Katherine E. Heim

Dr. Katherine E. Heim


Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 July 2019 in Inorganics
Verified
Journal Article
Open access
PDF file
SBSamuel Buxton
Samuel Buxton
EGEmily Garman
Emily Garman
KHKatherine E. Heim
Katherine E. Heim
TLTara Lyons-Darden
Tara Lyons-Darden
CSChristian E. Schlekat
Christian E. Schlekat
AOAdriana R. Oller
Adriana R. Oller
Nickel (Ni) metal and Ni compounds are widely used in applications like stainless steel, alloys, and batteries. Nickel is a naturally occurring element in water, soil, air, and living organisms, and is essential to microorganisms and plants. Thus, human and environmental nickel exposures are ubiquitous. Production and use of nickel and its compounds can, however, result in additional exposures to humans and the environment. Notable human health toxicity effects identified from human and/or animal studies include respiratory cancer, non-cancer toxicity effects following inhalation, dermatitis, and reproductive effects. These effects have thresholds, with indirect genotoxic and epigenetic events underlying the threshold mode of action for nickel carcinogenicity. Differences in human toxicity potencies/potentials of different nickel chemical forms are correlated with the bioavailability of the Ni2+ ion at target sites. Likewise, Ni2+ has been demonstrated to be the toxic chemical species in the environment, and models have been developed that account for the influence of abiotic factors on the bioavailability and toxicity of Ni2+ in different habitats. Emerging issues regarding the toxicity of nickel nanoforms and metal mixtures are briefly discussed. This review is unique in its covering of both human and environmental nickel toxicity data.

1 February 2020 in Regulatory Toxicology and Pharmacology
Verified
Journal Article
Open access
KHKatherine E. Heim
Katherine E. Heim
RDRuth Danzeisen
Ruth Danzeisen
VVViolaine Verougstraete
Violaine Verougstraete
FGFrédéric Gaidou
Frédéric Gaidou
TBTony Brouwers
Tony Brouwers
AOAdriana R. Oller
Adriana R. Oller
This study investigated nickel and cobalt ion release from the metals and several alloys in synthetic gastric, as well as interstitial and lysosomal lung fluids. Results were used to calculate the relative bioaccessible concentrations (RBCs) of the metals. Nickel release from SS 316L powder in gastric fluid was >300-fold lower than from a simple mixture of powders of the same bulk composition. Gastric bioaccessibility data showed 50-fold higher metal releases per gram of sample from powder than massive forms. RBCs of nickel and cobalt in the alloy powders were lower, equal, or higher in all fluids tested than their bulk concentrations. This illustrates the fact that matrix effects can increase or decrease the metal ion release, depending on the metal ingredients, alloy type, and fluid, consistent with research by others. Acute inhalation toxicity studies with cobalt-containing alloy powders showed that the RBC of cobalt in interstitial lung fluid predicted acute toxicity better than bulk concentration. This example indicates that the RBC of a metal in an alloy may estimate the concentration of bioavailable metals better than the bulk concentration, and the approach may provide a means to refine the classification of alloys for several human health endpoints.

17 May 2024 in Nanomaterials
Verified
Journal Article
Open access
PDF file
TLTara Lyons-Darden
Tara Lyons-Darden
KHKatherine E. Heim
Katherine E. Heim
LHLi Han
Li Han
LHLaura Haines
Laura Haines
CSChristie Sayes
Christie Sayes
AOAdriana R. Oller
Adriana R. Oller
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.

9 May 2023
Verified
Conference Paper
Closed access
GHGolara Honari
Golara Honari
KHKatherine E. Heim
Katherine E. Heim
KYKiana Yekrang
Kiana Yekrang
Nickel is the leading cause of contact allergy worldwide. A regulation to limit nickel exposure from consumer products that come in prolonged dir | POSTER