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61,005 resultsShowing papers similar to Surface Charges of Polystyrene Nanoplastics Affect Their Distribution in Mice
ClearPreferred Lung Accumulation of Polystyrene Nanoplastics with Negative Charges
Researchers investigated why certain nanoplastics preferentially accumulate in the lungs after entering the bloodstream. They found that negatively charged polystyrene nanoplastics attract specific blood proteins that promote uptake by lung blood vessel cells through a receptor-mediated pathway. The study suggests that the protein coating nanoplastics acquire in the blood plays a critical role in determining where they end up in the body.
Hepatotoxic mechanisms of functionalized nanopolystyrene: decoding the role of ionic surface groups
Researchers exposed mice to polystyrene nanoplastics with different surface charges via drinking water, finding that charged particles accumulate in liver sinusoids and induce hepatocyte ferroptosis through an endoplasmic reticulum stress cascade, while neutral particles cause endothelial cell senescence through lysosomal dysfunction.
Tissue accumulation of microplastics in mice and biomarker responses suggest widespread health risks of exposure
Researchers fed mice polystyrene microplastics of two sizes and tracked where the particles accumulated in the body, finding them in the liver, kidneys, and gut with distribution patterns depending on particle size. Biochemical analysis revealed that microplastic exposure disrupted energy and fat metabolism, caused oxidative stress, and altered markers of neurotoxicity in the blood. The study provides evidence that microplastics can accumulate in mammalian tissues and may pose widespread health risks.
Analysis of Biodistribution and in vivo Toxicity of Varying Sized Polystyrene Micro and Nanoplastics in Mice
This study found that smaller plastic particles spread more widely through the bodies of mice and caused more organ damage than larger ones, particularly in the liver, kidneys, and heart. Nanoplastics (under 1 micrometer) were especially concerning because they crossed biological barriers more easily than microplastics. The results suggest that the tiniest plastic particles in our environment may pose the greatest health risks.
[Exposure Pathways of Polystyrene Nanoplastics Mediate Their Cellular Distribution and Toxicity].
This study found that the route by which polystyrene nanoplastics enter the body determines which liver cell types accumulate the particles and what toxic effects occur, demonstrating that exposure pathway—not just dose—shapes nanoplastic toxicity in hepatic tissue.
Surface-charge-dependent ovarian toxicity of polystyrene microplastics: Insights into accumulation, mitochondrial damage, and macrophage polarization
Researchers investigated how polystyrene microplastics with different surface charges accumulate in and damage rat ovaries after oral exposure. Positively charged amino-modified microplastics accumulated most in ovarian tissue and caused the most severe effects, including hormonal disruption, oxidative stress, and mitochondrial damage. The study suggests that surface charge is a key factor determining how microplastics affect reproductive organs.
Charge-specific adverse effects of polystyrene nanoplastics on zebrafish (Danio rerio) development and behavior
Researchers exposed developing zebrafish to positively and negatively charged nanoplastics and found that the positively charged particles were significantly more toxic, accumulating in the brain and gut and causing developmental delays and brain cell death. The two types of nanoplastics affected different neurotransmitter pathways and interacted with different brain receptors, explaining their distinct behavioral effects. The study demonstrates that the surface charge of nanoplastics plays a critical role in determining their toxicity to developing organisms.
Comparing the effects and mechanisms of exposure to polystyrene nanoplastics with different functional groups on the male reproductive system
Scientists exposed male mice to polystyrene nanoparticles with different surface charges (unmodified, negatively charged, and positively charged) and found all three types damaged reproductive health by reducing sperm count, increasing sperm defects, and disrupting testicular tissue. The positively charged (amino-modified) nanoparticles were the most toxic, causing the greatest reproductive damage. This is important because as plastics age in the environment, they develop different surface charges that may make them more harmful to reproductive health than pristine plastic particles.
Size-Dependent PulmonaryToxicity and Whole-Body Distributionof Inhaled Micro/Nanoplastic Particles in Male Mice from Chronic Exposure
Researchers used a whole-body inhalation exposure system to chronically expose male mice to polystyrene micro- and nanoplastics at environmental concentrations and tracked particle distribution and lung toxicity. Nanoplastics (80 nm) showed greater tissue transport than microplastics (1 µm), with highest accumulation in lungs followed by blood and spleen, and both sizes disrupted oxidative balance and antioxidant defenses.
What Is on the Outside Matters—Surface Charge and Dissolve Organic Matter Association Affect the Toxicity and Physiological Mode of Action of Polystyrene Nanoplastics toC. elegans
Researchers investigated how surface charge and organic matter coatings affect the toxicity of polystyrene nanoplastics to the nematode C. elegans. Positively charged nanoplastics were over 60 times more toxic than negatively charged ones, and organic matter coatings reduced toxicity across all particle types. The findings suggest that surface chemistry plays a critical role in nanoplastic toxicity and should be considered when assessing environmental risks.
Size-dependent and tissue specific accumulation of polystyrene microplastics and nanoplastics in zebrafish
Researchers tracked size-dependent accumulation of polystyrene micro- and nanoplastics in multiple zebrafish tissues, finding that smaller particles distributed more broadly throughout the body compared to larger ones. Nanoplastics showed greater systemic distribution including into brain and reproductive tissues, raising concerns about size-dependent health risks.
In vitro study on the toxicity of nanoplastics with different charges to murine splenic lymphocytes
Researchers tested how nanoplastics with different surface charges affect immune cells from mouse spleens. They found that positively charged nanoplastics were significantly more toxic, causing greater cell death, more oxidative stress, and stronger inflammatory responses than negatively charged particles. The study suggests that the surface chemistry of nanoplastics plays a critical role in determining their impact on the immune system.
Role of nanoparticle surface charge in their toxicity
This study examined how surface charge (carboxyl vs. amino functionalization) affects the toxicity of polystyrene nanoparticles formed during plastic degradation, noting that nanoparticle toxicity can differ substantially from bulk material. Results highlighted that surface chemistry is a critical determinant of nanoparticle behavior in biological environments.
Tissue Distribution of Polystyrene or Mixed Polymer Microspheres and Metabolomic Analysis after Oral Exposure in Mice.
Mice orally exposed to polystyrene or mixed polymer microspheres showed plastic particle distribution across multiple tissues including the liver, kidney, and spleen, with metabolomic analysis revealing distinct alterations in lipid, amino acid, and energy metabolism pathways.
Differentially Charged Nanoplastics Induce Distinct Effects on the Growth and Gut of Benthic Insects (Chironomus kiinensis) via Charge-Specific Accumulation and Perturbation of the Gut Microbiota
Researchers exposed aquatic insect larvae to positively and negatively charged nanoplastics and found that the surface charge significantly affected how toxic the particles were. Positively charged nanoplastics caused more severe gut damage, greater accumulation in tissues, and bigger disruptions to gut bacteria. This matters because nanoplastics in the real environment carry various charges, and the findings suggest that charge is an important factor in determining health risks.
Polystyrene micro- and nanoplastics in a colitis mouse model – effects on biodistribution, macrophage polarization, and gut microbiome
Researchers studied the effects of polystyrene micro- and nanoplastics in a mouse model of colitis, examining biodistribution, immune cell responses, and gut microbiome changes. The study found that nanosized particles in particular showed distinct biodistribution patterns and affected macrophage polarization under inflammatory conditions, suggesting that intestinal inflammation may alter how the body handles micro- and nanoplastic particles.
Induction of Male Reproductive Toxicity in Mice by Differentially Charged Polystyrene Microplastics
This study exposed male mice to polystyrene microplastics carrying different surface charges (positive, negative, or neutral) and found that all types caused reproductive toxicity, including damage to sperm quality and testicular tissue. Surface charge influenced the severity and mechanism of harm, with positively charged particles showing the strongest effects, suggesting that the chemical surface properties of microplastics — not just particle size — determine their toxicity. These findings are concerning given widespread human exposure to microplastics via food, water, and air, and the ongoing global decline in male fertility.
Blood uptake and urine excretion of nano- and micro-plastics after a single exposure.
Mice exposed to polystyrene nanoparticles (100 nm) and microparticles (3 µm) via different routes showed that smaller particles appeared rapidly in blood and were detected in urine, while larger particles cleared more slowly. The study provides direct evidence that nanoplastics can cross biological barriers and enter circulation, with potential for distribution throughout the body.
Effects of size and surface charge on the sedimentation of nanoplastics in freshwater
Researchers investigated how size and surface charge of polystyrene nanoplastics affect their sedimentation behavior in freshwater, finding that both properties significantly influence aggregation dynamics and settling rates, with implications for predicting nanoplastic fate in aquatic environments.
Oppositely charged proteins lead to different effects on the bioaccumulation kinetics of polystyrene nanoplastics in zebrafish (Danio rerio)
Researchers studied how positively and negatively charged proteins in water affect the bioaccumulation of polystyrene nanoplastics in zebrafish. The study found that different protein types altered nanoplastic uptake kinetics in distinct ways, suggesting that the natural protein environment in water bodies plays an important role in determining how nanoplastics accumulate in aquatic organisms.
The biodistribution of polystyrene nanoparticles administered intravenously in the chicken embryo
Researchers injected polystyrene nanoplastics into chicken embryos and tracked where the particles traveled, finding high accumulations in the heart, liver, and kidneys, with particles crossing critical tissue barriers. This is an important advance in understanding how nanoplastics distribute throughout a developing organism, with potential implications for fetal health.
The size-dependence and reversibility of polystyrene nanoplastics-induced lipid accumulation in mice: Possible roles of lysosomes
This mouse study found that smaller nanoplastics (100 nm) cause more fat buildup in the liver than larger ones (500 nm), showing that size matters when it comes to health effects. Encouragingly, the liver damage was reversible after the mice stopped being exposed, suggesting the body can recover once nanoplastic intake is reduced. The damage appears to work by disrupting the cell's waste-recycling system (lysosomes).
In vivo impact assessment of orally administered polystyrene nanoplastics: biodistribution, toxicity, and inflammatory response in mice
Researchers orally administered polystyrene nanoplastics to mice for two weeks and tracked their distribution and biological effects. The nanoplastics accumulated primarily in the intestine, kidneys, and liver, triggering significant inflammatory responses and oxidative stress in these organs despite no visible tissue damage. The study provides evidence that even short-term oral exposure to nanoplastics can cause meaningful inflammatory changes in multiple organ systems.
Life cycle exposure to differentially charged polystyrene nanoplastics leads to gender-specific particle accumulation and neurotoxicity in zebrafish (Danio rerio)
Zebrafish exposed to nanoplastics with different surface charges throughout their entire life cycle showed brain damage, behavior changes, and disrupted brain chemistry. The effects depended on both the type of charge on the plastic and the sex of the fish, with positively charged nanoplastics accumulating most in the brain. This research suggests that the surface properties of nanoplastics matter for their neurotoxicity and that long-term exposure could affect brain health differently in males and females.