Orally ingested nanoparticles may overcome the gastrointestinal barrier, reach the circulatory system, be distributed in the organism and cause adverse health effects. However, ingested nanoparticles have to pass through different physicochemical environments, which may alter their properties before they reach the intestinal cells. In this study, silver nanoparticles are characterised physicochemically during the course of artificial digestion to simulate the biochemical processes occurring during digestion. Their cytotoxicity on intestinal cells was investigated using the Caco-2 cell model. Using field-flow fractionation combined with dynamic light scattering and small-angle X-ray scattering, the authors found that particles only partially aggregate as a result of the digestive process. Cell viabilities were determined by means of CellTiter-Blue (R) assay, 4',6-diamidino-2-phenylindole-staining and real-time impedance. These measurements reveal small differences between digested and undigested particles (1-100 mg/ml or 1-69 particles/cell). The findings suggest that silver nanoparticles may indeed overcome the gastrointestinal juices in their particulate form without forming large quantities of aggregates. Consequently, the authors presume that the particles can reach the intestinal epithelial cells after ingestion with only a slight reduction in their cytotoxic potential. The study indicates that it is important to determine the impact of body fluids on the nanoparticles of interest to provide a reliable interpretation of their nano-specific cytotoxicity testing in vivo and in vitro.
机构:
Capital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China
Chinese Acad Sci, Res Ctr Eco Environm Sci, State Key Lab Environm Chem & Ecotoxicol, Beijing 100085, Peoples R ChinaCapital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China
Ren, Quanzhong
Ma, Juan
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Chinese Acad Sci, Res Ctr Eco Environm Sci, State Key Lab Environm Chem & Ecotoxicol, Beijing 100085, Peoples R China
Univ Chinese Acad Sci, Coll Resources & Environm, Beijing 100049, Peoples R ChinaCapital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China
Ma, Juan
Li, Xiaobo
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Capital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R ChinaCapital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China
Li, Xiaobo
Meng, Qingtao
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Capital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R ChinaCapital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China
Meng, Qingtao
Wu, Shenshen
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Capital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R ChinaCapital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China
Wu, Shenshen
Xie, Yusa
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Chinese Acad Sci, Res Ctr Eco Environm Sci, State Key Lab Environm Chem & Ecotoxicol, Beijing 100085, Peoples R China
Univ Chinese Acad Sci, Coll Resources & Environm, Beijing 100049, Peoples R ChinaCapital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China
Xie, Yusa
Qi, Yu
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Chinese Acad Sci, Res Ctr Eco Environm Sci, State Key Lab Environm Chem & Ecotoxicol, Beijing 100085, Peoples R China
Univ Chinese Acad Sci, Coll Resources & Environm, Beijing 100049, Peoples R ChinaCapital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China
Qi, Yu
Liu, Sijin
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Chinese Acad Sci, Res Ctr Eco Environm Sci, State Key Lab Environm Chem & Ecotoxicol, Beijing 100085, Peoples R China
Univ Chinese Acad Sci, Coll Resources & Environm, Beijing 100049, Peoples R ChinaCapital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China
Liu, Sijin
Chen, Rui
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Capital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R ChinaCapital Med Univ, Beijing Key Lab Environm Toxicol, Beijing 100069, Peoples R China