Abstract
Cadmium (Cd) is a component in quantum dot 705 (QD705). Whether QD705 behaves similar to Cd in vivo is of great concern. We compared the distributional kinetics of cadmium chloride (CdCl2) and QD705 in mice after intravenous injection. QD705 showed a longer plasma and body retention than CdCl2 and could be detected in the brain during early exposure. While both the liver and spleen demonstrated a constant Cd concentration for 28 days after QD705 injection, it is likely that this represents intact QD705 stored in mononuclear phagocytes. The kidneys showed a time-dependent accumulation of Cd in the QD705-exposed animals. By day 28, Cd in the kidneys from QD705 was 3-fold that of CdCl2. QD705 and CdCl2 have very different kinetics in distribution and metabolism. The long body retention of QD705 in the kidneys may mean that QD705 has even more renal toxicity than CdCl2.
Declaration of interest : This work was supported by grant NM-098-PP08 from the Center for Nanomedicine Research, National Health Research Institutes, Taiwan. We appreciate the assistance of Dr Jen-Kun Chen for quantifying sulfur in QD705. The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.