首页 | 本学科首页   官方微博 | 高级检索  
     


Acute oral toxicity of nickel compounds
Authors:Rayetta G. Henderson  Jennifer Durando  Adriana R. Oller  Daniel J. Merkel  Palma Ann Marone  Hudson K. Bates
Affiliation:1. NiPERA, Inc., 2525 Meridian Parkway, Suite 240, Durham, NC 27713, USA;2. Product Safety Labs, 2394 US Highway 130, Suite E, Dayton, NJ 08810, USA
Abstract:Acute oral toxicity studies were conducted on samples of nine unique nickel compounds and two complex materials to comply with the data and classification requirements of the new Registration, Evaluation, and Authorization of Chemicals Regulation (REACH) in Europe. The samples tested in this study confirmed the overall low oral toxicity of nickel substances and demonstrated a wide range of LD50 values extending from 310 to >11,000 mg/kg. This variation highlights the differences in toxicological properties between various forms of nickel and underscores the importance of Ni(II) ion bioavailability in determining toxicity. The relative acute oral toxicity of the various nickel substances was found to be: nickel fluoride, nickel sulfate, nickel chloride, nickel acetate > nickel sulfamate > nickel hydroxycarbonate > nickel dihydroxide ?? nickel subsulfide, nickel oxides, nickel ash, nickel mattes. Based on these data, four nickel compounds would receive a Category 4 acute toxicity classification according to the European Regulation on Classification, Labelling and Packaging of Chemical Substances and Mixtures (CLP), while the rest of the nickel substances tested fit the criterion for no classification. These data also provided the in vivo verification needed to perform read-across for additional oral toxicity endpoints and nickel substances.
Keywords:Nickel   Metal   Acute toxicity   Oral   REACH   Read-across   Rat   Classification   Bioavailability   Bioaccessibility
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号