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Diss Factsheets
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EC number: 231-718-4 | CAS number: 7699-45-8
- 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
Dermal absorption
Administrative data
- Endpoint:
- dermal absorption in vivo
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- Not reported
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study well documented, meets generally accepted scientific principles, acceptable for assessment
- Justification for data waiving:
- other:
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 977
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The plasma zinc level was measured after topical application of zinc chloride in pregnant rats consuming a diet deficient in zinc.
- GLP compliance:
- no
Test material
- Reference substance name:
- Zinc chloride
- EC Number:
- 231-592-0
- EC Name:
- Zinc chloride
- Cas Number:
- 7646-85-7
- IUPAC Name:
- zinc dichloride
- Details on test material:
- - Name of test material (as cited in study report): Zinc chloride
Constituent 1
- Radiolabelling:
- no
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Simonsen Labs, Gilroy, Calif
- Housing: Housed individually in stainless steel cages
- Diet: Purified diet containing adequate zinc (100 ppm) before mating and purified diet deficient in zinc (less than 0.4 ppm) after mating during whole experimental period; ad libitum
- Water: Distilled deionized water; ad libitum
Administration / exposure
- Type of coverage:
- other: Covered with gauze and bandaged
- Vehicle:
- corn oil
- Duration of exposure:
- 8 or 24 h
- Doses:
- 0.4 mL of oil preparation containing 7,500 ppm zinc (as zinc chloride)
- No. of animals per group:
- 5-7
- Control animals:
- yes
- Details on study design:
- STUDY DESIGN: Females were mated with males night before experimental day. Copulation was determined by the presence of sperm in the vaginal
smear next morning. The animals were divided into following five groups:
-Normal control (1 group): Sacrificed at the beginning of the experiment (time zero) to obtain representative plasma zinc levels of animals consuming an adequate zinc diet.
-Untreated and fed zinc-deficient diet (2 groups): Oil preparation (containing less than 4 ppm zinc) applied for the full 24 h in one group, and for the last 8 h in the other.
-Treated and fed zinc-deficient diet (2 groups): Same as above except that zinc chloride was added to oil.
TEST SITE
- Preparation of test site: Test sites (dorsal thoracic surface along the spinal axis) treated with a depilatory agent to remove a patch of hair (approximately 3 x 4 cm2).
- Type of cover / wrap if used: Covered with gauze and bandaged
CONTROL FOR INGESTION: As a control for the possibility of oral intake of zinc, Oil Red O was added as a marker so that any oil seeping through the bandages would be seen.
SAMPLE COLLECTION
- Terminal procedure: Sacrificed with ether after 24 h
- Collection of blood: Cardiac puncture
PLASMA ZINC ANALYSIS
- Method type(s) for identification: Atomic absorption spectrophotometry
- Limits of detection: 0.02 ppm zinc - Details on in vitro test system (if applicable):
- Not applicable
Results and discussion
- Signs and symptoms of toxicity:
- not examined
- Dermal irritation:
- not examined
- Absorption in different matrices:
- Plasma:
Untreated and zinc-deficient diet group:
-8 and 24 h application: Plasma zinc values significantly lower than all other groups after 24 h in both the groups
Treated and zinc-deficient diet group:
-8 h application: Plasma zinc values similar to those of the control group fed an adequate zinc diet and significantly higher than those of rats that received no zinc application to the skin.
-24 h treatment: Plasma zinc values significantly higher than in any other group, including normal controls (See Table 1 for details) - Total recovery:
- Not determined
Percutaneous absorption
- Remarks on result:
- other: Not determined
- Conversion factor human vs. animal skin:
- Not applied
Any other information on results incl. tables
Table 1. Influence of topical zinc chloride on plasma zinc
Diet and topical application |
Treatment time (h) |
Rats (no.) |
Plasma zinc (µg/100 mL) |
|
|
Time |
Total duration |
|
|
Control diet |
0 |
0 |
5 |
114.6 ± 5.2* |
Zinc-deficient diet |
|
|
|
|
Oil |
16-24 |
8 |
5 |
74.6 ± 2.5 |
Oil |
0-24 |
24 |
6 |
63.2 ± 3.2 |
Oil + Zinc |
16-24 |
8 |
7 |
114.8 ± 3.7* |
Oil + Zinc |
0-24 |
24 |
6 |
182.5 ± 8.9* # @ |
*Significantly higher than groups receiving oil without zinc, P < 0.001
#Significantly higher than the group receiving oil plus zinc for 8 hr, P < 0.001
@Significantly higher than control group, P < 0.001
Other data: There was no trace of Oil Red O stain in the area outside of the bandage in any of the animals tested, indicating that leakage did not occur. Therefore, the possibility of oral intake of zinc was discounted. Food intake was similar among all groups.
Applicant's summary and conclusion
- Conclusions:
- In conclusion, zinc was absorbed in clinically significant amount after topical application of zinc chloride in pregnant rats consuming a zinc-deficient diet.
- Executive summary:
The effect (effect on plasma zinc concentration) of topical administration of zinc chloride was tested in pregnant rats consuming a diet deficient in zinc.
Four groups of rats were fed a zinc-deficient diet for 24 h. Half of the animals were treated during this period with a topical application of oil saturated with zinc chloride, for the full 24 h in one group, and for the last 8 h in the other. In the remaining two groups, oil without zinc chloride was applied under the same conditions as described above, and in all cases oral ingestion of the supplement was prevented. At the end of the 24 h period, the animals were sacrificed and plasma zinc was determined. An additional group of animals consuming a diet adequate in zinc was sacrificed without any treatment to provide control values of normal plasma zinc.
Rats consuming the deficient diet and without topical zinc supplementation had plasma zinc values significantly lower than all other groups after 24 h. Animals receiving zinc supplementation for 8 h had plasma levels similar to those of the control group fed an adequate zinc diet and significantly higher than those of rats that received no zinc application to the skin. In animals in which zinc was applied for 24 h, plasma zinc values were significantly higher than in any other group, including normal controls.
In conclusion, zinc was absorbed in clinically significant amount after topical application of zinc chloride in pregnant rats consuming a zinc deficient diet.
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