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Cytotoxicity of Poly(Alkyl Cyanoacrylate) Nanoparticles.
Sulheim, Einar; Iversen, Tore-Geir; To Nakstad, Vu; Klinkenberg, Geir; Sletta, Håvard; Schmid, Ruth; Hatletveit, Anne Rein; Wågbø, Ane Marit; Sundan, Anders; Skotland, Tore; Sandvig, Kirsten; Mørch, Ýrr.
Afiliación
  • Sulheim E; SINTEF Materials and Chemistry, Sem Sælands vei 2A, 7034 Trondheim, Norway. einar.sulheim@ntnu.no.
  • Iversen TG; Department of Physics, Norwegian University of Science and Technology, Høgskoleringen 5, 7491 Trondheim, Norway. einar.sulheim@ntnu.no.
  • To Nakstad V; Department of Molecular Cell Biology, Institute for Cancer Research, Oslo University Hospital-The Norwegian Radium Hospital, 0379 Oslo, Norway. Tore-Geir.Iversen@rr-research.no.
  • Klinkenberg G; Center for Cancer Biomedicine, Faculty of Medicine, University of Oslo, 0379 Oslo, Norway. Tore-Geir.Iversen@rr-research.no.
  • Sletta H; SINTEF Materials and Chemistry, Sem Sælands vei 2A, 7034 Trondheim, Norway. vu.nakstad@sintef.no.
  • Schmid R; SINTEF Materials and Chemistry, Sem Sælands vei 2A, 7034 Trondheim, Norway. geir.klinkenberg@sintef.no.
  • Hatletveit AR; SINTEF Materials and Chemistry, Sem Sælands vei 2A, 7034 Trondheim, Norway. havard.sletta@sintef.no.
  • Wågbø AM; SINTEF Materials and Chemistry, Sem Sælands vei 2A, 7034 Trondheim, Norway. ruth.b.schmid@sintef.no.
  • Sundan A; SINTEF Materials and Chemistry, Sem Sælands vei 2A, 7034 Trondheim, Norway. annerein.hatletveit@sintef.no.
  • Skotland T; SINTEF Materials and Chemistry, Sem Sælands vei 2A, 7034 Trondheim, Norway. ane.marit.wagbo@sintef.no.
  • Sandvig K; Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, 8905 MH, 7491 Trondheim, Norway. anders.sundan@ntnu.no.
  • Mørch Ý; Department of Molecular Cell Biology, Institute for Cancer Research, Oslo University Hospital-The Norwegian Radium Hospital, 0379 Oslo, Norway. tore.skotland@rr-research.no.
Int J Mol Sci ; 18(11)2017 Nov 18.
Article en En | MEDLINE | ID: mdl-29156588
ABSTRACT
Although nanotoxicology has become a large research field, assessment of cytotoxicity is often reduced to analysis of one cell line only. Cytotoxicity of nanoparticles is complex and should, preferentially, be evaluated in several cell lines with different methods and on multiple nanoparticle batches. Here we report the toxicity of poly(alkyl cyanoacrylate) nanoparticles in 12 different cell lines after synthesizing and analyzing 19 different nanoparticle batches and report that large variations were obtained when using different cell lines or various toxicity assays. Surprisingly, we found that nanoparticles with intermediate degradation rates were less toxic than particles that were degraded faster or more slowly in a cell-free system. The toxicity did not vary significantly with either the three different combinations of polyethylene glycol surfactants or with particle size (range 100-200 nm). No acute pro- or anti-inflammatory activity on cells in whole blood was observed.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cianoacrilatos / Nanopartículas Límite: Animals / Female / Humans / Male Idioma: En Revista: Int J Mol Sci Año: 2017 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cianoacrilatos / Nanopartículas Límite: Animals / Female / Humans / Male Idioma: En Revista: Int J Mol Sci Año: 2017 Tipo del documento: Article País de afiliación: Noruega
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