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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 vivo
Type of information:
other: Read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
weight of evidence
Study period:
July 2010
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Read Across from a GLP well conducted study on the supporting structural related substance
Justification for type of information:
The justification for the use of the similar substance is detailed in the Read Across document attached in section 13

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2010
Report date:
2010

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Reference substance name:
Oils, fish, oxidized, bisulfited, sodium salts
EC Number:
307-037-4
EC Name:
Oils, fish, oxidized, bisulfited, sodium salts
Cas Number:
97488-98-7
Molecular formula:
Not applicable, UVCB
IUPAC Name:
Oils, fish, oxidized, bisulfited, sodium salts
Test material form:
liquid
Details on test material:
- Name of test material (as cited in study report): FLL Sample 3
- Physical state: viscous liquid
- Purity: 90%
- Lot/batch No.: LS06921
- Expiration date of the lot/batch: 13 October 2010
- Storage condition of test material: room temperature, in the dark
- Other: amber coloured

Test animals / tissue source

Species:
rabbit
Strain:
New Zealand White
Details on test animals or tissues and environmental conditions:
TEST ANIMALS
- Source: Harlan Laboratories UK Limited, Hillcrest, Belton, Loughborough, UK
- Age at study initiation: 12-20 weeks
- Weight at study initiation: 2.40 or2.42 kg
- Housing: individually housed in suspended cages
- Diet (e.g. ad libitum): ad libitum to 2030 Teklad global rabbit diet
- Water (e.g. ad libitum): ad libitum
- Acclimation period: at least 5 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 17-23 degrees C
- Humidity (%): 30-70%
- Air changes (per hr): at least 15
- Photoperiod (hrs dark / hrs light): 12 / 12 dark-light

IN-LIFE DATES: not reported

Test system

Vehicle:
unchanged (no vehicle)
Controls:
yes, concurrent no treatment
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied: 0.1 ml

VEHICLE: Not applicable
Duration of treatment / exposure:
Test material was applied to eye, and the eyelids were held together for about 1 second and then released. Eyes were not rinsed after exposure.
Observation period (in vivo):
72 hours
Number of animals or in vitro replicates:
2
Details on study design:
REMOVAL OF TEST SUBSTANCE: Not applicable

SCORING SYSTEM: initial pain reaction from 6-point scale, Draize scale for scoring ocular irritation was used during the observation period. After scores were assigned, a modified version of Kay and Calandra (1962) was used to classify the ocular irritancy potential.

TOOL USED TO ASSESS SCORE: ophthalmoscope

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
cornea opacity score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
4
Irritation parameter:
iris score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
4
Irritation parameter:
conjunctivae score
Basis:
mean
Time point:
24/48/72 h
Score:
0.3
Max. score:
4
Irritation parameter:
chemosis score
Basis:
mean
Time point:
24/48/72 h
Score:
0.3
Max. score:
4
Irritant / corrosive response data:
See Table 1.
Other effects:
Body weight changes after 3 days: +0.05 kg

Any other information on results incl. tables

Table 1. Individual Scores and Individual Total Scores for Ocular Irritation

Rabbit number and sex

69221 Male

69239 Male

Time after treatment

1 hour

24 hours

48 hours

72 hours

1 hour

24 hours

48 hours

72 hours

Cornea

 E = Degree of opacity

0

0

0

0

0

0

0

0

 F = Area of Cornea involved

0

0

0

0

0

0

0

0

 Score (E x F) x 5

0

0

0

0

0

0

0

0

Iris

 D

0

0

0

0

0

0

0

0

 Score (D x 5)

0

0

0

0

0

0

0

0

Conjunctivae

 A = Redness

2

1

1

0

2

1

0

0

 B = Chemosis

2

1

0

0

2

1

0

0

 C = Discharge

2

1

0

0

2

1

0

0

 Score (A + B + C) x 2

12

6

2

0

12

6

0

0

Total Score

12

6

2

0

12

6

0

0

 

 

Applicant's summary and conclusion

Interpretation of results:
slightly irritating
Remarks:
Migrated information Criteria used for interpretation of results: other: modified Kay and Calandra 1962
Conclusions:
The test substance was determined to be a mild irritant (Class 4 on a 1 - 8 scale) to the rabbit eye according to a modified Kay and Calandra classification system.
Executive summary:

Introduction. The study was performed to assess the irritancy potential of the test material to the eye of the New Zealand White rabbit. The method was designed to meet the requirements of the following:

-      OECD guidelines for the testing of chemicals No. 405 “Acute Eye Irritation/Corrosion” (adopted 24 April 2002)

-      Method B.5 Acute Toxicity (Eye Irritation) of Commission Regulation (EC) No. 440/2008

 

Result. A single application of the test material to the non-irrigated eye of two rabbits produced moderate conjuctival irritation. Both treated eyes appeared normal at the 48 -Hour observation.

 

Conclusion. The test material produced a maximum group mean score of 12.0 and was classified as a mild irritant (Class 4 on a 1 to 8 scale) to the rabbit eye according to a modified Kay and Calandra classification system.