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

• Dong Ye,
• Mattia Bramini,
• Delyan R. Hristov,
• Sha Wan,
• Anna Salvati,
• Christoffer Åberg and
• Kenneth A. Dawson

Beilstein J. Nanotechnol. 2017, 8, 1396–1406, doi:10.3762/bjnano.8.141

• transport through them. Keywords: Caco-2; differentiation and polarisation; epithelial cell barrier; microscopy imaging; particle interaction; uptake and localisation; Introduction An overall conclusion from a multitude of nanoparticle-cell in vitro studies is that nanoparticle uptake into cells is

• nanoparticles such as microporous silicon [22], silica [23], poly(lactic-co-glycolic acid) [33] and carboxylated and aminated polystyrene [34]. We hypothesize that the low translocation observed in Caco-2 barriers results from a low uptake into the cells, an uptake that depends on cellular differentiation and

• polarisation. Additionally, though it is known that biomolecules adsorbed to nanoparticles affect their cell adherence [35], uptake [26][35] and translocation [34], we wish to clarify their role in the full process, from adherence to translocation, in both undifferentiated and mature Caco-2 barriers. To this