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Diss Factsheets
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EC number: 208-168-9 | CAS number: 513-78-0
- 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
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- No information
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study well documented, meets generally accepted scientific principles, acceptable for assessment
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- publication
- Title:
- Influence of inhaled cadmium microparticles on mouse influenza pneumonia.
- Author:
- Chaumard C, Quero AM, Bouley G, Girard F, Boudene C and German A
- Year:
- 1 983
- Bibliographic source:
- Environ. Res. 31(2):428-439
Materials and methods
- Principles of method if other than guideline:
- A study was conducted to study the effect of test material inhalation on the infectivity of an orthomyxovirus influenza strain in Swiss albino mice. A total of 132 animals were employed in this study. Animals were exposed to the test material microparticles at 9.02 mg Cd/m3 and observed for 17 d. 48 h after test material exposure, the animals were infected with an orthomyxovirus influenza strain.
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Cadmium oxide
- EC Number:
- 215-146-2
- EC Name:
- Cadmium oxide
- Cas Number:
- 1306-19-0
- IUPAC Name:
- oxocadmium
- Details on test material:
- - Name of test material (as cited in study report): CdO
- Impurity/Additive etc.: No information
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- Swiss
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River
- Weight at study initiation: 20.5 g
Administration / exposure
- Route of administration:
- inhalation
- Type of inhalation exposure:
- nose only
- Vehicle:
- other:
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- System of generating particulates/aerosols: CdO microparticles were generated in two apparatuses similar to that of Horstman et al 1973 and described in detail elsewhere (Boisset et al., 1978). Microparticle carrier atmospheres were cooled before being introduced into the exposure chambers.
- Method of particle size determination: On electron photomicrographs and analysed according to Raabe (1980)
- MMAD (Mass median aerodynamic diameter) / GSD (Geometric st. dev.): 1.79 µm with count median diameter of 0.33 µm
- Analytical verification of test atmosphere concentrations:
- yes
- Duration of exposure:
- 15 min
- Concentrations:
- 9.02 mg Cd/m³
- No. of animals per sex per dose:
- 132
- Control animals:
- yes
- Details on study design:
- - Duration of observation period following administration: 17 d
- Necropsy of survivors performed: Yes - Statistics:
- No statistics reported
Results and discussion
- Preliminary study:
- Not applicable
Effect levelsopen allclose all
- Sex:
- male
- Dose descriptor:
- LC50
- Effect level:
- > 9.02 mg/m³ air
- Exp. duration:
- 15 min
- Remarks on result:
- other: Reversible general (body weight) and local (local/body weight ratio) biometric disturbances
- Sex:
- male
- Dose descriptor:
- other: LOAEL
- Effect level:
- 9 mg/m³ air
- Exp. duration:
- 15 min
- Remarks on result:
- other: Reversible general (body weight) and local (local/body weight ratio) biometric disturbances
- Mortality:
- Number of deaths at each dose level: death rate:
Virus-control mice: 55/138 (40 %)
Non-infected exposed to Al2O3 controls: 67/132 (51 %)
CdO-infected mice: 25/133 (19%)
Time of death : Deaths occurred after the 7th day postexposure (to influenza) - Clinical signs:
- other: No information
- Body weight:
- No information.
- Gross pathology:
- No information.
- Other findings:
- - Other observations: Mice intoxicated by test material but not infected had reversible general (body weight) and local (local/body weight ratio) biometric disturbances. In intoxicated and infected animals, infectious death rate was significantly lower than in Al2O3 exposed animals or virus controls. Virus titration in lung confirmed the infectious death rate; at the Day 10 after infection, the virus titer in lung of test material exposed mice was lower than in virus controls.
Any other information on results incl. tables
None
Applicant's summary and conclusion
- Interpretation of results:
- other:
- Remarks:
- Criteria used for interpretation of results: expert judgment
- Conclusions:
- Hence, under the conditions of the test, the test material inhaled animals were found to be protected against the infection by the influenza virus.
- Executive summary:
A study was conducted to study the effect of test material inhalation on the infectivity of an orthomyxovirus influenza strain in Swiss albino mice.
A total of 132 animals were employed in this study. Animals were exposed to the test material microparticles at 9.02 mg Cd/m3 and observed for 17 d. 48 h after test material exposure, the animals were infected with an orthomyxovirus influenza strain.
Mice intoxicated by test material but not infected had reversible general (body weight) and local (local/body weight ratio) biometric disturbances. In intoxicated and infected animals, infectious death rate was significantly lower than in Al2O3 exposed animals or virus controls. Virus titration in lung confirmed the infectious death rate; at the Day 10 after infection, the virus titer in lung of test material exposed mice was lower than in virus controls.
Hence, under the conditions of the test, the test material inhaled animals were found to be protected against the infection by the influenza virus.
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