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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Endpoint:
basic toxicokinetics, other
Remarks:
Bio-elution
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
test procedure in accordance with generally accepted scientific standards and described in sufficient detail

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2020
Report date:
2020

Materials and methods

Objective of study:
bioaccessibility (or bioavailability)
Principles of method if other than guideline:
Bio-elution refers to the in vitro extraction methods used to assess the bio-accessibility of a substance. This technique quantifies the degree to which a substance (e.g. metal mixtures) is released in artificial biological fluids of defined
composition and pH: interstitial, alveolar, lysosomal, synovial, gastric and intestinal juice.

Test material

impurity 1
Reference substance name:
Total unspecified impurities
IUPAC Name:
Total unspecified impurities
Constituent 1
Reference substance name:
Cobalt Nickel Manganese Oxide
Cas Number:
37348-84-8
Molecular formula:
Ni1-x-yMnxCoyOz with Me=Ni+Mn+Co=1 and Ni/Me= 0.45-0.98 Mn/Me= 0.01-0.35 Co/Me= 0.01-0.35 O/Me= 1.00-1.33
IUPAC Name:
Cobalt Nickel Manganese Oxide
Test material form:
solid
Specific details on test material used for the study:
Batch PVX-089 PVX14
Nickel Manganese Cobalt ratio 8:1:1

Results and discussion

Any other information on results incl. tables

The bio-accessible fraction was calculated based on the comparison of the metal release with the metal bulk concentration of the compound. For the gastric bio-elution test, Co, Ni and Mn have different releases: Mn was released for 6%, Co for 57% and Ni for 82%. The coefficient of variance (CV) between the three replicas was less than 2% for the three metals, indicating a high reproducibility of the analytical results. For the lysosomal bio-elution test, a high reproducibility of the analytical results was noticed as well. The metal release of Co, Ni and Mn were found to be around 100%, i.e. all metals are fully bio-accessible in lysosomal fluid. In the alveolar bio-elution test, the release of Co, Mn and Ni were negligible. 

In the case of Nickel Cobalt Manganese Oxide (8:1:1), Co, Mn and Ni are completely bio-accessible in the lysosomal synthetic fluids, while these metals are only partially bio-accessible in gastric fluid and not bio-accessible in alveolar synthetic fluid. 

Applicant's summary and conclusion

Conclusions:
A bio-elution study to estimate the metal release of Nickel Cobalt Manganese Oxide (8:1:1) in three
artificial solutions was performed.
The results show different releases for Co, Mn and Ni from Nickel Cobalt Manganese Oxide (8:1:1)
for the gastric fluid. Mn was almost not released (only 6%), Co was 57% released and Ni have the
highest release of 82%. The intracellular (lysosomal) fluid show a similar release for CO, Mn and Ni
off 100%. No significant release in alveolar medium was measured.
Executive summary:

A bio-elution study to estimate the metal release of Nickel Cobalt Manganese Oxide (8:1:1) in three artificial solutions was performed.
The results show different releases for Co, Mn and Ni from Nickel Cobalt Manganese Oxide (8:1:1) for the gastric fluid. Mn was almost not released (only 6%), Co was 57% released and Ni have the highest release of 82%. The intracellular (lysosomal) fluid show a similar release for Co, Mn and Ni off 100%. No significant release in alveolar medium was measured.