Bioaccessibility of Metallic Nickel and Nickel Oxide Nanoparticles in Four Simulated Biological Fluids

Author:

Lyons-Darden Tara1ORCID,Heim Katherine E.1,Han Li2,Haines Laura2,Sayes Christie M.3,Oller Adriana R.4

Affiliation:

1. NiPERA, Inc., 2525 Meridian Parkway, Suite 240, Durham, NC 27713, USA

2. RTI International, 3040 E. Cornwallis Road, Research Triangle Park, NC 27709, USA

3. Department of Environmental Science, Baylor University, One Bear Place #97266, Waco, TX 76798, USA

4. Oller Consulting, 722 Gaston Manor Drive, Durham, NC 27703, USA

Abstract

Bioaccessibility of metals from substances and alloys is increasingly used as part of the assessment to predict potential toxicity. However, data are sparse on the metal bioaccessibility from nanoparticle (NP) size metal substances. This study examines nickel ion release from metallic nickel and nickel oxide micron particles (MPs) and NPs in simulated biological fluids at various timepoints including those relevant for specific routes of exposure. The results suggest that MPs of both metallic nickel and nickel oxide generally released more nickel ions in acidic simulated biological fluids (gastric and lysosomal) than NPs of the same substance, with the largest differences being for nickel oxide. In more neutral pH fluids (interstitial and perspiration), nickel metal NPs released more nickel ions than MPs, with nickel oxide results showing a higher release for MPs in interstitial fluid yet a lower release in perspiration fluid. Various experimental factors related to the particle, fluid, and extraction duration were identified that can have an impact on the particle dissolution and release of nickel ions. Overall, the results suggest that based on nickel release alone, nickel NPs are not inherently more hazardous than nickel MPs. Moreover, analyses should be performed on a case-by-case basis with consideration of various experimental factors and correlation with in vivo data.

Publisher

MDPI AG

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