Affiliation:
1. The School of Pharmacy, University of London, London WC1N 1AX
2. Department of Pharmacy, University of Strathclyde, Glasgow G1 1XW
3. Syntex Research Centre, Edinburgh EH14 4AP, UK
Abstract
Abstract
Non-ionic and carboxylated fluorescent polystyrene microspheres (100, 500 nm, 1 and 3 μm in diameter), were fed by gavage (2·5% w/v; 1·25 mg kg−1) daily for 10 days to female Sprague Dawley rats. Peyer’s patches, villi, liver, lymph nodes and spleen of animals fed the non-ionic microspheres from 100 nm to 1 μm showed unequivocal evidence of uptake and translocation of the particles. Heart, kidney and lung showed no evidence of the presence of microspheres. Carboxylated microspheres were taken up to a lesser degree than the non-ionised particles. Experiments with 125I radiolabeled 100 nm and 1 μm particles showed a higher uptake of the smaller particles, which were concentrated in GI tissue and liver. Particles were not distributed randomly in the tissues, but were concentrated at the serosal side of the Peyer’s patches and could be seen traversing the mesentery lymph vessels towards the lymph nodes. The results demonstrate a need to re-examine the possibilities of particulate oral delivery, as well as the potential toxicity of ingested particulates.
Publisher
Oxford University Press (OUP)
Subject
Pharmaceutical Science,Pharmacology
Cited by
349 articles.
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