Registration Dossier

Administrative data

Description of key information

In a skin irritation study conducted on rabbits and according to OECD 404, tungsten trioxide was deemed to be not irritating. In an eye irritation study conducted on rabbits and according to OECD 405, tungsten trioxide was deemed to be not irritating.

Key value for chemical safety assessment

Skin irritation / corrosion

Link to relevant study records

Referenceopen allclose all

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2002-06-24 to 2002-08-20
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
no
Qualifier:
according to
Guideline:
EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
GLP compliance:
yes
Species:
rabbit
Strain:
New Zealand White
Details on test animals and environmental conditions:
TEST ANIMALS
- Source: Charles River Wiga, D-97633
- Weight at study initiation: 1.8-2.0 kg
- Housing: Animals were housed singly in metal wire cages, type KK 016R
- Diet: Altromin 2023 diet for rabbits - ad libitum. Hay briquettes were offered additionally as a dietary supplement.
- Water: Tap water from an automatic watering system - ad libitum
- Acclimation period: 5 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): Average of 19.6 degree C
- Humidity (%): Average of 70.3%
- Air changes (per hr): 12/hr
- Photoperiod (hrs dark / hrs light): 12 dark/12 light (6 am to 6 pm)

IN-LIFE DATES: From: 2004-06-24 To: 2004-06-28
Type of coverage:
semiocclusive
Preparation of test site:
shaved
Vehicle:
other: deionised water
Controls:
other: surrounding untreated skin
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 g/ 2.5 cm X 2.5 cm patch

VEHICLE
- Amount(s) applied (volume or weight with unit): 1.0 mL
Duration of treatment / exposure:
4 hours
Observation period:
72 hours
Number of animals:
3 females
Details on study design:
TEST SITE
- Area of exposure: 2.5 cm X 2.5 cm on the clipped dorsal areas of the trunk of the rabbits.
- Type of wrap if used: cellulose patches and self adhesive non woven, hypoallergenic fabric

REMOVAL OF TEST SUBSTANCE
- Washing (if done): Residual test substance was wiped off with wet Kleenex tissues after 4 hour exposure period, if necessary.

SCORING SYSTEM: Erythema/Eschar and Oedema

- The skin was examined using a cold light source KL 1500 electronic
Irritation parameter:
erythema score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
4
Remarks on result:
no indication of irritation
Irritation parameter:
edema score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
4
Remarks on result:
no indication of irritation
Irritant / corrosive response data:
All areas to be treated with the test substance and all control areas were normal before the application and at each observation time.
Other effects:
No general toxic effects were noted.
Interpretation of results:
GHS criteria not met
Conclusions:
All areas to be treated with the test substance and all control areas were normal before the application and at each observation time. The mean scores for three of the animals at 24, 48 and 72 hrs. post application were 0.0 when observing for Erythema/Eschar and Oedema.
Endpoint:
skin irritation: in vitro / ex vivo
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
an in vitro skin irritation study does not need to be conducted because adequate data from an in vivo skin irritation study are available
Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (not irritating)

Eye irritation

Link to relevant study records

Referenceopen allclose all

Endpoint:
eye irritation: in vitro / ex vivo
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
an in vitro eye irritation study does not need to be conducted because adequate data from an in vivo eye irritation study are available
Endpoint:
eye irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2002-07-01 to 2002-08-20
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
Qualifier:
according to
Guideline:
EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
GLP compliance:
yes
Species:
rabbit
Strain:
New Zealand White
Details on test animals or tissues and environmental conditions:
TEST ANIMALS
- Source: Charles River Wiga
- Weight at study initiation: 2.1-2.2 kg
- Housing: Individual caging in metal wire cages (79 cm x 59 cm bottom area, 38 cm height, with a wooden rest shelf, 15 cm x 59 cm)
- Diet (e.g. ad libitum): Altromin 2023 diet for rabbits, ad libitum. Hay- briquettes were offered additionally as a dietary supplement.
- Water (e.g. ad libitum): Tap water from an automatic water system, ad libitum
- Acclimation period: 5 days (one animal), 12 days (two other animals)

ENVIRONMENTAL CONDITIONS
- Temperature (°C): average of 19.4 C
- Humidity (%): average of 66.7%
- Air changes (per hr): 12/hr
- Photoperiod (hrs dark / hrs light): 12 dark/12 light (6 am to 6 pm)

IN-LIFE DATES: From: 2002-07-01 To: 2002-07-12
Vehicle:
unchanged (no vehicle)
Controls:
other: The left eyes remained untreated and served as a control
Amount / concentration applied:
The approximate equivalent of 0.1 mL (~100 mg) of the test substance was administered per animal into the conjunctival sacs of the right eyes by gently pulling the lower lids away from the eyeballs for instillation. The eyes were held closed for about one second to prevent a loss of test substance.

Observation period (in vivo):
72 hours
Number of animals or in vitro replicates:
3 females
Details on study design:
SCORING SYSTEM: Scoring scheme for ocular lesions- examined the whole eye, the corneae, irises, and conjunctivae

TOOL USED TO ASSESS SCORE: otoscope lamp
Irritation parameter:
overall irritation score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Remarks on result:
no indication of irritation
Irritation parameter:
cornea opacity score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
4
Remarks on result:
no indication of irritation
Irritation parameter:
iris score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
2
Remarks on result:
no indication of irritation
Irritation parameter:
conjunctivae score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
3
Remarks on result:
no indication of irritation
Irritation parameter:
chemosis score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
4
Remarks on result:
no indication of irritation
Irritant / corrosive response data:
Both the untreated eyes and the eyes treated with the test substance, for all three animals, were normal at each observation point.
Other effects:
No general toxic effects of the test substance were observed.
Interpretation of results:
GHS criteria not met
Conclusions:
The administration of 100 mg of the test substance to the eyes of female rabbits, resulted in no signs of eye irritation. According to the Directive 2001/59/EC, the test substance is not "irritating to eyes."
Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (not irritating)

Respiratory irritation

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for classification or non-classification

Skin and eye irritation studies of sufficient quality and tested in accordance with standard methodology indicated that tungsten trioxide was not irritating to skin or eye. Therefore, no classification is required for the skin and eye irritation endpoint for tungsten trioxide.