Probing and preventing quantum dot-induced cytotoxicity with multimodal α-lipoic acid in multiple dimensions of the peripheral nervous system

Published on Mar 30, 2009in Nanomedicine: Nanotechnology, Biology and Medicine6.458
· DOI :10.2217/NNM.09.3
Manasi P Jain4
Estimated H-index: 4
(McGill University),
Angela O. Choi9
Estimated H-index: 9
+ 1 AuthorsDusica Maysinger63
Estimated H-index: 63
(McGill University)
Source
Abstract
Aim: Toxicity of nanoparticles developed for biomedical applications is extensively debated as no uniform guidelines are available for studying nanomaterial safety, resulting in conflicting data obtained from different cell types. This study demonstrates the varied toxicity of a selected type of nanoparticle, cadmium telluride quantum dots (QDs), in three increasingly complex cell models of the peripheral nervous system. Materials & methods: QD-induced cytotoxicity was assessed via cell viability assays and biomarkers of subcellular damage in PC12 cells and mixed primary dispersed dorsal root ganglia (DRG) cultures. Morphological analysis of neurite outgrowth was used to determine the viability of axotomized DRG explant cultures. Results & discussion: Cadmium telluride QDs and their core metals exert different degrees of toxicity in the three cell models, the primary dispersed DRGs being the most susceptible. α-lipoic acid is an effective, multimodal, cytoprotective agent that can act as an antioxidant, m...
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