| Literature DB >> 23630249 |
Annika Leifert1, Yu Pan, Anne Kinkeldey, Frank Schiefer, Julia Setzler, Olaf Scheel, Hera Lichtenbeld, Günter Schmid, Wolfgang Wenzel, Willi Jahnen-Dechent, Ulrich Simon.
Abstract
Understanding the mechanism of toxicity of nanomaterials remains a challenge with respect to both mechanisms involved and product regulation. Here we show toxicity of ultrasmall gold nanoparticles (AuNPs). Depending on the ligand chemistry, 1.4-nm-diameter AuNPs failed electrophysiology-based safety testing using human embryonic kidney cell line 293 cells expressing human ether-á-go-go-Related gene (hERG), a Food and Drug Administration-established drug safety test. In patch-clamp experiments, phosphine-stabilized AuNPs irreversibly blocked hERG channels, whereas thiol-stabilized AuNPs of similar size had no effect in vitro, and neither particle blocked the channel in vivo. We conclude that safety regulations may need to be reevaluated and adapted to reflect the fact that the binding modality of surface functional groups becomes a relevant parameter for the design of nanoscale bioactive compounds.Entities:
Keywords: complementarity; gold cluster; nanotoxicology; shape
Mesh:
Substances:
Year: 2013 PMID: 23630249 PMCID: PMC3657833 DOI: 10.1073/pnas.1220143110
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205