Journal of Toxicology and Environmental Health · 1980 · 63 citations · 22 references
PharmacyPharmacokineticsInnate ImmunityMucosal Drug DeliveryOral Drug DeliveryGastrointestinal AbsorptionIntestinal AbsorptionIntestinal Barrier FunctionMucosal AbsorptionMucosal Barrier FunctionMucosal PermeabilityGut Barrier PermeabilityIntestinal Barrier PermeabilityIntestinal Mucosa BarrierIntestinal Nutrient UptakeIntestinal Uptake
Intestinal barrier function in mice was assessed after acute or chronic oral administration of 15.8- and 5.7-micron synthetic spherical particles. The results failed to confirm previous reports that ingested particles rapidly appear in blood. Furthermore, 15.8-micron particles did not accumulate in intestinal Peyer's patches, mesenteric lymph nodes, or other organs of the reticuloendothelial system, even after the maximum dosage of 8 X 10(6) particles per day for 60 d. However, the 5.7-micron particles were demonstrated in Peyer's patches, mesenteric lymph nodes, and lungs after the maximum dosage of 4.5 X 10(8) particles per day for 60 d. At 77 d after the termination of ingestion, 5.7-micron particles were still present in these tissues. The 5.7-micron particles were not found in spleen; retention in liver was equivocal. The site of uptake of particles capable of penetrating the intestinal mucosa appears to be the Peyer's patches. It is suggested that most absorbed particles are sequestered in Peyer's patch macrophages. Particles that escape sequestration are transported by lymph rather than by portal blood. The findings indicate that hazards associated with intestinal uptake of large (> 5 micron) particulates exist, but that the frequency of such penetration is still unclear.
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Textbook of Medical Physiology
Annals of Internal Medicine · 1966 · 9.8K citations
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