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Diss Factsheets
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EC number: 914-459-8 | CAS number: -
- 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
Specific investigations: other studies
Administrative data
- Endpoint:
- mechanistic studies
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Acceptable, well-documented publication which meets basic scientific principles, for justification of read-across see Chapter 1 of CSR
Data source
Reference
- Reference Type:
- publication
- Title:
- Very long chain fatty acids (policosanols) and phytosterols affect plasma lipid levels and cholesterol biosynthesis in hamsters
- Author:
- Wang Y, Ebine N, Jia X, Jones P, Fairow C, Jaeger R
- Year:
- 2 005
- Bibliographic source:
- Metabolism Clinical and Experimental, Vol. 54: 508-514
Materials and methods
- Principles of method if other than guideline:
- Oral repeated dose study examinating the alterations in plasma lipid levels and cholesterol biosynthesis
- GLP compliance:
- not specified
- Type of method:
- in vivo
Test material
- Reference substance name:
- Very long chain fatty acids
- IUPAC Name:
- Very long chain fatty acids
- Details on test material:
- - Name of test material (as cited in study report): Licowax (derived from Montanwax, very long chain fatty acids (VLCFA))
- Composition of test material, percentage of components: 69% VLCFA (8% C24; 13% C26; 18% C28, 18% C30, 7% C32, 3% C34, 1% C36, 1% > C36)
Constituent 1
Test animals
- Species:
- hamster, Syrian
- Strain:
- not specified
- Sex:
- male
Administration / exposure
- Route of administration:
- oral: feed
- Vehicle:
- unchanged (no vehicle)
- Analytical verification of doses or concentrations:
- no
- Duration of treatment / exposure:
- 4 weeks
- Frequency of treatment:
- daily
Doses / concentrations
- Remarks:
- Doses / Concentrations:
25, 50 mg/kg bw/day
Basis:
nominal conc.
- No. of animals per sex per dose:
- 15 males
- Control animals:
- yes, plain diet
Results and discussion
- Details on results:
- TC levels and non-HDL-C levels were slightly increased in the groups treated with solely 25 or 50 mg/kg bw/day VLCFA, but the alterations were not significant. HDL-C was increased in both dosed groups, and this was significant in the 50 mg/kg bw/day group. The ratio of TC to HDL-C was not altered. The trigylceride levels were not affected in the treated groups (results presented in figures).
The exposure to VLCFA increased the rate of biosynthesis of cholesterol significantly at both doses, but there was no dose-response relationship.
Any other information on results incl. tables
Effects on cholesterol biosynthesis:
% newly synthesised cholesterol (2 h) | |
control group | 6.64 +/- 0.15 |
25 mg/kg bw/day | 6.85 +/- 0.25* |
50 mg/kg bw/day |
6.86 +/- 0.22* |
*: significantly different from control
There were no alterations in body weight or organ weights (liver, heart, kidneys, brain) due to exposure to the test substance.
Applicant's summary and conclusion
- Conclusions:
- Licowax (VLCFA) slightly increased the HDL-cholesterol and the cholesterol biosynthesis after repeated oral doses of 25 and 50 mg/kg bw/day. The alterations in cholestesterol biosynthesis were not dose-dependent. These effects are not considered to be adverse.
- Executive summary:
Groups of Syrian hamsters (15 males per group) were fed diets delivering body doses of 0, 25 or 50 mg/kg bw/day of very long chain fatty acids (VLCFA, Licowax). Body weights and the weight of liver, heart, kidneys and brain were unaffected by the treatment. Both treatments produced no alterations in the levels of trigycerides. A slight, but not significant increase of total cholesterol and non-HDL cholesterol was observed. HDL-C was increased in both dosed groups, and this effect was significant in the 50 mg/kg bw/day group. The ratio of TC to HDL-C was not altered. The exposure to VLCFA increased the rate of biosynthesis of cholesterol significantly at both doses, but there was no dose-response relationship.Therefore the effects are not considered to be adverse, the NOAEL of this study was >50 mg/kg/day.
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