| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5746227 | Chemosphere | 2017 | 9 Pages |
â¢MPA-CdTe QDs had a stronger effect on MPT than TGA-CdTe QDs.â¢The weaker effect of TGA-CdTe QDs on MPT might be owing to their better stability and thus less amount of released Cd2+.â¢Surface ligands play an important role in the toxicity of CdTe quantum dots at the sub-cellular level.
The potential toxicity of Quantum dots (QDs) should be assessed comprehensively for their fast spreading applications. Many studies have shown the toxicity of QDs is associated with their surface ligands. In this work, two analog ligands with one carbon difference, 2-mercaptoacetic acid (TGA) and 3-mercaptopropionic acid (MPA) were used as coating materials in the syntheses of two types of CdTe QDs with similar physicochemical properties. Then the biological effects of QDs on isolated mitochondria were studied. It was found that the two types of QDs could impair mitochondrial respiration and induce mitochondrial permeability transition (MPT). However, as compared with TGA-CdTe QDs, MPA-CdTe QDs had a stronger effect on MPT. The weaker effect of TGA-CdTe QDs on MPT might be owing to their better stability and thus less amount of released Cd2+, which could be further explained by the stronger affinity between the ligand (TGA) and the cadmium complexes in the crystal growth of QDs. These results highlighted the importance of ligands responsible for the toxicity of QDs at the sub-cellular level.
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