Search Results (20,655)

In this study, semi-interpenetrating polymer network (semi-IPN) hydrogels based on methacrylated dextran and native inulin were designed as biodegradable carriers for the colon-specific delivery of uracil as a model antitumor compound. The hydrogels were synthesized via free-radical polymerization, using diethylene glycol diacrylate (DEGDA) as a crosslinking agent at varying concentrations (5, 7.5, and 10 wt%), and their structural, thermal, and biological properties were systematically evaluated. Fourier transform infrared spectroscopy (FTIR) confirmed successful crosslinking and physical incorporation of uracil through hydrogen bonding. Concurrently, differential scanning calorimetry (DSC) revealed an increase in glass transition temperature (T_g) with increasing crosslinking density (149, 153, and 156 °C, respectively). Swelling studies demonstrated relaxation-controlled, first-order swelling kinetics under physiological conditions (pH 7.4, 37 °C) and high gel fraction values (84.75, 91.34, and 94.90%, respectively), indicating stable network formation. SEM analysis revealed that the hydrogel morphology strongly depended on crosslinking density and drug incorporation, with increasing crosslinker content leading to a more compact and wrinkled structure. Uracil loading further modified the microstructure, promoting the formation of discrete crystalline domains within the semi-IPN hydrogels, indicative of physical drug entrapment. All formulations exhibited high encapsulation efficiencies (>86%), which increased with increasing crosslinker content, consistent with the observed gel fraction values. Simulated in vitro gastrointestinal digestion showed negligible drug release under gastric conditions and controlled release in the intestinal phase, primarily governed by crosslinking density. Antimicrobial assessment against Escherichia coli and Staphylococcus epidermidis, used as an initial or indirect indicator of cytotoxic potential, revealed no inhibitory activity, suggesting low biological reactivity at the screening level. Overall, the results indicate that DEGDA-crosslinked dextran/inulin semi-interpenetrating (semi-IPN) hydrogels represent promising carriers for colon-targeted antitumor drug delivery. Full article

The synthesis of monocyclic and bicyclic compounds plays a fundamental role in organic chemistry, and the need for novel synthetic methodologies is still under investigation. In particular, α,β-unsaturated (bis)enones have emerged as valuable precursors for the formation of cyclic (both mono and bicyclic) structures through single-electron transfer (SET) processes. Single-electron transfer (SET) is a redox process where one electron moves from a donor species to an acceptor, generating radical ions or neutral radicals that drive unique reaction pathways. Thanks to the advent of radical chemistry, it was possible to discover an entirely new reactivity of α,β-unsaturated (bis)enones, which, after a SET event, undergo the formation of cyclic molecules, both in intra and inter-molecular reactions, under several possible pathways, including formal [2+2] cycloaddition reaction (22CA) and 5-exo-trig cyclization, for ring closure. Today, the generation of radical species can be broadly classified into three main approaches: photochemical and photocatalytic, metal-driven and electrochemical processes. In this review, we summarize the progress achieved to date in the synthesis of cyclic molecules from α,β-unsaturated (bis)enones via single-electron transfer events under these three main classes of processes. Whenever possible, the reaction pathway and fate of the radical species generated through SET is discussed. Full article

The anti-Markovnikov addition of thiyl radicals, generated via one-electron oxidation of thiols, to C=C double bonds is a useful method for synthesizing unsymmetrical sulfides and has been widely applied in the preparation of pharmaceuticals and functional materials. However, conventional radical thiol–ene reactions require metal-based photoinitiators or organic photosensitizers, raising concerns about product isolation and environmental impact. Herein, we demonstrate an initiator-free thiol–ene coupling via electrochemical oxidation of thiols. Using a microfluidic electrochemical reactor, the electrochemically generated thiyl radicals undergo rapid and selective addition to alkenes, affording thioethers in reasonable yields. Substrate scope studies involving 13 alkenes and 13 thiols indicate that thiol acidity (pK_a), alkene electronic properties, and steric effects play key roles in determining reaction efficiency. Although further optimization is required to improve yields and broaden substrate scope, this electrochemical approach highlights the potential of thiol–ene coupling as a sustainable tool in green synthetic chemistry. Full article

The widespread occurrence of pharmaceutical contaminants in aquatic environments poses significant risks to ecosystems and public health, necessitating the development of efficient and sustainable treatment technologies. Herein, a visible-light (VL)–active zinc single-atom catalyst supported on biochar (SAZn@BC) was synthesized via pyrolysis and applied for the degradation of ibuprofen (IBP), sulfamethoxazole (SMX), trimethoprim (TMP), and carbamazepine (CBZ) in water. Structural characterization confirmed the presence of g-C₃N₄ domains, abundant oxygen-containing functional groups, and atomically dispersed Zn sites with a Zn–N₄ coordination environment. Under VL irradiation, SAZn@BC achieved degradation efficiencies of 43.9%, 64.4%, and 61.9% for IBP, SMX, and TMP, respectively, within 30 min, while CBZ exhibited limited removal. Mechanistic investigations combining quenching experiments, electrochemical analyses, and X-ray photoelectron spectroscopy revealed that superoxide and hydroperoxyl radicals were the dominant reactive oxygen species, with hydroxyl radicals and singlet oxygen contributing to a lesser extent. In addition, a nonradical pathway involving direct interfacial electron transfer between oxygen functional groups on the biochar support and pharmaceutical molecules played a critical role, mediated by single-atom Zn sites and enhanced under VL irradiation. These findings demonstrate that SAZn@BC enables synergistic radical and nonradical pathways for pharmaceutical degradation and represents a promising strategy for water treatment applications. Full article

This study presents a comparative analysis of secondary metabolites and antioxidant, antimicrobial, and anticancer activities of acetone extracts obtained from the lichens Lepraria incana and Pertusaria amara. HPLC-UV analysis identified divaric acid, divaricatinic acid, norstictic acid, divaricatic acid and usnic acid in L. incana, and conprotocetraric acid, protocetraric acid, picrolichenic acid and atranorin in P. amara. Free radical scavenging capacity and reducing power assays were employed to assess the antioxidant activity of the extracts. The IC₅₀ values in the free radical scavenging assay were 664.23 μg/mL for L. incana and 750.50 μg/mL for P. amara, while reducing power absorbances varied between 0.0875–0.2562 and 0.0336–0.2011, respectively. Total phenolic contents in L. incana and P. amara extracts were 40.81 and 33.67 μg PE/mg of extract, while total flavonoid contents were 24.74 and 23.61 μg RE/mg of extract, respectively. Antimicrobial activity, determined by the microdilution method, ranged from 156 to 20 × 10³ μg/mL for L. incana and from 312 to 20 × 10³ μg/mL for P. amara. Cytotoxicity was tested using the MTT method. Among the tested samples, the L. incana extract showed the strongest cytotoxic activity toward A549 cells, with an IC₅₀ value of 47.53 μg/mL. Based on the results, the lichens examined demonstrate promise for future studies and potential development in biopharmaceutical applications. Full article

The rate constant k_OH for the reaction of 1,1,1,3,3,3-hexafluoroprop-2-imine with OH radicals was measured relative to two reference compounds, CH₃F and CH₃CHF₂, to be k_OH = (4.2 ± 1.1) × 10⁻¹⁴ cm³ molecule⁻¹ s⁻¹ at 295 K. This implies an atmospheric lifetime with respect to consumption by OH of 0.75 years. Reaction with Cl atoms yielded k_Cl = (7.9 ± 1.7) × 10⁻¹⁶ cm³ molecule⁻¹ s⁻¹ at 295 K, and reaction with O₃ has an upper limit of k_O3 < 4 × 10⁻²³ cm³ molecule⁻¹ s⁻¹, so that the atmospheric consumption by Cl and O₃ is negligibly slow. Absolute infrared cross sections of the imine yield a radiative efficiency of 0.34 W m⁻² ppb⁻¹, which is corrected to 0.23 W m⁻² ppb⁻¹ for the effects of atmospheric lifetime. The imine’s corresponding 100-year global warming potential is 64 ± 19. This value is an upper limit, given that heterogenous atmospheric removal paths, such as hydrolysis in water droplets, are not included. Full article

The automotive industry faces radical technological change, driven by the adoption of electrification, automation, and digitalization. As a leading industrial hub with key OEMs and suppliers, such as Volkswagen, Southeast Lower Saxony is disproportionately impacted by this structural transformation. As a consequence of these trends, the region’s automotive base faces economic uncertainties, local regulatory lag, and technological disruptions. In this study a scenario planning methodology is conducted, to identify three potential mobility futures for 2035: a Best-Case scenario, where innovation and favorable policies enable a stable growth environment for the local automotive industry; a Trend scenario, marked by incremental yet uneven progress, while maintaining the current status quo; and a Worst-Case scenario, defined by economic stagnation and regulatory impediments, leading to a slow degradation of the regional automotive industry. The scenarios are then evaluated based upon their impact and probability of occurrence, while individual impact factors were also prepared and categorized to support future decision-making on a topical basis. This study offers an overview of potential scenarios for the Southeast Lower Saxon automotive industry, supporting the strategic decision-making. Full article

This study aimed to systematically investigate the chemical constituents and bioactivities of the traditional wild tea plant Camellia kwangsiensis Chang. An HPLC method was first established to simultaneously quantify five major components. Subsequently, extensive isolation was performed using chromatographic techniques, and the structures of isolated compounds were elucidated by spectroscopic methods. Their biological potential was evaluated through antioxidant (DPPH and ABTS⁺ radical scavenging), α-glucosidase inhibitory, and anti-inflammatory (inhibition of nitric oxide production) assays. The LC-MS/MS analyses confirmed the absence of caffeine, theophylline, and theobromine. A total of 19 phenolic compounds were first isolated and identified, including one new proanthocyanidin, namely kwangsienin A (1), and 18 known phenolic components with six proanthocyanidins (2–7), one catechin (8), six flavonol glycosides (9–14), and five simple phenols (15–19). Notably, the proanthocyanidins displayed stronger or comparable antioxidant and α-glucosidase suppressive activity than the positive controls. In conclusion, C. kwangsiensis, rich in proanthocyanidins and naturally caffeine-free, represents a promising plant resource for developing decaffeinated functional tea beverages with antioxidant and hypoglycemic potential. Full article

Halide perovskites have many advantages in environmental remediation. The photocatalytic performance of halide perovskites is often hindered by low specific surface area and rapid photogenerated carrier recombination. The aim of this work is to prepare a green, novel photocatalyst in the form of biochar-anchored Cs₃Bi₂Br₉ perovskite composites. The rose-petal-derived biomass carbon (RC) provides adsorption sites and high electrical conductivity, while the perovskite Cs₃Bi₂Br₉ can efficiently capture visible right and degrade pollutants, and the reciprocal effect can enhance the photocatalytic efficiency of the composite. The results of scanning electron microscopy (SEM) showed the Cs₃Bi₂Br₉ particles were loaded on the surface of RC. Compared with bare Cs₃Bi₂Br₉, Cs₃Bi₂Br₉/RC composite has a more perfect structure, higher specific surface area, enhanced ability to absorb visible light, and reduced bandgap value. As visible-light-driven photocatalysts, the prepared Cs₃Bi₂Br₉/RC composites can enhance the removal efficiency of Rhodamine B. The Cs₃Bi₂Br₉/RC–0.2 composite displays the highest degradation efficiencies for RhB (10 mg/L), reaching 98% within 60 min. And the rate constant (k) is 1.9 times that of bare Cs₃Bi₂Br₉. The results of electrochemical impedance spectroscopy (EIS) show that the interaction between RC and Cs₃Bi₂Br₉ speeds up charge carrier separation and transfer. During photocatalytic process, holes (h⁺) and superoxide radicals (·O₂⁻) played major roles. The composites also showed excellent stability. It is meaningful to deal with a large number of withered rose petals to make them high-value products. This work not only provides a guideline for the construction of perovskite composites materials but also shows the promising prospects of biochar composites in deep treatment for contaminated water. Full article

High-temperature proton exchange membranes (HT-PEMs) are critical components of high-temperature fuel cells, facilitating proton transport and acting as a barrier to fuel and electrons; however, their performance is hampered by persistent issues of phosphoric acid leaching and oxidative degradation. Herein, a novel HT-PEM with abundant hydrogen bond network is constructed by incorporating nanoscale polyhedral oligomeric silsequioxane functionalized with eight pendent sulfhydryl groups (POSS-SH) into poly(4,4′-diphenylether-5,5′-bibenzimidazole) (OPBI) matrix. POSS, a cage-like nanostructured hybrid molecule, features a well-defined silica core and highly designable surface organic groups, offering unique potential for enhancing membrane performance at the molecular level. Through controlled reactions between sulfhydryl groups and allyl glycidyl ether (AGE), two functional POSS crosslinkers—octa-epoxide POSS (OE-POSS) and mixed sulfhydryl-epoxy POSS (POSS-S-E)—were synthesized. These were subsequently used to fabricate crosslinked OPBI membranes (OPBI-OE-POSS and OPBI-POSS-S-E) via epoxy–amine coupling. The OPBI-POSS-S-E membranes demonstrated exceptional oxidative stability, which is attributed to the free radical scavenging ability of the retained sulfhydryl groups on the nano-sized POSS framework. After soaking in Fenton’s reagent at 80 °C for 108 h, the OPBI-POSS-S-E-20% membrane retained 79.4% of its initial weight, significantly surpassing both the OPBI-OE-POSS-20% and pristine OPBI membranes. The PA-doped OPBI-POSS-S-E-20% membrane achieved a proton conductivity of 50.8 mS cm⁻¹ at 160 °C, and the corresponding membrane electrode assembly delivered a peak power density of 724 mW cm⁻², highlighting the key role of POSS as a nano-modifier in advancing HT-PEM performance. Full article

Aging and neurodegenerative diseases are characterized by common features involving bioenergetics deficiencies, oxidative stress and alterations of calcium buffering. Mechanisms of mitochondrial-targeted drugs include the modulation of electron transport chain and oxidative phosphorylation, the binding to mitochondrial lipids, free-radical scavenging, calcium signaling, and possible effects on mitochondrial biogenesis and dynamics and on the regulation of mitophagic pathways. One of the main sites of action of mitochondria-targeted drugs is the interaction with respiratory chain components. Mitochondrial-targeted compounds such as Mito-Q, and Mito-apocynin have been developed by conjugating triphenylphosphonium (TPP⁺) lipophilic cation group with natural molecules, therefore obtaining promising drugs for reestablishing the correct functioning of the mitochondrial respiratory chain. Stabilization of cardiolipin at the inner mitochondrial membrane by elamipretide or SkQ1 and mitochondria-targeted ROS scavengers can also offer a therapeutic approach to prevent bioenergetic impairment associated with several diseases. In addition, the modulation of calcium signaling can be achieved using both MCU agonists and antagonists representing another mitochondrial target for drug therapies development. Finally, potential strategies for treating neurodegenerative diseases based on the modulation of mitochondrial biogenesis, dynamics and/or mitophagic pathways are discussed. Full article

Background/Objectives: Pelvic exenteration is a radical procedure performed for recurrent gynecologic cancers. The goal of exenteration is to prolong survival, but this procedure also results in extensive tissue loss and consequently high morbidity. Reconstruction using vascularized flaps, particularly the VRAM flap, is crucial to restoring pelvic integrity and decreasing complications resulting from extensive tissue loss. With the rise of minimally invasive surgery, the traditionally open abdominal approach to exenteration and reconstruction can now be performed with the assistance of robotic platforms. This review aims to summarize available evidence, describe techniques, and propose future directions for robotic rectus flap reconstruction after pelvic exenteration. Methods: This narrative review was conducted following the SANRA guidelines for narrative synthesis. A comprehensive search of PubMed, Embase, Scopus, and Web of Science was conducted for studies published between January 2000 and November 2025 on pelvic exenteration followed by robotic rectus abdominis flap reconstruction in gynecologic oncology. Eligible studies were retrospective or prospective reports, technical descriptions, case series, or comparative analyses. Non-robotic techniques and animal studies were excluded. Although the primary focus was gynecologic oncology, technically relevant studies from other oncologic disciplines were included when the reconstructive approach was directly applicable to pelvic exenteration. Extracted data included patient demographics, surgical details, and perioperative and oncologic outcomes. Results: The literature search identified primarily case reports and small single-center series describing robot-assisted rectus muscle-based flap reconstruction after pelvic exenteration. Reported cases demonstrated technical feasibility and successful flap harvest using robotic platforms, with adequate pelvic defect coverage. Potential benefits, such as reduced wound morbidity and preservation of a minimally invasive workflow, have been described. However, patient numbers were small, techniques varied, and standardized outcome measures or comparative data with open approaches were lacking. Conclusions: Robotic rectus flap reconstruction represents a promising advancement in pelvic exenteration surgery, potentially reducing morbidity and improving recovery. Further research, including multicenter prospective studies, is needed to validate these findings and establish standardized protocols. Full article

China boasts abundant cultivated resources of pitahaya, with Guizhou Province being one of its core producing areas. Quality differences in red-fleshed pitahaya among local producing areas have not been fully clarified, and a standardized quantitative evaluation system for these differences remains lacking. This study seeks to identify the key factors influencing regional variations in quality and establish a comprehensive evaluation standard. In this study, 15 samples of red-fleshed pitahaya were collected from four major producing areas in Guizhou and used as research materials. Based on 15 quality characteristic indicators of the fruits, an analysis of quality differences and establishment of an evaluation system were carried out using multivariate statistical analysis. The results showed that 14 of the 15 quality indicators exhibited significant differences among pitahaya samples from different producing areas (p < 0.05), with the a* value being the sole exception. Cluster analysis classified the 15 samples into four groups. Principal component analysis (PCA) extracted four principal components, with a cumulative variance contribution rate of 81.07%, which clearly identified betacyanin, betaxanthin, 1,1-diphenyl-2-picrylhydrazyl (DPPH) free-radical scavenging rate, vitamin C, fruit shape index, and transverse diameter as the core evaluation indicators. This study systematically clarifies the differences in quality characteristics and the internal correlations among quality indicators of red-fleshed pitahaya from different major producing areas in Guizhou. It further provides an important scientific basis for pitahaya variety breeding, cultivation regulation, and market positioning in this region and fills the research gap existing in the field of comprehensive quality evaluation of pitahaya. This is of significant practical importance for promoting the standardized upgrading of local specialty fruit industries, enhancing the market competitiveness of products, and facilitating the high-quality development of the agricultural economy. Full article

Dysphania ambrosioides is a widely distributed species with a traditional use in folk medicine, but it exhibits marked chemical variability that limits its standardization. This study is the first to characterize the essential oil (EO) of three Ecuadorian populations—Arenillas (ARE), Pasaje (PAS) and Piñas (PIN)—using gas chromatography–mass spectrometry/flame ionization detection (GC-MS/FID), and to correlate its composition with edaphic properties and antioxidant activity. Chemical profiles revealed three distinct chemotypes: ARE (α-terpinene 65.35%, o-cymene 24.83% and ascaridole 3.30%), PAS (α-terpinene 56.31%, o-cymene 10.09% and ascaridole 10.84%) and PIN (α-terpinene 56.89%, o-cymene 17.07% and ascaridole 7.60%). The EO yield was low (0.030–0.064% w/w), coinciding with acidic and nutrient-poor soils. On the other hand, PAS, with its neutral soil and high nitrogen, produced the highest number of oxygenated compounds. Only PAS exhibited strong ABTS radical-scavenging activity (SC₅₀ = 37.99 ± 1.01 µg/mL). In contrast, ARE showed weak activity (SC₅₀ = 424 ± 1.01 µg/mL), while PIN showed moderate activity (SC₅₀ = 112.26 ± 1.01 µg/mL), which was correlated with its high total phenol content (298.48 mg EAG/L). The 2,2-diphenyl-1-picrylhydrazyl (DPPH) activity was low in all samples. Principal component analysis (PCA) confirmed clear separation of the chemotypes, which was linked to edaphic factors such as pH, heavy metals (Cu, Fe and Mn) and organic matter. These findings suggest that edaphic conditions may modulate the chemical composition and antioxidant activity of D. ambrosioides, indicating a potential approach for the sustainable selection of plant material. Full article

One of the major factors currently hindering the development of hemoglobin-based oxygen carriers (HBOCs) is the autoxidation of hemoglobin to inactive methemoglobin (MetHb). The effects of spermine on the stability, aggregation, structure, and function of adult hemoglobin (HbA) were studied. The interaction of spermine with HbA was elucidated by dynamic light scattering, colloid osmotic pressure measurements, thermal denaturation analysis, static light scattering, and oxygen dissociation assay. The antioxidant capacity of spermine was confirmed through UV–vis spectroscopic recordings, calculations of MetHb formation, and hydroxyl radical scavenging. The P50 value was determined by the oxygen dissociation curve to investigate the roles of spermine in increasing HbA’s oxygen affinity. The pH-dependent affinity between spermine and HbA was validated through surface plasmon resonance experiments. The transformation of HbA’s partial α-helix to a β-sheet structure induced by spermine was clarified using a microfluidic modulation spectrometer. The binding of spermine to βASP99, βGLU101, αTHR38, and αASN97 on HbA and the conformational shift in HbA towards the ‘R’ state were investigated via molecular docking and molecular dynamics simulations. In a word, spermine can enhance the oxygen affinity of HbA, effectively reduce autoxidation, and hold promise for applications in the research of HBOCs or hemoglobin modification. Full article