Background: Hair drying is a routine cosmetic practice; however, excessive heat exposure and non-uniform airflow can compromise cuticle integrity, degrade hair sensory properties, and induce scalp discomfort. This study aimed to (i) identify a practical thermal window that minimizes perturbation of hair fiber surface and quantify late-stage thermal amplification during the drying process using percentage-based analysis. Methods: Temperature-dependent hair fiber surface morphology was examined by scanning electron microscopy (SEM) after controlled exposure to 41°C, 60°C, 80°C, and 90°C using virgin and chemically damaged hair. The drying efficacy was assessed using the surface and internal moisture indices under airflow shaping (test) and uniform airflow (control) conditions. Hair fluttering (maximum angular displacement) was evaluated before and after drying under warm-cool alternating (60°C-80°C) versus constant hot airflow (80°C). Results: SEM revealed temperature-dependent cuticle disruption, with markedly greater surface perturbation at 90°C than at 80°C. Infrared thermography demonstrated pronounced late-stage thermal amplification: at 150 seconds, the surface temperature increased by 295% (from 24.2°C to 72.0°C) at 90°C, compared with 207% (from 24.2°C to 50.7°C) at 80°C. Airflow shaping promoted preferential surface moisture removal (–13.6%) while limiting internal dehydration (–9.4%), whereas the control condition exhibited minimal surface drying (–4.6%) but substantial internal moisture loss (–22.2%). Warm-cool modulation increased hair fluttering by +11.0%, whereas constant hot airflow reduced it (–3.7%). Conclusion These findings indicate that spatial and temporal control of heat delivery represents a clinically relevant design strategy beyond the nominal temperature specification in hair-drying devices.

Background: This study examined the effects of electroporation (EP) and sonophoresis (SP) on the skin permeation of various ingredients and the resulting changes in skin properties. Methods: Twenty participants used whitening and hyaluronic ampoules as adjunctive cosmetics. The intervention group used an EP with an SP device for application while the control group used their hands, both groups over a 4-week period. The outcomes measured included skin elasticity, gloss, pores, tone, and soothing.In addition, this study determined the absorption amount, absorption rate, and skin permeation of the cosmetic ampoules 30 minutes after applying the cosmetics in a clinical test. Results: Significant improvements in skin hydration, elasticity, tone, and pigmentation were observed in the intervention group. In particular, the most pronounced effects were observed immediately after use. In addition, application with EP and SP led to a more than 200% increase in the absorption amount, absorption depth, and absorption speed of cosmetics compared to hand application. Conclusion These findings suggest that simultaneous EP and SP significantly enhance skin permeability and cosmetic absorption, improving skin properties.

Background: The delivery of desired drugs through the skin can enhance the effectiveness of cosmetic treatments and further enhance skin recovery and collagen regeneration. This study evaluated the potential of a device to achieve noninvasive transdermal drug delivery using simultaneous electroporation (EP) and lowfrequency sonophoresis (SP). Methods: The percutaneous absorption after applying the device that administered EP and SP was evaluated using an ex vivo porcine skin model. Porcine skin tissue was placed on a polyurethane foam dressing impregnated with 3% povidone-iodine (PI). Four drops of ampoule were applied, and the device was applied to the skin for 3 minutes. The reaction between the penetrated whitening agents and 3% PI, indicated by color changes, was analyzed using an Antera 3D camera. Results: The simultaneous application of EP with SP to skin tissue at a specific ratio for 3 minutes resulted in a significant increase in the area that reacted with iodine after skin penetration. The results showed that exposure to hyaluronic acid ampoule (HAA) increases type I collagen synthesis in human dermal fibroblasts in a concentration- and time-dependent manner. In addition, treatment with HAA combined with the application of EP with SP increased cell proliferation and significantly increased type I collagen levels in human dermal fibroblasts, with device-assisted synthesis showing greater efficiency. Conclusion These results suggest that simultaneous EP and SP efficiently deliver large molecules, such as hyaluronic acid, deep into the skin without causing skin damage.

Background: Excessive heat from household styling devices denatures α-keratin, damages the cuticle, and degrades overall hair quality. Conventional blow-dryer temperatures often exceed 90°C, surpassing the safety threshold for keratin fibers. To determine whether combining focused airflow with rapid thermal cycling (peak temperatures ≤60°C) attenuates multiscale hair damage compared with continuous-heat drying. Methods: Human-hair tresses were assigned either to a focused-flow dryer operating in alternating cool/warm cycles or to a continuous-heat mode. Jet characteristics were quantified using planar particle-image velocimetry, and airflow temperatures were recorded using micro-thermocouples. Post-treatment analyses included scanning electron microscopy (cuticular surface roughness, Ra), single-fiber tensile testing, crosssectional densitometry (fiber compactness), and confocal Raman spectroscopy (α-helix/disulfide bond integrity). Results: Thermal cycling with focused airflow increased the central-core flow fraction from 37% to 64% and confined hair-surface peaks to 58°C-60°C. Alternating hot-cold drying reduced cuticlar surface roughness by approximately 7.3%, whereas continuous hat air drying increased roughness by 4.9%. Ultimate tensile strength was essentially preserved (–0.4%) under cycling but fell by 9.4% with uninterrupted heat (p = 0.003).Compactness loss was limited to 33% vs. 50%, and the S-S disulfide bond (~510 cm –1 )/C-H bending vibration band (~720 cm –1 ) ratio decreased by only 11% (vs. 19% under continuous heat). Conclusion Brief cooling intervals, when paired with a confined airflow, effectively prevented α-keratindenaturation and structural collapse. These findings support a clinically relevant approach to preserving hairfiber integrity during routine hair care and styling.

Background: We aimed to clarify the safety and efficacy of simultaneous skin exposure to blue, red, and infrared light. The purpose of this study was to confirm the mechanism by which multiple wavelengths increase hair development both in vivo and in vitro. Methods: Cultured human dermal papilla cells (hDPCs) were exposed to a 470/655/850 nm light-emitting diode (LED) array with a fixed energy density of 3.0 mW/cm 2 . We analyzed alkaline phosphatase (ALP) staining and activity. The relative expressions of ALP, VEGF, Shh, and OPN3 were examined using reverse transcriptasepolymerase chain reaction arrays 48 hours post-exposure and the protein levels related to extracellular signalregulated kinase (ERK)/protein kinase B (AKT)/glycogen synthase kinase 3 (GSK3)β signaling were assessed by western blotting. Next, we used H&E staining, hair growth scoring, skin thickness measurement, and the immunohistochemical analysis of the dorsal skin of C57BL/6 mice to investigate the effects of the mono- or combined-photobiomodulation (PBM) groups. Results: According to our findings, simultaneous irradiation with multi-wavelength LEDs at 470/655/850 nm increased the proliferation of hDPCs. Also, compared to the control group, the red wavelength and combined PBM groups had significantly improved skin thickness measurements. Overall, we concluded that the combined PBM therapy successfully induced the early onset of anagen and stimulated hair growth. Conclusion These results suggest that PBM therapy regulates hair growth by activating the ERK/AKT/GSK3βsignaling pathway. Thus, multiple-wavelength radiation from devices combining radiation emitted by lowpower lasers and LEDs could be a new approach for promoting PBM-induced beneficial effects.

Many of the fungicides and antibiotics currently available against plant pathogens are of limited use due to the emergence of resistant strains. In this study, we examined the effects of diphenyleneiodonium chloride (DPIC), an inhibitor of the superoxide producing enzyme NADPH oxidase, against fungal and bacterial plant pathogens. We found that DPIC inhibits fungal spore germination and bacterial cell proliferation. In addition, we demonstrated the potent antibacterial activity of DPIC using rice heads infected with the bacterial pathogen Burkholderia glumae which causes bacterial panicle blight (BPB). We found that treatment with DPIC reduced BPB when applied during the initial flowering stage of the rice heads. These results suggest that DPIC could serve as a new and useful antimicrobial agent in agriculture.
Agriculture ; Anti-Bacterial Agents ; Burkholderia ; Cell Proliferation ; Flowers ; Germination ; Head ; NADPH Oxidase ; Plants ; Spores, Fungal ; Superoxides

We identified two genes related to fungicide resistance in Fusarium fujikuroi through random mutagenesis. Targeted gene deletions showed that survival factor 1 deletion resulted in higher sensitivity to fungicides, while deletion of the gene encoding F-box/WD-repeat protein increased resistance, suggesting that the genes affect fungicide resistance in different ways.
Fusarium* ; Gene Deletion ; Mutagenesis

Cylindrocarpon destructans causes root rot disease in ginseng and can survive for a long time, producing chlamydospores. We optimized conditions to induce chlamydospore production from the conidia of C. destructans, isolated from Korean ginseng. This will provide the basis for testing the efficacy of control agents targeting these chlamydospores.
Korea* ; Panax* ; Spores, Fungal*

Fruiting bodies similar to those of the ascomycete fungi Podostroma cornu-damae and Cordyceps militaris were collected from Mt. Seunghak in Busan, Korea on August 21, 2012. The fruiting bodies were cylindrical, with tapered ends and golden red in color. The fruiting bodies contained abundant conidiophores bearing single-celled conidia, but no perithecia or asci. Pure culture of the fungal isolates was obtained through single-spore isolation. Analyses of morphological characteristics, including conidia shape, and phylogenetic traits, using internal transcribed spacer sequences, showed that these isolates belonged to the species Simplicillium lanosoniveum. Although this fungal species is known to be mycoparasitic, the isolates obtained in this study were unable to infect fungi. However, silkworms (Bombyx mori) inoculated with the fungal isolates died during the larval or pupal stages, as has been shown for the strongly entomopathogenic fungus Beauveria bassiana. This study is the first report of the entomopathogenicity of S. lanosoniveum and indicates its potential for use in biological control of insects.
Ascomycota ; Beauveria ; Bombyx ; Busan ; Cordyceps ; Fruit ; Fungi ; Insects ; Korea ; Spores, Fungal

The typical life cycle of filamentous fungi commonly involves asexual sporulation after vegetative growth in response to environmental factors. The production of asexual spores is critical in the life cycle of most filamentous fungi. Normally, conidia are produced from vegetative hyphae (termed mycelia). However, fungal species subjected to stress conditions exhibit an extremely simplified asexual life cycle, in which the conidia that germinate directly generate further conidia, without forming mycelia. This phenomenon has been termed as microcycle conidiation, and to date has been reported in more than 100 fungal species. In this review, first, we present the morphological properties of fungi during microcycle conidiation, and divide microcycle conidiation into four simple categories, even though fungal species exhibit a wide variety of morphological differences during microcycle conidiogenesis. Second, we describe the factors that influence microcycle conidiation in various fungal species, and present recent genetic studies that have identified the genes responsible for this process. Finally, we discuss the biological meaning and application of microcycle conidiation.
Fungi* ; Germination ; Hyphae ; Life Cycle Stages ; Spores ; Spores, Fungal