clearly more marked among the latter group. In addition to the bother and pain associated with repeated cystoscopies, these patients show low tolerance to the high incidence of urinary tract infections (UTIs) and transient urinary retention, the two most common adverse events. Fewer injection points may render treatments less painful, apparently without reducing efficacy, but will not avoid the need for repeated cystoscopies, and no studies have demonstrated that such modification increases adherence. Eventually, accessing the bladder wall for BoNT/A administration via a transabdominal approach, under real-time ultrasound guidance, may overcome trans-urethral limitations, but the technique’s reproducibility remains unknown. An intensive investigation is ongoing to identify aids that facilitate the passage of the large, fragile BoNT/A molecule across the urothelium to reach the bladder nerves without injections. Electromotive Drug Administration (EMDA) of BoNT/A demonstrated efficacy and safety over a 6-year follow-up in NDOi patients at a single center, but the results were not reproduced at other institutions. The application of shock waves to the bladder using shock waves generated by Extracorporeal Shock Wave Lithotripsy (ESWL) machines to tear the urothelium and facilitate the passage of BoNT/A instilled in the bladder is ingenious, but the experience is very limited. Dimethyl sulfoxide, liposomes, and thermal-reversal hydrogel to deliver the toxin failed in pilot trials. BoNT/A in nano-formulations has high heat stability, resistance to pH changes, and to enzymatic degradation. Extended efficacy in dermal and intramuscular pilot applications is promising but needs to be replicated in the bladder. Full article

This project investigates how the orientation of the carbon cathode with a single-sided microporous layer (MPL) affects battery performance through electrochemical tests, neutron tomography, and titration experiments. The titration experiment quantitatively assesses the amount of solid product (Li₂O₂) deposited on the electrode surface. In addition, neutron imaging with a 16 µm voxel resolution provides details on the spatial distribution of the solid product within the porous electrodes. Additionally, the performance impact of two electrolyte solvents, tetra ethylene glycol dimethyl ether (TEGDME) and dimethyl sulfoxide (DMSO), is evaluated when used to soak the carbon cathode. The cathode orientation where the MPL faces toward the electrolyte and separator reaches higher discharge and charge capacities and greater average discharge voltages compared to when the MPL faces away from the separator. Batteries discharged with DMSO as the solvent have a 64.86% decrease on average in discharge capacity compared to batteries using TEGDME as the solvent. Both the titration experiments and neutron imaging confirmed that the amount of solid products exhibits a linear correlation with the discharged capacity. Additionally, electrolytes with a high donor number, such as DMSO, were found to result in a smaller amount of Li₂O₂ deposited on the electrode surface. Full article

The packaging sector presents a significant sustainability challenge, particularly due to the prevalence of plastic packaging. There is a growing interest in sustainable packaging alternatives. The main challenge is to develop packaging with comparable and competitive characteristics. In this context, this manuscript aims to evaluate the performance of lignin-based polyurethane applied as a coating on recycled linerboard. Industrial softwood kraft lignin was fully characterized in terms of purity, functional groups (FTIR and ³¹P NMR) and molecular weight (GPC). Aiming at coating applications, the lignin sample was solubilized in dimethyl sulfoxide (DMSO) and used as a polyol substitute in the reaction, replacing polyethylene glycol (PEG) at levels of 70%, 80%, and 90%. Subsequently, hexamethylene diisocyanate (HDI) was added to initiate polyurethane formation. After polymerization, the coating was applied in multiple layers onto the linerboard paper. Regarding water resistance, all applications demonstrated effectiveness. The lignin-based polyurethane coating improved the Cobb1800 with reductions in the range of 1147.4 to 1155.8 g/m² compared to the uncoated paper. Water vapor permeability was reduced by more than 94%. In the evaluation of oil resistance, samples with three layers and 90% lignin replacement performed particularly well, achieving a high value in a kit test for oil and grease (kit test number 12). These results highlight a promising approach to paper-based packaging, with potential applications across a wide range of products. Full article

Donor–acceptor (D-A)-type conjugated porous polymers (CPPs) have emerged as highly competitive photocatalysts for aerobic oxidation reactions. Herein, we rationally design and synthesize a series of D-A structured photocatalysts by employing dibenzothiophene-S, S-dioxide (BTDO) as the acceptor unit, and 4,8-bis(thiophen-2-yl) benzo [1,2-b:4,5-b’] dithiophene (DBD) and pyrene (Py) as the donor units. The effects of acceptor content on the optoelectronic and photocatalytic properties are systematically investigated. With the gradual increase in BTDO proportion and the decrease in pyrene content, the photocatalysts exhibit gradually narrowed band gaps, significantly promoted charge separation efficiency, and broadened visible light absorption range. Among the five as-prepared photocatalysts, DBD-T displays superior catalytic performance toward blue light-driven aerobic oxidation. Under mild conditions, benzyl sulfide and benzyl amine are selectively converted into benzyl sulfoxide and benzyl imine with a high conversion efficiency up to 96%. Moreover, DBD-T shows good universality toward a wide range of substrates, together with excellent recyclability and long-term stability. This work demonstrates that enhancing the electron-withdrawing capability of the acceptor unit represents a feasible and effective strategy to boost the photocatalytic performance of D-A-type conjugated polymers. Full article

The chlorophyll molecule is considered a low-cost material, easy to synthesize, and easily extracted from plant leaves. It exhibits high chemical stability, structural flexibility, and high absorbance ability at the visible range of electromagnetic radiation. In this work, the geometrical, electronic, and optical properties of pure, dissolved, and doped chlorophyll (C1) natural organic dye were computed by density functional theory (DFT) and time-dependent density functional theory (TD-DFT). The solvents considered include water (H₂O), acetone (C₂H₆O), dichloromethane (CH₂Cl₂), chloroform (CH₃Cl), and dimethyl-sulfoxide (DMSO) (C₂H₆OS). The solar photovoltaic parameters, such as light-harvesting efficiency (LHE), oscillation strength (f), free energy of electron injection (${\Delta \mathrm{G}}_{\mathrm{I}\mathrm{n}\mathrm{j}.}$) and regeneration (${\Delta \mathrm{G}}_{\mathrm{R}\mathrm{e}\mathrm{g}.}$), open-circuit voltaic (V_OC), and efficiency ($\eta$), were also investigated. The evaluated energy gap slightly shifted from 1.920 eV to 1.980 eV based on the solvent polarity, while the UV-Visible absorption spectrum red-shifted from 422.3 nm to 439.8 nm, improving the overall efficiency up to 21.5% in DMSO solvent. The (LHE) and (${\Delta \mathrm{G}}_{\mathrm{I}\mathrm{n}\mathrm{j}.}$) properties regarding Cl molecules improved up to 69.1% and −1.384 eV when dissolved in chloroform and DMSO solvents, respectively. Doping C1 molecule via metal transition atoms such as zinc (Zn), nickel (Ni) and copper (Cu) further modified the optical and photovoltaic performance. Doped C1 molecule via Cu atom shows the best photonic results, including the highest open-circuit voltage (V_oc) and conversion efficiency ($\mathrm{Ƞ}$), while the Ni-doped C1 dye displays the longest lifetime, 1.699 µs, and the highest electronic coupling constant, 1.975 eV; thus, it has the superior photovoltaic performance. These results demonstrate that both solvents and transition metal atom modification significantly improve C1 performance, making metal-doped C1 a promising low-cost and eco-friendly sensitizer for dye-sensitized solar cells (DSSCs). Full article

The strong adhesion between cathode materials and aluminium (Al) foil substrates presents a significant challenge in the recycling of spent lithium-ion batteries (LiBs). Conventionally, high temperatures and high concentrations of costly organic solvents such as N-methyl-2-pyrrolidone (NMP), dimethylacetamide (DMAC), dimethylformamide (DMF), and dimethyl sulfoxide (DMSO) are used to enhance ultrasonication-based delamination. In this study, a novel, eco-efficient approach was demonstrated for delaminating cathode materials from Al foil using a low-concentration organic citric-acid-assisted low-power ultrasonic treatment coupled with a gentle, low-power-per-volume mechanical mixing system at room temperature. The separation mechanism was attributed to the structure disruption, possibly swelling, of the polyvinylidene fluoride (PVDF) binder using low-concentration citric acid and the cavitation effects induced by ultrasound. Key parameters influencing the delamination efficiency included the solvent type, temperature, ultrasonic power, and treatment duration. Under optimised conditions, citric acid was used as the sonication reagent, with a process temperature of 20 °C, 60 W ultrasonic power, and 80 min of ultrasonication; a delamination efficiency of approximately 92% was achieved. The recovered cathode materials exhibited low agglomeration, favouring subsequent leaching processes. This work proposes an environmentally friendly and effective method for cathode and Al foil recovery from spent LiBs, integrating manual dismantling, ultrasonic treatment, and material separation. Full article

Background: Mass spectrometry (MS)-based immunopeptidomics has emerged as the gold standard for profiling HLA-bound peptides, yet detection remains challenging due to their non-tryptic nature, variable lengths, and lack of basic residues, which limit ionisation and fragmentation efficiency. Methods: To address these limitations, we investigated the impact of incorporating 5% dimethyl sulfoxide (DMSO) into LC-MS/MS mobile-phase buffers on immunopeptidomic workflows. Using B-lymphoblastoid cell lines expressing HLA class I and II alleles and elastase-digested HeLa lysates as a surrogate for non-tryptic peptides, we assessed peptide identification, ionisation efficiency, charge state distribution, and fragmentation quality. Results: DMSO significantly increased peptide identifications across all sample types, with gains of ~1.33 folds for HLA class I, ~1.55 folds for HLA class II, and ~1.24 folds for elastase digests. Improvements were systematic and reproducible, driven by enhanced electrospray ionisation, higher charge states, and superior MS2 spectral quality, evidenced by ~2-fold increase in b- and y-ion intensities. Importantly, DMSO did not introduce major sequence bias, preserving motif integrity and predicted binding characteristics. Conclusions: Overall, these findings establish DMSO as a robust additive for improving sensitivity and reliability in immunopeptidomics, particularly for low-input or clinically derived samples. Full article

The preparation of the novel optically active sulfoxides (-)-(S)-1,1,1,3,3,3-hexafluoro-2-[o-(p-tolylsulfinyl)phenyl]propan-2-ol 1, (-)-(S)-1,1,1,3,3,3-hexafluoro-2-[o-(methylsulfinyl)phenyl]propan-2-ol 2 and (-)-(S)-1,1,1,3,3,3-hexafluoro-2-[o-(t-butyl-sulfinyl)phenyl]propan-2-ol 3 according to the Andersen methodology and their spectroscopic characterization is presented. The NMR and CD spectroscopic evidence of the existence of the equilibrium between sulfoxide and hypervalent sulfurane forms of these compounds in solution and attempts at the isolation of corresponding sulfuranes are shown. For compound 3, the unprecedented subsequent irreversible transformation in solution into corresponding cyclic sulfinate ester–sultine 17 was established on the basis of NMR spectroscopy measurements. The mechanism of this transformation was investigated by means of GC-MS analysis and confirmed on the basis of synthesized long alkyl chain analog 23 transformation in solution. Moreover, the oxidation properties of obtained sulfoxides 2 and 3 for the selected compounds are described. Full article

Cold recycled asphalt mixtures incorporate a high amount of reclaimed asphalt pavement (RAP), which offers more economic and environmental advantages than hot recycling techniques. Nevertheless, the presence of aged RAP binder frequently leads to reduced low-temperature performance and uncertainty in mechanical response. The influence of slack wax on full-depth reclamation (FDR) mixtures with bitumen emulsion is assessed in this study using a dual-scale approach. The approach integrates both chemical and rheological binder-scale characterization with mixture-scale mechanical performance with variability assessment. At the binder scale, the binder beam rheometer (BBR), dynamic shear rheometer (DSR), and Fourier transform spectroscopy (FTIR) indicated that the addition of 10% recycling agent improved the low-temperature properties. The improvement at lower temperatures shifted the BBR temperature from −23 °C to −30 °C, which ultimately resulted in a less negative ΔT_c, from −0.7 °C to −0.3 °C, and moderately improved high-temperature stiffness. Moreover, the FTIR analysis indicated a reduction in oxidation-related chemical markers, as evidenced by the reduced carbonyl and sulfoxide indices. At the mixture scale, complex modulus shows a systematic decrease in stiffness, particularly at lower temperatures of −25 °C and −15 °C, and a reduced phase angle, suggesting higher elastic dominance. The reduction is observed at all temperatures and frequencies. Rutting resistance of both formulations remains below 3% after 30,000 cycles. The complex modulus coefficient of variability was found to be 8–12%, comparable to that of hot mix asphalt. In conclusion, the findings suggest that the recycling agent provides a controlled restoration of viscoelastic properties in cold recycled mixtures without compromising structural integrity. This underscores the significance of multi-scale evaluation and variability assessment when characterizing high RAP recycling agents under the studied materials and dosage. Full article

During the early pupal stage in butterflies, the peripheral portion of wing tissue undergoes apoptosis to finalize adult wing morphology, and wing color patterns are determined coordinately. We hypothesized that the development of wing morphology and color patterns may involve NADPH oxidase (NOX). To test this hypothesis, we treated pupae of the blue pansy butterfly Junonia orithya with NOX inhibitors. When VAS2870, isuzinaxib, or diphenyleneiodonium chloride (DPI) in dimethyl sulfoxide (DMSO) was topically applied to the pupal wing tissue via the sandwich method, wing morphology and color pattern elements, including eyespots, parafocal elements, submarginal bands, and marginal bands, were severely deformed as if the marginal area were surgically removed. The topical application of DMSO alone mildly deformed and enlarged eyespots without affecting other color patterns and wing morphology. When systemically injected into pupae, VAS2870 increased eyespots in males but decreased eyespots in females, likely due to the sexual dimorphism of this species. These results suggest that NOX and probably hydrogen peroxide play important roles in wing morphogenesis and color pattern fate determination in butterfly wings. Sexually dimorphic eyespot size in this species may also be explained by the sexually differential activities of NOX. Full article