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Prasad, BR,Mullins, G,Nikolskaya, N,Connolly, D,Smith, TJ,Gerard, VA,Byrne, SJ,Davies, GL,Gun'ko, YK,Rochev, Y
2012
January
Journal Of Nanobiotechnology
Effects of long-term exposure of gelatinated and non-gelatinated cadmium telluride quantum dots on differentiated PC12 cells
Published
Altmetric: 2WOS: 14 ()
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CdTe Quantum Dots Differentiated PC12 cells Cytotoxicity Neuronal Growth Factor Apoptosis CYTOPLASMIC CALCIUM LEVELS OXIDATIVE STRESS INTRACELLULAR-TRANSPORT HIPPOCAMPAL-NEURONS CYTOCHROME-C CDTE SURFACE CDSE NANOCRYSTALS CYTOTOXICITY
10
4
Background: The inherent toxicity of unmodified Quantum Dots (QDs) is a major hindrance to their use in biological applications. To make them more potent as neuroprosthetic and neurotherapeutic agents, thioglycolic acid (TGA) capped CdTe QDs, were coated with a gelatine layer and investigated in this study with differentiated pheochromocytoma 12 (PC12) cells. The QD - cell interactions were investigated after incubation periods of up to 17 days by MTT and APOTOX-Glo Triplex assays along with using confocal microscopy.Results: Long term exposure (up to 17 days) to gelatinated TGA-capped CdTe QDs of PC12 cells in the course of differentiation and after neurites were grown resulted in dramatically reduced cytotoxicity compared to non-gelatinated TGA-capped CdTe QDs.Conclusion: The toxicity mechanism of QDs was identified as caspase-mediated apoptosis as a result of cadmium leaking from the core of QDs. It was therefore concluded that the gelatine capping on the surface of QDs acts as a barrier towards the leaking of toxic ions from the core QDs in the long term (up to 17 days).
10.1186/1477-3155-10-4
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