Acc. Chem. Res.
http://pubs.acs.org/doi/abs/10.1021/ar300040z
In one of my previous post, a quantum dot toxicity study on primates
showed limited short-term toxicity and unknown long-term toxicity. In
this account, various QD toxicity studies were summarized. They were
trying to explore the causes of the discrepancy in "in vitro" and "in
vivo" QD toxicological data. They believe dosing provides one
explanation for these findings. Under
culture conditions, a cell experiences a constant QD dose, but the in
vivo QD concentration can vary, and the organ-specific dose may not be
high enough to induce detectable toxicity. Because QDs are retained
within animals, long-term toxicity may be a problem but has not been
established.
Finally, they suggest that in future QD toxicity studies more specific toxicological questions should be asked. For
example: “At what dose are 5 nm CdSe QDs that are stabilized with
mercaptoacetic acid and conjugated to the antibody herceptin toxic to
HeLa cells?” rather than “Are QDs toxic?”
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