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Toxicological information

Skin irritation / corrosion

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Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
07.09.1981 to 11.09.1981
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The study was conducted according to a test protocol that is comparable to the appropriate OECD test guideline. It was not compliant with GLP, but underwent a quality assurance audit.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1982
Report Date:
1982

Materials and methods

Test guideline
Qualifier:
equivalent or similar to
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
yes
Remarks:
24 hour exposure
GLP compliance:
no

Test material

Reference
Name:
Unnamed
Type:
Constituent

Test animals

Species:
rabbit
Strain:
New Zealand White
Details on test animals and environmental conditions:
TEST ANIMALS
- Source: Buckshire Corporation, Perkasie, Pennsylvannia.
- Age at study initiation: No data
- Weight at study initiation: No data
- Housing: Individually in suspended steel wire mesh cages
- Diet (e.g. ad libitum): Ad libitum
- Water (e.g. ad libitum): Ad libitum
- Acclimation period: 12 days.


ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 ±2
- Humidity (%): 50± 5
- Air changes (per hr): No data
- Photoperiod (hrs dark / hrs light): 12/12


IN-LIFE DATES: From: 07.09.1981 to 11.09.1981

Test system

Type of coverage:
semiocclusive
Preparation of test site:
shaved
Vehicle:
unchanged (no vehicle)
Controls:
not required
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 ml
Duration of treatment / exposure:
24 hour(s)
Observation period:
72 hours
Number of animals:
6
Details on study design:
TEST SITE
- Area of exposure: No data
- % coverage: No data
- Type of wrap if used: No wrap used. The treated patch of gauze was secured on two opposing edges with narrow strips of surgical tape.


REMOVAL OF TEST SUBSTANCE
- Washing (if done): Not done


SCORING SYSTEM: Draize

Results and discussion

In vivo

Results
Irritation parameter:
primary dermal irritation index (PDII)
Basis:
mean
Time point:
other: 24, 48 and 72 hours
Score:
1.94
Max. score:
8
Reversibility:
fully reversible within: 8 days
Irritant / corrosive response data:
All six animals developed well-defined erythema (grade 2) 24 or 48 hours after application, which remained in all animals to 96 hours. One animal had persistent erythema (grade 1) to 168 hours. There was no oedema.
Other effects:
None reported.

Any other information on results incl. tables

No irritation was observed at the untreated sites of all animals. Significant irritation was observed in the positive
control animals which had a PII score of 5.22

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
In a skin irritation study (reliability score 2) conducted using a protocol similar to OECD 404, but not to GLP, Prylog was mildly irritating to the skin of rabbits following 24 hours exposure. Based on the available information, the substance does not meet the current EU criteria for classification as a skin irritant.
Executive summary:

In a skin irritation study (reliability score 2) conducted using a protocol similar to OECD 404, but not to GLP, Prylog was mildly irritating to the skin of rabbits following 24 hours exposure.