Search Results (876)

Background/Objectives: Wound healing requires simultaneous pain control, inflammation management, infection prevention, and tissue regeneration. This study aimed to develop and evaluate in vitro a non-contact thermosensitive spray hydrogel combining lidocaine for rapid analgesia and allantoin for tissue repair. Methods: The effects of chitosan and Poloxamer 407 on viscosity, spray diameter, and bioadhesion ability of hydrogels were optimized using response surface methodology. Lead formulations (S1 and S2) were selected via a desirability function within the software. The pH, gelation temperature (T_G), rheological behavior, sprayability, bioadhesion, and lidocaine release using the dialysis bag method were assessed. The in vitro cytotoxicity, anti-inflammatory activity (TNF-α), and cell migration (scratch assay) of the formulations were investigated. Results: The viscosity values (42.7–58.7 mPa·s) indicated suitability for spraying at room temperature. T_G was 28.7 ± 0.6 °C (S1) and 29.3 ± 0.3 °C (S2), enabling rapid sol–gel transition at skin temperature. The lidocaine release reached 95–100% within 120 min. S2 exhibited lower viscosity and wider spray diameter, improving applicability on larger wound areas. In vitro cytotoxicity, scratch assay, and inflammatory marker analyses demonstrated that the optimized sprayable hydrogels exhibited a biocompatible and cell-healing profile. Conclusions: The developed thermosensitive spray hydrogel enables the combined delivery of lidocaine and allantoin, rapid gelation at body temperature, and touch-free administration. Its suitable viscosity and sprayability, and fast lidocaine release profile indicate high patient compliance and a significant advantage over conventional cream/ointment formulations, particularly regarding painless application, reduced contamination risk, enhanced therapeutic potential, and confirmed in vitro biocompatibility with supportive effects on keratinocyte behavior. Full article

Polyethylene terephthalate-derived fluorescent carbon quantum dots (PET-CQDs) are promising nanomaterials for sensing and biomedical uses, yet their biological interactions after metal doping require careful evaluation. Here, we report an in silico assessment of pristine and dual-site (via graphitic [G] and carbonyl [O]) metal-doped PET-CQDs (Ca, Mg, Fe, Zn) using molecular docking against eight human proteins: HSA (distribution), CYP3A4 (metabolism), hemoglobin (systemic biocompatibility), transferrin (uptake), GST (detoxification), ERα (endocrine regulation), IL-6 (inflammation), and caspase-3 (cytotoxic signaling) together with ADMET profiling and DFT–docking correlation analysis. Docking affinities were compared with controls and ranged from −7.8 to −10.4 kcal·mol⁻¹ across systems, with binding stabilized by π–π stacking, hydrogen bonding and metal–ligand coordination involving residues such as arginine, tyrosine and serine. Importantly, top-performing CQD variants differed by target: PET-CQDs, MgG_PET-CQDs and FeG_PET-CQDs were best for GST; ERα interacted favorably with all doped variants; IL-6 bound best to CaO_PET-CQDs and FeO_PET-CQDs (≈−7.1 kcal·mol⁻¹); HSA favored CaG_PET-CQDs (−10.0 kcal·mol⁻¹) and FeO_PET-CQDs (−9.9 kcal·mol⁻¹); CYP3A4 bound most strongly to pristine PET-CQDs; hemoglobin favored MgG_PET-CQDs (−9.6 kcal·mol⁻¹) and FeO_PET-CQDs (−9.3 kcal·mol⁻¹); transferrin favored FeG_PET-CQDs; caspase-3 showed favored binding overall (pristine −6.8 kcal·mol⁻¹; doped −7.4 to −7.6 kcal·mol⁻¹). ADMET predictions indicated high GI absorption, improved aqueous solubility for some dopants (~18.6 mg·mL⁻¹ for Ca-O/Mg-O), low skin permeability and no mutagenic/carcinogenic flags. Regression analysis showed frontier orbital descriptors (HOMO/LUMO) partially explain selective affinities for ERα and IL-6. These results support a target-guided selection of PET-CQDs for biomedical applications, and they call for experimental validation of selected dopant–target pairs. Full article

Radiation shielding in medical settings has traditionally relied on fixed structural models, with thicknesses and material composition determined by their shielding effect against direct X-rays. However, clinical practice increasingly demands lightweight and biocompatible shielding tools that can be locally applied to specific anatomical regions. Such tools should allow rapid installation and removal, skin protection, and disposable as well as continuous shielding. As a potential solution, this study aimed to improve the effectiveness of a cream-type material that directly coats the skin with shielding agents. A modeling pack was fabricated using bismuth oxide, an eco-friendly shielding material; zinc oxide, commonly utilized in cosmetics for ultraviolet protection; and alginate, which enhances skin adhesion by evaporating moisture. The effects of varying bismuth oxide and zinc oxide ratios on porosity and shielding performance were evaluated to establish assessment criteria for future commercialization. The experimental results demonstrated that higher proportions of bismuth oxide enhanced the shielding effect, while a linear change in shielding rate was observed at a thickness of 1.0 mm. Although pore structure variations were minimal, optimizing inter-particle arrangement may further improve skin adhesion. These findings suggest that cream-type radiation-shielding materials are highly promising for medical applications. Full article

The increasing demand for advanced cosmetic formulations based on natural biopolymers has stimulated the design of multifunctional and sustainable skin care products. Hyaluronic acid (HA) and silk proteins are widely recognized for their hydrating, barrier-supportive, and biocompatible properties. This study aimed to develop a novel topical formulation, integrating low- and medium molecular weight hyaluronic acid (LMW-HA and MMW-HA), encapsulated sodium hyaluronate (NaHA), silk, and hydrolyzed silk as active components, aiming to enhance skin barrier function and biocompatibility. The formulation was subjected to comprehensive physicochemical characterization including evaluation of appearance, odor, color, pH, viscosity, and stability, all assessed over 30 days and microbiological stability testing under controlled storage conditions. Safety evaluation followed a dual-phase strategy: (i) in silico toxicological screening of individual ingredients, including sensitization, and mutagenicity predictions, and (ii) in vivo skin compatibility assessment in 25 human volunteers using a semi-occlusive patch test. The formulation demonstrated good physicochemical stability, as pH remained stable, and viscosity showed no significant changes, confirming structural integrity, indicating preserved structural and microbiological stability throughout the study period. The in silico assessment indicated no mutagenic and/or sensitizing alerts and favorable safety margins for all components, confirming the safety profile of each ingredient, supporting their suitability for dermocosmetic use, while in vivo evaluation revealed no significant adverse effects, with irritation scores indicating no skin reaction (erythema or edema) across the test population. These findings support the potential of this novel biopolymer-based formulation as a safe and well-tolerated dermocosmetic product, aligning with principles of sustainable development and biomimetic design. Full article

Functionalized hydrogels represent an emerging class of smart materials being explored for advancing next-generation wearable technologies, owing to their flexibility, biocompatibility, stimuli-responsiveness, and tunable properties. This review provides an overview of recent developments in hydrogel-based wearables, highlighting their potential to enhance adaptive, multifunctional, and environmentally sustainable devices and textiles. It begins by examining progress in wearable sensors, energy storage and harvesting, biosignal monitoring, and smart textiles, as well as the associated challenges, including limited battery life, inadequate skin adhesion, user discomfort, and constrained functionality. The review further explores the synthesis, fabrication techniques, properties, and types of hydrogels tailored for wearable technologies, followed by a detailed discussion of their applications in smart batteries, supercapacitors, sensors, nanogenerators, fabrics and hybrid systems. It also highlights integrating artificial intelligence (AI) and the Internet of Things (IoT) to improve designs; enhance performance through real-time monitoring, data analytics, and user interaction; and expand functionality. Also, it analyzes key limitations of current hydrogels—particularly in energy density, dehydration resistance, fatigue behaviour, and large-scale reproducibility—and outlines strategies based on hierarchical material design, sustainable and biodegradable formulations, and standardized testing and regulatory alignment. The review concludes by affirming the role of hydrogel-based technologies in shaping the future of wearable innovations across healthcare, lifestyle, and beyond and outlines promising research directions. Full article

Background: Conventional insulin injections cannot mimic physiological pancreatic function and often lead to dangerous hypoglycemic events that glucose-responsive systems aim to prevent. Glucose-responsive microneedles (MNs) offer a promising closed-loop alternative. We developed an enzyme-free, glucose-responsive MN patch composed of a PVA/Dextran hydrogel dynamically crosslinked with borax, and evaluated its performance, biosafety, and in vivo efficacy. Methods: MNs were fabricated from PVA/Dextran via micromolding and crosslinked with borax. The formulation was systematically optimized based on mechanical properties and glucose-responsive release kinetics. Physicochemical properties, biosafety (cytotoxicity, skin barrier recovery, boron leaching), and in vivo efficacy in a type 1 diabetic mouse model were evaluated in comparison to a subcutaneous (SC) insulin injection. Results: The optimized MNs showed robust mechanics (per-needle fracture force approximately 1.0 N) for reliable skin penetration. The system demonstrated clear glucose sensitivity, with a release flux ratio ≥1.5 between hyperglycemic (e.g., 400 mg·dL⁻¹) and normoglycemic (100 mg·dL⁻¹) conditions and exhibited excellent reversibility under alternating glucose levels. The patch was highly biocompatible, with >95% cell viability, the only transient skin barrier disruption that fully recovered within 24 h, and had low boron release from patches in vitro. In vivo, the optimized sI-MN patch demonstrated a sustained, glucose-responsive release profile, maintaining blood glucose in diabetic mice near 100 mg·dL⁻¹ for approximately 8 h. This pharmacokinetic profile contrasts markedly with the rapid hypoglycemic nadir and rebound hyperglycemia observed with a standard subcutaneous insulin bolus, highlighting the patch’s potential for mitigating hypoglycemia. Conclusions: The enzyme-free PVA/Dextran/borax MN patch enables autonomous, glucose-responsive insulin delivery. It provides more stable and safer glycemic control than conventional injections by mitigating the risk of hypoglycemia. By mitigating the hypoglycemic risk associated with bolus injections, this systematically optimized platform represents a potential step toward a safer, patient-friendly diabetes therapy, though significant challenges in duration and dose scaling remain. Full article

Background/Objectives: Polymeric microneedles are an innovative drug delivery form combining the benefits of both transdermal and intravenous administration. However, their practical application is limited by fabrication challenges. To address this, the study explores a novel approach for the rapid, precise, and customized production of polymeric microneedles of diverse geometries by utilizing Liquid Crystal Display (LCD) 3D printing technology, marking the first reported use of this technique for microneedle mold fabrication. Methods: LCD 3D printing technology was applied to prepare resin biocompatible microneedle molds. The method developed was optimized by identifying and controlling the critical process parameters (CPPs) through implementing statistical experimental design techniques within the Quality by Design regulatory framework for pharmaceutical development. The optimized molds were subsequently utilized to produce polyvinyl alcohol microneedles with customized shapes and geometries. Representative designs were then loaded with Ropinirole Hydrochloride as a model drug and evaluated in relation to their morphology, drug content, skin insertion depth, and permeability. Results: The application of a Central Composite Design identified layer height and exposure time as the critical process parameters affecting mold fabrication. The optimized design space enabled the selection of printing conditions that maximized dimensional accuracy. Employing these optimum LCD 3D printing parameters, microneedles of various shapes and dimensions were successfully fabricated, exhibiting highly dimensional accuracy. Additionally, tuning skin permeability was proven to be feasible by adjusting microneedle geometry. Conclusions: This work demonstrates the successful use of LCD 3D printing technology in producing biocompatible molds for customized microneedle fabrication, facilitating the development of transdermal delivery systems with personalized drug permeation profiles. Full article

Pectin is widely used in different areas like biomedical, pharmaceutical, food, and environmental industries thanks to its gelling properties. Pectin hydrogels are of great interest because of their wide biomedical applications in drug delivery, tissue engineering, wound healing, the food industry, agriculture, and cosmetic products because of their biocompatibility, biodegradability, and non-toxic nature. This review provides an understanding of pectin-based hydrogels and their applications in various industrial areas. In addition, an overview of emerging technologies and recent applications of pectin hydrogels is provided, including the controlled and targeted release of bioactive compounds or drugs. They are used as a scaffold for cell growth, as a wound dressing to promote healing, as a fat replacer in food, and as a texturizer in skin-care products. It also serves as a coating for seeds to improve their germination and growth. This paper also identifies knowledge gaps and future research direction for optimizing pectin hydrogels. Full article

Objectives: Pseudomonas aeruginosa is an opportunistic pathogen of high clinical relevance due to its ability to form biofilms, its inherent virulence regulated by quorum-sensing systems, and its multidrug resistance. In the present study, we evaluated the inhibitory potential of nine extracts from Inula species (chloroform and methanolic fractions, including a sesquiterpene lactone-enriched fraction) against biofilm formation and virulence-associated traits of P. aeruginosa PAO1 and three multidrug-resistant clinical isolates, as well as their cytotoxicity, biocompatibility, and ability to affect cytokine and nitric oxide production in infected skin explants. Methods: The following methods were applied: fractionation and extraction of plant extracts; cytotoxicity assessment on HFF cells; crystal violet assay for determining antibiofilm activity; fluorescence microscopy for evaluating biofilm viability; electron microscopy for assessing the 3D structure of biofilms and morphological alterations; inhibition assays of pyocyanin pigment, protease activity, bacterial motility, interleukin-17, and nitric oxide production; histological analysis of mouse skin explants. Results: Quantitative analyses of antibiofilm activity revealed that five of the tested extracts inhibited biofilm formation by more than 50%. Structural and functional analyses using confocal laser scanning microscopy and scanning electron microscopy demonstrated a substantial reduction in biofilm thickness, exfoliation of biofilm biomass, the presence of isolated bacterial clusters, metabolically inactive cell populations, and morphological abnormalities associated with cell elongation, invaginations, and polar deformations as a consequence of treatment. In addition, the plant extracts strongly affected virulence factors regulated by quorum sensing. The methanolic fractions from I. britannica and I. bifrons significantly suppressed pyocyanin synthesis. In contrast, the chloroform fractions from I. helenium and I. spiraeifolia produced the largest inhibition zones in assays for extracellular protease activity. Furthermore, all chloroform extracts suppressed bacterial motility, with the lowest swarming diameter observed for the chloroform and lactone-enriched fractions from I. britannica. The chloroform extracts of I. helenium and I. bifrons, methanolic extracts of I. britannica, and chloroform and methanolic extracts of I. spiraeifolia showed relatively low toxicity to normal diploid human fibroblasts. Methanolic and chloroform fractions from I. britannica disrupted biofilm integrity and reduced IL-17A and nitric oxide production in infected skin explants. Conclusions: All these findings indicate a possible synergistic action of the chemical constituents within the fractions on quorum-sensing regulation, biofilm formation, cellular viability, and modulation of host inflammatory responses. Full article

Microneedle (MN) patches comprise a promising platform for transdermal delivery of macromolecular therapeutics. However, achieving sufficient mechanical strength for skin penetration while maintaining high biocompatibility and efficient antibody loading remains a major challenge. In this study, we designed and developed a core–shell-structured hydrogel MN patch composed of a silk fibroin core and a protein-based shell layer for antibody loading and potential transdermal release. The latter was constructed using a fusion protein consisting of the B and C domains of Staphylococcus aureus protein A (BC) and a tyrosine-rich mussel adhesive protein (MAP), thereby enabling antibody binding via the BC domains. By harnessing biomimetic design strategies, the BC-MAP shell facilitates antibody immobilization via specific affinity interactions, while the silk fibroin core provides substantial mechanical strength: the MN patch demonstrated a penetration force approximately 4.2 times greater than that required to pierce porcine skin. Collectively, our core–shell-structured hydrogel MN patch is a promising platform for transdermal antibody delivery. Full article

Wound healing is a complicated process that involves hemostasis, antibacterial defense, and tissue regeneration. Conventional treatment methods, such as surgical suturing, have inherent limitations, necessitating the exploration of new ones. Hydrogels can create a moist environment that facilitates wound healing, making them an ideal material for wound healing. In this study, a procoagulant polysaccharide mixture (carboxymethyl chitosan/sodium alginate/fucoidan; CAF) was designed. Hydrogels were prepared using CAF and an oxidized starch/tannic acid blend (OT) at different ratios. Through comprehensive evaluations, such as gelation time, swelling capacity, and antibacterial efficacy, an optimal hydrogel (COT) was identified. This COT hydrogel was formed by mixing 3% CAF and OT solutions at a ratio of 2:1 (v/v). The associated gelation process occurred rapidly within 13 s. COT hydrogel exhibited self-healing properties, and a high swelling rate (~3109 ± 74%). It also demonstrated high antibacterial activity, facilitating enhanced protection against infection. Additionally, COT hydrogel exhibited biocompatibility and biosafety. COT hydrogel demonstrated low cytotoxicity on mice fibroblast cells (L929) and good hemocompatibility in vitro. Moreover, in vivo evaluations revealed that it did not cause skin irritation or allergic reactions. Importantly, COT hydrogel significantly outperformed the commercially available hydrogel with its hemostatic and wound healing performance (p < 0.001, p < 0.01). Full article

Background: Hyaluronan, or hyaluronic acid (HA), is a glycosaminoglycan with structural and signaling functions playing key roles in human skin homeostasis. It ensures hydration and biomechanical properties of this tissue as well as regulates cell adhesion, migration, proliferation, and inflammation. Its biocompatibility, viscoelastic properties, biological functions, and large-scale sustainable bioproduction made this polysaccharide a hero molecule of the cosmetic industry. Methods: A literature search was conducted to discuss the skin and hair benefits of the external use of HA and its derivatives. Four main questions were addressed: What are the different forms of HA in cosmetic formulations? What about their safety? Does HA penetrate human skin and hair? What are the benefits and mode of actions of HA, and its derivatives, in the fields of cosmetic and dermatology? Results: The analysis revealed HA below 100 kDa to penetrate skin, and lower molecular weight being able to reach the dermis. The safety of HA-containing formulations has been evaluated in several clinical trials and is supported by independent reports of commercial ingredients. We described HA molecules having beneficial effects on skin and hair, as well as their mode of action. Conclusions: This review provides comprehensive information on the nature and efficacy of topical HA, and its derivatives, in cosmetic applications, with an emphasis on hair care. New areas of research were highlighted as the vectorization of high-molecular-weight HA. Full article

This study investigates electrospinning methodologies using distilled water as an environmentally friendly and non-toxic solvent for fabricating nanofibers composed of fish collagen (COL) and pullulan (PUL). The underlying hypothesis is that incorporating PUL will enhance the spinnability of the electrospun solution through the formation of hydrogen bonds with COL, thereby facilitating improved fiber development within an aqueous system. This study examined the interactions between COL and PUL molecules, focusing on hydrogen bonding and the consequential alterations in secondary structural conformation, to elucidate their effects on the spinnability and stability of COL in water-based solutions. Furthermore, this study emphasizes the advantages of needle-free electrospinning, which enables the efficient production of nanofibers and offers scalability potential for industrial applications. The architecture and properties of the resultant ultra-thin COL/PUL fibers were comprehensively characterized, underscoring their suitability for various biomedical applications. The development of PUL-based skin nanofibers represents a significant advancement in the field of biomaterials, offering a biocompatible and biodegradable alternative for dermatological applications, including skin regeneration, wound healing, drug delivery, tissue engineering, and cosmetic science. The benefits of needle-free electrospinning, such as enhanced production efficiency and scalability, are particularly emphasized, demonstrating its potential for the large-scale commercial manufacturing of biocompatible nanofibers. This study aimed to address the research gap regarding the use of distilled water as an eco-friendly and safe solvent for electrospinning nanofibers made from collagen and pullulan. This study aimed to investigate the unexplored potential of distilled water for this application. Full article

Hydrogels have gained significant attention as effective vehicles for transdermal applications offering significant advantages in pharmaceutical and cosmetic applications. Their unique polymeric network structure enables efficient encapsulation and controlled release of active ingredients, making them ideal for therapeutic drug delivery systems (TDDs) and topical skincare formulations. In pharmaceutical approaches, hydrogels facilitate the transdermal transport of therapeutic agents into systemic circulation, improving bioavailability and patient compliance. In cosmetics, they enhance skin hydration and support the delivery of bioactive compounds, contributing to improved product performance and user satisfaction. Among various hydrogel-forming polymers, Hyaluronic Acid (HA) stands out as the most often used polymer in this field due to its biocompatibility, moisture-retention properties, and ability to penetrate the skin. This review explores the dual role of HA-based hydrogels in pharmaceutical and cosmetic application, detailing their structural characteristics, preparation methods, and mechanisms of active ingredient loading and release. Furthermore, the review presents the details on hydrogels and how they are used as TDDs. Special attention is given to hyaluronic acid (HA) in this field, and this review discusses the properties, preparation methods, and applications of HA-based hydrogels as a delivery system, including methods of loading the actives and the releasing of these actives from them. Full article

Background/Objective: The effectiveness of blue-light phototherapy (PT) is mainly dependent on the total dose of light (time under PT and amount of skin exposed) received by infants. The primary aim of this study was the development of a novel, flexible, and stretchable device to provide continuous PT treatment, avoiding temporary interruptions that are often observed in practice, such as during breastfeeding, for example. This study evaluated the biocompatibility of a novel, low-cost blanket equipped with light-emitting diode (LED) lamps designed to maintain therapeutic efficacy while facilitating uninterrupted skin-to-skin contact. Methods: Fourteen New Zealand White rabbits, weighing approximately 2.9 kg and aged 4 months, were randomly assigned to an experimental group (TG, n = 7) or a control group (CG, n = 7). The TG received phototherapy directly on the skin (irradiance: 19.3 [13.0–22.0] µW/cm⁻²/nm⁻¹) during two 12 h sessions over consecutive days, while the CG remained under identical conditions with the device turned off. Biochemical, hematological, dermatological, and histological parameters, as well as rectal and skin temperatures, were assessed. Results: The results showed no differences in clinical appearance or histological analysis of skin tissue between the groups. Blood analysis indicated a reduction in absolute monocyte counts in the TG compared to the CG (p = 0.049), though levels remained within normal ranges. Skin temperature was consistently higher in the TG, except during the initial measurement. Rectal temperatures were similar on the first day but lower in the TG on the second day (mean 40.3 ± 0.21 °C vs. 40.7 ± 0.32 °C; p = 0.039). Conclusions: Temperature levels remained within physiological limits for both groups throughout the study. The device demonstrated biocompatibility and caused no adverse dermatological, hematological, or biochemical effects. Full article