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For the compounds within AD, their toxicity can be more accurately predicted.
No mechanism of toxicity can be considered as generic for all NP [126].
This toxicity can be measured on in vitro models, using different measurements.
With ZnS shells on the CdTe/CdS QDs, its toxicity can be greatly decreased.
However, some general conclusions about CNT toxicity can be drawn from the reviewed studies.
This to observe if a better consensus between calculated and measured toxicity can be established.
Aldehyde toxicity can be entirely circumvented by performing aldehyde biosynthesis in non-cellular systems.
Human toxicity can be determined using adequate in vitro test designs.
Toxicity can be manifested in platelet activation as it has been shown for SWCNTs.
Neurological toxicity can be acute, requiring dose adaptation or a change of drugs.
The ROS toxicity can be eliminated via combination of the ROS electrophilic groups with the NAC sulfhydryl group.
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