| Literature DB >> 26051544 |
Bénédicte Pradines1, Vanessa Lievin-Le Moal2, Christine Vauthier3, Gilles Ponchel3, Philippe M Loiseau2, Kawthar Bouchemal4.
Abstract
Nanoparticles composed of poly(isobutylcyanoacrylate) core coated with a mixture of chitosan and thiolated chitosan have already shown promising results in terms of mucoadhesion and permeation enhancement properties of pharmaceutical active drugs delivered via mucosal routes. In the present work, the cytotoxicity of these nanoparticles was first investigated using direct contact assay on undifferentiated human cervix epithelial HeLa cells. The results showed strong toxicity in HeLa cells for the two investigated concentrations 25 and 50 μg/mL. The cytotoxic effect was mainly attributed to the poly(isobutylcyanoacrylate) core since no significant differences in nanoparticle cytotoxicity were reported when nanoparticle shell composition was modified by adding chitosan or thiolated chitosan. In contrast, lower nanoparticle toxicity was reported using human fully-differentiated enterocyte-like Caco-2/TC7, and fully-differentiated mucus-secreting HT-29/MTX cells forming monolayer in culture mimicking an intestinal epithelial barrier. This study demonstrated that the toxicity of poly(isobutylcyanoacrylate) nanoparticles is highly cell line-dependent.Entities:
Keywords: Cytotoxicity; Nanoparticles; Poly(isobutylcyanoacrylate); Thiolated chitosan
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Year: 2015 PMID: 26051544 DOI: 10.1016/j.ijpharm.2015.06.001
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875