Search Results (2,720)

This study proposes an innovative silver-nanoparticle-assisted electrochemical etching method for the fabrication of porous silicon Bragg reflectors with multi-wavelength reflection characteristics. By introducing silver nanoparticles at varying concentrations (0.1–10 mg/mL) into the conventional HF–ethanol electrolyte and applying periodically modulated current densities (40/100 mA/cm²), the transition from single-peak to multi-peak reflection spectra was successfully achieved. The results demonstrate that at a concentration of 10 mg/mL silver nanoparticles, up to four distinct reflection bands can be obtained. A systematic investigation was conducted on the influence of etching cycles (4–20 cycles) and silver nanoparticle concentration on the optical performance and microstructure. SEM analysis revealed well-defined periodic multilayer structures, while XPS analysis confirmed the presence of metallic silver on the porous silicon surface. This work provides a simple, controllable, and cost-effective approach to the development of multifunctional photonic devices, with promising applications in laser optics, solar cells, chemical sensing, and surface-enhanced Raman scattering. Full article

Background: The human acellular amniotic membrane (HAAM) is widely used as a decellularized bioscaffold in tissue engineering to promote wound healing, but its clinical application is limited by poor mechanical properties, rapid degradation, and handling difficulties. This study aimed to develop a modified amniotic membrane-based composite material loaded with vascular endothelial growth factor (VEGF) and the Notch signaling inhibitor N-[N-(3,5-difluorophenacetyl)-Lalanylhydrazide]-Sphenylglycine t-butyl ester (DAPT) to enhance wound healing by modulating macrophage polarization and cytokine secretion. Methods: VEGF-loaded gellan gum-hyaluronic acid (GG-HA) hydrogels (VEGF-GG-HA) and DAPT-loaded HAAM (DAPT-HAAM) were prepared and combined to form a novel composite material (VEGF-GG-HA & DAPT-HAAM). The morphology and microstructure of the materials were characterized using scanning electron microscopy. In vitro studies were conducted using the human monocytic cell line (Tohoku Hospital Pediatrics-1, THP-1) to evaluate the effects of the materials on cell viability, cytokine secretion, and protein expression. Assessments included CCK-8 assays, ELISA, quantitative real-time PCR, Western blot analysis, and immunohistochemical staining. Results: The composite material VEGF-GG-HA & DAPT-HAAM exhibited good biocompatibility and significantly promoted THP-1 cell proliferation compared to control and single-component groups. It enhanced the secretion of IL-10, TNF-α, TGF-β, MMP1, and MMP3, while suppressing excessive TGF-β overexpression. The material also modulated macrophage polarization, showing a trend toward anti-inflammatory M2 phenotypes while maintaining pro-inflammatory signals (e.g., TNF-α) for a balanced immune response. Conclusions: The modified amniotic membrane hydrogel composite promotes wound healing through a phased immune response: it modulates macrophage polarization (balancing M1 and M2 phenotypes), enhances cytokine and matrix metalloproteinase secretion, and controls TGF-β levels. These effects contribute to improved vascular remodeling, reduced fibrosis, and prevention of scar formation, demonstrating the potential for enhanced wound management. Full article

Reliable methods for the isolation and culture of human eccrine sweat gland cells (SGCs) are essential for studying glandular biology and developing tissue-engineered skin substitutes (TESs) that restore full skin function. However, maintaining the glandular phenotype of SGCs in vitro remains a major challenge. In this study, we present an optimized isolation protocol combining enzymatic digestion with mechanical separation to improve SGC yield and purity, while also enabling keratinocyte isolation from a single human skin biopsy. We then evaluated two culture strategies, 2D monolayers and 3D spheroids, to determine their impact on SGC identity and proliferation. While 2D culture supported cell expansion, SGCs and keratinocytes exhibited highly similar marker expression profiles, with the absence of functional SGC markers (AQP5, α-SMA) reflecting a shift toward less differentiated phenotypes. In contrast, SGCs cultured in 3D spheroids preserved the expression of SGC-specific markers (AQP5, K18, α-SMA), distinguishing them from keratinocytes; however, their growth and structural organization were suboptimal under these 3D conditions. Moreover, SGCs expanded in 2D did not regain their glandular features when reintroduced into 3D culture, suggesting potential limitations in phenotype recovery. These results highlight the need for improved culture systems that maintain SGC identity while supporting expansion. Advancing such methods is a critical step toward integrating functional sweat glands into TESs and achieving complete skin regeneration for clinical applications. Full article

Three-dimensional (3D) hepatic tissue engineering holds great potential for liver regeneration, disease modeling, and drug screening. These applications require densely layered hepatic tissues that mimic native 3D liver architecture. However, limited oxygen supply and reduced cell viability in densely layered hepatic constructs remain key challenges. To overcome this, this study developed a photo-crosslinkable, oxygen-releasing hydrogel composed of methacrylated hyaluronic acid (MeHA) and calcium peroxide (CPO). The MeHA/CPO hydrogel exhibited favorable rheological properties and sustained oxygen release. Induced pluripotent stem cell-derived hepatocyte (iHep) sheets were cultured with or without MeHA/CPO hydrogel in single- and double-layer formats. The hydrogel enhanced structural integrity and supported the formation of a multilayer (~33 µm). Double-layered iHep sheets with MeHA/CPO showed the significantly increased expression of paracrine factors (HGF, VEGF, Alb) and improved albumin secretion without loss of hepatocyte identity (AFP, HNF4α). This oxygen-releasing system effectively alleviates hypoxic stress, supporting the structural and functional viability of multilayered iHep sheets. Our platform provides a promising approach for engineering metabolically active hepatic tissues and may serve as a foundation for 3D hepatic tissue engineering. Full article

Rigid–flexible coupled robots hold significant potential for operating in unstructured environments, but a systematic analysis of their actuation strategies across diverse physical fields is notably lacking in the literature. This review addresses this gap by introducing a novel taxonomy based on field-controlled evolutionary pathways—mechanical → electromagnetic → chemical → biohybrid—and critically examining over 100 seminal studies through a six-dimensional framework encompassing design, dynamics, and performance. We demonstrate that hybrid field integration (e.g., pneumatic-chemical synergy) improves grasping robustness by 40% in cluttered environments compared to single-field systems. Notably, biohybrid actuators, which integrate living cells, exhibit over 90% motion similarity to biological models, while phase-transition materials allow for adaptive stiffness tuning (0.1–5 N·mm⁻¹) in medical applications. Radar chart analysis further reveals fundamental trade-offs between energy efficiency, response speed, and scalability across the various fields. These insights provide a clear roadmap for the development of next-generation robots with embodied intelligence, emphasizing multi-field synergies and bio-inspired adaptability. Full article

Patchoulene, the characteristic sesquiterpene of patchouli essential oil, is highly valued in the perfume industry for its distinctive woody note and fixative properties. Beyond its olfactory applications, patchoulene has demonstrated promising biological activities, including anti-inflammatory, antimicrobial, and neuroprotective effects. Current production relies mainly on extraction from Pogostemon cablin plants, which requires long growth cycles (≥8 months), exhibits low yields, and imposes significant environmental constraints. To overcome these limitations, this study aimed to enhance the Whole-cell yield of patchoulene synthase (PcPTS) through structure-informed protein engineering. A semi-rational design approach was employed, combining homology modeling, molecular docking, evolutionary analysis, and molecular dynamics simulations to identify functional residues within the enzyme active site. Ala-scanning mutagenesis highlighted Thr532 as essential for catalytic activity, and coevolutionary analysis indicated synergistic effects between Phe456 and Thr532. Site-directed mutagenesis was conducted to generate single (F456M, T532Y) and double (F456M/T532Y, designated M2) mutants. The double mutant M2 showed a 3.62-fold increase in patchoulene production compared to the wild-type enzyme. In silico analyses suggested that the enhanced performance of M2 originates from improved substrate positioning, reduced structural flexibility, and strengthened molecular interactions, collectively contributing to a lower energy barrier for catalysis. This study provides an effective strategy for the rapid optimization of terpenoid synthases and facilitates the development of microbial cell factories for sustainable and high-yield production of plant-derived terpenoids. Full article

The search for alternatives to fossil fuels has led to hydrogen becoming an important factor in the powering means of transportation. Its most effective application is in fuel cells. A single fuel cell is not a sufficient source of power, which is why a stack of fuel cells is the more common solution. Fuel cells are tested using single units, as this allows all cell parameters (the current density, flow rates and efficiency) to be evaluated. Therefore, the scalability of fuel cells is an essential factor. This paper analyses the scalability of fuel cells with a power of approximately 100 kW and 1.2 kW. Road tests of the fuel cells were compared with stationary tests, which allowed the load to be reproduced and scaled. This provided a representation of the scaled current and the scalable power of the fuel cell. The research provided voltage–current characteristics of fuel cell stacks and their individual equivalents. It was concluded that regardless of the power scaling or current values, the characteristics obtain similar patterns. A very important element of the research is the awareness of the properties of these cells (the number of cells and active charge exchange area) in order to compare the unit characteristics of fuel cells. Full article

Persistent Enterococcus faecalis infections represent a major cause of endodontic treatment failure, highlighting the need for innovative disinfection strategies beyond conventional irrigation. This in vitro study evaluated the antimicrobial potential of pulsed electric fields (PEF) as a non-thermal and non-chemical adjunctive method for root canal disinfection. Fifty-two extracted mandibular premolars with single canals were standardized to 16 ± 0.1 mm, inoculated with E. faecalis, and incubated for 28 days to establish mature biofilms. The teeth were subsequently exposed to PEF under varying electrical parameters using sterile water as the irrigant, and bacterial viability and metabolic activity were assessed post-treatment. Confocal laser scanning microscopy (CLSM) was performed to visualize bacterial distribution within dentinal tubules, with particular attention to the apical region, which is most resistant to disinfection. PEF application significantly reduced bacterial viability and metabolic activity compared with baseline (p < 0.05), although complete elimination was not achieved. CLSM images revealed both red-stained non-viable cells, reflecting irreversible electroporation, and green-stained viable cells, indicating reversible electroporation and residual bacterial survival. These findings demonstrate that PEF can inactivate microorganisms through electroporation while maintaining tissue compatibility, and its antimicrobial effect may be enhanced when combined with sodium hypochlorite. Optimization of electrical parameters and evaluation in polymicrobial biofilm models are warranted to establish clinical relevance and support translation into practice. Full article

Lipids are spatiotemporally organized in cell membranes, where they play indispensable roles in regulating diverse biological processes. Their distribution and dynamics are intricately coupled to signal transduction, membrane trafficking, and host–pathogen interactions. The past decade has seen substantial progress in the development of lipid probes and imaging techniques, which have greatly advanced our understanding of lipid-mediated regulation in living cells. Chemically optimized lipid analogs conjugated with hydrophilic fluorophores have enabled the faithful visualization of raftophilic lipids, such as sphingomyelin, gangliosides, and cholesterol, while minimizing artifacts. In parallel, genetically encoded lipid sensors derived from lipid-binding protein domains have been established. These sensors selectively report the localization and dynamics of diverse lipid species, including phosphoinositides, cholesterol, sphingomyelin, and phosphatidylserine, in their native contexts. Combined with state-of-the-art advanced microscopy approaches, including ultrafast single-molecule imaging and super-resolution microscopy, these probes facilitate high-resolution and quantitative analyses of lipid organization. This review summarizes recent advances in both synthetic lipid probes and genetically encoded lipid sensors, emphasizing their applications in mechanistic studies of membrane biology. We further discuss current challenges and future directions toward the comprehensive and minimally perturbative visualization of lipids. Full article

Cell-based therapeutics are redefining interventions for vision loss by enabling tissue replacement, regeneration, and neuroprotection. This review surveys contemporary cellular strategies in ophthalmology through the lenses of therapeutic effectiveness, translational readiness, and governance. We profile principal sources—embryonic and induced pluripotent stem cells, mesenchymal stromal cells, retinal pigment epithelium, retinal progenitor and limbal stem cells—and enabling platforms including extracellular vesicles, encapsulated cell technology and biomaterial scaffolds. We synthesize clinical evidence across age-related macular degeneration, inherited retinal dystrophies, and corneal injury/limbal stem-cell deficiency, and highlight emerging applications for glaucoma and diabetic retinopathy. Delivery routes (subretinal, intravitreal, anterior segment) and graft formats (single cells, sheets/patches, organoids) are compared using standardized structural and functional endpoints. Persistent barriers include GMP-compliant derivation and release testing; differentiation fidelity, maturation, and potency; genomic stability and tumorigenicity risk; graft survival, synaptic integration, and immune rejection despite ocular immune privilege; the scarcity of validated biomarkers and harmonized outcome measures and ethical, regulatory, and health-economic constraints. Promising trajectories span off-the-shelf allogeneic products, patient-specific iPSC-derived grafts, organoid and 3D-bioprinted tissues, gene-plus-cell combinations, and cell-free extracellular-vesicle therapeutics. Overall, cell-based therapies remain investigational. With adequately powered trials, methodological harmonization, long-term surveillance, scalable xeno-free manufacturing, and equitable access frameworks, they may eventually become standards of care; at present, approvals are limited to specific products/indications and regions, and no cell therapy is the standard of care for retinal disease. Full article

Efficient control of HIV-1 infection relies on highly active antiretroviral therapy (HAART). However, this therapy is not curative and requires continuous drug administration. Application of HIV-1 defective interfering particles (DIPs), engineered with ablations in key viral protein expressions (e.g., Tat, Rev, Vpu, and Env), suggests a therapeutic potential transforming them into Therapeutic Interfering Particles (TIPs). A recent animal HIV model study in non-human primates reports a substantial reduction in viral load after a single intravenous injection of TIPs. In contrast, human clinical trials demonstrate no beneficial effect of defective interfering particles (DIPs) in people living with HIV-1. This discrepancy highlights the importance of further investigation of HIV-TIP interactions. A quantitative view of intracellular replication for HIV-1 in the presence of TIPs is still missing. Here, we develop a high-resolution mathematical model to study various aspects of the interference of a specific engineered TIP-2 particle characterized by a 2.5-kb deletion in the HIV pol-vpr region with HIV-1 replication within infected CD4+ T cells. We define the conditions in terms of the number of homozygous HIV-1 virions and TIP-2 particles that enable the reduction of the wild-type virus replication number to the value of about one. The deterministic model predicts that at a ratio of 1 HIV-1 to 10 TIP-2 particles, the infected cell still produces some viruses, although in a minor quantity, i.e., about two virions per cycle. Pre-activation of the interferon type I (IFN-I) system results in a complete block of HIV-1 production by TIP-2 co-infected cells. Overall, the modelling results suggest that to improve the effectiveness of TIPs in reducing HIV infection, their combination with other types of antiviral protection should be considered. Our results can be used in the development of combination therapy aimed at treating HIV-1 infection. Full article

The introduction of Maritime Autonomous Surface Ships (MASS) and the accelerating digitalization of ports require precise and dynamic analysis of traffic conditions. However, conventional marine traffic analyses have been limited to low-resolution grids and static density visualizations without fully integrating vessel direction and speed. To address this limitation, this study proposes a traffic flow visualization model that incorporates dynamic maritime traffic structure. The model integrates density, dominant direction, and average speed into a single symbol, thereby complementing the limitations of static analyses. In addition, high-resolution grids of approximately 90 m were applied to enable detailed analysis. AIS data collected between 2022–2023 from the coastal waters of Mokpo, South Korea, were preprocessed, aggregated into grid cells, and analyzed to estimate representative directions (at 10° intervals) as well as average speeds. These results were visualized through color, thickness, length, and direction of arrows. The analysis showed high-density, low-speed traffic patterns and starboard-passage behavior in port approaches and narrow channels, while irregular directions with low density were observed in non-standard routes. The proposed model provides a visual representation of dynamic traffic structures that cannot be revealed by density maps alone, thus offering practical applicability for MASS route planning, VTS operation support, and risk assessment. Full article

Wharton’s Jelly-derived mesenchymal stem cell (WJ-MSC) secretome contains diverse bioactive factors with potential for skin regeneration, but its clinical efficacy is limited by poor transdermal delivery. In this study, we developed a dual-delivery system by nanoencapsulating WJ-MSC secretome and coating it onto marine sponge-derived spicules. Physicochemical characterization, in vitro assays (fibroblast and keratinocyte proliferation, keratinocyte migration, type I procollagen secretion, and antioxidant activity), and in vivo penetration studies were conducted. A single-arm clinical trial evaluated dermal absorption, pore characteristics, skin texture, wrinkles, and pigmentation following topical application. Transdermal penetration efficiency was significantly higher in the nano-coated spicule group than in the uncoated secretome control. In vitro, secretome treatment promoted fibroblast and keratinocyte activity, accelerated wound closure, and increased collagen synthesis. Clinically, a single application enhanced dermal absorption and significantly reduced pore number, while two weeks of treatment decreased wrinkles and pigmentation. Spicule-based nanoencapsulation effectively overcomes the skin barrier, enhances the regenerative activity of WJ-MSC secretome, and induces measurable clinical improvements in skin rejuvenation. This platform represents a promising cosmetic and therapeutic strategy in dermatology. Full article

Limited access to electricity and high levels of CO₂ emissions—over 35 billion metric tons in recent years—highlight the urgent need for sustainable energy solutions, particularly in rural areas dependent on polluting fuels. To address this challenge, three single-chamber microbial fuel cells (MFCs) with carbon anodes and zinc cathodes were designed and operated for 35 days in a closed circuit. Voltage, current, pH, conductivity, ORP, and COD were monitored. FTIR-ATR spectroscopy (range 4000–400 cm⁻¹) was applied to identify structural changes, and polarization curves were constructed to estimate internal resistance. The main FTIR peaks were observed at 1027, 1636, 3237, and 3374 cm⁻¹, indicating the degradation of polysaccharides and hydroxyl groups. The maximum voltage reached was 0.961 ± 0.025 V, and the peak current was 3.052 ± 0.084 mA on day 16, coinciding with an optimal pH of 4.977 ± 0.058, a conductivity of 194.851 ± 2.847 mS/cm, and an ORP of 126.707 ± 6.958 mV. Connecting the three MFCs in series yielded a total voltage of 2.34 V. Taxonomic analysis of the anodic biofilm revealed a community dominated by Firmicutes (genus Lactobacillus: L. acidophilus, L. brevis, L. casei, L. delbrueckii, L. fermentum, L. helveticus, and L. plantarum), along with Bacteroidota and Proteobacteria (electrogenic bacteria). This microbial synergy enhances electron transfer and validates the use of carrot waste as a renewable source of bioelectricity for low-power applications. Full article

Dendritic cells (DCs) are the most highlighted cell population for cancer immunotherapy development. Currently, DC-derived exosomes show promising anti-cancer activity. Exosomes are a subpopulation of extracellular vesicles (EVs) and originate from endosomes. It transports dynamic molecular cargos such as DNA, RNA, protein, and lipid. This cellular cargo exchange reprograms the recipient cell naturally. In cancer research, DC-derived exosomes (DEXs) are used as a therapeutic tool. There are some approaches followed in the application of DEX in cancer as a therapeutic tool. DEX-based drug delivery, tumor antigen-loaded DEX, and modified DEX are applicable approaches in cancer therapy. DEXs are biocompatible, nontoxic, and have ability-specific targeting. On the other hand, this method faces some challenges, such as large-scale production, isolation, and heterogeneity. A multidisciplinary approach (advanced nanotechnology, multi-omics, and single-exosome profiling) comes up with a solution to this issue. This review provides a comprehensive overview of the DEX approach, tracing its developmental journey and therapeutic application in cancer immunotherapy. It examines key findings from clinical trials and outlines the challenges and future research directions in this field, ultimately underscoring the potential of DC-derived exosomes as a research-backed, cell-free solution for the next generation of cancer immunotherapies. Full article