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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
Basic toxicokinetics
Administrative data
- Endpoint:
- basic toxicokinetics in vivo
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- Not reported
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- significant methodological deficiencies
Data source
Reference
- Reference Type:
- publication
- Title:
- Powdered Tantalum as a Medium for Bronchography in Canine and Human Lungs
- Author:
- Nadel JA, Wolfe WG & Graf PD
- Year:
- 1 968
- Bibliographic source:
- Invest. Radiol. Vol. 3: 229-238
Materials and methods
- Objective of study:
- distribution
- excretion
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The immediate and long term effects on the lungs of dogs after insufflating with powdered tantalum were investigated. The lungs of dogs were artificially ventilated. Transpulmonary pressure, airflow, volume, pulmonary resistance and dynamic pulmonary compliance were measured. Blood samples were taken and carbon dioxide and oxygen tensions measured. Bronchograms were obtained by stopping ventilation temporarily and insufflating tantalum powder into the lungs. Deposition of tantalum in the lungs was monitored with a fluoroscope. The weight of tantalum at the start and the amount recovered from the apparatus after the bronchogram was measured and it was assumed that the weight lost was deposited in the lungs. Chest roentgenograms were obtained following bronchography and during various studies at the same time the mechanical properties of the lungs were measured. The roentgenograms followed the time course of excretion of powdered tantalum from the lungs after the bronchogram. Dogs were necropsied and the lungs studied microscopically.
- GLP compliance:
- not specified
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
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- - Name of test material (as cited in study report): pure tantalum powder
Constituent 1
Test animals
- Species:
- dog
- Strain:
- not specified
Administration / exposure
- Route of administration:
- inhalation: dust
- Vehicle:
- unchanged (no vehicle)
- Details on exposure:
- TYPE OF INHALATION EXPOSURE: other:
-Immediate effects
The lungs were ventilated artificially with a Harvard respiratory pump connected to a tracheostomy tube.
-Long term effects
In this group, two methods were used: firstly, the animals were intubated temporarily with a cuffed endotracheal tube (No. 38-12F); secondly a polyethylene catheter (No. PE 260) was inserted into a bronchus.
GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus:
-Immediate effects
Air flow from a compressed air tank (range 0.65 to 1.35 L/s) was allowed to flow into a closed 1 L container that contained 80 g of powdered tantalum. The jet of air stirred the powder into a fine cloud; the tantalum powder flowed into the lungs via the tracheostomy tube and was deposited in the airways.
-Long term effects
In the first group, the tantalum powder was deposited into the lungs as part of a sterile bronchography procedure.
In the second group, a compressive rubber bulb was attached to a catheter which enters a 50 mL closed glass bottle containing powdered tantalum. When the insufflator bulb is squeezed, the airflow stirs the powder into a cloud and particles leave the bottle via a second catheter (in the airway of the animal) and deposit it in the airways. The powder deposits within 1 cm of the catheter tip; by moving it around, powder can be deposited selectively in various airways.
TEST ATMOSPHERE (if not tabulated)
- Particle size distribution: mean particle diameter by weight, 2.5 µm (range 0.33 - 3.7 µm) - Duration and frequency of treatment / exposure:
- Each animal was subjected to a single bronchography procedure.
Doses / concentrations
- Remarks:
- Doses / Concentrations:
8 - 16 g of tantalum (0.5 - 1.0 mL) was required to outline the airways; this amount of material was deposited during 3 - 5 lung inflations in less than 2 minutes.
- No. of animals per sex per dose / concentration:
- 31 animals in total were subjected to bronchography:
-20 animals were in the immediate effects category
-11 animals were in the long term effects group; of these, 4 took part in the endotracheal procedure and 7 via catheterisation. - Control animals:
- no
Results and discussion
- Preliminary studies:
- The article reports on the inertness of tantalum stating that the lack of solubility and chemical inertness suggest that there should be little foreign-body or systemic reaction to tantalum.
Toxicokinetic / pharmacokinetic studies
- Details on distribution in tissues:
- Airways of both lungs from trachea to bronchioles less than 1 mm in diameter were outlined without any evidence of tantalum in the alveoli. Bronchograms showed that total lung resistance increased as did dynamic pulmonary compliance and arterial pH whereas arterial CO2 and O2 decreased. None of these changes were viewed as significant.
Microscopic sections of airways taken immediately after bronchography showed a fine coating of tantalum outlining the airways with no evidence of inflammation. All animals recovered from bronchography without evidence of respiratory infection and survived until killed for pathologic examination.
Roentgenograms of the lungs showed that tantalum was cleared from airways larger than 1 mm in 2 -3 days, during which time tantalum was found in the stomach and intestines indicating that it had been carried up the airways and swallowed. In the walls of some airways less than 1 mm in diameter, there were small clusters of macrophages containing tantalum particles. These areas did not contain fibroblasts. In dogs killed at 23 and 38 days, small amounts of tantalum in peribronchiolar tissue of airways less than 1 mm in diameter were seen. There was no sign of tissue reaction in any area and lymph nodes did not contain tantalum.
- Details on excretion:
- Sequential roentgenograms showed complete clearing of the tantalum from the lungs within 4 days. Roentgenologic examination of the lungs post mortem confirmed the absence of tantalum in airways and lung parenchyma, and microscopic examination of the lungs 8 - 21 days after bronchography revealed no evidence of inflammation in airways or lung parenchyma.
Applicant's summary and conclusion
- Conclusions:
- In an experimamental inhalation study using dogs, tantalum was not found to cause unfavourable tissue reaction. When inhaled, there was no evidence of either acute or chronic inflammatory response in the airways or pulmonary tissue. Powdered tantalum delivered to the large airways was carried up the airways and cleared by ciliary activity and by coughing within 4 days. Some of this tantalum was swallowed and excreted. The tantalum reaching the gastrointestinal tract produced no untoward effects. Thus it was found that tantalum in the conducting airways was completely eliminated without significant inflammatory effects or absorption. Tantalum delivered to peripheral airways was cleared slowly via phagocytosis. During the phagocytic process, no evidence of fibroblastic or inflammatory response in the pulmonary tissue was noted. Thus it was found that modes of lung clearance of tantalum depend on deposition. Neither airways nor lung parenchyma showed adverse responses to tantalum.
- Executive summary:
An experimental study was performed to determine the fate and metabolism of inhaled tantalum to dogs. During the study, dogs were insufflated with powdered tantalum and its retention and clearance monitored with bronchograms and roentgenograms.
Under the conditions of the study, tantalum was not found to cause unfavourable tissue reaction. When inhaled, there was no evidence of either acute or chronic inflammatory response in the airways or pulmonary tissue. Powdered tantalum delivered to the large airways was carried up the airways and cleared by ciliary activity and by coughing within 4 days. Some of this tantalum was swallowed and excreted. The tantalum reaching the gastrointestinal tract produced no untoward effects.
Thus it was found that tantalum in the conducting airways was completely eliminated without significant inflammatory effects or absorption. Tantalum delivered to peripheral airways was cleared slowly via phagocytosis. During the phagocytic process, no evidence of fibroblastic or inflammatory response in the pulmonary tissue was noted. Thus it was found that modes of lung clearance of tantalum depend on deposition. Neither airways nor lung parenchyma showed adverse responses to tantalum.
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