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Nano-sized Al(2)O(3) reduces acute toxic effects of thiacloprid on the non-biting midge Chironomus riparius

This study focuses on interactions between nanoparticles and a pesticide. The aim was to investigate how nano-sized aluminum oxide (410 nm) can alter the toxic effects of thiacloprid, even if no sorption between particles and the insecticide takes place. Thus, our study investigated a rather unexplo...

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Detalles Bibliográficos
Autores principales: Lorenz, Carla S., Wicht, Anna-J., Guluzada, Leyla, Luo, Leilei, Jäger, Leonie, Crone, Barbara, Karst, Uwe, Triebskorn, Rita, Liang, Yucang, Anwander, Reiner, Haderlein, Stefan B., Huhn, Carolin, Köhler, Heinz-R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413047/
https://www.ncbi.nlm.nih.gov/pubmed/28464012
http://dx.doi.org/10.1371/journal.pone.0176356
Descripción
Sumario:This study focuses on interactions between nanoparticles and a pesticide. The aim was to investigate how nano-sized aluminum oxide (410 nm) can alter the toxic effects of thiacloprid, even if no sorption between particles and the insecticide takes place. Thus, our study investigated a rather unexplored interaction. We conducted our research with larvae of Chironomus riparius and used thiacloprid as test substance as its toxicity to C. riparius is well described. The used nano-Al(2)O(3) particles where chosen due to their suitable properties. For testing the acute effects of the interaction, we exposed larvae to thiacloprid (0.5, 1.0, 2.0, and 5.0 μg/L) and nano-Al(2)O(3) (300 and 1000 mg/L), either solely or in binary mixtures. While thiacloprid resulted in elevated mortality, nano-Al(2)O(3) solely did not exert any effects. Moreover, we observed an aggregation of nano-Al(2)O(3) within the lumen of the intestinal tract of the larvae. Further results showed a significantly reduced mortality of fourth instar larvae when they were exposed to mixtures of nanoparticles and the pesticide, compared to thiacloprid alone. With increasing nano-Al(2)O(3) concentration, this effect became gradually stronger. Additionally, chemical analyses of internal thiacloprid concentrations implicate reduced uptake of thiacloprid in animals exposed to mixtures. However, as larvae exposed to thiacloprid concentrations > 0.5 μg/L showed severe convulsions, independent of the presence or concentration of nano-Al(2)O(3,) we assume that nano-Al(2)O(3) leads to a delay of mortality and does not entirely prevent it. As sorption measurements on pristine or defecated nano-Al(2)O(3) did not reveal any sorptive interaction with thiacloprid, we can exclude sorption-based reduction of thiacloprid bioavailability as a mechanism behind our results. Even though we used test substances which might not co-occur in the environment in the tested concentrations, our study gives evidence for an interaction besides adsorption, which is important to generally understand how nanoparticles might affect biota.