TY - JOUR
T1 - Eco-, geno- and human toxicology of bio-active nanoparticles for biomedical applications
AU - Robbens, Johan
AU - Vanparys, Caroline
AU - Nobels, Ingrid
AU - Blust, Ronny
AU - Van Hoecke, Karen
AU - Janssen, Colin
AU - De Schamphelaere, Karel
AU - Roland, Kathleen
AU - Blanchard, Gersande
AU - Silvestre, Frédéric
AU - Gillardin, Virginie
AU - Kestemont, Patrick
AU - Anthonissen, Roel
AU - Toussaint, Olivier
AU - Vankoningsloo, Sébastien
AU - Saout, Christelle
AU - Alfaro-Moreno, Ernesto
AU - Hoet, Peter
AU - Gonzalez, Laetitia
AU - Dubruel, Peter
AU - Troisfontaines, Paul
PY - 2010
Y1 - 2010
N2 - Gene delivery has become an increasingly important strategy for treating a variety of human diseases, including infections, genetic disorders and tumours. To avoid the difficulties of using viral carriers, more and more non-viral gene delivery nanoparticles are developed. Among these new approaches polyethylene imine (PEI) is currently considered as one of the most effective polymer based method solution and considered as the gold standard. The toxicity of nanoparticles is a major concern when used for medical application. In this study we chose two nanoparticles for an in depth toxicological and ecotoxicological evaluation, one well characterized, PEI, and another novel polymer, poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA). In the present study we have assessed the toxicity of these cation nanoparticles as such and of the polyplexes - nanoparticles covered with DNA. As these nanoparticles are also frequently used in high volumes in various industries and as such may enter in the environment, we also made an initial assessment of ecotoxicological effects assessment. The following nanoparticles related aspects have been studied during the project: development and characterization, ecotoxicity, general toxicity and specific toxicity. To this end a battery of different tests was used. The conclusion of these tests is that toxicity is varying between different nanoparticles and between different DNA covering ratios. In general, in the different systems tested, the PEI polymer is more toxic than the PDMAEMA polymer. The same difference is seen for the polyplexes and the higher the charge ratio, the more toxic are the polyplexes. Our study also clearly shows the need for a broad spectrum of toxicity assays for a comprehensive risk assessment. Our study has performed such a comprehensive analysis of two biomedical nanoparticles.
AB - Gene delivery has become an increasingly important strategy for treating a variety of human diseases, including infections, genetic disorders and tumours. To avoid the difficulties of using viral carriers, more and more non-viral gene delivery nanoparticles are developed. Among these new approaches polyethylene imine (PEI) is currently considered as one of the most effective polymer based method solution and considered as the gold standard. The toxicity of nanoparticles is a major concern when used for medical application. In this study we chose two nanoparticles for an in depth toxicological and ecotoxicological evaluation, one well characterized, PEI, and another novel polymer, poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA). In the present study we have assessed the toxicity of these cation nanoparticles as such and of the polyplexes - nanoparticles covered with DNA. As these nanoparticles are also frequently used in high volumes in various industries and as such may enter in the environment, we also made an initial assessment of ecotoxicological effects assessment. The following nanoparticles related aspects have been studied during the project: development and characterization, ecotoxicity, general toxicity and specific toxicity. To this end a battery of different tests was used. The conclusion of these tests is that toxicity is varying between different nanoparticles and between different DNA covering ratios. In general, in the different systems tested, the PEI polymer is more toxic than the PDMAEMA polymer. The same difference is seen for the polyplexes and the higher the charge ratio, the more toxic are the polyplexes. Our study also clearly shows the need for a broad spectrum of toxicity assays for a comprehensive risk assessment. Our study has performed such a comprehensive analysis of two biomedical nanoparticles.
KW - Abnormalities, Drug-Induced
KW - Animals
KW - Biomedical Enhancement
KW - Cell Line
KW - Cytokines
KW - Environmental Pollutants
KW - Escherichia coli
KW - Eukaryota
KW - Gene Expression
KW - Gene Expression Profiling
KW - Gene Transfer Techniques
KW - Hepatocytes
KW - Humans
KW - Nanoparticles
KW - Polyethyleneimine
KW - Polymethacrylic Acids
KW - Skin
KW - Toxicity Tests
KW - Xenopus
U2 - 10.1016/j.tox.2009.11.002
DO - 10.1016/j.tox.2009.11.002
M3 - A1: Web of Science-article
C2 - 19944128
SN - 0340-5761
VL - 269
SP - 170
EP - 181
JO - Archives of Toxicology
JF - Archives of Toxicology
IS - 2-3
ER -