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EC number: 231-135-5 | CAS number: 7440-25-7
- 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
Direct observations: clinical cases, poisoning incidents and other
Administrative data
- Endpoint:
- direct observations: clinical cases, poisoning incidents and other
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- not reported
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Report with an insufficient level of information to assess the findings presented.
Data source
Reference
- Reference Type:
- publication
- Title:
- Tantalum inhalation and pulmonary function
- Author:
- Smith P, Stitik F, Smith J, Rosenthal R, Menkes H
- Year:
- 1 977
- Bibliographic source:
- American Review of Respiratory Disease, Vol. 115, No. 4, April 1977 p 378
Materials and methods
- Study type:
- study with volunteers
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The effects of tantalum inhalation was studied in 14 volunteers. During the study, tantalum aerosol was inhaled through an oropharyngeal tube. Pulmonary function was tested before and within 15 minutes of inhalation. Roentgenograms of the subjects were taken and measurements of closing volume, closing capacity, total lung capacity and residual volume were taken. Specific airway conductance (SGaw) and forced expired volume (FEV1) were determined.
- GLP compliance:
- not specified
- Remarks:
- (not reported)
Test material
- Reference substance name:
- Tantalum
- EC Number:
- 231-135-5
- EC Name:
- Tantalum
- Cas Number:
- 7440-25-7
- Molecular formula:
- Ta
- IUPAC Name:
- tantalum
- Details on test material:
- - Name of test material (as cited in study report): tantalum aerosol
Constituent 1
Method
- Type of population:
- not specified
- Subjects:
- 14 normal volunteers.
- Route of exposure:
- inhalation
- Reason of exposure:
- intentional
- Exposure assessment:
- not specified
- Details on exposure:
- Tantalum aerosol was inhaled through an oropharyngeal tube. No further information provided.
Results and discussion
Any other information on results incl. tables
None of the groups showed changes in closing volume, closing capacity, slope of phase III, total lung capacity, or residual volume. In groups 2 and 3, neither specific airway conductance (SGaw) nor forced expired volume in one second (FEV1) changed significantly; however, bothe SGaw and FEV1 fel significantly in Group 3: 25 -45% and 9 -13% respectively. Even though there was no change in FEV1 with air in Group 2, the FEV1 with helium in all four subjects tested in Group 2 fell 2 -5%. To test whether subjects in Group 3 had more reactive airways, challenges with metacholine were performed in all 3 groups. No significant differences between groups were detected.
Applicant's summary and conclusion
- Conclusions:
- During the course of the study the airway response to tantalum was seen to be variable in normal volunteers and thought, in part, to be related to depth of particle deposition. Pulmonary changes (SGaw, FEV1) were correlated with bronchoconstriction seen on roentgenograms, although changes in FEV1 with helium in Group 2 suggest that small airways constrict distal to those visualised by tantalum. Methacholine failed to detect differences in airway reactivity and thus failed to predict airways response to tantalum inhalation. This indicated that the airway responsiveness to an inert metal seen in Group 3 is not related to an individual's response to vagal agonists.
- Executive summary:
The effects of tantalum inhalation was studied in 14 volunteers. During the study, tantalum aerosol was inhaled through an oropharyngeal tube. Pulmonary function was tested before and within 15 minutes of inhalation. Roentgenograms of the subjects were taken and measurements of closing volume, closing capacity, total lung capacity and residual volume were taken. Specific airway conductance (SGaw) and forced expired volume (FEV1) were determined. During the course of the study the airway response to tantalum was seen to be variable in normal volunteers and thought, in part, to be related to depth of particle deposition. Pulmonary changes (SGaw, FEV1) were correlated with bronchoconstriction seen on roentgenograms, although changes in FEV1 with helium in Group 2 suggest that small airways constrict distal to those visualised by tantalum. Methacholine failed to detect differences in airway reactivity and thus failed to predict airways response to tantalum inhalation. This indicated that the airway responsiveness to an inert metal seen in Group 3 is not related to an individual's response to vagal agonists.
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