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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Skin irritation / corrosion

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Administrative data

Endpoint:
skin irritation: in vitro / ex vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2009
Report date:
2009

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: OECD guideline 431
Deviations:
no
Principles of method if other than guideline:
In vitro skin corrosion test: "Human Skin Model Test", April 2004 B.40 bis
3-D human skin model (EPI-200)

Evaluation criteria: The OD values obtained of each sample are used for calculating the percentage viability compared to the negative control, which is defined to be 100%. Based on this percentage of viable cells and the criteria defined below the test item is classified to be corrosive or non-corrosive.
Considered corrosive: viability after 3 min of exposure is <50%
Considered corrosive: viability after 3 min of exposure is >=50% and the viability after 1 hr of exposure is <15%
Considered non-corrosive: viability after 3 min of exposure is >=50% and the viability after 1 hr of exposure is >=15%

There were no modifications to the test procedure.

Test doses: approx. 50 µl per insert (tissue diameter: 8 mm; culture area: 0.6 cm2)

No other effects observed.
GLP compliance:
yes (incl. QA statement)

Test material

Reference
Name:
Unnamed
Type:
Constituent
Details on test material:
The pasty test item was applied by using an applicator made from a 1 ml disposable syringe. The application of the test item was difficult. A complete removal of the residues of the test item was not possible. --- Negative control: Distlled water (water for injections; Serumwerk Bernburg AG); Positve control: KOH as 8 N solution (preparation: 2.24 g in 5 ml distilled water)

Results and discussion

In vitro

Results
Irritation / corrosion parameter:
other: other: in vitro assay; cell viability (MTT assay)
Value:
ca. 2.23
Remarks on result:
other:
Remarks:
Time point: 3 min and 1 hr. Max. score: 2.49. Remarks: OECD 431. (migrated information)

In vivo

Irritant / corrosive response data:
The test item is non-corrosive.

Exposure time 3 min
Viability negative control: 100%
Viability positive control: 38%
Test item: 97%

Exposure time 1 hr
Viability negative control: 100%
Viability positive control: 9%
Test item: 90%

Reproducibility was very good (n=3)

Applicant's summary and conclusion

Conclusions:
Cell viability in test item group (in % of untreated control)
after 3 min: 97%; after 1 hr: 90%

OD mean score
3 min: 2.194 in test item group (negative control: 2.264; positive control: 0.857)
1 hr: 2.271 in test item group (negative control: 2.531; positive control: 0.223)

The test item is non-corrosive.