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61,005 resultsShowing papers similar to Cellular internalization and release of polystyrene microplastics and nanoplastics
ClearCorrelation between cellular uptake and cytotoxicity of polystyrene micro/nanoplastics in HeLa cells: A size-dependent matter
Researchers tested polystyrene particles of various sizes on human cells and found that only the smallest nanoplastics, those under about 25 nanometers in radius, could enter cells and cause toxic effects. Larger microplastic particles did not penetrate the cell membrane and showed no toxicity even at very high concentrations. The study provides a clear explanation for why smaller plastic particles tend to be more harmful, directly linking cell entry to cellular damage.
Bioaccumulation of differently-sized polystyrene nanoplastics by human lung and intestine cells
Researchers examined how human lung and intestine cells take up polystyrene nanoplastics of different sizes, finding that smaller particles were internalized in greater numbers but at lower total mass compared to larger ones. When compared on a surface area basis, the uptake rates were similar across sizes, suggesting that surface interactions with cell membranes play a key role. The findings indicate that particle size is an important factor to consider when evaluating the health risks of nanoplastic exposure.
Size-dependent internalization of polystyrene microplastics as a key factor in macrophages and systemic toxicity
Researchers systematically tested how the size of polystyrene microplastics affects their uptake and toxicity in immune cells and mice. Smaller particles (0.5 micrometers) were taken up much more readily by immune cells and caused more damage, including mitochondrial dysfunction and cell death, compared to larger 5-micrometer particles. In living mice, smaller microplastics accumulated more in organs and caused broader changes in blood and metabolic markers, confirming that particle size is a key factor in microplastic toxicity.
Endocytosis, Distribution, and Exocytosis of Polystyrene Nanoparticles in Human Lung Cells
Researchers studied how polystyrene nanoparticles of 50 and 100 nanometers enter and exit human lung cells. They found that cellular uptake increased with exposure time and dose, with the smaller particles being taken up more readily and primarily accumulating in lysosomes. The study reveals that while lung cells can expel some ingested nanoplastics, a significant portion remains inside the cells, raising concerns about long-term respiratory exposure.
Cellular interactions with polystyrene nanoplastics—The role of particle size and protein corona
Researchers investigated how polystyrene nanoplastics interact with mammalian cells, finding that particle size and the protein corona that forms around particles in biological fluids strongly influence cellular uptake and toxicity. Smaller nanoplastics penetrated cell membranes more readily and caused greater disruption, suggesting that the tiniest plastic particles may pose the greatest biological risk.
The internal dose makes the poison: higher internalization of polystyrene particles induce increased perturbation of macrophages
Researchers exposed human macrophages, key immune cells, to polystyrene particles of different sizes and found that smaller particles were internalized more readily and caused greater cellular disruption. Nanoscale plastics triggered stronger inflammatory responses and more oxidative stress than larger microplastics. The study suggests that the amount of plastic actually absorbed by immune cells, not just the amount present in the environment, determines how harmful the exposure is.
Defining the size ranges of polystyrene nanoplastics according to their ability to cross biological barriers
Researchers systematically examined polystyrene nanoplastics of different sizes to define the size ranges at which they can cross biological barriers, providing a more precise definition of nanoplastic dimensions relevant to toxicological assessment.
Human neurons are susceptible to the internalization of small-sized nanoplastics
Researchers studied how human neurons take up nanoplastics and found that the cells readily absorbed 50-nanometer polystyrene particles through specific cellular pathways. The nanoplastics accumulated in cell compartments and, at higher concentrations, triggered oxidative stress and reduced cell survival. The study provides evidence that very small plastic particles can enter human brain cells, raising concerns about potential neurological effects of nanoplastic exposure.
Effects of bisphenol A and nanoscale and microscale polystyrene plastic exposure on particle uptake and toxicity in human Caco-2 cells
Researchers studied how human intestinal Caco-2 cells take up polystyrene plastic particles of five different sizes ranging from 300 nanometers to 6 micrometers. The study found that smaller particles were taken up at higher rates and that co-exposure with bisphenol A increased cellular toxicity, suggesting that nanoscale plastics may pose a greater risk to human intestinal cells than larger microplastics.
The potential effects of microplastic pollution on human digestive tract cells
Researchers tested polystyrene particles of four different sizes on human colon and small intestine cells to assess the potential effects of microplastic ingestion. They found that the smallest nanoscale particles were more readily taken up by cells and caused greater reductions in cell viability and increased oxidative stress. The study suggests that smaller plastic particles may pose a greater risk to the human digestive tract than larger ones.
Cell uptake of mixtures of different-sized nanoplastics: Interplay and mechanism
Researchers studied how two sizes of polystyrene nanoplastics interact during cellular uptake, finding that larger 100 nm particles can pull smaller 50 nm particles into cells via clathrin-mediated endocytosis, while smaller particles alter the protein corona of larger ones in serum, either enhancing or inhibiting uptake depending on concentration ratios.
Nano-plastics and gastric health: Decoding the cytotoxic mechanisms of polystyrene nano-plastics size
Researchers examined how different sizes of polystyrene nanoplastics affect human stomach cells in the laboratory. They found that smaller nanoplastics were more readily taken up by the cells and caused greater damage, including increased oxidative stress and reduced cell survival. The study suggests that nanoplastic particle size plays a critical role in determining their potential impact on gastrointestinal health.
Size-dependent translocation of polystyrene nanoplastics across biological barriers in mammals
This study tracked radiolabeled nanoplastic particles in rats and found that smaller 20-nanometer particles could cross biological barriers that larger 100-nanometer particles could not, including reaching the brain. Both sizes were transferred from mothers to offspring, but through different pathways, revealing that nanoplastic size plays a critical role in determining which organs and tissues are exposed.
Uptake and Toxicity of Polystyrene NPs in Three Human Cell Lines
Researchers tested three sizes of polystyrene nanoparticles on human gut and liver cell lines and found that smaller particles (30 nm) were more toxic than larger ones (100 nm). Despite significant uptake by all cell types, the overall toxicity was low at tested concentrations. Interestingly, the nanoparticles entered cells mainly through a scavenger receptor pathway rather than the commonly assumed routes, which could change how scientists predict nanoplastic behavior in the human body.
Multi-endpoint toxicological assessment of polystyrene nano- and microparticles in different biological models in vitro
Researchers assessed the toxicity and transport of polystyrene nano- and microparticles using multiple human cell models, including intestinal and placental barrier systems. They found that while neither size was acutely toxic, the nanoparticles were able to cross the intestinal barrier and showed some embryotoxic potential. The study suggests that nanoplastics may pose greater health concerns than microplastics due to their ability to penetrate biological barriers.
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.
Uptake and toxicity of polystyrene micro/nanoplastics in gastric cells: Effects of particle size and surface functionalization
Researchers evaluated the uptake and toxicity of polystyrene micro- and nanoplastics in human gastric cells, comparing different sizes and surface treatments. The study found that smaller 50-nanometer particles were taken up at significantly higher rates, with positively charged aminated particles being the most toxic, causing cytotoxicity at lower concentrations and higher rates of cell death.
Biological interactions of polystyrene nanoplastics: Their cytotoxic and immunotoxic effects on the hepatic and enteric systems
Researchers exposed mouse and human liver cells and live mice to polystyrene nanoplastics of five different sizes and found that the smallest particles were most toxic in lab dishes, while medium and large particles caused the most liver damage in living animals. The larger particles triggered immune responses by recruiting inflammatory cells to the liver and intestines, causing tissue damage. This study reveals that nanoplastic size matters in unexpected ways, and that lab tests alone may not predict which particles are most dangerous in the body.
Tissue distribution of polystyrene nanoplastics in mice and their entry, transport, and cytotoxicity to GES-1 cells
Scientists tracked polystyrene nanoplastics in mice after oral exposure and found the particles accumulated in the stomach, intestines, and liver tissues. In human gastric cells, the nanoplastics entered through multiple pathways and were transported through the cell's internal trafficking system, ultimately reducing cell growth and increasing cell death. The study provides detailed evidence of how nanoplastics can cross biological barriers and cause cellular damage in mammalian systems.
Hazard assessment of different-sized polystyrene nanoplastics in hematopoietic human cell lines
Researchers tested how different sizes of polystyrene nanoplastics (50, 200, and 500 nm) affect human blood cell lines. While none of the sizes caused direct cell death, all three were taken up by cells and disrupted mitochondrial function in immune-related cell types. The study suggests that even without killing cells outright, nanoplastics may interfere with important cellular energy processes, with effects varying by particle size and cell type.
Quantification of Polystyrene Uptake by Different Cell Lines Using Fluorescence Microscopy and Label-Free Visualization of Intracellular Polystyrene Particles by Raman Microspectroscopic Imaging
Scientists tested how human cells take up polystyrene microplastic particles using three cell types that represent the lung lining, intestinal lining, and immune system. All three cell types absorbed the microplastic beads, with immune cells showing different uptake patterns compared to the barrier cells of the lungs and gut. This study confirms that microplastics can enter human cells through multiple exposure routes, including breathing and eating, and that immune cells may play a special role in processing these particles.
Uptake and effects of orally ingested polystyrene microplastic particles in vitro and in vivo
Researchers studied the uptake and effects of orally ingested polystyrene microplastic particles using human intestinal cell models and rodent experiments. They found that smaller microplastics were taken up by intestinal cells and could cross the gut barrier, though the majority passed through the digestive system. The study suggests that while most ingested microplastics are excreted, a fraction can be absorbed, warranting further investigation into long-term health effects.
Mechanisms of ingested polystyrene micro-nanoplastics (MNPs) uptake and translocation in an in vitro tri-culture small intestinal epithelium
Researchers used a sophisticated laboratory model of the human small intestine to study how micro- and nanoplastics cross the gut barrier after simulated digestion. They found that smaller nanoplastics were absorbed more efficiently than larger microplastics, and the particles used multiple cellular pathways to cross the intestinal lining. The study provides new evidence about the mechanisms by which ingested plastic particles could potentially reach the bloodstream.
Internalization and toxicity of polystyrene nanoplastics on inmortalized human neural stem cells
Researchers tested 30-nanometer polystyrene particles on human neural stem cells grown in the lab and found the particles entered the cells, accumulated inside them, and triggered cell death. The nanoplastics also slowed cell growth but did not penetrate the cell nucleus. This study provides direct evidence that nanoplastics could harm the brain's stem cells, raising concerns about potential effects on brain development.