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EC number: 201-204-4 | CAS number: 79-41-4
- 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 vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- test procedure in accordance with generally accepted scientific standards and described in sufficient detail
Data source
Reference
- Reference Type:
- other: thesis
- Title:
- Using physiologically based pharmacokinetic modelling to predict the pharmacokinetics and toxicity of methacrylate esters
- Author:
- Jones O
- Year:
- 2 002
- Bibliographic source:
- A Thesis submitted to Univ. of Manchester for the degree of Doctor of Philosophy
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- A physiologically based pharmacokinetic model has been formulated to predict the pharmacokinetics and systemic disposition of alkylmethacrylate esters in rats and humans. Several kinetic parameters were determined experimentally - including dermal absorption.
- GLP compliance:
- no
Test material
- Reference substance name:
- Methacrylic acid
- EC Number:
- 201-204-4
- EC Name:
- Methacrylic acid
- Cas Number:
- 79-41-4
- Molecular formula:
- C4H6O2
- IUPAC Name:
- methacrylic acid
- Test material form:
- liquid
Constituent 1
Test animals
- Species:
- other: rat and human
- Strain:
- other: Wistar/Fischer F344/ not applicable
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- Epidermal membrane absorption studies
Skin was used from male rats of the Wistar-derived strain (supplied by Charles River UK Ltd, Margate, Kent, UK.) aged 28 days ± 2 days
Whole skin absorption studies
Skin was taken from male Fisher F344 (supplied by Harlan Olac) rats weighing between 200 and 250 g.
Human epidermal membrane absorption studies
Extraneous tissue was removed from human abdominal whole skin samples obtained post mortem in accordance with local ethical guidelines
Administration / exposure
- Type of coverage:
- occlusive
- Vehicle:
- unchanged (no vehicle)
- Duration of exposure:
- up to 48 h
- Doses:
- 100 µL/cm2
- No. of animals per group:
- 3 (human: 2)
Results and discussion
Percutaneous absorptionopen allclose all
- Key result
- Time point:
- 8 h
- Dose:
- 100 µl/cm2
- Parameter:
- percentage
- Absorption:
- ca. 36.5 %
- Remarks on result:
- other: whole rat skin; peak absorption period 5-8 h
- Key result
- Time point:
- 4 h
- Dose:
- 100 µl/cm2
- Parameter:
- percentage
- Absorption:
- 81 %
- Remarks on result:
- other: rat epidermis; peak absorption period 0.5-4h;
- Time point:
- 24 h
- Dose:
- 100 µL/cm2
- Parameter:
- percentage
- Absorption:
- ca. 93 %
- Remarks on result:
- other:
- Remarks:
- rat epidermis; peak absorption rate 0.5-4 h
- Dose:
- 100 µL/cm2
- Parameter:
- percentage
- Absorption:
- >= 70 %
- Remarks on result:
- other: 24 h
- Remarks:
- rat whole skin, peak absorption rate 5-8 h
- Conversion factor human vs. animal skin:
- Based on the experimentally supported model, the peak rate of absorption in for human vs. rat epidermis is predicted to 3.1 % while the peak rate for whole human vs whole rat skin is predicted to 7.1 %.
Any other information on results incl. tables
Rat epidermis
The fastest rate of absorption of MAA through rat epidermal membrane was recorded as being 23825μg*cm-2*hr-1 and this occurred between 0.5 and 4 hrs following application of the chemical. After 24 h, 93 % of the applied dose appeared in the receptor chamber indicating a practically complete absorption through rat epidermis within 24 h.
Human epidermis
Experimental data are only available for methyl-, n-butyl- and 2-ethylhexyl methacrylate. With the model developed with these experimental data the peak rate of absorption of methacrylic acid through human skin was estimated being 812 μg*cm-2*hr-1. The rates of absorption through human epidermis are considerably slower than those measured for MAA through rat epidermis.
Whole rat skin
Of the methacrylates whose rate of absorption through whole rat skin was investigated, methacrylic acid is the most rapidly absorbed chemical - faster than all esters, triggered by the small molecular volume. The peak rate of appearance of MAA occurred between 5 and 8 hrs and was calculated as 4584 μg cm-2 hr-1. While the esters are partly or completely hydrolysed by carboxylesterases present in the viable tissue, MAA passes the tissue almost quantitatively. Of the original dose applied to the whole skin, 70% appeared in the receptor chamber within 24 hrs.
Applicant's summary and conclusion
- Conclusions:
- Epidermal studies
The fastest rate of absorption of MAA through rat epidermal membrane was recorded as being 23825 μg*cm-2*hr-1 and this occurred between 0.5 and 4 hrs following application of the chemical. Methacrylic acid absorption through human skin was estimated being 812 μg*cm-2*hr-1, based on a model developed with experimental data on rat and human skin with MMA, n-BMA and 2-EHMA.. The rates of absorption through human epidermis are considerably slower than those measured through rat epidermis.
Whole rat skin
Of the methacrylates whose rate of absorption through whole rat skin was investigated, methacrylic acid is the most rapidly absorbed chemical - faster than all esters. While the esters are partly or completely hydrolysed by carboxylesterases present in the viable tissue, MAA passes the tissue almost quantitatively. The peak rate of appearance of MAA, which occurred between 5-8 hrs was calculated to be 4584 μg*cm-2*hr-1. Of the original dose applied to the whole skin, 70% appeared in the receptor chamber within 24 hrs. - Executive summary:
The in vivo and in vitro investigations as well as the PBPK models developed from the data showed that methacrylic acid and the lower alkyl-methacrylate esters are rapidly absorbed and the esters are hydrolyzed at exceptionally high rates to methacrylic acid by high capacity, ubiquitous carboxylesterases. Further, the removal of the hydrolysis product, methacrylic acid, also is very rapid (minutes).
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