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EC number: 201-377-6 | CAS number: 81-81-2
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- Ecotoxicological Summary
- Aquatic toxicity
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- Short-term toxicity to fish
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- Toxicological Summary
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- Acute Toxicity
- Irritation / corrosion
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- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
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- Additional toxicological data

Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 994
- Report date:
- 1994
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- GLP compliance:
- not specified
Test material
- Reference substance name:
- 129-06-0
- IUPAC Name:
- 129-06-0
- Reference substance name:
- Warfarin sodium
- EC Number:
- 204-929-4
- EC Name:
- Warfarin sodium
- Cas Number:
- 129-06-6
- IUPAC Name:
- sodium 2-oxo-3-(3-oxo-1-phenylbutyl)-2H-chromen-4-olate
- Details on test material:
- -Purity: not reported
Constituent 1
Constituent 2
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Age at study initiation: young adult females
- Weight at study initiation: 2336 g, 2166 g
- Housing: singly in suspended wire-mesh cages
- Diet (e.g. ad libitum): approx. 125 g high fiber rabbit chow
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 2 weeks
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18-22°C
- Humidity (%): 40-60%
- Air changes (per hr): not reported
- Photoperiod (hrs dark / hrs light): 12 hr light/12 hr dark
Test system
- Vehicle:
- not specified
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.01 g - Duration of treatment / exposure:
- 20 sec
- Observation period (in vivo):
- 1 hr, 4 hr and days 1, 2, 3 and 7
- Number of animals or in vitro replicates:
- 2
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): yes
- Time after start of exposure: 20 sec after exposure
SCORING SYSTEM: Draize scale
TOOL USED TO ASSESS SCORE: hand-slit lamp / biomicroscope / fluorescein
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- not specified
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- not specified
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Reversibility:
- not specified
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Reversibility:
- not specified
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 1.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 7 days
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- fully reversible within: 7 days
- Irritant / corrosive response data:
- The test substance produced mild chemosis and moderate conjunctival redness with hemorrhaging of the conjunctiva and nictitating membrane in the treated washed and unwashed rabbit eyes. In addition, moderate iritis and copious blood-tinged discharge were observed in the treated unwashed eye. Both treated eyes were normal 7 days following treatment.
- Other effects:
- Both rabbits pawed their treated eye and 1 rabbit vocalized after instillation of the test substance.
Any other information on results incl. tables
Individual eye irritation Draize scores are presented below.
Rabbit Number 29045 (Unwashed) |
1 Hour |
4 Hours |
1 Day |
2 Days |
3 Days |
7 Days |
Cornea Opacity |
0 |
0 |
0 |
0 |
0 |
0 |
Cornea Area |
0 |
0 |
0 |
0 |
0 |
0 |
Iris |
0 |
1 |
0 |
0 |
0 |
0 |
Conjunctiva Redness |
2 |
2 |
2C |
2C |
2C |
0 |
Conjunctiva Chemosis |
2 |
2 |
2 |
1 |
1 |
0 |
Conjunctiva Discharge |
2H |
3H |
1H |
0 |
0 |
0 |
Rabbit Number 29046 (Washed) |
1 Hour |
4 Hours |
1 Day |
2 Days |
3 Days |
7 Days |
Cornea Opacity |
0 |
0 |
0 |
0 |
0 |
0 |
Cornea Area |
0 |
0 |
0 |
0 |
0 |
0 |
Iris |
0 |
0 |
0 |
0 |
0 |
0 |
Conjunctiva Redness |
2 |
2 |
2C |
2C |
2C |
0 |
Conjunctiva Chemosis |
2 |
2 |
1 |
1 |
1 |
0 |
Conjunctiva Discharge |
0 |
0 |
0 |
0 |
0 |
0 |
H = Hemastix evaluations positive for blood
C = Hemorrhaging of the conjunctiva and the nictitating membrane
Applicant's summary and conclusion
- Interpretation of results:
- moderately irritating
- Remarks:
- Migrated information
- Conclusions:
- Under the conditions of this study, the test substance was a moderate eye irritant.
- Executive summary:
The test substance was evaluated for acute eye irritation potential in 2 rabbits. Approximately 0.01 g of the test substance was instilled into the lower conjunctival sac of the right eye of each rabbit. Approximately 20 seconds after instillation, the treated and control eyes of 1 rabbit were washed. The treated and control eyes of the remaining rabbit were not washed. The eyes of the rabbits were examined on the day of treatment and on days 1, 2, 3, and 7 following treatment.
The test substance produced mild chemosis and moderate conjunctival redness with hemorrhaging of the conjunctiva and nictitating membrane in the treated washed and unwashed rabbit eyes. In addition, moderate iritis and copious blood-tinged discharge were observed in the treated unwashed eye. Both treated eyes were normal 7 days following treatment.
Under the conditions of this study, the test substance was a moderate eye irritant.
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