Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Eye irritation

Currently viewing:

Administrative data

Endpoint:
eye irritation: in vitro / ex vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP study meeting generally accepted scientific standards and documented in detail

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2012
Report date:
2012

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
The present test is based on the experience that irritant chemicals produce cytotoxicity in human reconstructed cornea after a short term topical exposure. After application of 50µl of the test material to the surface of the three dimensional human cornea model "EpiOcular" for 30minutes, the test substance is removed. After a 2h post-exposure period, the induced cytotoxicity (= loss of viability) is measured as the reduction of mitochondrial dehydrogenase activity using MTT. A chemical is considered as irritant, if the mean viability of smaller or equal 50%, and as not-irritant, if the mean viability is above 60%. In the range between 50% and 60% no prediction can be made.

Though there are no official national or international guidelines for the EpiOcularTM test yet, the study was performed according to the methods described in the following publications:
- MatTek Corporation, Ashland, MA 01721, USA: EpiOcularTM human cell construct: Procedure details, Version 3.1a of February 10, 2010.
- Harbell J.W. et al. (2009): COLIPA Program on Optimization of Existing In Vitro Eye Irritation Assays for Entry into Formal Validation: Technology Transfer and Intra/Inter Laboratory Evaluation of EpiOcular Assay for Chemicals. Poster # 378, Society of Toxicology, March 2009.
In addition the study follows the testing strategy for determination of eye irritation/corrosion as given in the following OECD guideline:
- OECD Guideline for Testing of Chemicals No. 405, April 24, 2002 (“Acute Eye Irritation/Corrosion”)
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
Fatty acids, C18-unsatd., dimers, compds. with coco alkylamines
EC Number:
614-682-8
Cas Number:
68647-95-0
Molecular formula:
Not applicable (UVCB substance)
IUPAC Name:
Fatty acids, C18-unsatd., dimers, compds. with coco alkylamines
Details on test material:
- Name of test material (as cited in study report): Fatty acids, C18-unsatd., dimers, compds. with coco alkylamines
- Physical state: highly viscous liquid
- Analytical purity: The test item is a complex mixture of isomers and homologues components, so no purity can be stated. (For details see analytical report BASF study-No.: 11S05363)
- Purity test date: 2012-08-08
- Lot/batch No.: BI514173
- Expiration date of the lot/batch: 2013-04-18
- Storage condition of test material: room temperature

Test animals / tissue source

Species:
other: human cornea model
Details on test animals or tissues and environmental conditions:
Three dimensional human cornea model EpiOcular OCL-200
- Source: MatTek corp., Ashland MA, USA
- Culture Medium: DMEM
- Cell death detection agent: 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) (MatTek corp., Ashland MA, USA / Sigma,Germany)
- duplicate cultures
The test substance is not able to reduce MTT directly.

Test system

Vehicle:
unchanged (no vehicle)
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 50µl
Duration of treatment / exposure:
30min
Details on study design:
Negative control: De-ionized water
Positive control: Methyl acetate (98%+)

Incubation times:
Pre-incubation in culture medium: 16-24h
Pre-treatment with PBS to wet the tissue surfact for 30min
Exposure time: 30min
Post-incubation period: 2h (after washing)
MTT incubation: 3h

REMOVAL OF TEST SUBSTANCE
- Washing (if done): with PBS and medium subsequently at the end of the exposure time. After soaking for 12minutes in medium, the tissues were dried on absorbant paper.

Results and discussion

In vivo

Results
Irritation parameter:
other: cell viability
Basis:
mean
Remarks on result:
other: 65% (not irritating)

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information