Low uptake of silica nanoparticles in Caco-2 intestinal epithelial barriers

被引:25
|
作者
Ye, Dong [1 ,2 ]
Bramini, Mattia [1 ,3 ]
Hristov, Delyan R. [1 ]
Wan, Sha [1 ]
Salvati, Anna [1 ,4 ]
Aberg, Christoffer [1 ,4 ]
Dawson, Kenneth A. [1 ]
机构
[1] Univ Coll Dublin, Ctr BioNano Interact, Sch Chem & Chem Biol, Dublin 4, Ireland
[2] AbbVie Deutschland GmbH & Co KG, Brain Delivery Neurosci Discovery, Knollstr, D-67061 Ludwigshafen, Germany
[3] Ist Italiano Tecnol, Ctr Synapt Neurosci & Technol, Lgo Rosanna Benzi 10, I-16132 Genoa, Italy
[4] Univ Groningen, Groningen Res Inst Pharm, Antonius Deusinglaan 1, NL-9713 AV Groningen, Netherlands
来源
基金
爱尔兰科学基金会;
关键词
Caco-2; differentiation and polarisation; epithelial cell barrier; microscopy imaging; particle interaction; uptake and localisation; PROTEIN CORONA; POLYSTYRENE NANOPARTICLES; POLYMERIC NANOPARTICLES; DRUG PERMEABILITY; IN-VITRO; SIZE; TRANSPORT; NANOTECHNOLOGY; TOXICITY; IMPACT;
D O I
10.3762/bjnano.8.141
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Cellular barriers, such as the skin, the lung epithelium or the intestinal epithelium, constitute one of the first obstacles facing nanomedicines or other nanoparticles entering organisms. It is thus important to assess the capacity of nanoparticles to enter and transport across such barriers. In this work, Caco-2 intestinal epithelial cells were used as a well-established model for the intestinal barrier, and the uptake, trafficking and translocation of model silica nanoparticles of different sizes were investigated using a combination of imaging, flow cytometry and transport studies. Compared to typical observations in standard cell lines commonly used for in vitro studies, silica nanoparticle uptake into well-developed Caco-2 cellular barriers was found to be very low. Instead, nanoparticle association to the apical outer membrane was substantial and these particles could easily be misinterpreted as internalised in the absence of imaging. Passage of nanoparticles through the barrier was very limited, suggesting that the low amount of internalised nanoparticles was due to reduced uptake into cells, rather than a considerable transport through them.
引用
收藏
页码:1396 / 1406
页数:11
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