Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 481-880-7 | CAS number: 949495-68-5
- 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
Endpoint summary
Administrative data
Description of key information
Skin corrosion / irritation: Standard quality (Item 2) is not corrosive (OECD431, GLP, K, rel.2). Standard quality (Items 1, and 4) and high alpha pinene quality (item 5) are not irritant (OECD 439, GLP, K, rel.1)
Eye damage/irritation: Standard quality (Item 2) is not irritant (similar to OECD 437, GLP, K, rel.2)
Key value for chemical safety assessment
Skin irritation / corrosion
Link to relevant study records
- Endpoint:
- skin corrosion: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 23-28 April 2008
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- GLP study conducted according to OECD test Guideline No. 431. However, functional model conditions and references to historical control data are not included in the report.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 431 (In Vitro Skin Corrosion: Reconstructed Human Epidermis (RHE) Test Method)
- Version / remarks:
- Adopted April 13, 2004
- Deviations:
- yes
- Remarks:
- functional model conditions and references to historical control data are not included in the report.
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.40 (In Vitro Skin Corrosion: Transcutaneous Electrical Resistance Test (TER))
- Deviations:
- yes
- Remarks:
- functional model conditions and references to historical control data are not included in the report.
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- yes
- Remarks:
- UK GLP Compliance Programme (inspected on 05 July 2016 / signed on 28 October 2016)
- Test system:
- human skin model
- Source species:
- human
- Cell type:
- non-transformed keratinocytes
- Justification for test system used:
- Following the REACH bottom-up strategy, the EpiDerm™ Human Skin Model method was used to assess skin corrosion as recommended in the OECD test guideline No. 431.
- Vehicle:
- unchanged (no vehicle)
- Details on test system:
- RECONSTRUCTED HUMAN EPIDERMIS (RHE) TISSUE
- Model used: Epi-200-Kit, MatTek Corporation (Ashland, MA 01721, USA).
- Lot number: 10504 Kit N
- Production Date: no data
- Shipping date: no data
- Delivery date: no data
- Date received: April 24, 2008
- Date of initiation of testing: April 25, 2008
TEMPERATURE USED FOR TEST SYSTEM
- Temperature used during treatment / exposure: 3 and 60 minutes at 37 °C in a humidified atmosphere of 5% CO2
- Temperature of post-treatment incubation: 3 h at 37 °C in a humidified atmosphere of 5% CO2
REMOVAL OF TEST MATERIAL AND CONTROLS
- Volume and number of washing steps: At the end of the exposure period the first insert was removed from the 6-well plate. Using a wash bottle the tissue was gently rinsed with PBS Rinse Solution to remove any residual test material. Excess PBS Rinse Solution was removed by gently shaking the insert and
blotting the lower surface with blotting paper.
- Observable damage in the tissue due to washing: none reported
- Modifications to validated SOP: none reported
MTT DYE USED TO MEASURE TISSUE VIABILITY AFTER TREATMENT / EXPOSURE
- MTT concentration: 1.0 mg/mL MTT solution
- Incubation time: 3 hours at 37 °C, 5% CO2 in air
- Spectrophotometer: Versamax® Molecular Devices, D-85737 Ismaning
- Wavelength: 570 nm
- Filter: without reference filter
- Linear OD range of spectrophotometer: not reported
FUNCTIONAL MODEL CONDITIONS WITH REFERENCE TO HISTORICAL DATA
Not reported
NUMBER OF REPLICATE TISSUES: Duplicate tissues for test item, negative and positive controls
CONTROL TISSUES USED IN CASE OF MTT DIRECT INTERFERENCE
Not needed
NUMBER OF INDEPENDENT TEST SEQUENCES / EXPERIMENTS TO DERIVE FINAL PREDICTION: 1
PREDICTION MODEL / DECISION CRITERIA
- The test substance is considered to be corrosive to skin if the viability after 3 minutes exposure is less than 50%, or if the viability after 3 minutes exposure is greater than or equal to 50 % and the viability after 1 hour exposure is less than 15%.
- The test substance is considered to be non-corrosive to skin if the viability after 3 minutes exposure is greater than or equal to 50% and the viability after 1 hour exposure is greater than or equal to 15%. - Control samples:
- yes, concurrent negative control
- yes, concurrent positive control
- Amount/concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 50 µL of the undiluted test item.
NEGATIVE CONTROL
- Amount(s) applied (volume or weight): 50 μL of sterile distilled water was used as supplied
POSITIVE CONTROL
- Amount(s) applied (volume or weight): 50 μL of 8.0 N Potassium Hydroxide was used as supplied - Duration of treatment / exposure:
- 3 and 60 minutes.
- Duration of post-treatment incubation (if applicable):
- not applicable
- Number of replicates:
- Duplicate tissues for test item, negative and positive controls
- Irritation / corrosion parameter:
- % tissue viability
- Run / experiment:
- 3 minutes exposure
- Value:
- 92.6
- Vehicle controls validity:
- not applicable
- Negative controls validity:
- valid
- Remarks:
- 100%
- Positive controls validity:
- valid
- Remarks:
- 26.4%
- Remarks on result:
- other: No indication of corrosion
- Irritation / corrosion parameter:
- % tissue viability
- Run / experiment:
- 60 minutes exposure
- Value:
- 85.5
- Vehicle controls validity:
- not applicable
- Negative controls validity:
- valid
- Remarks:
- 100%
- Positive controls validity:
- valid
- Remarks:
- 12.4%
- Remarks on result:
- other: No indication of corrosion
- Other effects / acceptance of results:
- - OTHER EFFECTS:
- Visible damage on test system: none reported
- Direct-MTT reduction: none.
DEMONSTRATION OF TECHNICAL PROFICIENCY: not included in the report
ACCEPTANCE OF RESULTS:
- Acceptance criteria met for negative control: The mean OD570 for the negative control treated tissues was 1.637 for the 3 Minute exposure period and 1.703 for the 60 Minute exposure period. The negative control acceptance criteria were therefore satisfied (≥ 0.8).
- Acceptance criteria met for positive control: The relative mean tissue viability for the positive control treated tissues was 26.4% and 12.4% relative to the negative control following the 3 and 60 Minute exposure period, respectively. The positive control acceptance criterion was therefore satisfied (≤ 30%). - Interpretation of results:
- other: Non-corrosive base don GHS criteria
- Conclusions:
- Under the experimental conditions of this study, the test substance is not classified as corrosive, according to EU CLP Regulation (EC) No 1272/2008 and to the GHS.
- Executive summary:
An in vitro skin irritation study was performed according to the OECD Guideline 431 and in compliance with GLP, using the EpiDerm™ Human Skin Model.
Duplicate tissues were treated with 50 µL of the undiluted test item for exposure periods of 3 and 60 minutes. Negative and positive control groups were treated for each exposure period. At the end of the exposure period the test item was rinsed from each tissue before each tissue was taken for MTT‑loading. After MTT loading each tissue was placed in 2 mL Isopropanol for MTT extraction. At the end of the formazan extraction period each well was mixed thoroughly and triplicate 200 mL samples were transferred to the appropriate wells of a pre-labeled 96‑well plate. The optical density (OD) was measured at 570 nm. Data are presented in the form of percentage viability (MTT reduction in the test item treated tissues relative to negative control tissues).
The relative mean viability of the test item treated tissues was 92.6% and 85.5% after 3 and 60 minutes exposure, respectively. The relative mean viability of the positive control treated tissues was 26.4% and 12.4% after 3 and 60 minutes exposure. The quality criteria required for acceptance of results in the test were satisfied.
Under the experimental conditions of this study, the test substance is not classified as corrosive according to EU CLP Regulation (EC) No 1272/2008 and to the GHS.
This study is considered as acceptable and satisfies the requirement for skin corrosion endpoint.
- Endpoint:
- skin irritation: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 11-29 May 2017
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 439 (In Vitro Skin Irritation: Reconstructed Human Epidermis Test Method)
- Version / remarks:
- adopted 28 July 2015
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.46 (In Vitro Skin Irritation: Reconstructed Human Epidermis Model Test)
- Version / remarks:
- 23 July 2009
- Deviations:
- no
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- UK GLP Compliance Program (inspected on July 05, 2016 / Signed on October 28, 2016)
- Specific details on test material used for the study:
- Storage conditions: Room temperature in the dark until 19 January 2017 thereafter approximately 4°C in the dark
- Test system:
- human skin model
- Source species:
- human
- Cell type:
- non-transformed keratinocytes
- Justification for test system used:
- Following the REACH top-down strategy, the EPISKIN™ Reconstructed Human Epidermis Model method was used to assess skin irritation as recommended in the OECD test guideline No. 439.
- Vehicle:
- unchanged (no vehicle)
- Details on test system:
- RECONSTRUCTED HUMAN EPIDERMIS (RHE) TISSUE
- Model used: EPISKIN™ Reconstructed Human Epidermis Model Kit, SkinEthic Laboratories, Lyon, France
- Tissue batch number(s): 17-EKIN-019
- Production date: not reported
- Shipping date: not reported
- Delivery date: 10 May 2017
- Expiry date: 15 May 2017
- Date of initiation of testing: 11 May 2017
TEMPERATURE USED FOR TEST SYSTEM
- Temperature used during treatment / exposure: room temperature
- Temperature of post-treatment incubation (if applicable): 37°C
REMOVAL OF TEST MATERIAL AND CONTROLS
- Volume and number of washing steps: At the end of the exposure period, each tissue was removed from the well using forceps and rinsed using a wash bottle containing DPBS with Ca++ and Mg++. Rinsing was achieved by filling and emptying each tissue insert for approximately 40 seconds using a constant soft stream of DPBS to gently remove any residual test item. The rinsed tissues were transferred to the second column of 3 wells containing 2 mL of maintenance medium in each wellsidual test or control items and then incubated in 2mL maintenance medium for 42 h at 37 °C, 5 % CO2 in air. Number of washing steps not reported.
- Observable damage in the tissue due to washing: none reported
- Modifications to validated SOP:
Deviation 1
Due to unusual variation noted in the untreated killed control group, it was considered necessary to repeat the killed tissue groups.
Deviation 2
An assessment found the test item was able to directly reduce MTT. Therefore, an additional procedure using water killed tissues was performed. However, the results obtained showed that no interference due to direct reduction of MTT occurred. It was therefore considered unnecessary to use the results of the water killed tissues for quantitative correction of results or for reporting purposes.
MTT DYE USED TO MEASURE TISSUE VIABILITY AFTER TREATMENT / EXPOSURE
- MTT concentration: 0.3 mg/mL
- Incubation time: 3 hours
- Spectrophotometer: Labtech LT 4500 microplate reader
- Wavelength: 570 nm
- Filter: without reference filter
- Linear OD range of spectrophotometer: not reported
FUNCTIONAL MODEL CONDITIONS WITH REFERENCE TO HISTORICAL DATA
- Barrier function: IC50 = 1.8 mg/ml ( ≥ 1.5 mg/ml)
- Morphology: Well-differenciated epidermis consisting of a basal layer, several spinous and granular layers and a thinck stratum corneum
- Contamination: absence of bacteria, fungus and mycoplasma
- Reproducibility: All of the values for the negative and positive control groups fell within the historical ranges of the testing laboratory obtained in the previous six months. This was taken to show the correct functioning of the test system.
CONTROL TISSUES USED IN CASE OF MTT DIRECT INTERFERENCE:
- Fresh tissues / killed tissues: skin irritation potential performed in parallel on viable and water killed tissues for quantitative correction of the results
- Procedure used to prepare the killed tissues (if applicable): Water-killed tissues were prepared prior to the study by placing untreated EPISKINTM tissues in a 12 well plate containing 2.0 mL of sterile distilled water in each well. The tissues were incubated at 37°C, 5% CO2 in air for 48 +/- 1 hours. At the end of the incubation the water was discarded. Once killed the tissues were stored in a freezer (-14 to +30 °C) for up to 6 months. Before use each tissue was thawed by placing in 2.0 mL of maintenance medium for approximately 1 hour at room temperature.
- N. of replicates : 3 (test item + untreated)
- Method of calculation used: the results obtained showed that no interference due to direct reduction of MTT occurred. It was therefore considered unnecessary to use the results of the water killed tissues for quantitative correction of results or for reporting purposes.
NUMBER OF INDEPENDENT TEST SEQUENCES / EXPERIMENTS TO DERIVE FINAL PREDICTION: 1
PREDICTION MODEL / DECISION CRITERIA
- The test substance is considered to be irritating to skin if relative mean tissue viability is ≤ 50% after 15 minutes of exposure.
- The test substance is considered to be non-irritating to skin if relative mean tissue viability is > 50% after 15 minutes of exposure. - Control samples:
- yes, concurrent negative control
- yes, concurrent positive control
- Amount/concentration applied:
- TEST MATERIAL
- The test item was used as supplied (undiluted).
- Amount(s) applied (volume or weight with unit): 10 ± 2 mg of the test substance (powder) was dispensed over each tissue. The tissues were wetted with 5 μL of purified water prior to application of the test substance.
NEGATIVE CONTROL
- Amount(s) applied (volume or weight): 10 μL
- Concentration (if solution): DPBS
POSITIVE CONTROL
- Amount(s) applied (volume or weight): 10 μL
- Concentration (if solution): Sodium Dodecyl Sulphate (SDS) at a 5% (w/v) aqueous solution - Duration of treatment / exposure:
- 15 minutes
- Duration of post-treatment incubation (if applicable):
- 42 hours
- Number of replicates:
- Triplicate tissues for test substance, negative and positive controls
- Irritation / corrosion parameter:
- % tissue viability
- Run / experiment:
- 15 minute exposure period and 42 h post-exposure incubation period
- Value:
- 95.9
- Vehicle controls validity:
- not applicable
- Negative controls validity:
- valid
- Remarks:
- 100%
- Positive controls validity:
- valid
- Remarks:
- 12.2%
- Remarks on result:
- no indication of irritation
- Other effects / acceptance of results:
- - OTHER EFFECTS:
- Visible damage on test system: none reported
- Direct-MTT reduction: yes, an assessment found the test item was able to directly reduce MTT. Therefore, an additional procedure using water killed tissues was performed. However, the results obtained showed that no interference due to direct reduction of MTT occurred. It was therefore considered unnecessary to use the results of the water killed tissues for quantitative correction of results or for reporting purposes.
- Colour interference with MTT: no
DEMONSTRATION OF TECHNICAL PROFICIENCY: yes
ACCEPTANCE OF RESULTS:
- Acceptance criteria met for negative control: The mean OD570 for the negative control treated tissues was 0.656 and the standard deviation value of the viability was 7.3%.
- Acceptance criteria met for positive control: The relative mean tissue viability for the positive control treated tissues was 12.2% relative to the negative control treated tissues and the standard deviation value of the viability was 0.7%.
- Acceptance criteria met for variability between replicate measurements: The standard deviation calculated from individual tissue viabilities of the three identically test item treated tissues was 11.5%.
- Reference to historical values: All of the values for the negative and positive control groups fell within the historical ranges of the testing laboratory obtained in the previous six months. This was taken to show the correct functioning of the test system. - Interpretation of results:
- other: CLP criteria not met
- Conclusions:
- Under the experimental conditions of this study, the test substance is not classified for skin irritation according to Regulation (EC) No. 1272/2008 (CLP).
- Executive summary:
An in vitro skin irritation study was performed according to the OECD Guideline 439 and in compliance with GLP, using the EPISKINTM reconstructed human epidermis model.
Triplicate tissues were treated with the test item for an exposure period of 15 minutes. At the end of the exposure period each tissue was rinsed before incubating for 42 hours. The test item was found to directly reduce MTT and therefore additional non-viable tissues were incorporated into the testing for correction purposes. At the end of the post‑exposure incubation period each tissue was taken for MTT-loading. The maintenance medium from beneath each tissue was transferred to pre‑labeled micro tubes and stored in a freezer for possible inflammatory mediator determination. After MTT-loading a total biopsy of each epidermis was made and placed into micro tubes containing acidified isopropanol for extraction of formazan crystals out of the MTT‑loaded tissues. At the end of the formazan extraction period each tube was mixed thoroughly and duplicate 200 µL samples were transferred to the appropriate wells of a pre‑labeled 96‑well plate. The optical density was measured at 570 nm.
The relative mean viability of the test item treated tissues was 95.9% after the 15‑Minute exposure period and 42‑Hours post‑exposure incubation period.
The relative mean tissue viability for the positive control treated tissues was 12.2% relative to the negative control treated tissues and the standard deviation value of the viability was 0.7%. The positive control acceptance criteria were therefore satisfied.
The mean OD570 for the negative control treated tissues was 0.656 and the standard deviation value of the viability was 7.3%. The negative control acceptance criteria were therefore satisfied.
The standard deviation calculated from individual tissue viabilities of the three identically test item treated tissues was 11.5%. The test item acceptance criterion was therefore satisfied.
All of the values for the negative and positive control groups fell within the historical ranges of the testing laboratory obtained in the previous six months. This was taken to show the correct functioning of the test system.
Under the experimental conditions of this study, the test substance is not classified for skin irritation according to Regulation (EC) No. 1272/2008 (CLP).
This study is considered as acceptable and satisfies the requirement for skin irritation endpoint.
- Endpoint:
- skin irritation: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From January 30 to February 4, 2019
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- GLP study conducted according to OECD test Guideline No. 439.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 439 (In Vitro Skin Irritation: Reconstructed Human Epidermis Test Method)
- Version / remarks:
- adopted 28 July 2015
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.46 (In Vitro Skin Irritation: Reconstructed Human Epidermis Model Test)
- Version / remarks:
- 23 July 2009
- Deviations:
- no
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- UK GLP Compliance Program (inspected on August 21, 2018 / Signed on November 19, 2018)
- Test system:
- human skin model
- Source species:
- human
- Cell type:
- non-transformed keratinocytes
- Justification for test system used:
- Following the REACH top-down strategy, the EPISKIN™ Reconstructed Human Epidermis Model method was used to assess skin irritation as recommended in the OECD test guideline No. 439.
- Vehicle:
- unchanged (no vehicle)
- Details on test system:
- RECONSTRUCTED HUMAN EPIDERMIS (RHE) TISSUE
- Model used: EPISKIN™ Reconstructed Human Epidermis Model Kit, SkinEthic Laboratories, Lyon, France
- Tissue batch number(s): 19-EKIN-005
- Production date: not reported
- Shipping date: not reported
- Delivery date: 29 January 2019
- Expiry date: 4 February 2019
- Date of initiation of testing: 30 January 2019
TEMPERATURE USED FOR TEST SYSTEM
- Temperature used during treatment / exposure: room temperature
- Temperature of post-treatment incubation (if applicable): 37°C
REMOVAL OF TEST MATERIAL AND CONTROLS
- Volume and number of washing steps: At the end of the exposure period, each tissue was removed from the well using forceps and rinsed using a wash bottle containing DPBS with Ca++ and Mg++. Rinsing was achieved by filling and emptying each tissue insert for approximately 40 seconds using a constant soft stream of DPBS to gently remove any residual test item. The rinsed tissues were transferred to the second column of 3 wells containing 2 mL of maintenance medium in each wellsidual test or control items and then incubated in 2mL maintenance medium for 42 h at 37 °C, 5 % CO2 in air. Number of washing steps not reported.
- Observable damage in the tissue due to washing: none reported
- Modifications to validated SOP:
Deviation 1
An assessment found the test item was able to directly reduce MTT. Therefore, an additional procedure using water killed tissues was performed. However, the results obtained showed that no interference due to direct reduction of MTT occurred. It was therefore considered unnecessary to use the results of the water killed tissues for quantitative correction of results or for reporting purposes.
MTT DYE USED TO MEASURE TISSUE VIABILITY AFTER TREATMENT / EXPOSURE
- MTT concentration: 0.3 mg/mL
- Incubation time: 3 hours
- Spectrophotometer: Labtech LT 4500 microplate reader
- Wavelength: 570 nm
- Filter: without reference filter
- Linear OD range of spectrophotometer: not reported
FUNCTIONAL MODEL CONDITIONS WITH REFERENCE TO HISTORICAL DATA
- Barrier function: IC50 = 1.9 mg/ml ( ≥ 1.5 mg/ml)
- Morphology: Well-differenciated epidermis consisting of a basal layer, several spinous and granular layers and a thinck stratum corneum
- Contamination:
absence of bacteria, fungus and mycoplasma
absence of HIV1 & 2 & hepatitis C antibodies; absence of hepatitis B antigen HBs
- Reproducibility: All of the values for the negative and positive control groups fell within the historical ranges of the testing laboratory obtained in the previous six months. This was taken to show the correct functioning of the test system.
CONTROL TISSUES USED IN CASE OF MTT DIRECT INTERFERENCE:
An assessment found the test item was able to directly reduce MTT. Therefore, an additional procedure using water killed tissues was performed. However, the results obtained showed that no interference due to direct reduction of MTT occurred. It was therefore considered unnecessary to use the results of the water killed tissues for quantitative correction of results or for reporting purposes.
NUMBER OF INDEPENDENT TEST SEQUENCES / EXPERIMENTS TO DERIVE FINAL PREDICTION: 1
PREDICTION MODEL / DECISION CRITERIA
- The test substance is considered to be irritating to skin if relative mean tissue viability is ≤ 50% after 15 minutes of exposure.
- The test substance is considered to be non-irritating to skin if relative mean tissue viability is > 50% after 15 minutes of exposure. - Control samples:
- yes, concurrent negative control
- yes, concurrent positive control
- Amount/concentration applied:
- TEST MATERIAL
- The test item was used as supplied (undiluted).
- Amount(s) applied (volume or weight with unit): 10 µL
NEGATIVE CONTROL
- Amount(s) applied (volume or weight): 10 μL
- Concentration (if solution): DPBS
POSITIVE CONTROL
- Amount(s) applied (volume or weight): 10 μL
- Concentration (if solution): Sodium Dodecyl Sulphate (SDS) at a 5% (w/v) aqueous solution - Duration of treatment / exposure:
- 15 minutes
- Duration of post-treatment incubation (if applicable):
- 42 hours
- Number of replicates:
- Triplicate tissues for test substance, negative and positive controls
- Irritation / corrosion parameter:
- % tissue viability
- Run / experiment:
- 15 minute exposure period and 42 h post-exposure incubation period
- Value:
- 96.1
- Vehicle controls validity:
- not applicable
- Negative controls validity:
- valid
- Remarks:
- 100%
- Positive controls validity:
- valid
- Remarks:
- 3.9%
- Remarks on result:
- no indication of irritation
- Other effects / acceptance of results:
- - OTHER EFFECTS:
- Visible damage on test system: none reported
- Direct-MTT reduction: yes, an assessment found the test item was able to directly reduce MTT. Therefore, an additional procedure using water killed tissues was performed. However, the results obtained showed that no interference due to direct reduction of MTT occurred. It was therefore considered unnecessary to use the results of the water killed tissues for quantitative correction of results or for reporting purposes.
- Colour interference with MTT: no
DEMONSTRATION OF TECHNICAL PROFICIENCY: yes
ACCEPTANCE OF RESULTS:
- Acceptance criteria met for negative control: The mean OD570 for the negative control treated tissues was 0.846 and the standard deviation value of the viability was 6.8%. The negative control acceptance criteria were therefore satisfied.
- Acceptance criteria met for positive control: The relative mean tissue viability for the positive control treated tissues was 12.2% relative to the negative control treated tissues and the standard deviation value of the viability was 0.7%.
- Acceptance criteria met for variability between replicate measurements: The standard deviation calculated from individual tissue viabilities of the three identically test item treated tissues was 13.8%. The test item acceptance criterion was therefore satisfied. - Interpretation of results:
- other: CLP criteria not met
- Conclusions:
- Under the experimental conditions of this study, the test substance is not classified for skin irritation according to Regulation (EC) No. 1272/2008 (CLP).
- Executive summary:
An in vitro skin irritation study was performed according to the OECD Guideline 439 and in compliance with GLP, using the EPISKINTM reconstructed human epidermis model.
Triplicate tissues were treated with the test item for an exposure period of 15 minutes. At the end of the exposure period each tissue was rinsed before incubating for 42 hours. The test item was found to directly reduce MTT and therefore additional non-viable tissues were incorporated into the testing for correction purposes. At the end of the post‑exposure incubation period each tissue was taken for MTT-loading. The maintenance medium from beneath each tissue was transferred to pre‑labeled micro tubes and stored in a freezer for possible inflammatory mediator determination. After MTT-loading a total biopsy of each epidermis was made and placed into micro tubes containing acidified isopropanol for extraction of formazan crystals out of the MTT‑loaded tissues. At the end of the formazan extraction period each tube was mixed thoroughly and duplicate 200 µL samples were transferred to the appropriate wells of a pre‑labeled 96‑well plate. The optical density was measured at 570 nm.
The relative mean viability of the test item treated tissues was 96.1% after the 15‑Minute exposure period and 42‑Hours post‑exposure incubation period.
The relative mean tissue viability for the positive control treated tissues was 3.9% relative to the negative control treated tissues and the standard deviation value of the viability was 1.3%. The positive control acceptance criteria were therefore satisfied.
The mean OD570 for the negative control treated tissues was 0.846 and the standard deviation value of the viability was 6.8%. The negative control acceptance criteria were therefore satisfied.
The standard deviation calculated from individual tissue viabilities of the three identically test item treated tissues was 13.8%. The test item acceptance criterion was therefore satisfied.
All of the values for the negative and positive control groups fell within the historical ranges of the testing laboratory obtained in the previous six months. This was taken to show the correct functioning of the test system.
Under the experimental conditions of this study, the test substance is not classified for skin irritation according to Regulation (EC) No. 1272/2008 (CLP).
This study is considered as acceptable and satisfies the requirement for skin irritation endpoint.
- Endpoint:
- skin irritation: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From January 30 to February 4, 2019
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- GLP study conducted according to OECD test Guideline No. 439.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 439 (In Vitro Skin Irritation: Reconstructed Human Epidermis Test Method)
- Version / remarks:
- adopted 28 July 2015
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.46 (In Vitro Skin Irritation: Reconstructed Human Epidermis Model Test)
- Version / remarks:
- 23 July 2009
- Deviations:
- no
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- UK GLP Compliance Program (inspected on August 21, 2018 / Signed on November 19, 2018)
- Test system:
- human skin model
- Source species:
- human
- Cell type:
- non-transformed keratinocytes
- Justification for test system used:
- Following the REACH top-down strategy, the EPISKIN™ Reconstructed Human Epidermis Model method was used to assess skin irritation as recommended in the OECD test guideline No. 439.
- Vehicle:
- unchanged (no vehicle)
- Details on test system:
- RECONSTRUCTED HUMAN EPIDERMIS (RHE) TISSUE
- Model used: EPISKIN™ Reconstructed Human Epidermis Model Kit, SkinEthic Laboratories, Lyon, France
- Tissue batch number(s): 19-EKIN-005
- Production date: not reported
- Shipping date: not reported
- Delivery date: 29 January 2019
- Expiry date: 4 February 2019
- Date of initiation of testing: 30 January 2019
TEMPERATURE USED FOR TEST SYSTEM
- Temperature used during treatment / exposure: room temperature
- Temperature of post-treatment incubation (if applicable): 37°C
REMOVAL OF TEST MATERIAL AND CONTROLS
- Volume and number of washing steps: At the end of the exposure period, each tissue was removed from the well using forceps and rinsed using a wash bottle containing DPBS with Ca++ and Mg++. Rinsing was achieved by filling and emptying each tissue insert for approximately 40 seconds using a constant soft stream of DPBS to gently remove any residual test item. The rinsed tissues were transferred to the second column of 3 wells containing 2 mL of maintenance medium in each wellsidual test or control items and then incubated in 2mL maintenance medium for 42 h at 37 °C, 5 % CO2 in air. Number of washing steps not reported.
- Observable damage in the tissue due to washing: none reported
- Modifications to validated SOP:
Deviation 1
An assessment found the test item was able to directly reduce MTT. Therefore, an additional procedure using water killed tissues was performed. However, the results obtained showed that no interference due to direct reduction of MTT occurred. It was therefore considered unnecessary to use the results of the water killed tissues for quantitative correction of results or for reporting purposes.
MTT DYE USED TO MEASURE TISSUE VIABILITY AFTER TREATMENT / EXPOSURE
- MTT concentration: 0.3 mg/mL
- Incubation time: 3 hours
- Spectrophotometer: Labtech LT 4500 microplate reader
- Wavelength: 570 nm
- Filter: without reference filter
- Linear OD range of spectrophotometer: not reported
FUNCTIONAL MODEL CONDITIONS WITH REFERENCE TO HISTORICAL DATA
- Barrier function: IC50 = 1.9 mg/ml ( ≥ 1.5 mg/ml)
- Morphology: Well-differenciated epidermis consisting of a basal layer, several spinous and granular layers and a thinck stratum corneum
- Contamination:
absence of bacteria, fungus and mycoplasma
absence of HIV1 & 2 & hepatitis C antibodies; absence of hepatitis B antigen HBs
- Reproducibility: All of the values for the negative and positive control groups fell within the historical ranges of the testing laboratory obtained in the previous six months. This was taken to show the correct functioning of the test system.
CONTROL TISSUES USED IN CASE OF MTT DIRECT INTERFERENCE:
An assessment found the test item was able to directly reduce MTT. Therefore, an additional procedure using water killed tissues was performed. However, the results obtained showed that no interference due to direct reduction of MTT occurred. It was therefore considered unnecessary to use the results of the water killed tissues for quantitative correction of results or for reporting purposes.
NUMBER OF INDEPENDENT TEST SEQUENCES / EXPERIMENTS TO DERIVE FINAL PREDICTION: 1
PREDICTION MODEL / DECISION CRITERIA
- The test substance is considered to be irritating to skin if relative mean tissue viability is ≤ 50% after 15 minutes of exposure.
- The test substance is considered to be non-irritating to skin if relative mean tissue viability is > 50% after 15 minutes of exposure. - Control samples:
- yes, concurrent negative control
- yes, concurrent positive control
- Amount/concentration applied:
- TEST MATERIAL
- The test item was used as supplied (undiluted).
- Amount(s) applied (volume or weight with unit): 10 µL
NEGATIVE CONTROL
- Amount(s) applied (volume or weight): 10 μL
- Concentration (if solution): DPBS
POSITIVE CONTROL
- Amount(s) applied (volume or weight): 10 μL
- Concentration (if solution): Sodium Dodecyl Sulphate (SDS) at a 5% (w/v) aqueous solution - Duration of treatment / exposure:
- 15 minutes
- Duration of post-treatment incubation (if applicable):
- 42 hours
- Number of replicates:
- Triplicate tissues for test substance, negative and positive controls
- Irritation / corrosion parameter:
- % tissue viability
- Run / experiment:
- 15 minute exposure period and 42 h post-exposure incubation period
- Value:
- 81.3
- Vehicle controls validity:
- not applicable
- Negative controls validity:
- valid
- Remarks:
- 100%
- Positive controls validity:
- valid
- Remarks:
- 3.7%
- Remarks on result:
- no indication of irritation
- Other effects / acceptance of results:
- - OTHER EFFECTS:
- Visible damage on test system: none reported
- Direct-MTT reduction: yes, an assessment found the test item was able to directly reduce MTT. Therefore, an additional procedure using water killed tissues was performed. However, the results obtained showed that no interference due to direct reduction of MTT occurred. It was therefore considered unnecessary to use the results of the water killed tissues for quantitative correction of results or for reporting purposes.
- Colour interference with MTT: no
DEMONSTRATION OF TECHNICAL PROFICIENCY: yes
ACCEPTANCE OF RESULTS:
- Acceptance criteria met for negative control: The mean OD570 for the negative control treated tissues was 0.839 and the standard deviation value of the viability was 1.1%. The negative control acceptance criteria were therefore satisfied.
- Acceptance criteria met for positive control: The relative mean tissue viability for the positive control treated tissues was 3.7% relative to the negative control treated tissues and the standard deviation value of the viability was 1.1%. The positive control acceptance criteria were therefore satisfied.
- Acceptance criteria met for variability between replicate measurements: The standard deviation calculated from individual tissue viabilities of the three identically test item treated tissues was 1.8%. The test item acceptance criterion was therefore satisfied. - Interpretation of results:
- other: CLP criteria not met
- Conclusions:
- Under the experimental conditions of this study, the test substance is not classified for skin irritation according to Regulation (EC) No. 1272/2008 (CLP).
- Executive summary:
An in vitro skin irritation study was performed according to the OECD Guideline 439 and in compliance with GLP, using the EPISKINTM reconstructed human epidermis model.
Triplicate tissues were treated with the test item for an exposure period of 15 minutes. At the end of the exposure period each tissue was rinsed before incubating for 42 hours. The test item was found to directly reduce MTT and therefore additional non-viable tissues were incorporated into the testing for correction purposes. At the end of the post‑exposure incubation period each tissue was taken for MTT-loading. The maintenance medium from beneath each tissue was transferred to pre‑labeled micro tubes and stored in a freezer for possible inflammatory mediator determination. After MTT-loading a total biopsy of each epidermis was made and placed into micro tubes containing acidified isopropanol for extraction of formazan crystals out of the MTT‑loaded tissues. At the end of the formazan extraction period each tube was mixed thoroughly and duplicate 200 µL samples were transferred to the appropriate wells of a pre‑labeled 96‑well plate. The optical density was measured at 570 nm.
The relative mean viability of the test item treated tissues was 81.3% after the 15‑Minute exposure period and 42‑Hours post‑exposure incubation period.
The relative mean tissue viability for the positive control treated tissues was 3.7% relative to the negative control treated tissues and the standard deviation value of the viability was 1.1%. The positive control acceptance criteria were therefore satisfied.
The mean OD570 for the negative control treated tissues was 0.839 and the standard deviation value of the viability was 1.1%. The negative control acceptance criteria were therefore satisfied.
The standard deviation calculated from individual tissue viabilities of the three identically test item treated tissues was 1.8%. The test item acceptance criterion was therefore satisfied.
All of the values for the negative and positive control groups fell within the historical ranges of the testing laboratory obtained in the previous six months. This was taken to show the correct functioning of the test system.
Under the experimental conditions of this study, the test substance is not classified for skin irritation according to Regulation (EC) No. 1272/2008 (CLP).
This study is considered as acceptable and satisfies the requirement for skin irritation endpoint.
Referenceopen allclose all
Table 7.3.1/1: Mean OD570 Values and Viabilities for the Negative Control Item, Positive Control Item and Test Item
Dose group |
Treatment Interval |
Absorbance 570 nm Tissue 1* |
Absorbance 570 nm Tissue 2* |
Mean Absorbance of 2 Tissues |
Rel. Absorbance [% of Negative Control]** |
Negative Control |
3 min |
1.628 |
1.647 |
1.637 |
100.0
|
Positive Control |
3 min |
0.494 |
0.369 |
0.432 |
26.4 |
Pink Pepper (ST 08 C 08) |
3 min |
1.547 |
1.486 |
1.517 |
92.6
|
Negative Control |
1 hour |
1.755 |
1.650 |
1.703 |
100.0
|
Positive Control |
1 hour |
0.191 |
0.231 |
0.211 |
12.4
|
Pink Pepper (ST 08 C 08) |
1 hour |
1.436 |
1.477 |
1.456 |
85.5
|
* Mean of three replicate wells after blank correction
** relative absorbance [rounded values]: 100 x (absorbance test item) / (absorbance negative control)
Table 7.3.1/1: EpiSkin™ results
Item |
OD570of tissues |
Mean OD570of triplicate tissues |
±SDof OD570 |
Relative individual tissue viability (%) |
Relative mean viability (%) |
± SD of Relative mean viability (%) |
Negative Control Item |
0.661 |
0.656 |
0.048 |
100.8 |
100* |
7.3 |
0.701 |
106.9 |
|||||
0.606 |
92.4 |
|||||
Positive Control Item |
0.084 |
0.080 |
0.005 |
12.8 |
12.2 |
0.7 |
0.081 |
12.3 |
|||||
0.075 |
11.4 |
|||||
Test Item |
0.549 |
0.629 |
0.076 |
83.7 |
95.9 |
11.5 |
0.640 |
97.6 |
|||||
0.699 |
106.6 |
OD=Optical Densit
SD= Standard deviatio
*= The mean viability of the negative control tissues is set at 100%
Table 7.3.1/1: EpiSkin™ results
Item |
OD570of tissues |
Mean OD570of triplicate tissues |
±SDof OD570 |
Relative individual tissue viability (%) |
Relative mean viability (%) |
± SD of Relative mean viability (%) |
Negative Control Item |
0.814 |
0.846 |
0.058 |
96.2 |
100* |
6.8 |
0.812 |
96.0 |
|||||
0.913 |
107.9 |
|||||
Positive Control Item |
0.046 |
0.033 |
0.011 |
5.4 |
3.9 |
1.3 |
0.029 |
3.4 |
|||||
0.025 |
3.0 |
|||||
Test Item |
0.937 |
0.813 |
0.117 |
110.8 |
96.1 |
13.8 |
0.705 |
83.3 |
|||||
0.797 |
94.2 |
OD=Optical Density
SD= Standard deviation
*= The mean viability of the negative control tissues is set at 100%
Table 7.3.1/1: EpiSkin™ results
Item |
OD570of tissues |
Mean OD570of triplicate tissues |
±SDof OD570 |
Relative individual tissue viability (%) |
Relative mean viability (%) |
± SD of Relative mean viability (%) |
Negative Control Item |
0.847 |
0.839 |
0.009 |
101.0 |
100* |
1.1 |
0.839 |
100.0 |
|||||
0.830 |
98.9 |
|||||
Positive Control Item |
0.037 |
0.031 |
0.010 |
4.4 |
3.7 |
1.1 |
0.020 |
2.4 |
|||||
0.036 |
4.3 |
|||||
Test Item |
0.680 |
0.682 |
0.015 |
81.0 |
81.3 |
1.8 |
0.668 |
79.6 |
|||||
0.698 |
83.2 |
OD=Optical Density
SD= Standard deviation
*= The mean viability of the negative control tissues is set at 100%
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Link to relevant study records
- Endpoint:
- eye irritation: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 24 April 2008
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
- Remarks:
- GLP study conducted prior to the adoption of the OECD test Guideline No. 437 but followed the SOP used to validate the model. The absence of references to historical control data reduce the reliability of this assay, but this deviation is considered not to have affected the conclusions (unequivocal results)
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 437 (Bovine Corneal Opacity and Permeability Test Method for Identifying Ocular Corrosives and Severe Irritants)
- Deviations:
- yes
- Remarks:
- historical control data are not reported, some information on eye collection and preparation are missing
- Qualifier:
- according to guideline
- Guideline:
- other: INVITTOX (UK) protocol no.98 "The Bovine Corneal Opacity and Permeability Assay"
- Version / remarks:
- February 1994
- Deviations:
- no
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- yes
- Species:
- cattle
- Strain:
- not specified
- Details on test animals or tissues and environmental conditions:
- SOURCE OF COLLECTED EYES
- Source: Odenwaldschlachthof Brensbach, D-64395 Brensbach
- Number of animals: not reported
- Characteristics of donor animals (e.g. age, sex, weight): not reported
- Storage, temperature and transport conditions of ocular tissue (e.g. transport time, transport media and temperature, and other conditions): Freshly isolated bovine eyes were collected from the abattoir. Excess tissue was removed from the excised eyes and they were contained and transported in Hank’s BSS supplemented with streptomycin / penicillin at room temperature.
- Time interval prior to initiating testing: The bovine eyes were fetched from the slaughterhouse and stored in the refrigerator at about 2 - 8 °C until preparation of the corneas on the same day,
- indication of any existing defects or lesions in ocular tissue samples: none reported. All eyes were carefully examined macroscopically for defects. Those presenting defects such as vascularization, pigmentation, opacity and scratches were discarded.
- Indication of any antibiotics used: Hank’s BSS supplemented with streptomycin / penicillin - Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent vehicle
- yes, concurrent positive control
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit):1 mL of test item was applied on each cornea. - Duration of treatment / exposure:
- 10 minutes ± 30 seconds at 32 ± 2 °C in a horizontal position
- Duration of post- treatment incubation (in vitro):
- 2 hours
- Number of animals or in vitro replicates:
- Total: 9 corneas - 3 corneas/group for test item, negative and positive controls
- Details on study design:
- SELECTION AND PREPARATION OF CORNEAS
All eyes were carefully examined macroscopically for defects. Those presenting defects such as vascularization, pigmentation, opacity and scratches were discarded. The cornea was carefully removed from the eye using scalpel and rounded scissors. A rim of about 2 mm of tissue (sclera) was left for stability and handling of the isolated cornea. All corneas used in the experiment were collected in Hank’s BSS supplemented with streptomycin / penicillin and checked finally with a view box for defects listed above.
Each cornea was mounted in a cornea holder with the endothelial side against the sealing ring (O-ring) of the posterior part of the holder. The cornea was gently flattened over the Oring but stretching was avoided. After the anterior part of the holder was positioned on top of the cornea and fixed in place with screws, both compartments of the holder were filled with complete minimum essential medium (cMEM). The posterior compartment was filled first to return the cornea to its natural convex position. Care was taken to assure no air bubbles were present within the compartments.
For equilibration, the corneas in the holder were incubated in a vertical position for about one hour at 32 ± 2 °C in a water-bath.
At the end of the incubation period, the medium was removed from both compartments and replaced with fresh cMEM, and the basal opacity was determined (t0). For measurement, the posterior compartment was plugged and the anterior compartment was unplugged.
The bovine eyes were fetched from the slaughterhouse and stored in the refrigerator at about 2 - 8 °C until preparation of the corneas on the same day,
The cornea of the freshly delivered eye was removed as described earlier and inserted in pre-cooled preservation medium. The corneas were stored individually in a minimum volume of 5 mL. The preservation medium was composed of Medium 199 supplemented with Lglutamine, Na-bicarbonate and Taurine. Shortly before use, Dextran was added.
QUALITY CHECK OF THE ISOLATED CORNEAS : macroscopic examination
NUMBER OF REPLICATES : 3 corneas/group
NEGATIVE CONTROL USED : 0.9% (v/v) saline
POSITIVE CONTROL USED : Ethoxyethanol
APPLICATION DOSE AND EXPOSURE TIME : Fresh cMEM was placed in the posterior compartment, while the anterior compartment received the test item or negative or positive control at a volume of 1.0 mL on the surface of the corneas and was incubated at 32 ± 2 °C in the water-bath, while the corneas were in a horizontal position.
TREATMENT METHOD: closed chamber
POST-INCUBATION PERIOD: No
REMOVAL OF TEST SUBSTANCE:
- Number of washing steps after exposure period: After the test item was rinsed off from the application side by changing cMEM several times, in minimum three times, fresh cMEM was added and opacity was measured (t10).
- POST-EXPOSURE INCUBATION: The corneas were then incubated at 32 ± 2 °C for further two hours in a vertical position, followed by a third opacity reading (t120).
METHODS FOR MEASURED ENDPOINTS:
- Corneal opacity: The opacitometer determines changes in the light transmission passing through the corneas, and displays a numerical opacity value. This value was recorded in a table. The opacitometer was calibrated as described in the manual and the opacity of each of the corneas was determined by reading each holder placed in the photoreceptor compartment for treated cornea.
After recording the basal opacity of all corneas, the mean value of all corneas were taken and any cornea deviating from this by more than 3 units, also –3 units is possible, was discarded. Sets of three corneas were used for treatment with the test item and the negative and positive controls.
- Corneal permeability: Following to the opacity readings, the permeability endpoint was measured as an indication of the integrity of the epithelial cell sheets. After the final opacity measurement was performed, the medium was removed from the anterior compartment and replaced by 1 mL of a 0.5% (v/v) fluorescein solution. Corneas were incubated again in a horizontal position for about 90 minutes in a water-bath at 32 ± 2 °C. Medium from the posterior compartment was removed with a 5 mL-syringe, well mixed and the optical density at 490 nm (OD490) was determined with a spectrophotometer.
SCORING SYSTEM: In Vitro Irritancy Score (IVIS)
DECISION CRITERIA:
0-3 Non eye irritant
3.1-25 Mild eye irritant
25.1-55 Moderate eye irritant
55.1-80 Severe eye irritant
> 80.1 Very severe eye irritant - Irritation parameter:
- in vitro irritation score
- Run / experiment:
- mean/3 corneas
- Value:
- 0.13
- Vehicle controls validity:
- not applicable
- Negative controls validity:
- valid
- Remarks:
- IVIS = 0.92
- Positive controls validity:
- valid
- Remarks:
- IVIS = 45.06
- Remarks on result:
- no indication of irritation
- Other effects / acceptance of results:
- OTHER EFFECTS:
- Visible damage on test system: the test item did not cause any opacity or permeability of the corneas compared with the results of the negative control
DEMONSTRATION OF TECHNICAL PROFICIENCY: not included in the report
ACCEPTANCE OF RESULTS:
- Acceptance criteria met for negative control: cannot be assessed
- Acceptance criteria met for positive control: yes
- Range of historical values if different from the ones specified in the test guideline: not reported - Interpretation of results:
- GHS criteria not met
- Conclusions:
- With an IVIS < 3, the test item does not require classification for eye irritation or serious eye damage according to the Regulation (EC) No. 1272/2008 and to the GHS.
- Executive summary:
An in vitro eye irritation study was performed prior to the adoption of the OECD Guideline 437 (but follows the SOP used to validate the model), and in compliance with GLP to assess the corneal damage potential of test substance by means of the BCOP assay using fresh bovine corneae.
After a first opacity measurement of the fresh bovine corneas (t0), the neat test item , the positive, and the negative controls were applied to corneas and incubated for 10 minutes at 32 ± 2 °C in cMEM (complete Minimum Essential Medium), supplemented with 10% FCS (Fetal Calf Serum). After the incubation phase the test item, the positive, and the negative controls were each rinsed from the corneas and opacity was measured again (t10). Further, the corneas were incubated for another 120 minutes at 32 ± 2 °C in medium, and opacity was measured a third time (t120).
The opacity measurement permeability of the corneas was determined by application of 1 mL of a fluorescein solution for about 90 minutes at 32 ± 2 °C. The liquid in the posterior chamber was measured spectrophotometrically.
The negative control (0.9% NaCl solution) showed neither an increase of opacity nor permeability of the corneas. The in vitro score was calculated as 0.92.
The positive control (2-Ethoxyethanol) showed clear opacity and distinctive permeability of the corneas and therefore, is classified as moderate eye irritant. The in vitro score was calculated as 45.06. The positive controlelicited an In Vitro Irritancy Score of 45.06. Even if below the cut-off value of 53, it is close to the treshold and the since the negative control and test item results were not equivocal, the study was considered to be acceptable.
The test item did not cause any opacity or permeability of the corneas compared with the results of the negative control. The calculated in vitro score was 0.13 and therefore, the test item was classified as non eye irritant.
With an IVIS < 3, the test item does not require classification for eye irritation or serious eye damage according to the Regulation (EC) No. 1272/2008 and to the GHS.
The study is acceptable and satisfies the requirement for an in vitro eye irritation assay.
Reference
Table 7.3.2/1: Individual and Mean Corneal Opacity and Permeability Measurements
Test Group |
Opacity value = Difference (t120-t0) of Opacity |
Permeability at 490 nm (OD490)* |
In vitro Score |
Mean in vitroScore |
Proposed in vitro Irritation Scale |
||
|
|
Mean |
|
Mean |
|
|
|
Negative Control |
0 |
0 |
0.049 |
0.061 |
0.74 |
0.92 |
Non eye irritant |
Negative Control |
0 |
0.046 |
0.69 |
||||
Negative Control |
0 |
0.088 |
1.32 |
||||
Positive control |
32 |
0.566 |
40.49 |
Moderate eye irritant |
|||
Positive control |
30 |
1.180 |
47.70 |
||||
Positive control |
28 |
1.265 |
46.98 |
||||
Test item |
0 |
0.000 |
-1.05 |
Non eye irritant |
|||
Test item |
0 |
0.104 |
1.56 |
||||
Test item |
0 |
0.059 |
-0.12 |
Assay validity
The positive control elicited an In Vitro Irritancy Score of 45,06. Even if below the cut-off value of 53, it is close to the treshold and the since the negative control and test item results were not equivocal, the study was considered to be acceptable.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Skin irritation/corrosion:
A key study was identified for skin corrosion. This in vitro skin corrosion study (RCC, 2008, Rel.2) was performed according to the OECD Guideline 431 and in compliance with GLP, using the EpiDerm™ Human Skin Model. The relative mean viability of the test item (Item 2) treated tissues was 92.6% and 85.5% after 3 and 60 minutes exposure, respectively. The quality criteria required for acceptance of results in the test were satisfied.With a tissue viability > 15% after 60 minutes of exposure, the test material was considered not to be corrosive to skin.
The testing and assessment strategy, as described in ECHA R.7a Endpoint specific guidance (December 2016), was used to evaluate the skin irritation potential of the registered substance:
Element |
Information |
Conclusion |
Comments |
|
Existing data on physico |
1a |
Is the substance spontaneously flammable in contact with air (pyrophoric) or water at room temperature? |
NO |
|
1b |
Is the substance an organic hydroperoxide or an organic peroxide? |
NO |
||
1c |
Is the pH of the substance ≤ 2.0 or ≥ 11.5? |
NO |
||
1d |
Are there other physical or chemical properties that |
NO |
||
Existing human data |
2 |
Are there adequate existing human data which provide evidence that the substance is a corrosive |
NO |
|
Existing animal data from corrosion/irritation studies |
3 |
Are there data from existing studies on corrosion and irritation in laboratory animals, which provide sound conclusive evidence that the substance is a corrosive, irritant or non-irritant? |
NO |
|
Existing data from general toxicity studies via the dermal route and from sensitisation studies |
4a |
Is the substance classified as fatal in contact with skin (LD50 ≤ 50 mg/kg bw, CLP hazard statement |
NO |
|
4b |
Has the substance proven to be a corrosive, irritant or non-irritant in a suitable acute dermal toxicity test? |
NO |
||
4c |
Has the substance proven to be a corrosive or an irritant in sensitisation studies or after repeated |
NO |
No local effects were reported in acute oral study at 2000 mg/kg bw (in PEG 300) |
|
Existing/new (Q)SAR data and read |
5a |
Are there structurally related substances (suitable “read-across” or grouping), which are classified as corrosive to the skin (Skin Corrosive Cat. 1), or do suitable (Q)SAR methods indicate corrosion |
NO |
|
5b |
Are there structurally related substances (suitable “read-across” or grouping), which are classified as irritant to the skin (Skin Irritant Cat. 2), or indicating that the substance is non-irritant, or do suitable (Q)SAR methods indicate irritant or non-irritant potential of the substance? |
NO |
||
Existing in vitro data |
6a |
Has the substance demonstrated corrosive properties in an EU/OECD adopted in vitro test? |
NO |
The substance is not corrosive (OECD 431, GLP, Rel.2) |
6b |
Has the substance demonstrated irritant or non-irritant properties in an EU/OECD adopted |
NO |
(at the initiation of the dossier, no test was available) |
|
6c |
Are there data from a non-validated suitable in vitro test(s), which provide sound conclusive evidence that the substance is corrosive/ irritant? |
NO |
||
Weight-of- Evidence analysis |
7 |
The “elements” described above may be arranged as appropriate. Taking all available existing and |
NO |
|
New in vitro test for irritation |
8 |
Does the substance demonstrate irritating or non-irritating properties in (an) EU/OECD adopted in vitro test(s) for skin irritation? |
YES |
=> an Episkin test for irritation was initiated (Top-down strategy) on Items 1, 4 and 5. The substances are not irritant to skin. |
New in vitro test for corrosivity |
9 |
Does the substance demonstrate corrosive properties in (an) EU/OECD adopted in vitro test(s) for skin corrosion? |
NO |
|
New in vivo test for corrosion/irritation |
10 |
To be used only as a last resort |
NO |
In vivo testing should not be conducted in this case since the substance falls under the scope of the specific in vitro tests performed, and there are no substance-specific limitations on use of those tests. An adaptation according to Annex XI to the REACH Regulation is included in this dossier. |
Following the REACH top-down, in vitro skin irritation studies (Envigo, 2017 / Covance, 2019 / Covance, 2019) were performed on Items 1, 3 and 4 according to the OECD Guideline 439 and in compliance with GLP, using the EPISKIN reconstructed human epidermis model.
The relative mean viability of the test item treated tissues was 95.9% for Item 1, 96.1% for Item 4 and 81.3% for Item 5, after the 15‑Minute exposure period and 42‑Hours post‑exposure incubation period.
The quality criteria required for acceptance of results in the test were satisfied.With a tissue viability > 50%, the test items were considered to be not irritant to skin.
Eye irritation:
A key study was identified on Item 2 (RCC, 2008, rel.2). This in vitro eye irritation study was performed prior to the adoption of the OECD Guideline 437 (but follows the SOP used to validate the model), and in compliance with GLP to assess the corneal damage potential of test substance by means of the BCOP assay using fresh bovine corneae.
The negative control (0.9% NaCl solution) showed neither an increase of opacity nor permeability of the corneas. The in vitro score was calculated as 0.92.
The positive control (2-Ethoxyethanol) showed clear opacity and distinctive permeability of the corneas and therefore, is classified as moderate eye irritant. The in vitro score was calculated as 45.06. The positive controlelicited an In Vitro Irritancy Score of 45.06. Even if below the cut-off value of 53, it is close to the treshold and the since the negative control and test item results were not equivocal, the study was considered to be acceptable.
The test item did not cause any opacity or permeability of the corneas compared with the results of the negative control. The calculated in vitro score was 0.13 and therefore, the test item was classified as non eye irritant.
With an IVIS < 3, the test item does not require classification for eye irritation or serious eye damage.
Justification for classification or non-classification
Harmonized classification:
The substance has no harmonized classification according to the Regulation (EC) No. 1272/2008 (CLP).
Self-classification:
Based on the available data no additional self-classification is proposed for the substance (all qualities, see Section 13 for further details on composition) regarding skin and eye irritation according to the CLP and to the GHS.
No data was available regarding respiratory irritation, however the substance not being classified for skin and eye irritation, no classification is expected for respiratory irritation.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.