Search Results (1,214)

Microplastics and nanoplastics (MNPs) have been recognized as ubiquitous emerging global pollutants, which are extensively detectable in diverse environmental media and food matrices. Increasing evidence indicates that the intestine is a primary target of orally ingested MNPs and a critical initiating hub for systemic toxicity. Once ingested orally, MNPs can interact with the intestinal mucus layer and epithelial barrier, induce gut microbiota dysbiosis, remodel bile acid and short-chain fatty acid metabolism, and activate oxidative stress, inflammation, apoptosis, and immune imbalance. These gut-derived disturbances may subsequently propagate adverse signals to distal organs through the gut-liver, gut-brain, gut-kidney, gut-lung, gut-reproductive, and gut-mammary axes. Intestinal barrier dysfunction, endotoxin translocation, abnormal microbial metabolites, and microbiota-derived immune signals constitute common mediating pathways linking local intestinal injury to multi-organ toxicity. In addition, smaller particle size, surface oxidation, environmental aging, bio-corona/plastisphere formation, and co-exposure with other contaminants can further modulate the intensity and specificity of gut-organ axis disruption. Prior reviews are limited to separate analyses of single-organ toxicity or isolated gut-organ pathways. To fill this gap, this work synthesizes contemporary mechanistic and experimental evidence to establish a gut-initiated systemic toxicology framework for MNPs. We differentiate direct particle translocation from gut-derived indirect signaling, evaluate the varying robustness of supporting evidence for each gut-organ axis, and underscore nanoscale biointerface properties as key modulators of MNPs systemic toxic potency. Full article

The exponential rise in global plastic production has resulted in the widespread environmental dissemination of micro- and nanoplastics (MNPs) across air, water, and biological systems. Inhalation of airborne MNPs represents a biologically plausible pathway of pulmonary exposure, particularly within indoor and occupational environments. Experimental evidence indicates that inhaled MNPs deposit within distal lung compartments, where their small aerodynamic diameter and surface reactivity may favor cellular uptake, oxidative stress induction, inflammatory activation, and prolonged biopersistence. Experimental studies further indicate that MNP exposure may induce DNA damage, chromosomal instability, and the dysregulation of signaling pathways involved in genomic integrity, thereby providing additional mechanistic support for their potential role in carcinogenesis. Chronic redox imbalance, macrophage dysfunction, inflammasome activation, epithelial–mesenchymal transition, and dysregulated cell adhesion collectively resemble mechanisms implicated in inflammation-associated carcinogenesis. Emerging in vitro and in vivo data further suggest that nanoplastics may function as tumor promoters or co-carcinogenic modifiers, particularly under chronic low-dose exposure or in combination with other airborne toxicants. However, human epidemiological evidence remains limited, and causality has not been established. This review synthesizes current mechanistic evidence regarding inhaled MNPs as potential modifiers of lung carcinogenesis, compares them with established inhaled carcinogens, and outlines critical research priorities necessary to clarify exposure–response relationships and clinical relevance. Current evidence supports biological plausibility rather than confirmed carcinogenic classification. Full article

The round window membrane (RWM) presents a major barrier to local drug delivery into the inner ear. Although magnetically guided superparamagnetic iron oxide nanoparticles (SPIONs) have shown promise for enhancing transport across the RWM, the effectiveness of magnetic-field-driven delivery decreases rapidly with distance from the magnet, limiting clinical applicability. In this study, PEGylated SPIONs were investigated as externally actuated carriers for enhanced transport across membrane barriers using magnetic, photothermal, ultrasonic, and vibrational stimulation. Nanoparticle transport was evaluated using a custom dual-chamber benchtop platform containing porcine small intestinal submucosa (SIS) membranes as a model transport barrier. Transport studies demonstrated that magnetic-field-assisted delivery significantly increased magnetic nanoparticle (MNP) transport rates relative to passive diffusion; however, transport enhancement decreased sharply with increasing magnet-to-membrane distance. To overcome this limitation, alternative external actuation strategies were explored. Laser-induced photothermal heating, ultrasonication, and mechanical vibration all significantly enhanced MNP transport, even in the absence of magnetic fields. Among the conditions examined, combined magnetic and photothermal stimulation produced the highest transport rates, indicating synergistic enhancement. These results show that MNP transport can be effectively enhanced through magnetic, thermal, and mechanical mechanisms. The findings establish a multimodal transport-engineering framework for improving drug delivery across the RWM and suggest clinically translatable alternatives to magnetic-field-only approaches for inner-ear therapy. Full article

Iron oxide-based nanomaterials have attracted considerable interest owing to their unique magnetic properties and potential biomedical and environmental applications. In this study, starch-coated superparamagnetic Fe₃O₄ nanoparticles (Sta-MNP) were synthesized and comprehensively characterized using electron microscopy (TEM, SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), vibrating sample magnetometry (VSM), attenuated total reflectance Fourier-transform infrared spectroscopy (ATR-FTIR), and nanoparticle tracking analysis (NTA). The results confirmed the formation of a magnetite-based iron oxide nanoparticles sample with a median physical diameter of 12.24 nm, superparamagnetic behavior with a saturation magnetization of 59.81 emu/g, and effective starch coating on the nanoparticle surface. The biological effects of Sta-MNP were assessed in Triticum aestivum L. using the mitotic index (MI) and aberration index (AI) as cytogenetic endpoints, respectively. Exposure-induced concentration-dependent increases in both parameters across the tested volume fractions (0–200 µL/L), suggesting a significant interaction between Sta-MNP and dividing cells. Overall, this study provides a comprehensive physicochemical profile of starch-coated magnetite nanoparticles and demonstrates their potential cytogenetic impact in a plant model system, supporting further investigation of their environmental interactions and potential agricultural applications. Full article

Occupational chronic obstructive pulmonary disease (O-COPD) represents a lung disorder attributable to occupational exposures that are characterized by early development of airway remodeling and pulmonary fibrosis. O-COPD is poorly recapitulated by existing preclinical models. This study aimed to perform comparative characterization of an O-COPD patient cohort exposed to industrial aerosols and to develop a relevant murine model that accurately mirrors the human pathology. In the patient cohort, it was shown that the O-COPD phenotype is associated with the chemical composition of industrial aerosols and mediated by a specific inflammatory pattern with predominant obstructive changes and increased bronchial reactivity upon exposure to metal particles, as well as irreversible fibrotic changes in the lungs upon exposure to silicon dioxide. In the murine model, silica nanoparticles (SiNPs) or magnetic nanoparticles (MNPs) were utilized. Repeated intranasal SiNP administrations have been shown to reflect one of the main features of O-COPD—progressive airway remodeling and fibrosis, observed even after elimination of SiNPs. Administration of MNPs in the same regimen did not result in fibrotic changes in the lungs, partially recapitulating the human pathology resulting from exposure to the complex composition of industrial aerosols as well as the specific properties of chemically synthesized nanoparticles. Thus, the integrative data from the human cohort and animal model provides a reflective platform to advance the investigation of O-COPD mechanisms and development of interventions for fibrotic lung pathology. Full article

Background: Micro- and nanoplastics (MNPs) are emerging contaminants increasingly detected in human tissues and biological fluids. Their presence in blood, vascular tissues, thrombi, and atherosclerotic plaques raises concern about their possible association with cardiovascular disease. This systematic review synthesized evidence on associations between MNPs and cardiovascular pathology. Methods: A systematic search was conducted in October 2025 in PubMed, Scopus, Web of Science, and Embase according to PRISMA guidelines and a PICOS-based strategy. Original human studies from the last 10 years were eligible. Fourteen studies were included. Due to methodological heterogeneity, a narrative synthesis was performed. Risk of bias was assessed using ROBINS-E, and certainty of evidence was evaluated using a GRADE-informed approach. Results: MNPs were detected in multiple cardiovascular-related matrices. Included studies suggested possible associations with major adverse cardiovascular events, acute coronary syndrome, myocardial infarction, arterial stenosis, vascular calcification, thromboembolic disease, hypertension, inflammatory markers, coagulation-related parameters, and lipid profiles. However, the certainty of evidence was very low, and most studies had a high or very high risk of bias. Conclusions: Current evidence suggests a possible association between MNPs and cardiovascular pathology, but causality remains unproven. Larger prospective studies using standardized detection protocols, rigorous contamination control, and adjustment for confounders are needed. Full article

Micro- and nanoplastics (MNPs) are now pervasive in human tissues, yet their biological behavior remains unexplained within conventional pharmacokinetic frameworks. Here, we propose that MNP distribution may follow a bioenergetic logic governed by cellular turnover and metabolic demand, rather than passive diffusion alone. Integrating the human autopsy literature datasets with programmatic biological parameters suggests that MNPs persist intracellularly and are propagated through cycles of cell death and renewal, establishing a previously unrecognized system of retention-driven recirculation. By integrating tissue-specific metabolic rates, macrophage abundance, and intracellular vulnerability indices across 19 organs, we define a hierarchy of susceptibility, with highest accumulation in the spleen, intestinal epithelium, lung, and bone marrow. This hierarchy maps onto clinical patterns of tissue dysfunction and supports a unifying mechanism in which oxidative stress, energetic instability, and chronic inflammation emerge as convergent responses to MNP burden. We further identify a minimal circulating signature—lactate, high-sensitivity C-reactive protein (hsCRP), and lactate dehydrogenase (LDH)—that reflects systemic bioenergetic disruption associated with MNP exposure. Together, this framework offers a conceptual shift from diffusion-limited to turnover-driven accumulation models, providing testable hypotheses for future prospective validation. Full article

Plastic pollution has emerged as a major environmental concern due to its persistence and widespread accumulation in terrestrial ecosystems. The extensive utilization of plastics across a diverse range of products, from packaging to healthcare, construction, and transportation, poses a significant risk due to their enduring and non-biodegradable nature. Micro/nanoplastics (MNPs) derived either from the fragmentation of larger plastics or direct release are increasingly detected in agricultural soils, where they interact with plant systems. In addition, chronic exposure of MNPs alters soil structure, microbial diversity, and nutrient cycling, further impacting agroecosystem functioning. Plants have been shown to absorb MNPs mostly from contaminated soil and irrigated water through their root systems, allowing their subsequent translocation to aerial tissues. MNPs can enter plants through the aquaporins, apoplast pathways, crack entry modes, and leaf stomata, disrupting nutrient uptake, photosynthesis, and growth processes, ultimately affecting crop productivity and quality, while their accumulation in edible tissues raises concerns regarding food safety and trophic transfer. To address these challenges, it is crucial to have standard detection methods for identifying MNPs and to bridge the gap for further mitigation. This review further discussed effective mitigation strategies, including nanomaterial and phytohormone-based interventions under increasing plastic contamination. Full article

Micro- and nanoplastics (MNPs) are emerging global pollutants that pose a significant threat to living organisms due to their widespread presence, ingestion by aquatic species, and ability to cross biological barriers, including the blood–brain barrier. Zebrafish is a well-established and convenient model for ecotoxicological research because of its small size, optical transparency, fully sequenced genome, high genetic homology to humans, ease of breeding, and short life cycle. Exposure to MNPs affects multiple organ systems in zebrafish, including the brain, eyes, liver, intestine, gills, and reproductive system. These particles can induce oxidative stress, inflammation, and interference with diverse biomolecules, leading to adverse biological effects. An analysis of transcriptomic alterations induced by MNPs exposure can contribute to understanding the mechanisms of these adverse effects. In this narrative review, we classify existing studies on MNPs exposure in zebrafish by affected organ system and summarize the gene expression-based evidence of MNP-induced toxicity with a particular focus on high-throughput approaches such as RNA sequencing and single-cell RNA sequencing. Full article

Magnetic hyperthermia relies on the ability of magnetic nanoparticles (MNPs) to dissipate heat under alternating magnetic fields, with the heating efficiency commonly quantified through the specific loss power (SLP). Accurate estimation of SLP requires realistic modeling of the dynamic magnetic response of nanoparticle ensembles, particularly in the ferromagnetic single-domain regime where hysteresis losses dominate. In the present work, we developed a computational framework in Mathematica based on the thermally activated Stoner–Wohlfarth model to simulate dynamic hysteresis loops and estimate SLP in ensembles of non-interacting magnetic nanoparticles. The model incorporates experimentally relevant distributions of particle diameter, magnetic anisotropy, and easy-axis orientation, enabling realistic representation of nanoparticle polydispersity and orientation disorder. Thermal activation was introduced through Arrhenius-type Néel switching probabilities, while the dynamic magnetization evolution was obtained numerically through solution of the corresponding rate equations. The framework was tested for magnetite nanoparticles, one of the most widely used materials in magnetic hyperthermia, considering typical single-domain ferromagnetic particle sizes in the range of 15–30 nm and effective anisotropy K_eff values representative, 3 kJ/m³ < K_eff < 20 kJ/m³ of experimentally reported systems. Simulations were performed under clinically relevant alternating magnetic fields with amplitudes up to 24 kA/m and frequencies ranging from 100 to 765 kHz. The model successfully reproduced dynamic hysteresis loop evolution and enabled systematic investigation of the influence of nanoparticle size, anisotropy, and orientation distributions on loop shape, symmetry, and SLP. The developed code provides a computationally accessible tool for researchers working in magnetic hyperthermia, allowing direct connection between microscopic nanoparticle properties and macroscopic heating performance. By enabling parametric mapping of dynamic hysteresis behavior and SLP dependence, the framework may support the rational optimization of magnetic nanoparticle systems for biomedical hyperthermia applications. Full article

The increasing prevalence of antimicrobial resistance (AMR) has promoted the development of advanced biomaterials capable of overcoming the limitations of conventional antibiotics. In this context, metal nanoparticle hybrid hydrogels (MNHHs) have emerged as multifunctional platforms that integrate the high water-retention capacity and biocompatibility of hydrogels with the antimicrobial properties of metallic nanoparticles (MNPs). This review critically analyzes recent advances in the design, physicochemical properties, antimicrobial mechanisms, and biomedical applications of these systems. Current evidence demonstrates that MNHHs can achieve antimicrobial efficiencies above 98–99%, with minimum inhibitory concentrations as low as 0.78 µg mL⁻¹ and inhibition zones of up to 25 mm against clinically relevant pathogens. Furthermore, the incorporation of MNPs significantly improves the mechanical properties of hydrogels and enables controlled and sustained metal ion release for periods of up to 14 days. Despite these promising results, important challenges remain regarding cytotoxicity, release control, the lack of experimental standardization, and the limited understanding of long-term biological effects. Overall, MNHHs represent a promising strategy for infection control, regenerative medicine, and controlled drug delivery; however, their clinical translation still requires the development of reproducible, safe, scalable, and highly biocompatible systems. Full article

To clarify the microbial contamination and wood degradation risk of the Nanhai No. 1 shipwreck hull and verify on-site antibacterial agent effectiveness, microbial samples were collected and analyzed via SEM, metagenomic sequencing, bacterial isolation, enzyme activity detection, and antibacterial experiments. The results showed that Actinomycetota was the dominant phylum, and Brachybacterium, Microbacterium, and Brevibacterium were the dominant genera. Seven bacterial strains were isolated and purified, among which Brevibacterium sp. (NH.SH-B6) had the strongest wood degradation ability, possessing cellulase, LiP, MnP, and Lac activities. When cultured with hull wood as the sole carbon source, LiP was the dominant degrading enzyme of NH.SH-B6, and its maximum enzyme activity was achieved under the optimal conditions of pH = 7, 10% NaCl, 1000 mg/L FeSO₄, and no PEG400 added. 50 mg/mL cinnamaldehyde and 0.5% isothiazolinone K100 had good inhibitory effects on the isolated bacteria, and bacterial proliferation was due to incomplete antibacterial agent spraying. This study clarifies the microbial degradation risk of the Nanhai No. 1 shipwreck hull and provides a scientific basis for optimizing the on-site protection strategy of the shipwreck. Full article

Melittin (Mel) is a membrane-active peptide with potential anticancer activity, but its direct therapeutic application may be limited by nonspecific toxicity and delivery-related challenges. The study aimed to assess melittin-functionalized magnetic nanoparticles (MNPs-Mel) as a strategy to enhance antitumor activity in Caco-2 cells, with/without magnetic hyperthermia (MH) association. BJ fibroblasts were used as a normal human in vitro cellular model. The effects of free Mel (2.5 µg/mL), MNPs, and MNPs-Mel (50 µg/mL both) + MH (30 min at 355 kHz and 25 kA/m) were assessed using colorimetry (for viability), luminescence (ATP), and spectrophotometry (lactate) following different exposure conditions. The mechanism of apoptosis induction was evaluated by ELISA (caspase 8 and 9 levels). Transmission electron microscopy (TEM) was also used to evaluate nanoparticle morphology and treatment-associated cellular ultrastructural changes. Free Mel reduced viability in both cell lines, with Caco-2 cells showing greater sensitivity at lower concentrations. MNPs (with/without MH) produced limited and less consistent effects, whereas MNPs-Mel significantly reduced Caco-2 viability and ATP levels and increased LDH and caspase 9. MH further enhanced the effects of MNPs-Mel: reduced viability (57–58% of the control at 24 h and 72 h), decreased ATP levels (67% of the control at 24 h and 53% at 72 h), increased LDH levels (206% of the control at 24 h and 301% at 72 h), and induced the mitochondrial apoptotic pathway (caspase 9 increased with 2164% of the control at 72 h). TEM proved the internalization of both MNPs and MNPs-Mel and revealed extensive ultrastructural alterations concerning mitochondria and lysosomes produced by MNPs-Mel, particularly in the Caco-2 cells. These modifications were heavily increased by MNPs-Mel + MH exposure. Overall, these findings demonstrate that Mel functionalization increases the antitumor activity of Mel at lower doses and that MH further potentiates this effect in Caco-2 cells. Full article

Cancer remains one of the most formidable health challenges worldwide. Extensive research has shown that tumor progression is not driven solely by malignant cells but is profoundly shaped by the tumor microenvironment (TME), which influences cancer initiation, immune evasion, and metastatic spread. Consequently, the TME has become an increasingly compelling therapeutic target. Nanotechnology has transformed cancer diagnostics and therapy, with metallic nanoparticles (mNPs) gaining particular attention due to their distinctive physicochemical properties and broad therapeutic potential. However, their interactions within the TME remain insufficiently understood, particularly with the non-cancerous cellular components, such as Cancer-Associated Fibroblasts (CAFs), Tumor-Associated Macrophages (TAMs), Dendritic Cells (DCs), Natural Killer (NK) cells, and T cells. Most existing reviews emphasize nanoparticle interactions with non-cellular TME components, such as the extracellular matrix, while far less attention has been given to their effects on cellular constituents (a gap this work specifically addresses). Although several molecular pathways through which mNPs modulate TME-resident cells have been identified, these likely represent only a small portion of the underlying mechanisms explored in this review. Progress in the field is further hindered by the limited availability of physiologically relevant experimental models; current in vitro and in vivo systems often fail to capture the complexity and dynamic heterogeneity of the TME. These limitations highlight the urgent need for more comprehensive and mechanistically grounded studies to validate the TME as a viable therapeutic target for nanoparticle-based cancer interventions. In particular, deeper insights into how mNPs influence immune regulation, stromal remodeling, and metabolic reprogramming within the TME will be essential for unlocking their full therapeutic potential in oncology. Full article

Magnetic fields (MFs) represent an emerging modality in cancer therapy, encompassing static, low-frequency, pulsed, and nanoparticle-mediated alternating fields. These interventions have demonstrated the capacity to modulate proliferation, apoptosis, ferroptosis, migration, and epithelial-to-mesenchymal transition (EMT) in tumor cells, often through reactive oxygen species (ROS) modulation, ion channel regulation, membrane receptor dynamics, and lysosomal membrane permeabilization. Magnetic nanoparticle hyperthermia (MHT) has reached clinical application, showing promising outcomes in glioblastoma and prostate cancer, while pulsed electromagnetic fields (PEMFs) and magneto-mechanical approaches are under preclinical investigation. The mechanistic diversity of MFs allows synergistic combination with chemotherapy, radiotherapy, and immunotherapy. However, parameter sensitivity, field standardization, and long-term safety remain challenges. Here, we review mechanistic insights, signaling pathways, and experimental and clinical evidence for MF-based cancer therapies, highlighting translational potential and the need for rigorous optimization to realize clinical efficacy. Full article