Search Results (1,613)

Light-converting polymer coatings and films are emerging passive photonic materials for spectral engineering in sustainable and protected agriculture. By absorbing ultraviolet or weakly used spectral components and re-emitting in visible bands that overlap with photosynthetic pigments and plant photoreceptor action regions, these materials can modify the radiation environment without additional electrical energy input. This critical narrative review analyses light-converting polymer films and coatings from a materials and coatings perspective, with emphasis on photophysical mechanisms, polymer matrices, luminophore families, coating fabrication routes, optical transparency, photoluminescence, aggregation phenomena, photostability and scalability. The photobiological background is included as a concise framework that justifies the spectral targets of the conversion process. Rare-earth complexes, inorganic phosphors, quantum dots, aggregation-induced-emission systems and organic dyes are compared as candidate luminophores. Particular attention is devoted to the general challenges associated with organic luminescent coatings, including dispersion, aggregation, optical transparency, photostability, and scalability. A PMMA/PDI coating system is discussed only as an illustrative case study demonstrating these broader materials-design considerations. Extrusion, solution casting, spin-coating, dip-coating and sol–gel processing are evaluated as fabrication strategies for laboratory and large-area greenhouse applications. The work concludes by identifying the main gaps that must be addressed before practical deployment: quantitative UV–Vis and photoluminescence characterization, absolute quantum yield, haze and scattering, thickness and morphology mapping, accelerated UV aging, weathering resistance, toxicity assessment and crop-specific validation. Full article

Radiation-based treatments have emerged as important environmental and postharvest regulatory tools for improving the quality of edible mushrooms. Visible light, ultraviolet (UV) radiation, gamma irradiation, and pulsed-light treatments influence mushroom growth, morphogenesis, nutrient accumulation, antioxidant capacity, and storage performance through distinct physiological and molecular mechanisms. However, current findings remain fragmented, and a comprehensive synthesis of their regulatory effects and underlying mechanisms is lacking. This systematic review was conducted following the PRISMA 2020 framework. A structured literature search was performed in the Web of Science, PubMed, and CNKI databases. After screening and eligibility assessment, 111 studies were included in the qualitative synthesis. The available evidence indicates that radiation-based treatments exert stage-dependent and species-specific effects on edible mushrooms. Visible light primarily regulates morphogenesis through photoreceptor-mediated signaling pathways, whereas UV radiation promotes vitamin D₂ biosynthesis and antioxidant accumulation through photochemical and reactive oxygen species (ROS)-related mechanisms. Gamma irradiation and pulsed-light treatments are mainly applied during postharvest handling to suppress microbial contamination, delay browning and senescence, and extend shelf life. Based on the available evidence, a unified mechanistic framework linking signal perception, ROS regulation, transcriptional reprogramming, metabolic responses, and quality formation is proposed. Despite these advances, substantial challenges remain, including limited mechanistic understanding, insufficient integration of multi-omics evidence, lack of standardized treatment protocols, and difficulties in industrial-scale implementation. Future research should focus on multi-radiation synergistic strategies, precision environmental regulation, and intelligent cultivation systems. Overall, this review provides a comprehensive synthesis of current evidence regarding radiation-mediated quality regulation in edible mushrooms and offers a theoretical basis for optimizing mushroom production and developing sustainable postharvest preservation technologies. Full article

Ultraviolet (UV) light exposure is a recognised risk factor for dermal haemangiosarcoma (HSA) in dogs and dermal squamous cell carcinoma (SCC) in dogs and cats. These tumours cause substantial local disease and often require repeated surgery due to recurrence or de novo lesions, creating a notable welfare and financial burden. Research on preventing harmful UV exposure in pets is still in its infancy, particularly in relation to the safety of UV filters used in sunscreens. This review summarises the current evidence on UV-induced carcinogenesis, strategies to reduce UV exposure, and the safety of sunscreen ingredients in dogs and cats. UV light is strongly implicated in a range of dermatoses, from actinic keratosis to dermal HSA and SCC in dogs and cats, and the risk is likely higher in Australian pets. Indoor confinement during peak UV periods, shade, and sun-protective clothing can reduce exposure, with sunscreen an additional strategy. Sunscreen is relevant because UV-associated cancers typically develop in sparsely haired or hairless regions such as the nose and ventrum, making these areas suitable for targeted sunscreen application. Sunscreens containing non-nanoparticle zinc oxide appear safe for dogs and cats when ingestion is prevented or minimised, whereas the safety of organic UV filters remains unclear due to limited safety data in both humans and animals. Non-nanoparticle titanium dioxide is a possible alternative to zinc oxide and organic filters, but there is currently little information on its safety when ingested by dogs and cats. Overall, the available evidence supports sunscreen as a necessary component of UV-reduction strategies in pets, but substantial research is needed to determine the safety profiles of different UV filters and to establish evidence-based guidelines for their safe use. Full article

Advanced oxidation processes using titanium dioxide (TiO₂) have emerged as a promising approach for the photocatalytic degradation of contaminants in water and have drawn extensive research attention despite limited translation of this technology to large-scale applications. The limitations of this technology include immobilization of the photocatalyst, scalability, and compatibility with available light sources. Using 3D printing to immobilize TiO₂-based photocatalysts, we systematically evaluated the rates of photocatalytic degradation of methylene blue (MB) with different light-emitting diode (LED) ultraviolet (UV) light sources and modified TiO₂-based photocatalytic materials. The UV LED lights successfully decreased the MB concentrations with half-lives ranging from 0.9 to 2.4 h, with relative photocatalytic performance of UVA-365 > UVA-395 > UVC-280. The photocatalytic degradation rates under UV LEDs were slower (0.9–2.4 h) than those achieved using a low-pressure mercury UV-C lamp (0.5 h) and were also lower than those observed under solar simulated lights (0.6 h). The TiO₂ modified by an alkyl silane entity and embedded in a polylactic acid polymeric system with 3D printing exhibited the fastest methylene blue (MB) removal among the three TiO₂-based structures evaluated, with a half-life of 0.6 h compared to the 1.6–17.7 h for the other materials. This research demonstrated that 3D printing enables the integration of functionalized photocatalysts, and, when paired with low-cost, low-energy UV LED lights, can achieve environmentally relevant rates of performance. Ultimately, these findings represent an incremental step toward improving the performance of 3D-printed photocatalytic materials. Full article

Osseointegration is defined as the structural and functional integration between alveolar bone and a dental implant. Photo-functionalization (PF) refers to ultraviolet (UV)-induced surface modifications of titanium implants, including changes in physicochemical properties and biological responsiveness. The aim of this study was to evaluate the effects of PF on early osteoblast responses related to osseointegration on titanium dental implants in vitro. We hypothesized that PF applied to titanium implants enhances early osteoblast responses related to osseointegration. Sixteen titanium dental implants were divided into two equal groups of eight: untreated (PF−) and PF-treated (PF+). PF+ implants were exposed to UV light at 172 nm for 10 s. An additional cell-only control group was incubated without an implant. All groups were cultured in vitro with SAOS-2 human osteoblast-like cells. Cell proliferation and viability were assessed using standard in vitro assays, and DNA damage was evaluated using the Terminal deoxynucleotidyl transferase [TdT] dUTP Nick End Labeling (TUNEL) assay. Early cellular responses related to osseointegration were assessed by evaluating adhesion-related vinculin levels and alkaline phosphatase (ALP) activity. After 24 h of incubation, cell proliferation was comparable between the groups, whereas after 48 h, cell number was significantly lower in the PF− group compared with the PF+ group and the control group (p = 0.039). Osteoblast viability was significantly lower in the PF− group than in the control group (53% vs. 94%, p = 0.002), while the PF+ group showed a numerically higher viability value than the PF− group (70% vs. 53%). TUNEL assay showed no statistically significant difference in DNA damage among the groups, although the PF− group showed a slightly higher TUNEL-positive cell ratio (p = 0.563). Vinculin levels were significantly higher in the PF+ group at both 24 and 48 h compared with the PF− group and control group (p < 0.0001). ALP activity increased significantly over time in cells incubated with PF-treated implants (p < 0.0001). Within the limitations of this exploratory pilot in vitro study, UV photo-functionalization was associated with more favorable early osteoblast-like cell responses on titanium dental implants, particularly in terms of proliferation, adhesion-related vinculin levels, and ALP response. PF did not increase TUNEL-positive cell ratios compared with untreated implants under the present experimental conditions. These findings should be interpreted as preliminary biological evidence and require confirmation through larger experimental designs, detailed physicochemical surface characterization, and in vivo validation. Full article

The oral cavity harbors a complex microbial community where pathogens implicated in dental caries and periodontitis can heavily colonize toothbrushes, transforming them into persistent sources of contamination that threaten both oral and systemic health. Consequently, this study evaluated the bactericidal efficacy of 275 nm ultraviolet light-emitting diode (UV-LED) irradiation against common oral bacteria in vitro and its practical utility for extraoral toothbrush sanitization. Suspensions of Streptococcus mutans, Streptococcus sanguinis, Porphyromonas gingivalis, and Fusobacterium nucleatum were irradiated for 3 min, 6 min, and 9 min. Bacterial growth and bactericidal effects were measured using growth curve and colony-forming unit assays, respectively. LIVE/DEAD staining and crystal violet staining were used to evaluate the bacterial viability and multispecies biofilm formation after irradiation. Additionally, the sanitization effects of a 275 nm UVC-based portable device on used toothbrushes were investigated. Direct UVC irradiation at 275 nm exhibited strong bactericidal effects against common oral bacteria in vitro. UVC irradiation also showed great sanitization effects on used toothbrushes. In summary, the vulnerability of common oral bacteria to 275 nm UVC, combined with its sanitizing efficacy on used toothbrushes, establishes a solid basis for extraoral sanitization, offering a reliable strategy to mitigate the risk of oral pathogen transmission from contaminated toothbrushes. Full article

Protein kinases have key roles in cells as they regulate diverse signal transduction pathways. Mitogen-activated protein kinase (MAPK) signaling route modulates several processes, such as cell proliferation, cell programming, metabolic changes and stress responses. Within the group of proteins participating in this pathway, the MAPK kinase (MEK1) is a dimeric, 393-residue-long, dual-specificity protein kinase that phosphorylates both tyrosine and threonine residues. In this study, we explored the conformational changes occurring during the unfolding of MEK1, by using orthogonal biophysical techniques. Intrinsic fluorescence, extrinsic 8-anilinonapthalene-1-sulfonic acid (ANS) fluorescence, dynamic light scattering (DLS), and far-ultraviolet (UV) circular dichroism (CD) showed that the protein acquired a native-like conformation within a narrow pH range (8.0 to 9.0). Urea and guanidinium hydrochloride (GdmCl) denaturations followed by intrinsic and ANS fluorescence and far-UV CD, at pH 8.1, where the protein acquired a native-like conformation, showed that: (i) the apparent conformational stability of isolated MEK1 was low; and (ii) the unfolding occurred through the presence of intermediates. The presence of several unfolding intermediates was also evidenced through: (i) differential scanning calorimetry (DSC) in the absence of the ligand ATP; and (ii) unfolding simulations with the help of computational techniques based on constraint network analysis (CNA). We propose that the apparent low stability of this protein was related to its flexibility and modulates its ability to interact with diverse molecular partners. Full article

Conventional oxidative hair dyes rely on aromatic amines, raising concerns about human health and environmental safety. This study reports a natural hair-coloring system using size-controlled ink particles (SIPs, ~170 nm in diameter) from cuttlefish ink and chitosan. Because both SIPs and hair surfaces carry negative charges near neutral pH, original SIPs exhibited poor deposition onto hair. Polyelectrolyte complexation with chitosan reversed the SIP surface charge under acidic conditions (maximum ζ ≈ +41 mV at pH 2.4), enabling electrostatic deposition onto hair fibers. Dynamic light scattering (DLS) revealed pH-responsive aggregation at pH 1.6–1.8 and redispersion at pH 2.8–4.3, while ultraviolet–visible (UV–Vis) spectra confirmed that the broadband absorption of melanin was preserved, consistent with predominantly noncovalent interactions. Scanning electron microscopy (SEM) showed a particle-based composite coating on hair fibers. An optimal SIP:chitosan weight ratio of 10:1 at pH ~4.7 yielded the darkest and most uniform coloration (L* = 32.89, ΔE*_ab = 55.89) without metallic mordants, achieving darker coloration than representative plant-based natural colorants reported in the literature. These results demonstrate a marine-biomass-derived approach to natural black hair coloration with strong darkening performance. Full article

Ultraviolet (UV) light is emerging as an important tool for biosensing, biomedical signal readout, and dose monitoring because of its strong and selective interactions with nucleic acids, proteins, and other biological components. This review summarizes recent progress in UV sensing-guided biomedical systems, with emphasis on three interconnected directions: label-free and surface-weighted imaging, wearable and embedded UV dosimetry, and sensor-assisted therapeutic guidance. Representative examples include ultraviolet photoacoustic microscopy (UV-PAM) for label-free nuclear imaging, microscopy with ultraviolet surface excitation (MUSE) for rapid slide-free histology-like readout, epidermal and flexible UV dosimeters for skin-level exposure quantification, and UV therapeutic platforms that are increasingly supported by sensing, dosimetry, and feedback for safer dose delivery. Across these applications, we emphasize the shared biosensing principles of signal generation, optical or acoustic transduction, quantitative readout, calibration, and feedback-informed decision support. We also discuss the role of artificial intelligence in virtual staining, image enhancement, domain correction, dose prediction, and decision support. The review concludes with key translational challenges in standardization, uncertainty quantification, multimodal integration, and feedback-driven system design. Overall, this sensing-centered perspective helps define the role of UV technologies more clearly within biosensors-oriented biomedical engineering. Full article

High-power 355 nm ultraviolet (UV) lasers, leveraging their short wavelength, high photon energy, and high absorption across a broad range of materials, have become indispensable light sources for precision manufacturing, semiconductor processing, and laser direct imaging (LDI). In this paper, we demonstrate a high-power 355 nm UV laser system based on a narrow-linewidth polarization-maintaining (PM) Yb-doped fiber laser and cascaded frequency conversion. A single-frequency semiconductor laser is employed as the seed source, with its spectral linewidth broadened to 0.32 nm (full width at half maximum, FWHM) via phase modulation to suppress stimulated Brillouin scattering (SBS). Through a PM master oscillator power amplifier (MOPA) architecture, a maximum average output power of 899 W at 1064 nm is achieved with a beam quality factor of M² = 1.12 (M²_x = 1.11, M²_y = 1.13). By employing lithium triborate (LiB₃O₅, LBO) crystals for extracavity cascaded second-harmonic generation (SHG) and sum-frequency generation (SFG), a maximum green output power of 613.7 W at 532 nm is obtained, corresponding to a SHG conversion efficiency of 68.2%, and a maximum UV output power of 227.1 W at 355 nm is achieved, with a total conversion efficiency of 25.2%. At the maximum output power, the UV beam quality factors are M² = 1.16 (M²_x = 1.24 and M²_y = 1.09), and the power fluctuation is better than ±1.5% root-mean-square (RMS) over 8 h of continuous operation. These results indicate that the cascaded frequency conversion approach based on narrow-linewidth PM fiber lasers possesses the capability for further scaling to higher-power single-path high-brightness UV output and can provide high-brightness UV sources for applications such as flexible printed circuit (FPC) laser cutting, flat-panel display laser direct imaging, and semiconductor wafer scribing. Full article

The disinfection process in wastewater treatment is key to the discharge and/or reuse of high-quality effluent. However, disinfection using ultraviolet (UV) light may be inefficient because bacteria possess mechanisms for repairing damaged DNA. This study aimed to assess the photoreactivation and dark repair of total coliform (TC) in wastewater effluent after UV-C disinfection treatment. Four UV-C doses (28.8, 53.1, 57.6, and 106.2 mJ/cm²) and two post-irradiation conditions (light vs. darkness) were applied. Reactivation was monitored after 2, 4, 6 and 24 h (25 °C). Similar TC inactivation efficiencies were observed for the three lowest UV-C doses, whereas the 106.2 mJ/cm² dose achieved the greatest reduction (1.1 Log of TC), decreasing TC concentrations from 3.1 × 10⁵ ± 3.5 × 10⁵ to 1.2 × 10⁵ ± 1.4 × 10⁵ MPN/100 mL. Reactivation assays revealed substantial bacterial recovery after UV treatment, with 24 h survival rates up to 2.3 × 10³ under light and 9.2 × 10² in darkness. Photoreactivation and dark repair assays revealed substantial variability in bacterial recovery after UV treatment depending on UV-C dose, post-irradiation condition and incubation time. In general, bacterial recovery was still detected even at the 106.2 mJ/cm² dose, particularly after 24 h of incubation (178–604%). These findings suggest that effective organic matter removal before UV-C disinfection is critical to improve UV transmittance, reduce shielding effects, and limit subsequent bacterial recovery. Full article

Ascorbic acid plays an important role in the human body due to its antioxidant and anti-inflammatory properties, as well as its involvement in collagen synthesis, enzymatic regulation, and the biosynthesis of corticosteroids and selected neurotransmitters. Owing to these diverse functions, it is used both in the prevention and supportive treatment of several disorders and as a mild, non-toxic reducing agent in the synthesis of gold nanoparticles (AuNPs). In the present study, a method for synthesizing gold nanoparticles was developed using second-generation poly(amidoamine) dendrimers (PAMAM G2) with an ethylenediamine core as stabilizing agents and ascorbic acid as the reducing agent. The synthesis was performed using two techniques: sonication and microwave irradiation. A comparative analysis was conducted for colloidal systems obtained at various molar ratios of PAMAM G2 dendrimers to chloroauric acid (ranging from 1:1 to 1:5). The presence of gold nanoparticles was confirmed using ultraviolet–visible spectroscopy (UV–Vis). Nanoparticle diameters and zeta potentials were determined by dynamic light scattering (DLS). The sizes of the metallic cores were estimated using scanning transmission electron microscopy (STEM). Furthermore, the morphology and topography of entire complexes deposited on silicon substrates were visualized using atomic force microscopy (AFM). For cytotoxicity studies on human breast adenocarcinoma and human osteosarcoma cell lines, the most stable colloids—those obtained at a PAMAM G2:HAuCl₄ molar ratio of 1:3—were selected. Results indicate that the synthesized nanoparticles exhibit slightly higher cytotoxicity compared with AuNPs/PAMAM G2 complexes reduced with sodium citrate, as evidenced by lower EC₅₀ values (the concentration responsible for reducing cell viability to 50%). It should be emphasized, however, that AuNPs/PAMAM G2 reduced with ascorbic acid are significantly smaller, with diameters of approximately 10 nm, whereas citrate-reduced nanoparticles exhibit diameters of around 20 nm. These results indicate that nanoparticle size, rather than the chemical nature of the reducing agent, is a dominant factor governing the cytotoxic response of AuNPs/PAMAM G2 complexes. Full article

Green synthesis of gold nanoparticles is an effective approach to create biocompatible nanomaterials. In this study, gold nanoparticles (BC-AuNPs) were prepared by reducing chloroauric acid with black corncob (BC) extract at relatively low temperatures. The optimal preparation conditions were obtained through a single-factor experiment, which included 5 mL of black corncob extract and 0.12 mL of 3% HAuCl₄ solution at a pH of 5.0, and the reaction was carried out at 50 °C in a water bath for 3 h. The prepared BC-AuNPs were characterized by ultraviolet–visible (UV-Vis) spectroscopy, Fourier-transform infrared (FTIR) analysis, transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), dynamic light scattering (DLS), and Zeta-potential measurement, which showed that they were dispersed spherical particles with an average size of approximately 23.0 nm and their surfaces were covered with various black corncob active components. The photothermal performance test indicated a good photothermal effect with a conversion efficiency of 41.3%. Antibacterial experiments revealed that BC-AuNPs had excellent antibacterial activity. The minimum inhibitory concentrations (MICs) for E. coli and Salmonella were 25.00 and 50.00 µg/mL, respectively. Overall, this study proved a potential application for gold nanoparticles in photothermal antibacterial fields. Full article

The identification of the chemical species responsible for the anomalous near-ultraviolet (UV) opacity in the Venusian cloud for “unknown absorber” remains a paramount challenge in planetary science. This study presents a comprehensive quantum chemical investigation into a broad suite of candidate molecules, including isomers of thiosulfeno (S₂O₂), the hydroxysulfonyl radical (HSO₃), disulfur monoxide (S₂O), disulfur dichloride (S₂Cl₂), iron(III) chloride (FeCl₃), phosphine (PH₃), and structural isomers of polysulfur oxides (S₃O). Utilizing Time-Dependent Density Functional Theory (TD-DFT) at the CAM-B3LYP/def2-TZVPP level of theory, we systematically mapped electronic transitions across three distinct environmental phases: gas-phase (without solvent), supercritical CO₂, and concentrated H₂SO₄ aerosols. To establish confidence in the predicted results, our TD-DFT approach was rigorously benchmarked against high-level theoretical methods (CCSD(T), EOM-CCSD, and MRCI+Q) from recent literature. All these electronic transitions were modeled via the Solvation Model based on Density (SMD). Our results demonstrate a profound topological and environmental dependence on spectral signatures. Among the candidates, trans-OSSO (t-OSSO) emerged as the most viable near-UV absorber candidate, exhibiting a highly allowed π → π* transition at 379.37 nm (f = 0.1140) in H₂SO₄, providing a near-perfect alignment with the observed 365 nm planetary albedo drop. Conversely, the polysulfur oxide cis-S₃O was acknowledged as a primary visible-light chromophore, with an intense absorption at 436.31 nm (f = 0.1280) responsible for the characteristic yellow tint of the planet. Additionally, the photochemically maintained SSCl₂ isomer was identified as a critical broadband near-UV absorber. Species such as S₂O and planar S₃O were found to function as critical mid-UV shields (270–300 nm). This work establishes a multi-chromophore model of the Venusian atmosphere, where a chemically stratified network of sulfur-oxygen chains and chlorine-sulfur reservoirs, tuned by the acidic aerosol matrix, collectively governs radiative balance and atmospheric super-rotation of the planet. Furthermore, to account for massive continuum tailing into the visible region (>400 nm), we employed a semi-classical Reflection Principle approach to model 1D vibronic broadening. This analysis revealed that while standard solvent effects induce minor solvatochromic shifts, ground-state structural fluxionality in the OSSO isomers drives intense, symmetry-allowed transitions deep into the visible spectrum, an effect absent in structurally constrained or rigid control species. Full article

Stellar irradiation is thought to be a significant contributor to the origin of life. Ultraviolet (UV) light interacting with iron cyanide complexes may play an important role in prebiotic chemistry. The UV–Visible (UV–Vis) spectra of these iron cyanide complexes can be measured by the same source that drives the chemistry, providing a real-time in situ quantitative analysis of prebiotically relevant, UV-driven photochemistry. We measure the UV–Vis absorbances of ferrocyanide and nitroprusside, and relate these absorbances to known concentrations. We show that these absorbances can be combined to accurately predict the concentrations of ferrocyanide–nitroprusside mixtures that could be generated from ferrocyanide and nitroxyl salts irradiated by ultraviolet light. The ferrocyanide molar attenuation coefficients were found to be maximal at the following: ${\epsilon }_{ferrocyanide}\left(340\mathrm{nm}\right)=(2.2\pm 0.4)\times {10}^3{\mathrm{dm}}^2{\mathrm{mol}}^{-1}$. Nitroprusside peaks show the following values: ${\epsilon }_{nitroprusside}\left(340\mathrm{nm}\right)=(4.1\pm 0.3)\times {10}^2{\mathrm{dm}}^2{\mathrm{mol}}^{-1}$, ${\epsilon }_{nitroprusside}\left(400\mathrm{nm}\right)=(1.71\pm 0.05)\times {10}^2{\mathrm{dm}}^2{\mathrm{mol}}^{-1}$, and ${\epsilon }_{nitroprusside}\left(500\mathrm{nm}\right)=62.1\pm 1.7{\mathrm{dm}}^2{\mathrm{mol}}^{-1}$. With the help of our measured absorbances, we consider ferrocyanide and nitroprusside to function as sunscreens. In the absence of continuous ferrocyanide sources, UV-sensitive compounds could be protected on timescales of months. This would allow for compounds like nicotinamide adenine dinucleotide, NADH, to survive for over a year at depths of 5 m, compared to a lifetime of 6 months when unprotected. Our toy model constrains the photochemical survival of compounds of interest to the origin of life community across a comprehensive spectral range and can be used to constrain the survival using different exoplanetary irradiative conditions; thus, we are able to explore the UV environment with the presence of ferrocyanide and nitroprusside and contribute to the wider discussion surrounding the prevalence of the origin of life in the Universe. Full article