Registration Dossier

Administrative data

Endpoint:
skin sensitisation
Remarks:
in vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
July 10 - August 4, 1995
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: see 'Remark'
Remarks:
The sensitisation test, performed in the year 1995, did not follow the OECD. However the conditions applied in the study are acceptable and the result shows that the substance is not sensitising. Eucarol AGE SS (D-Glucopyranose, oligomeric, 6-(hydrogen 2-sulfobutanedioate), 1- (coco alkyl) ethers, sodium salts) was old name for EUCAROL AGE SS/ND before REACH regulatory - new nomenclature. The substance was identified with: CAS: 151911-53-4 EC: 500-331-5

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1995
Report Date:
1995

Materials and methods

Principles of method if other than guideline:
Kligman Magnusson
GLP compliance:
no
Type of study:
other: Kligman Magnusson

Test material

Reference
Name:
Unnamed
Type:
Constituent

In vivo test system

Test animals

Species:
guinea pig
Strain:
Hartley
Sex:
female
Details on test animals and environmental conditions:
TEST ANIMALS
- Source: Padre Antonio - Mariano Comense (CO)
- Weight at study initiation: 200 - 300 g
- Housing: the animals were caged, in groups of ten, in transparent polycarbonate cages
- Diet (e.g. ad libitum): pellet diet
- Water (e.g. ad libitum): filtered water from an automatic watering system
- Acclimation period: animals were kept in quarantine for one week

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22+/- 2 °C
- Humidity (%): 55% +/- 15%
- Air changes (per hr): at least 25 times per hour
- Photoperiod (hrs dark / hrs light): 12 h/day

Study design: in vivo (non-LLNA)

Induction
Route:
intradermal and epicutaneous
Vehicle:
unchanged (no vehicle)
Challenge
Route:
epicutaneous, occlusive
Vehicle:
unchanged (no vehicle)
No. of animals per dose:
10 animals treated with test material
5 animals treated with distilled water
Details on study design:
RANGE FINDING TESTS:

MAIN STUDY
A. INDUCTION EXPOSURE
- Test groups: 10 guinea pigs treated with 3 double intradermal injections (Freud complete adjuvant in distilled water 1:1, test material and test material in FCA 1:1) . After 6 days a topical application of 0,5 ml of sodium lauril solfatum 105 was made.
After 7 days the eluated of the test material (dose 0,5 ml/animal) was applied for a period of 48 h.
- Control group: 5 guinea pigs treated with the same pairs of injection but in the 2nd one only distilled water were used.

B. CHALLENGE EXPOSURE
- Day(s) of challenge: 21 days after the beginning of treatment
- Exposure period: 24 h
- Concentrations: 0,5 ml of the test material on the left side and distilled water on the right side
- Evaluation (hr after challenge): 48 and 72 h

Results and discussion

In vivo (non-LLNA)

Results
Reading:
1st reading
Hours after challenge:
48
Group:
test group
Dose level:
0.5 ml
No. with + reactions:
0
Total no. in group:
10
Remarks on result:
other: Reading: 1st reading. . Hours after challenge: 48.0. Group: test group. Dose level: 0.5 ml. No with. + reactions: 0.0. Total no. in groups: 10.0.

Applicant's summary and conclusion

Interpretation of results:
not sensitising
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
On the basis of the results the test material can be considered non sensitizing.