Search Results (1,678)

This work introduces a non-isolated high step-up dc-dc interleaved boost converter combining magnetic coupling and voltage multiplier cells (VMCs). The proposed topology features a transformer with two primary windings of equal turns, interconnected to each other, enabling improved current sharing, and multiple secondary windings that contribute to extending the voltage gain. A three-winding coupled inductor is integrated into the design, while VMCs not only boost the output voltage but also significantly reduce the voltage stresses on the switches, eliminating the need for extreme duty ratios. The converter exhibits inherent modularity, allowing for voltage gain adjustments either through the turns ratio of the coupled inductor or by incorporating additional VMCs. An in-depth analysis of the topology is derived, and an experimental prototype rated at 48 V/400 V, 25 kHz, and 1 kW is implemented to verify and validate the theoretical claims, achieving an efficiency of 95.12% at full-load conditions. Full article

Driven by the growing demand for sustainable resource utilization, the recovery of valuable constituents from spent lithium-ion batteries (LIBs) has attracted considerable attention, whereas conventional recycling processes remain energy-intensive, inefficient, and environmentally detrimental. Herein, an efficient and environmentally benign separation strategy integrating dielectrophoresis (DEP) and magnetophoresis (MAP) is proposed for isolating the primary components of “black mass” from spent LIBs, i.e., lithium iron phosphate (LFP) and graphite microparticles. A coupled electric–magnetic–fluid dynamic model is established to predict particle motion behavior, and a custom-designed microparticle separator is developed for continuous LFP–graphite separation. Numerical simulations are performed to analyze microparticle trajectories under mutual effects of DEP and MAP and to evaluate the feasibility of binary separation. Structural optimization revealed that the optimal separator configuration comprised an electrode spacing of 2 mm and a ferromagnetic body length of 5 mm with 3 mm spacing. Additionally, a numerical study also found that an auxiliary flow velocity ratio of 3 resulted in the best particle focusing effect. Furthermore, the effects of key operational parameters, including electric and magnetic field strengths and flow velocity, on particle migration were systematically investigated. The findings revealed that these factors significantly enhanced the lateral migration disparity between LFP and graphite within the separation channel, thereby enabling complete separation of LFP particles with high purity and recovery under optimized conditions. Overall, this study provides a theoretical foundation for the development of high-performance and environmentally sustainable LIBs recovery technologies. Full article

Background/Objectives: Gluteal medius tendon tears (GTT) are a common cause of greater trochanteric pain and functional impairment. Accurate preoperative imaging is critical for diagnosis and surgical decision-making. This study aimed to evaluate and compare the diagnostic accuracy of four imaging modalities—X-ray, ultrasound (US), magnetic resonance imaging (MRI), and bone scan (BS)/SPECT/CT—in detecting and grading GTT, using perioperative findings as the reference standard. Methods: In this prospective study, a cohort of 45 patients (41 women, 4 men; mean age 62.9) with suspected GTT and failed conservative treatment had open surgical treatment by augmentation of the gluteus medius tendon. All patients underwent preoperative imaging with X-ray, US, MRI, and BS. Imaging results were compared with intraoperative findings. Results: MRI demonstrated the highest sensitivity (98%) and strong PPV (91.1%), correctly identifying nearly all true positives. Ultrasound showed similar sensitivity (95%) but yielded more false positives. X-ray and BS exhibited perfect specificity and PPV (100%) but poor sensitivity (21% and 38%, respectively), limiting their utility in ruling out GTT. Conclusions: MRI is the most sensitive and reliable single modality for diagnosing GTT, though false positives remain a concern in surgical decision-making. Ultrasound, while sensitive, lacks specificity and should not be used in isolation for surgical decision-making. A multimodal imaging approach, particularly combining MRI with X-ray and BS, may offer high diagnostic certainty and help prevent unnecessary surgical interventions. Full article

Primary human endothelial cells represent an essential tool to model endothelial dysfunction and to screen interventions for its treatment. Here, we developed a protocol for the synchronous isolation of primary human saphenous vein endothelial cells (HSaVEC), human internal thoracic artery endothelial cells (HITAEC), and human microvascular endothelial cells (HMVEC) from SV and ITA utilized as conduits during coronary artery bypass graft surgery and from subcutaneous adipose tissue excised while providing an access to the heart. Treatment by collagenase type IV and magnetic separation with anti-CD31-antibody-coated beads ensured relatively high efficiency of the isolation (≈60% for HSaVEC, ≈50% for HITAEC, and ≈20% for HMVEC) and high purity (≥99%) of isolated ECs within ≈2 weeks (HSaVEC), ≈2–3 weeks (HITAEC), and ≈3–4 weeks (HMVEC). A colorimetric assay of cell viability and proliferation, as well as real-time bioimpedance monitoring using the xCELLigence instrument, demonstrated high proliferative activity in HSaVEC, HITAEC, and HMVEC, whilst the in vitro tube formation assay indicated their angiogenic potential. The isolation of HSaVEC, HITAEC, and HMVEC from patients undergoing coronary artery bypass graft surgery is a promising option to investigate endothelial heterogeneity, to interrogate endothelial responses to various stresses, and to pinpoint the optimal approaches for restoring endothelial homeostasis, thereby reproducing them within the bedside-to-bench-to-bedside concept. Full article

Three previously undescribed clerodane diterpenoids, including two cis-clerodanes, solidagolactone IX (1) and solidagoic acid K (2), and one trans-clerodane, solidagodiol (3), along with two known cis-clerodane diterpenoids, (−)-(5R,8R,9R,10S)-15,16-epoxy-ent-neo-cleroda-3,13,14-trien-18-ol (4) and solidagoic acid J (5), were isolated and comprehensively characterized from the ethanolic and ethyl acetate root extract of Solidago gigantea Ait. (giant goldenrod). Compound 4 has previously been reported from the roots of this species, whereas compound 5 was identified from the leaves of S. gigantea but not from the roots. The bioassay-guided isolation involved thin-layer chromatography–direct bioautography (TLC–DB) with a Bacillus subtilis antibacterial assay, preparative flash column chromatography, and TLC–mass spectrometry (MS). The chemical structures of the isolated compounds (1–5) were elucidated through extensive in-depth spectroscopic and spectrometric analyses, including one- and two-dimensional nuclear magnetic resonance (NMR) spectroscopy, high-resolution tandem mass spectrometry (HRMS/MS), and attenuated total reflectance Fourier-transform infrared (ATR–FTIR) spectroscopy. Their antimicrobial activities were evaluated using in vitro microdilution assays against B. subtilis and different plant pathogens. Compound 3 was the most active against the tested Gram-positive strains, exerting particularly potent effects against Clavibacter michiganensis with a minimal inhibitory concentration (MIC) value of 5.1 µM as well as B. subtilis and Curtobacterium flaccumfaciens pv. flaccumfaciens (MIC 21 µM for both). Compound 4 also strongly inhibited the growth of C. michiganensis (MIC 6.3 µM). Compounds 2, 4, and 5 displayed moderate to weak activity against B. subtilis and C. flaccumfaciens pv. flaccumfaciens with MIC values ranging from 100 to 402 µM. Rhodococcus fascians bacteria were moderately inhibited by compounds 3 (MIC 41 µM) and 4 (MIC 201 µM). Bactericidal activity was observed for compound 3 against C. michiganensis with a minimal bactericidal concentration (MBC) value of 83 µM. Compounds 2 and 3 demonstrated weak antifungal activity against Fusarium graminearum. Our findings underscore the value of bioassay-guided approaches in discovering previously undescribed bioactive compounds. Full article

The grain boundary diffusion (GBD) process is currently the relatively effective method for utilizing heavy rare earth (HRE) elements in NdFeB magnets, especially for magnetic sheets. However, due to a highly uneven microstructure, the recovery of GBD magnets was considered difficult. In this work, our study prioritized short-loop recycling of GBD NdFeB sheet magnets to prepare block magnets. A comparative investigation was conducted between GBD-processed NdFeB magnets and the conventional sintered magnets, with particular emphasis on their recyclability characteristics. Among them, the Tb content of GBD magnets of 0.4 wt.% was significantly lower than sintered magnets of 1.73 wt.%. When two waste magnets were supplemented with the same amount of rare earth, it was found that the coercivity of the block magnets regenerated from GBD sheet magnets was higher. Microstructural analysis revealed that the core–shell grains originally located in the surface layer of GBD magnets were uniformly mixed and diffused with the ordinary particles originally located inside during the regeneration sintering process. The regenerated GBD magnets exhibited a more uniform core–shell microstructure with submicron shells of Tb elements along with reduced areas of RE-rich phase enrichment which facilitated the formation of a continuous and uniform thin-layer grain boundary, thereby enhancing the magnetic isolation effect. Apart from the significance of recycling, these block magnets regenerated from GBD magnets also provides a new approach to solving the challenge of high coercivity and low HRE elements in bulk magnets. Full article

Background/Objectives: Selective inhibition of bacterial virulence factors is a promising strategy to convert pathogenic bacteria into non-pathogenic commensals, circumventing the challenge of antibiotic resistance. This approach enables the host immune system to eliminate virulence-attenuated pathogens. Methods: In this study, we evaluated the effects of Lindera obtusiloba Blume extract and cinnamtannin B1, the active component of the ethyl acetate fraction, on the type III secretion system (T3SS) of Yersinia enterocolitica. Results: The ethyl acetate fraction, at 100 mg/L, effectively suppressed all three T3SS components—the flagellar, Ysa, and Ysc T3SSs. Cinnamtannin B1, isolated from the ethyl acetate fraction through separation and identified through nuclear magnetic resonance spectrometer analysis, significantly inhibited flagellar and Ysa T3SS secretion, while selectively inhibiting expression of key effector proteins YopH and YopO in the Ysc T3SS. Additionally, cinnamtannin B1 reduced Y. enterocolitica-induced RAW 264.7 macrophage mortality and prevented poly (ADP-ribose) polymerase degradation, a marker of apoptosis. Conclusions: These findings suggest cinnamtannin B1 from L. obtusiloba as a selective T3SS-targeting compound with mechanistic potential for anti-virulence intervention. Further in vivo validation will be necessary to evaluate its therapeutic applicability. Full article

Phytopathogenic fungi represent a significant biotic stress affecting global agriculture, often causing severe diseases and, in some cases, leading to plant death. They have been isolated from economically important crops, including cereals, legumes, and fruits. Among the compounds produced by fungi, phytotoxins play a key role in disease development by interfering with host physiological processes. In this study, organic extracts from Cercospora kikuchii, Cercospora nicotianae, Cercospora sojina, Diaporthe longicolla, Septoria glycines, Pyrenophora teres, and Pyrenophora tritici-repentis, isolated from three major Argentine crops, were first screened for the in vitro production of phytotoxic metabolites. Subsequently, selected metabolites were dereplicated using liquid chromatography-tandem mass spectrometry (LC-MS/MS) and nuclear magnetic resonance (NMR) spectroscopy. The phytotoxins identified varied according to the fungal species and extraction conditions. Cercosporin, putaminoxin, scytalone, and isosclerone were identified. These findings underscore the need for further chemical investigation to comprehensively characterize the metabolome of these phytopathogens and clarify their roles in plant–pathogen interactions. Full article

Access to safe water remains a vital public health challenge, especially in low- and middle-income countries like Colombia, where untreated sources lead to severe diarrheal diseases in children under five. Escherichia coli (E. coli), a key indicator of fecal contamination, is often detected using culture-based methods that are time-consuming and rely on specialized infrastructure. To overcome these limitations, we developed an aptamer-based isolation system targeting environmental E. coli. Aptamers were obtained using a Cell-SELEX protocol, and after six enrichment rounds, two candidates—APT-EC-1 and its truncated version APT-EC-MUT—were synthesized and attached to carboxyl-functionalized magnetic nanoparticles (MNP-COOH). Both complexes demonstrated a strong binding affinity and high specificity, successfully isolating E. coli from environmental and ATCC reference strains in the laboratory. Sensitivity tests detected E. coli at dilutions up to 1:10,000, showing reliable performance. In early in-field testing with environmental water samples, APT-EC-1 consistently identified E. coli colonies, while APT-EC-MUT struggled with low bacterial levels, illustrating performance differences. These findings demonstrate the promise of aptamer-functionalized MNPs as the basis for quick, affordable, and portable biosensors for water quality testing, especially in resource-scarce areas. Future efforts will add colorimetric or electrochemical readouts to allow real-time, on-site detection of fecal contamination. Full article

The increasing penetration of electrified vehicles is accelerating the evolution of on-board and off-board charging systems, which must deliver higher efficiency, power density, safety, and bidirectionality under increasingly demanding constraints. This article presents a system-level review of state-of-the-art charging architectures, with a focus on galvanically isolated power conversion stages, wide-bandgap-based switching devices, battery pack design, and real-world implementation trends. The analysis spans the full energy path—from grid interface to battery terminals—highlighting key aspects such as AC/DC front-end topologies (Boost, Totem-Pole, Vienna, T-Type), high-frequency isolated DC/DC converters (LLC, PSFB, DAB), transformer modeling and optimization, and the functional integration of the Battery Management System (BMS). Attention is also given to electrochemical cell characteristics, pack architecture, and their impact on OBC design constraints, including voltage range, ripple sensitivity, and control bandwidth. Commercial solutions are examined across Tier 1–3 suppliers, illustrating how technical enablers such as SiC/GaN semiconductors, planar magnetics, and high-resolution BMS coordination are shaping production-grade OBCs. A system perspective is maintained throughout, emphasizing co-design approaches across hardware, firmware, and vehicle-level integration. The review concludes with a discussion of emerging trends in multi-functional power stages, V2G-enabled interfaces, predictive control, and platform-level convergence, positioning the on-board charger as a key node in the energy and information architecture of future electric vehicles. Full article

Background: Ephedra przewalskii Stapf stems are a traditional Mongolian medicine commonly used to treat infectious diseases. Previous in vitro experiments have shown that the extract powder derived from its stems possesses antiviral activity. However, the active compounds responsible for this activity in E. przewalskii Stapf have not yet been identified or evaluated. This study aimed to identify the active components in E. przewalskii that exhibit antiviral effects against SARS-CoV-2 in vitro and validate their antiviral activity. Methods: E. przewalskii stem extracts were subjected to high-performance liquid chromatography with varying methanol ratios in the mobile phase to obtain fractions with different polarities. Antiviral activity was assessed by infecting VeroE6/TMPRSS2 cells with the SARS-CoV-2 Delta strain and treating them with the obtained fractions. Infectious titers were measured using the 50% tissue culture infective dose (TCID₅₀) method, and half-maximal inhibitory concentration (IC₅₀) values were calculated for each fraction. The active components in the two fractions with the highest antiviral activity were identified and structurally characterized by nuclear magnetic resonance analysis. The antiviral activity of these compounds was confirmed by adding them to SARS-CoV-2-infected cells and measuring their infectious titers using the TCID₅₀ method. The IC₅₀ values were also calculated. Viral-particle inactivation assays were conducted by mixing the extracts with SARS-CoV-2 and measuring infectious titers. Results: (−)-Catechin, (+)-epigallocatechin-(2α→O→7,4α→8)-(−)-epicatechin, and ent-epicatechin-(4α→8;2α→O→7)-catechin were isolated from E. przewalskii. These compounds exhibited significant antiviral activity against SARS-CoV-2 but demonstrated minimal direct virucidal effects. Conclusion: (−)-Catechin, (+)-epigallocatechin-(2α→O→7,4α→8)-(−)-epicatechin, and ent-epicatechin-(4α→8;2α→O→7)-catechin exhibit antiviral activity against SARS-CoV-2 in infected cells. Full article

Structural analysis of glycosphingolipids provides novel insights into organismal classification and reveals conserved functional roles that transcend taxonomic boundaries. To elucidate the structural characteristics of acidic glycosphingolipids (AGLs) in the adductor muscle of the Japanese giant scallop (Patinopecten yessoensis), AGLs were isolated and purified by column chromatography using anion exchange resin and silica gel. Structural characterization was performed using mass spectrometry, proton nuclear magnetic resonance spectroscopy, and immunological techniques. The sugar chain structure was identified as GlcA4Meβ1-4(GalNAc3Meα1-3)Fucα1-4GlcNAcβ1-2Manα1-3Manβ1-4Glcβ1-Cer, consistent with the mollu-series core reported for mollusks. In addition to uronic acid, the structure was distinguished by internal fucose and methylated sugars, features commonly found in bivalves. The presence of xylose in the sugar chains of AGLs was also suggested. In contrast, the ceramide moiety was composed primarily of fatty acids C16:0 and C18:0 and the long-chain base d16:1. This chemical structure provides valuable insights into the biological classification of P. yessoensis and the mollu-series glycolipids containing fucose and methylated sugars, which may serve as bioactive components shared across species in the phylum Mollusca and class Bivalvia. Full article

Soybean oil has recently emerged as the most widely consumed genetically modified (GM) vegetable oil globally. DNA-based methods offer considerable advantages for monitoring GM-derived products; however, their efficacy strongly depends on the quality and quantity of extracted DNA. Owing to intensive processing, refined oils typically contain extremely low concentrations of severely fragmented DNA, making DNA extraction highly challenging. To address this issue, we introduce an innovative magnetic bead-based DNA extraction protocol specifically tailored to refined soybean oils. Optimal DNA adsorption was achieved using 300 nm carboxyl (-COOH)-modified magnetic beads under optimized conditions, including 1 M guanidine isothiocyanate (GITC) buffer at pH 6.0, combined with ethanol at a 1:1 ratio. Subsequently, we developed a cetyltrimethylammonium bromide (CTAB)-magnetic bead method in which DNA was efficiently transferred from the oil phase to the aqueous phase, concentrated via precipitation, resuspended in GITC buffer, and finally purified using magnetic beads. Comparative evaluations using nested polymerase chain reaction (PCR) and real-time PCR confirmed that this method significantly outperformed traditional CTAB-based methods (CTAB alone, CTAB-hexane) and two representative silica membrane-based extraction kits. Spike recovery experiments further demonstrated its superior efficacy, achieving a DNA recovery rate of 76.37%. The proposed protocol is simple, user-friendly, cost-effective, and highly efficient, markedly reducing reliance on large volumes of organic solvents (e.g., hexane and chloroform) and minimizing the required centrifugation steps. This novel method established an effective approach for DNA extraction from refined vegetable oils, facilitating the development of rapid and reliable GM detection. Full article

While numerous bioactive polysaccharides have been identified from mushrooms, their mechanisms of action, particularly through the induction of oxidative stress in tumor cells, remain underexplored. This study isolates a novel polysaccharide, LSPS2, derived from Laetiporus sulphureus, followed by the elucidation of its distinctive structural features and specific antitumor activity in A549 lung carcinoma cells. LSPS2 was composed primarily of glucose (88.1%) and minor amounts of mannose (8.0%) and galactose (3.9%). Methylation and one-dimensional/two-dimensional nuclear magnetic resonance (1D/2D NMR) analysis results indicated that LSPS2 was composed of (1→3)-linked-D-β-glucopyran residues and (1→4)-linked-D-α-glucopyran residues as the main chain. The side chains were connected to O-6 and O-3 of glucopyranose (Glcp) residues with terminal Glcp. It differs from previous reports on L. sulphureus polysaccharides. Functionally, LSPS2 markedly suppressed A549 cell viability in a manner that depended on both exposure duration and concentration. LSPS2 upregulated malondialdehyde (MDA) and downregulated reduced glutathione (GSH), demonstrating that LSPS2 induces oxidative stress in A549 cells. The results of superoxide dismutase (SOD) activity assays further indicated that LSPS2 downregulates SOD activity, which may be the mechanism by which LSPS2 induces oxidative stress and, consequently, apoptosis in A549 cells. This targeted downregulation of a key antioxidant enzyme highlights a potential pathway for polysaccharide-induced tumor cell death. Our findings not only identify LSPS2 as a structurally distinct biopolymer but also elucidate its mode of action, underscoring its prospective application in tumor therapy and functional foods, warranting further investigation. Full article

Breast and colon cancers are leading causes of death worldwide. There is a need for improved treatment strategies. South African medicinal plants, including Clerodendrum glabrum (C. glabrum) and Combretum nelsonii (C. nelsonii), are known for their cytotoxic properties. This study aimed to isolate and characterize terpenoids and stilbenes from the roots of C. glabrum and C. nelsonii and evaluate their anticancer potential against colorectal adenocarcinoma (Caco-2) and hormone receptor-positive breast cancer (MCF-7) cell lines. Spectroscopic techniques including nuclear magnetic resonance spectroscopy (NMR) were used to characterize the isolated compounds. Repeated column chromatography of C. glabrum extract led to the isolation of ferruginol (1), royleanone (2), and β-amyrin palmitate (3). C. nelsonii extract afforded combretastatin A-1 (4), a mixture of combretastatin A-1-2′-O-β-D-glucopyranoside (5a) and combretastatin B-1-2′-O-β-D-glucopyranoside (5b). Compounds 1, 2, 4, 5a, and 5b were isolated for the first time from the plant species. C. glabrum extract showed good anticancer properties with LC₅₀ of 1.30 × 10³ µg/mL (CaCo-2) and 2790 µg/mL (MCF-7). Compound (1) exhibited high toxicity against the Caco-2 at LC₅₀ of 24.3 µg/mL and moderate activity against MCF-7 at 48.4 µg/mL. Compound (4) and the mixture (5a and 5b) showed moderate activity against the MCF-7 at LC₅₀ 72.0 and 44.1 µg/mL, respectively. These findings highlight C. glabrum and C. nelsonii as promising sources of anticancer lead compounds. Full article