Nanoparticle uptake by the rat gastrointestinal mucosa: quantitation and particle size dependency
- PMID: 1983142
- DOI: 10.1111/j.2042-7158.1990.tb07033.x
Nanoparticle uptake by the rat gastrointestinal mucosa: quantitation and particle size dependency
Abstract
Polystyrene microspheres in the size range 50 nm to 3 microns were fed by gavage to female Sprague Dawley rats daily for 10 days at a dose of 1.25 mg/kg-1. Previous histological evidence of the uptake of these particles and their absorption across the gastrointestinal tract and passage via the mesentery lymph supply and lymph nodes to the liver and spleen was confirmed by analysis of tissues for the presence of polystyrene by gel permeation chromatography. Measurement of radioactivity of tissues following administration of 100 nm and 1 micron I125-labelled polystyrene latex particles for 8 days was corroborative although less secure because of the potential lability of the labelled particles. The extent of absorption of 50 nm particles under the conditions of these experiments was 34% and of the 100 nm particles 26% (as measured by determination of polystyrene content), of which total, about 7% (50 nm) and 4% (100 nm), was in the liver, spleen, blood and bone marrow. Particles larger than 100 nm did not reach the bone marrow, and those larger than 300 nm were absent from blood. No particles were detected in heart or lung tissue.
Similar articles
-
The uptake and translocation of latex nanospheres and microspheres after oral administration to rats.J Pharm Pharmacol. 1989 Dec;41(12):809-12. doi: 10.1111/j.2042-7158.1989.tb06377.x. J Pharm Pharmacol. 1989. PMID: 2576440
-
Factors affecting the oral uptake and translocation of polystyrene nanoparticles: histological and analytical evidence.J Drug Target. 1995;3(1):65-70. doi: 10.3109/10611869509015936. J Drug Target. 1995. PMID: 7655823
-
Tissue distribution of 20 nm, 100 nm and 1000 nm fluorescent polystyrene latex nanospheres following acute systemic or acute and repeat airway exposure in the rat.Toxicology. 2009 Sep 19;263(2-3):117-26. doi: 10.1016/j.tox.2009.07.002. Epub 2009 Jul 15. Toxicology. 2009. PMID: 19615422
-
A commentary on morphological and quantitative aspects of microparticle translocation across the gastrointestinal mucosa.J Drug Target. 1995;3(1):57-60. doi: 10.3109/10611869509015934. J Drug Target. 1995. PMID: 7655821 Review.
-
Major determinants in hepatic disposition of polystyrene nanospheres: implication for rational design of particulate drug carriers.Crit Rev Ther Drug Carrier Syst. 2002;19(4-5):277-306. doi: 10.1615/critrevtherdrugcarriersyst.v19.i45.10. Crit Rev Ther Drug Carrier Syst. 2002. PMID: 12661696 Review.
Cited by
-
Styrene maleic acid-encapsulated paclitaxel micelles: antitumor activity and toxicity studies following oral administration in a murine orthotopic colon cancer model.Int J Nanomedicine. 2016 Aug 17;11:3979-91. doi: 10.2147/IJN.S110251. eCollection 2016. Int J Nanomedicine. 2016. PMID: 27574427 Free PMC article.
-
Nanosized Drug Delivery Systems in Gastrointestinal Targeting: Interactions with Microbiota.Pharmaceuticals (Basel). 2016 Sep 29;9(4):62. doi: 10.3390/ph9040062. Pharmaceuticals (Basel). 2016. PMID: 27690060 Free PMC article. Review.
-
A Critical Review of the Use of Surfactant-Coated Nanoparticles in Nanomedicine and Food Nanotechnology.Int J Nanomedicine. 2021 Jun 9;16:3937-3999. doi: 10.2147/IJN.S298606. eCollection 2021. Int J Nanomedicine. 2021. PMID: 34140768 Free PMC article. Review.
-
Past, present, and future technologies for oral delivery of therapeutic proteins.J Pharm Sci. 2008 Jul;97(7):2497-523. doi: 10.1002/jps.21183. J Pharm Sci. 2008. PMID: 17918721 Free PMC article. Review.
-
Size-dependent bioadhesion of micro- and nanoparticulate carriers to the inflamed colonic mucosa.Pharm Res. 2001 Jun;18(6):788-93. doi: 10.1023/a:1011032328064. Pharm Res. 2001. PMID: 11474782
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources