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EC number: 264-885-7 | CAS number: 64417-98-7
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1999-03-08 to 1999-05-24
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- Non-GLP study.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 999
- Report date:
- 1999
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- other: Maximization Test of the Guideline for Toxicity Studies of Drugs (Notification No. 1-24 of Pharmaceuticals and Cosmetics Division dated September 11, 1989)
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- GLP compliance:
- not specified
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- Study was performed before the LLNA method became the preferred method for skin sensitisation testing.
Test material
- Reference substance name:
- Yttrium zirconium oxide
- EC Number:
- 264-885-7
- EC Name:
- Yttrium zirconium oxide
- Cas Number:
- 64417-98-7
- Molecular formula:
- (ZrO2)x (Y2O3)y 0.59 < x < 1.0 and 0 < y < 0.41
- IUPAC Name:
- zirconium(4+) yttrium dioxidandiide
- Test material form:
- solid: particulate/powder
- Details on test material:
- - Name of test material (as cited in study report): zirconium oxide (5.15 wt% yttrium oxide intercrystallised)
- Molecular formula (if other than submission substance): 97ZrO2 3Y2O3 (mole fraction)
- Molecular weight (if other than submission substance): 126
- Smiles notation (if other than submission substance): no data
- InChl (if other than submission substance): no data
- Structural formula attached as image file (if other than submission substance): no data
- Substance type: no data
- Physical state: white powder
- Stability under test conditions: nonreactive to water
- Storage condition of test material: stored at room temperature
- Other: no data
- Further details on test material confidential
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Charles River Laboratories Japan, Inc.
- Age at study initiation: 4 weeks old
- Weight at study initiation: 272 g - 302 g
- Housing: Five guinea pigs were kept together in each aluminum bracket cage (360 W x 520 D x 330 H mm, Bottom: 320 W x 480 D mm) until the elicitation treatment, then were kept individually in aluminum bracket cages (220 W x 380 D x 250 H mm) after the elicitation treatment. The cages were changed once a week.
- Diet: Solid feed (RC4, Oriental Yeast Col, Ltd)
- Water: Hita municipal water supply was used for water, which was provided freely by automatic water-supply equipments.
- Acclimation period: no data
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 23+/- 2 degrees C
- Humidity (%): 55 +/- 15%
- Air changes (per hr): 10 ~ 15 ventilation per hour
- Photoperiod (hrs dark / hrs light): 12 hour light and dark period (light on at 7 am - off at 7 pm)
IN-LIFE DATES: From: 1999-02-23 To: 1999-05-24
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- intradermal
- Vehicle:
- physiological saline
- Concentration / amount:
- 2.5% w/v in physiological saline
Amount applied: 0.1 mL per injection - Day(s)/duration:
- Day 1
- Adequacy of induction:
- not specified
- Route:
- epicutaneous, occlusive
- Vehicle:
- other: distilled injection water
- Concentration / amount:
- 25% w/v in distilled injection water
Amount applied: 0.2 mL - Day(s)/duration:
- Day 8, 48 h of exposure
- Adequacy of induction:
- non-irritant substance, but skin pre-treated with 10% SDS
Challenge
- No.:
- #1
- Route:
- epicutaneous, occlusive
- Vehicle:
- other: distilled injection water
- Concentration / amount:
- 25% and 2.5% w/v in distilled injection water
Amount applied: 0.1 mL - Day(s)/duration:
- Day 22, 24 h of exposure
- Adequacy of challenge:
- not specified
- No. of animals per dose:
- Control group: 5 animals
Test agent group: 10 animals
Positive conrol group: 5 animals - Details on study design:
- Intradermal sensitisation:
Suprascapular fur was shaved by an electric clipper in order to establish 2x4 cm sensitisation regions, and with the midline as the axis of symmetry, 0.1 mL of below preparations were injected per region of each left-right pair.
1) Test agent group
E-FCA
2.5% test agent
2.5% test agent/FCA emulsion
2) Control group
E-FCA (2 pairs in total)
3) Positive control group
E-FCA
0.1% DNCB/olive oil
0.1% DNCB/FCA emulsion
Patch sensitisation:
Six days after the intradermal sensitisation, the fur in the sensitisation regions of the animals in the control groups and the test agent group were shaved by an electric clipper and an electric shaver, then sodium lauryl sulfate (contains 10% petrolatum) was applied. Seven days after the intradermal sensitisation, the control group was applied with distilled injection water, the test agent group with 25% test agent, and the positive control group with 0.5% DNCB, by placing 2x4 cm lints (Nankai Sangyou Co.) moistened with 0.2 mL each of the preparation on the shaved sensitisation regions and by covering them with rubber dam sheets (Nihon Rikagaku Industry Co., Ltd.), then the trunks were wrapped with Dermicel (Johnson & Johnson K.K.) for 48 hours for occlusive dressing.
Elicitation treatment (challenge):
Fourteen days after the start of the patch sensitisation, the flank fur of the animals was shaved by an electric clipper and an electric shaver, and for the control group and the test agent group, the areas were applied with 25% test agent and 2.5% test agent to each group, respectively, by placing 2x2 cm lints moistened with 0.1 mL of the preparation, and by covering them with oil paper and rubber dam sheets, then the trunks were wrapped with Dermicel (Johnson & Johnson K.K.) for 24 hours for occlusive dressing. For the positive control group, 0.1% DNCB was applied by placing 2x2 cm lints moistened with 0.1 mL of the preparation and by covering them with rubber dam sheets, then the trunks were wrapped with Dermicel (Johnson & Johnson K.K.) for 24 hours for occlusive dressing. - Challenge controls:
- 25% test agent
- 2.5 g of the test agent was suspended in distilled injection water to make 10 mL.
2.5% test agent
- 0.25 g of the test agent was suspended in distilled injection water to make 10 mL.
0.1% DNCB (2,4-dinitrochlorobenzene, positive control substance)
- 0.01 g of DNCB was dissolved in ethanol to make 10 mL. - Positive control substance(s):
- yes
- Remarks:
- DNCB (2,4-dinitrochlorobenzene)
Results and discussion
- Positive control results:
- 0.1% DNCB elicited region: Diffuse moderate erythema or severe erythema and oedema were acknowledged in every sample 24 and 48 hours after the elicitation patch removal. Furthermore, scab formations were acknowledged in 4/5 cases after both 24 and 48 hours, and desquamation was acknowledged in all cases after 48 hours. The average scores 24 and 48 hours after the elicitation patch removal were 3.0 and 2.8, respectively.
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 25% w/v in distilled injection water
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- none
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 25% w/v in distilled injection water
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- none
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 2.5% w/v in distilled injection water
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- none
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 2.5% w/v in distilled injection water
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- none
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 25% w/v in distilled injection water
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Clinical observations:
- none
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 25% w/v in distilled injection water
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Clinical observations:
- none
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 2.5% w/v in distilled injection water
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Clinical observations:
- none
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 2.5% w/v in distilled injection water
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Clinical observations:
- none
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 0.1% w/v DNCB in ethanol
- No. with + reactions:
- 5
- Total no. in group:
- 5
- Clinical observations:
- Diffuse moderate erythema or severe erythema and oedema were acknowledged in every animal. Furthermore, scab formations were acknowledged in 4 out of 5 animals.
- Remarks on result:
- positive indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 0.1% w/v DNCB in ethanol
- No. with + reactions:
- 5
- Total no. in group:
- 5
- Clinical observations:
- Diffuse moderate erythema or severe erythema and oedema were acknowledged in every animal. Furthermore, scab formations were acknowledged in 4 out of 5 animals, and desquamation was acknowledged in all cases.
- Remarks on result:
- positive indication of skin sensitisation
Any other information on results incl. tables
Skin Reaction
2.1 Test Agent Group
1) 25% test agent elicited region
No skin reaction was acknowledged 24 and 48 hours after the elicitation patch removal.
The average scores 24 and 48 hours after the elicitation patch removal were both 0.
2) 2.5% test agent elicited region
No skin reaction was acknowledged 24 and 48 hours after the elicitation patch removal.
The average scores 24 and 48 hours after the elicitation patch removal were both 0.
2.2 Control Group
1) 25% test agent elicited region
No skin reaction was acknowledged 24 and 48 hours after the elicitation patch removal.
The average scores 24 and 48 hours after the elicitation patch removal were both 0.
2) 2.5% test agent elicited region
No skin reaction was acknowledged 24 and 48 hours after the elicitation patch removal.
The average scores 24 and 48 hours after the elicitation patch removal were both 0.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Since no skin reaction was acknowledged in the elicited region of either the test agent group or the control group, it was concluded that the test substance does not have skin sensitising potential under the conditions of this test. On the other hand, it was confirmed that 2,4-dinitrochlorobenzene, the positive control agent, has an extreme skin sensitising potential.
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