Search Results (964)

Calcium peroxide nanoparticles (CaO₂ NPs) have recently attracted increasing attention as oxygen-generating nanomaterials with potential biomedical applications. Their ability to release molecular oxygen and reactive oxygen species (ROS) in aqueous environments enables modulation of hypoxic and oxidative microenvironments, which play critical roles in infection control, tumor progression, and tissue regeneration. Despite growing interest in oxygen-releasing biomaterials, the literature specifically addressing CaO₂ nanomaterials remains comparatively limited and fragmented, particularly when compared with the extensive body of work on calcium oxide-based systems. This review provides a comprehensive overview of CaO₂ nanoparticles, focusing on synthesis strategies, physicochemical properties, and emerging biomedical applications. Conventional bottom-up synthesis routes based on calcium salts, calcium hydroxide, and calcium oxide are critically compared, highlighting the influence of reaction parameters and stabilizing agents on particle size, morphology, crystallinity, and colloidal stability. Surface modification strategies, including polyethylene glycol, polyvinylpyrrolidone, and hyaluronic acid, are also discussed for their role in improving nanoparticle stability, regulating decomposition kinetics, and enhancing biocompatibility. The mechanisms governing oxygen and ROS generation are analysed in relation to antibacterial activity, hypoxia alleviation in tumor microenvironments, and oxygen-supplying biomaterials for tissue engineering and wound healing. In addition, key challenges associated with oxidative stress responses are discussed. Finally, the review outlines current limitations and perspectives regarding the clinical translation of CaO₂-based nanotherapeutic systems. Overall, this work aims to consolidate the currently dispersed knowledge on CaO₂ nanoparticles and provide a critical framework to guide future research in oxygen-releasing nanomedicine. Full article

Hemostatic biomaterial agents are widely used during surgery and trauma care to control bleeding, yet their effects on wound healing remain incompletely understood. This study evaluated the impact of oxidized non-regenerated cellulose (ONRC), oxidized regenerated cellulose (ORC), and a gelatin-based hemostat (GELA) on wound healing at 14 and 30 days in a mouse model. Full-thickness wounds were created in C57BL/6J mice (n = 192) and compared to sham controls. Tissue samples were analyzed histologically, supported by immunohistochemistry for Ki-67 and α-SMA and qPCR for VEGF, TGF-β, and FGF-2. Histology demonstrated preserved tissue architecture across groups with progressive resorption of cellulose-based materials, whereas GELA showed localized fibrous structures and enhanced extracellular matrix formation. At day 14, no significant differences were observed in proliferation, contraction, VEGF, or FGF-2 expression; however, TGF-β was significantly reduced in the ORC group. By day 30, GELA significantly increased epidermal proliferation, while contraction markers were elevated in both GELA and ORC. VEGF expression was reduced in GELA and ORC, whereas ONRC showed increased TGF-β expression. FGF-2 remained unchanged across groups. All investigated hemostatic materials were well tolerated during the early postoperative phase (up to day 14), indicating short-term biocompatibility within the scope of this model. In contrast, material-specific differences in cellular activity and growth factor expression became apparent during the later remodeling phase (day 30). These findings suggest differential effects on cellular and molecular aspects of tissue remodeling; however, no conclusions can be drawn regarding overall healing quality or clinical safety, as no quantitative macroscopic or functional outcome measures were assessed. Full article

Treatment of postsurgical osteosarcoma remains one of the major challenges in orthopedic clinics. Conventional implants often fail to address complex pathological issues, including irregular bone defects, residual tumor cells, and delayed bone regeneration. Herein, this study reports a multifunctional shape-memory polyurethane (SMPU)/manganese dioxide (MnO₂) composite that provides adaptive support, antitumor activity, and osteogenic bioactivity. SMPU was synthesized by introducing 1,4-butanediol (BDO) and dimethylolpropionic acid (DMPA) as chain extenders at a specific ratio. Commercial MnO₂ nanoparticles were incorporated as both a photothermal agent and a bioactive component to achieve multifunctionality. As designed, a coordination system was formed between the polymer chains and MnO₂ nanoparticles within the composites. The influence of MnO₂ content was systematically investigated. Although increasing MnO₂ amounts improved photothermal and mechanical performance, excessive incorporation adversely affected the molecular structure and compromised the composite’s biocompatibility. By adjusting the MnO₂ content, the composites were demonstrated to possess robust mechanical performance, good shape-memory behavior, and controllable Mn²⁺ release. Additionally, the composites exhibited tunable photothermal performance under near-infrared (NIR) irradiation. Furthermore, in vitro studies confirmed that the composites containing 4 wt% MnO₂ could eliminate tumor cells via photothermal effects and promote the osteogenic differentiation of human bone marrow-derived mesenchymal stem cells (hBMSCs). Overall, the SMPU/MnO₂ composites had superior multifunction for treating irregular bone defects following bone tumor surgery. Full article

The management of complex acute and chronic wounds remains a formidable challenge in modern medicine, underscoring the urgent need for advanced therapeutic strategies that accelerate healing, prevent infection, and promote functional tissue regeneration. Electrospun nanofibers have attracted considerable attention in the biomedical field due to their extracellular matrix-like architecture, high surface area, interconnected porosity, and tunable physicochemical composition, which drive advances in wound regeneration, tissue engineering, and biopolymer-based therapeutics. In wound healing, nanofibrous dressings composed of natural polymers such as chitosan, gelatin, collagen, and cellulose promote cell attachment and proliferation, support angiogenesis, and enable infection control while delivering bioactive agents, thereby addressing significant challenges related to inflammation, biocompatibility, and antimicrobial resistance. In tissue engineering, aligned and hierarchically organized scaffolds fabricated from biopolymers such as collagen, gelatin, chitosan, and cellulose enhance the guided orientation of cells, differentiation, and functional regeneration of neural, musculoskeletal, vascular, and skin tissues. In addition to their conventional regenerative applications, recent studies have demonstrated that electrospun biopolymer nanofibers can be used in multifunctional biomedical platforms, including smart and stimuli-responsive systems for drug delivery, biosensing, regenerative interfaces, and wearable medical technologies. The integrated constructs that incorporate diagnostic or therapeutic functionalities, hybrid fabrication approaches that combine 3D printing with electrospinning, and intelligent biopolymer frameworks that enable telemedicine, real-time physiological monitoring, and personalized regenerative therapies offer new opportunities for developing improved biomedical systems. Overall, these advances position electrospun nanofiber systems as promising biomaterials for next-generation biomedical innovation. This review summarizes recent progress in tissue-engineered scaffolds, wound dressings, fabrication strategies for integrative therapeutics, and wearable devices with transformative potential for biomedical applications. Finally, the review addresses significant challenges related to scalability and clinical translation. It offers perspectives on future directions, including the integration of artificial intelligence and the regeneration of complex skin appendages, which will shape the next generation of nanofiber-based wound-healing therapies. Full article

Benchmark-driven evaluation helps distinguish between planning quality and interface reliability when large language models are utilized for embodied reasoning in simulation. Our submission to the Embodied Agent Interface Challenge (EAI) is evaluated across four stages of the pipeline. These being goal interpretation, subgoal decomposition, action sequencing, and transition modeling. The tasks run in the BEHAVIOR and VirtualHome simulators, which use constrained action vocabularies, fixed-object inventories and symbolic state representations within a standard evaluation protocol. Our system accesses the OpenAI API using GPT-4.1 for BEHAVIOR, GPT-4.1-mini for VirtualHome, and GPT-5-mini in later exploratory experiments across both environments. The schemas for each task determine how the outputs are structured, and outputs are regenerated when they do not follow the specification. On the final public leaderboard, our system ranked eighteenth overall with a score of 57.92, achieving 68.88 on BEHAVIOR and 46.96 on VirtualHome. In this paper, we describe our approach and discuss what these observations suggest about the strengths and limitations of current language models when used for embodied reasoning. Full article

Oxidized cellulose (OC) and oxidized regenerated cellulose (ORC) are bioabsorbable polysaccharide-based materials widely used in surgery for topical hemostasis. Beyond their established hemostatic role, increasing attention has been directed toward their potential antimicrobial activity, primarily attributed to local acidification following carboxyl group dissociation. Discussing the possible implications of the antibacterial properties of OC/ORC in veterinary surgical practice, this review critically examines the existing evidence. In vitro studies show that viable bacterial counts are significantly reduced in both Gram-positive and Gram-negative pathogens, including antibiotic-resistant strains. Historical in vivo animal models further support a reduction in bacterial recovery in contaminated tissues treated with OC. However, contemporary veterinary clinical trials specifically evaluating surgical site infection (SSI) outcomes remain limited. Documented limitations include variability in formulation, quantity-dependent degradation kinetics, and the potential for foreign body reactions when excessive material is retained. Current evidence suggests that OC may provide adjunctive antimicrobial effects under controlled experimental conditions, primarily in vitro and in standardized animal models, but these properties should be interpreted with caution, and its role should be integrated within comprehensive infection prevention strategies rather than considered a substitute for established perioperative protocols. Full article

Chitosan-coated sand has been developed as a sustainable, environmentally friendly, and cost-effective water treatment method for removing nitrate anions, leveraging the adsorption properties of chitosan. When applied to sand using glutaraldehyde as a cross-linking agent, this adsorbent removes nitrate anions with an adsorption capacity (q_e) of 154.41 mg g⁻¹. This approach is particularly advantageous due to its low cost, high adsorption capacity, and effectiveness over a wide range of pH and temperatures, although its performance is optimal under slightly acidic to neutral conditions (pH = 6) due to electrostatic attraction and ion exchange, as the positively charged amino groups of chitosan bind to the negatively charged nitrate ions. Nitrate adsorption is also described by the Langmuir isotherm and follows the pseudo-second-order model. Furthermore, the adsorbent remains highly stable even after five regeneration cycles, demonstrating its long-term effectiveness and durability, while offering a cost-effective and environmentally friendly solution in accordance with the principles of sustainable development. Full article

The Numidian cypress (Cupressus sempervirens var. numidica, C. numidica hereafter) is a rare, almost unknown, endemic taxon of Tunisia whose conservation has long been hampered by human activities, taxonomic uncertainty and limited ecological knowledge, with only 64.33 ha of its populations remaining. Although recent genetic studies have confirmed its native status and long-term isolation, detailed information on its distribution, population structure and threats remain lacking. This study provides the first comprehensive assessment of C. numidica across its remaining range. Field surveys revealed that the species persists in only three small, fragmented forests, Bou Abdallah, Sidi Amer, and Dir Satour, covering a total of 64.33 ha. Soil analysis revealed some differences among sites, with Bou Abdallah showing higher clay content and Dir Satou exhibiting the highest levels of nitrogen, organic carbon, Olsen P, and available Mn and Mo. Climatic analyses indicate a semi-arid Mediterranean environment with pronounced summer droughts and a clear warming trend. Trees showed widespread damages, due to intensive grazing, tree cutting, crown dieback (drought), and pest and pathogen attacks. Natural regeneration was limited, and the condition of affected trees ranged from moderate to severe, with Bou Abdallah showing the highest levels of degradation. Notably, the severe fungal pathogen Seiridium cardinale, causal agent of cypress canker, was detected on C. numidica for the first time, highlighting an urgent conservation concern. Our results point to a staged conservation approach over time. In the immediate term (within 1 year), urgent monitoring and management of S. cardinale is needed. In the short term, efforts should focus on protecting carefully selected areas, about 5–10 regeneration microsites per forest, from grazing to support natural regeneration, reduce ongoing soil degradation, and establish clonal and seed-production plantations along with long-term seed storage. In the long term, the survival of C. numidica will only be possible with the active involvement of local communities, through awareness campaigns, adapting traditional practices such as gdel, and developing small-scale ecotourism that provides sustainable livelihoods while reinforcing support for conservation. Full article

Critical-sized bone defects pose significant challenges in orthopedic surgery. The introduction of 3D printing technology in bone grafting offers a promising solution by creating customized grafts that mimic the natural bone structure. This study aimed to reconstruct long-segment bone defects in the rabbit radius using a 3D-printed material composed of hydroxyapatite (HAP) and poly(lactide-co-glycolide) (PLGA), referred to as ALBO-OS, and to evaluate its potential to support bone healing without the use of stem cells or growth factors. Six rabbits underwent computed tomography scanning to create patient-specific 3D models of the radius. Custom-designed ALBO-OS implants were 3D-printed and used to fill segmental defects corresponding to one-third of the bone length in each rabbit, created by osteotomy. Over a 12-week observation period, graft integration, osteointegration, and overall bone regeneration were assessed through histological and histomorphometric analyses. The implanted scaffolds demonstrated encouraging bone healing, with significant bone regeneration observed within the defect areas. Histological evaluation revealed significant new bone formation and vascularization, with minimal inflammatory response. The findings demonstrated the potential of 3D-printed HAP/PLGA-based materials as a promising strategy for the reconstruction of large bone defects, eliminating the need for exogenous biological agents. Full article

The α-gal epitope is synthesized in non-primate mammals and New-World monkeys by the glycosylation enzyme α1,3galactosyltransferase (α1,3GT), encoded by the GGTA1 gene. Ancestral Old-World monkeys and apes synthesizing α-gal epitopes underwent extinction 20–30 million years ago. Their mutated offspring, with the inactivated GGTA1 gene, survived and produced the natural anti-Gal antibody, specifically binding α-gal epitopes. Anti-Gal protected the surviving offspring from lethal viruses presenting α-gal epitopes, which killed α-gal-synthesizing parental primates. Anti-Gal constitutes ~1% of human immunoglobulins and is also produced in Old-World monkeys and apes. α-Gal epitopes can serve as therapeutic agents in several clinical disciplines: 1. Cancer immunotherapy: Engineering cancer cells to express α-gal epitopes results in anti-Gal binding to these cells and localized activation of the complement system that kills these cancer cells and recruits the antigen-presenting cells (APCs) dendritic cells and macrophages. Anti-Gal bound to cancer cells targets them for robust uptake by APCs, which process internalized tumor antigens (TAs) and transport them to lymph nodes for activation of cytotoxic T-cells. These T-cells kill TA-presenting metastatic tumor cells. Clinical trials demonstrated that such engineering is achieved by intra-tumoral injection of α-gal glycolipids, the use of recombinant α1,3GT, or the use of oncolytic viruses containing the GGTA1 gene. 2. Viral vaccines: Inactivated whole-virus vaccines presenting α-gal epitopes bind anti-Gal, which targets them for extensive uptake by APCs, thereby increasing their immunogenicity by ~100-fold. 3. Injured-tissue regeneration: Anti-Gal binding to α-gal-presenting nanoparticles administered to wounds, into the post-myocardial infarction (MI) injured myocardium and into injured spinal cord, activates the complement system that recruits pro-regenerative macrophages, which orchestrate regeneration by recruiting stem cells and the secretion of pro-regenerative cytokines. All these findings suggest that α-gal/anti-Gal antibody interaction can serve as a novel therapeutic approach, applicable to various clinical settings. Full article

Bisphosphonate-related osteonecrosis of the jaw (BRONJ) is characterized by exposed necrotic bone that often progresses with increasing pain and impaired quality of life. Zoledronate, the most potent and widely used bisphosphonate, has been strongly associated with BRONJ development following invasive dental procedures. Given the rising incidence of BRONJ, understanding and implementing effective preventive strategies have become imperative. Biomaterials based on synthetic hydroxyapatite and beta-tricalcium phosphate have been investigated as potential preventive agents. Their therapeutic rationale is supported by two key principles: the well-documented chemical interaction of calcium phosphates with bisphosphonates when used as drug carriers, and the established clinical use of synthetic calcium phosphate biomaterials in dentistry for bone regeneration. This review examines the underlying mechanisms of this preventive therapeutic strategy and evaluates studies investigating synthetic calcium phosphate biomaterials for BRONJ prevention through zoledronate adsorption at jaw wound sites, thereby reducing soft tissue toxicity and promoting healing. The evidence supports the protective effect of these biomaterials as a scientifically grounded preventive approach for BRONJ. Full article

In this study, a series of SiO₂-based biomaterials synthesized via the sol-gel technique was developed by integrating different weight percentages (10_wt% and 15_wt%) of ferulic acid (FA) and varying weight percentages (6_wt%, 12_wt%, and 24_wt%) of polyethylene glycol (PEG). Chemical characterization of the materials was performed by FTIR-ATR spectroscopy to confirm the incorporation of the functional agents and the matrix structure. Biocompatibility was assessed through cell-based assays and gene expression analysis, highlighting a positive effect of the materials on cell proliferation and the regulation of key markers for tissue regeneration. Finally, the ability to induce hydroxyapatite (HA) formation was verified using simulated body fluid (SBF) following the Kokubo test, demonstrating the bioactive potential of the treated surfaces. The obtained results indicate that the combination of SiO₂, FA, and PEG via sol-gel represents a promising platform for applications in the field of bone regeneration and functional biomaterials. Full article

Enrofloxacin (ENR), as a widely used antimicrobial agent in aquaculture, poses potential risks to ecosystems and human health due to its environmental persistence. Therefore, it is of great significance to explore efficient methods for removing ENR from aquaculture wastewater. In this study, a series of shrimp shell-derived aerogel (MBC300–MBC700) were fabricated from Litopenaeus vannamei shells through chemical modification followed by pyrolysis at 300–700 °C, and their adsorption performance and mechanisms toward ENR were systematically investigated. The modified porous materials exhibited a well-developed micro–mesoporous structure, high specific surface area, and abundant surface functional groups. Meanwhile, MBC400 demonstrated the highest adsorption capacity for ENR, reaching 14.56 mg/g, with a corresponding specific surface area of 77.71 m²/g. The adsorption kinetics followed the pseudo-second-order model, and the isothermal data were better fitted by the Freundlich model, indicating a chemisorption-dominated, heterogeneous multilayer adsorption process. Thermodynamic analysis revealed that the adsorption was spontaneous (ΔG < 0) and endothermic (ΔH > 0). In regeneration experiments, 30% ethanol solution achieved the best desorption efficiency for MBC400, with adsorption efficiency remaining above 75% after three cycles. Based on the characterization and adsorption results, adsorption mechanism of ENR on MBC400 was elucidated as a synergistic effect of hydrogen bonding, π–π stacking, electrostatic interaction, and surface complexation. This study provides a novel strategy and theoretical basis for the high-value utilization of shrimp shell waste and for the efficient removal of fluoroquinolone antibiotics from aquaculture effluents. Full article

Neuroinflammation is a central hallmark of numerous neurological disorders, including Alzheimer’s disease, Parkinson’s disease, traumatic brain injury, and spinal cord damage. Its persistent and dysregulated nature not only accelerates neuronal loss but also impedes endogenous repair, posing a major challenge for effective therapeutic intervention. Recent advances in nanobiotechnology have opened transformative opportunities to modulate neuroinflammation with unprecedented precision while simultaneously supporting neural regeneration. This review highlights emerging nanomaterial-based strategies including lipid-based, polymeric, inorganic nanoparticles designed to traverse the blood–brain barrier (BBB), deliver anti-inflammatory agents, modulate immune cell behavior, and attenuate glial activation. Extending beyond nanoparticle-based delivery systems, recent advances also emphasize the integration of nanomaterials into biomimetic architectures to provide structural and functional cues for neural repair. We further summarize how these functional nanostructured scaffolds, such as extracellular matrix (ECM) mimetic, nanofibrous and conductive hydrogels, are being leveraged in neural tissue engineering to direct stem cell fate, promote axonal outgrowth, and rebuild damaged neuroarchitectures. Moreover, pharmacokinetics, biodistribution, safety, clinical trials, regulatory considerations and limitations of nanotherapeutics in neurodegenerative diseases are discussed. By outlining the current progress, mechanistic insights, and translational challenges, this review underscores the potential of nanobiotechnology-enabled therapeutics to revolutionize the treatment of neuroinflammatory conditions and advance next-generation neural repair technologies. Full article

Landfill leachate, a byproduct of municipal solid waste treatment, typically contains hazardous substances such as toxic metals (e.g., lead) and eutrophication agents (e.g., phosphate). This study addresses the pressing challenge of polishing complex wastewater, such as landfill leachate, through the development of a novel ternary layered double hydroxide (LDH). As CaFe-LDHs are known to have an affinity for anions, and CoFe-LDHs have shown an affinity for toxic metal cations, CoCaFe-LDH was proposed to integrate both functionalities. The LDH was anchored on activated biochar to synthetize the novel composite adsorbent CoCaFe-LAB. Key operational parameters (including initial pH, adsorbent dosage, contact time, initial adsorbate concentration, presence of coexisting ions, and regeneration capability) were systematically evaluated. Kinetic and equilibrium analyses revealed that Elovich and Sips models, respectively, best described the adsorption behavior of Pb²⁺ and PO₄³⁻, indicating a heterogeneous adsorption system. Maximum adsorption capacities in synthetic solutions reached 140.81 mg Pb²⁺ g⁻¹ and 25.19 mg PO₄³⁻ g⁻¹ at 45 °C. The CoCaFe-LAB composite proved highly effective, particularly for lead removal. In real effluent tests, the adsorbent achieved complete phosphate removal (100%) from electro-oxidized landfill leachate at a dosage of 2.0 g L⁻¹, confirming its practical applicability and efficiency. Full article