1. Biochemical mechanisms of dose-dependent cytotoxicity and ROS-mediated apoptosis induced by lead sulfide/graphene oxide quantum dots for potential bioimaging applications.
- Author
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Ayoubi M, Naserzadeh P, Hashemi MT, Reza Rostami M, Tamjid E, Tavakoli MM, and Simchi A
- Subjects
- Cell Survival drug effects, Glutathione metabolism, Humans, Leukocytes, Mononuclear cytology, Leukocytes, Mononuclear drug effects, Lipid Peroxidation drug effects, Lysosomes drug effects, Lysosomes metabolism, Mitochondria drug effects, Mitochondria metabolism, Nanoparticles chemistry, Nanoparticles ultrastructure, Semiconductors, Sulfhydryl Compounds metabolism, Apoptosis drug effects, Diagnostic Imaging, Graphite toxicity, Lead toxicity, Quantum Dots toxicity, Reactive Oxygen Species metabolism, Sulfides toxicity
- Abstract
Colloidal quantum dots (CQD) have attracted considerable attention for biomedical diagnosis and imaging as well as biochemical analysis and stem cell tracking. In this study, quasi core/shell lead sulfide/reduced graphene oxide CQD with near infrared emission (1100 nm) were prepared for potential bioimaging applications. The nanocrystals had an average diameter of ~4 nm, a hydrodynamic size of ~8 nm, and a high quantum efficiency of 28%. Toxicity assay of the hybrid CQD in the cultured human mononuclear blood cells does not show cytotoxicity up to 200 µg/ml. At high concentrations, damage to mitochondrial activity and mitochondrial membrane potential (MMP) due to the formation of uncontrollable amounts of intracellular oxygen radicals (ROS) was observed. Cell membrane and Lysosome damage or a transition in mitochondrial permeability were also noticed. Understanding of cell-nanoparticle interaction at the molecular level is useful for the development of new fluorophores for biomedical imaging.
- Published
- 2017
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