Non-volatile extract of Ginger, obtained from the roots of Zingiber officinalis (Zingiberaceae) by supercritical CO2 extraction

Skin irritation / corrosion

Administrative data

Endpoint:

skin irritation: in vitro / ex vivo

Type of information:

experimental study

Adequacy of study:

key study

Study period:

01 Feb 2018 to 26 March 2018

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2018

Report date:

2018

Materials and methods

Test guideline

Test guideline 1

Qualifier:

according to guideline

Guideline:

OECD Guideline 439 (In Vitro Skin Irritation: Reconstructed Human Epidermis Test Method)

Version / remarks:

2015

Deviations:

no

Test guideline 2

Qualifier:

according to guideline

Guideline:

EU Method B.46 (In Vitro Skin Irritation: Reconstructed Human Epidermis Model Test)

Version / remarks:

2012

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Remarks:

08 May 2017

Test material

Test material information

Constituent 1

Reference substance name:

Non-volatile extract of Ginger, obtained from the roots of Zingiber officinalis (Zingiberaceae) by supercritical CO2 extraction

IUPAC Name:

Non-volatile extract of Ginger, obtained from the roots of Zingiber officinalis (Zingiberaceae) by supercritical CO2 extraction

Test material form:

liquid

Details on test material:

Batch number: 861213

In vitro test system

Test system:

human skin model

Source species:

human

Cell type:

non-transformed keratinocytes

Cell source:

other: MatTek Corporation

Justification for test system used:

The test method is based on reconstructed human epidermis models, which closely mimic the biochemical and physiological properties of the upper parts of the human skin, i.e. the epidermis. The procedure described under this test method allows the hazard identification of irritant substances in accordance with UN GHS Category 1 or Category 2, and is in line with the OECD 439 test guidance.

Vehicle:

unchanged (no vehicle)

Details on test system:

TEMPERATURE USED FOR TEST SYSTEM
- Temperature used during treatment / exposure: 37°C for the first 35 minutes followed by 25 minutes at room temperature under a sterile hood
- Temperature of post-treatment incubation (if applicable): 37°C, 5% CO2 and 95% relative humidity

REMOVAL OF TEST MATERIAL AND CONTROLS
- Washing: untill all test item was removed

MTT DYE USED TO MEASURE TISSUE VIABILITY AFTER TREATMENT / EXPOSURE
- MTT concentration: 1 mg/mL
- Incubation time: 3h
- Spectrophotometer: Tecan Sunrise Magellan Version 7.2
- Wavelength: 540 nm

FUNCTIONAL MODEL CONDITIONS WITH REFERENCE TO HISTORICAL DATA
- Viability: The MTT conversion assay is a quantitative validated method, which is used to measure cell viability.
- Barrier function: The barrier function is assessed by determination of the concentration at which a marker substance reduces the viability of the tissues by 50% (IC50) after a fixed exposure time, or by determination of the exposure time required to reduce cell viability by 50% (ET50) upon application of the marker substance at a specified, fixed concentration.
- Contamination: The skin model was free of contamination by bacteria, viruses, mycoplasma, or fungi.

NUMBER OF REPLICATE TISSUES: 3

CONTROL TISSUES USED IN CASE OF MTT DIRECT INTERFERENCE
- Fresh tissues / killed tissues : killed tissues
- Procedure used to prepare the killed tissues (if applicable): freeze-killed
- N. of replicates : 3
- Method of calculation used:
True viability = Viability of treated tissue – Interference from test chemical = OD tvt – OD kt
where OD kt = (mean OD tkt – mean OD ukt)
tvt = treated viable tissue kt = killed tissues
tkt = treated killed tissue ukt = untreated killed tissue (NC treated tissue)


NUMBER OF INDEPENDENT TEST SEQUENCES / EXPERIMENTS TO DERIVE FINAL PREDICTION: 1

PREDICTION MODEL / DECISION CRITERIA (choose relevant statement)
- The test substance is considered to be irritant to skin if the mean relative tissue viability of three individual tissues exposed to the test substance is reduced below or equal to 50% of the mean viability of the negative controls.
- The test substance is considered to be non-irritant to skin if the mean relative tissue viability of three individual tissues exposed to the test substance is >50% of the mean viability of the negative controls.

Control samples:

yes, concurrent negative control

yes, concurrent positive control

Amount/concentration applied:

TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 30µL
- Concentration (if solution): undiluted

NEGATIVE CONTROL
- Amount(s) applied (volume or weight): 30µL
- Concentration (if solution): undiluted D-PBS

POSITIVE CONTROL
- Amount(s) applied (volume or weight): 30µL
- Concentration (if solution): 5% aqueous sodium dodecyl sulphate (SDS)

Duration of treatment / exposure:

60 minutes

Duration of post-treatment incubation (if applicable):

42 hours

Number of replicates:

The measurements were made for three tissues per condition in 2 replicates.

Results and discussion

In vitro

Results

Irritation / corrosion parameter:

% tissue viability

Run / experiment:

Main experiment

Value:

0

Vehicle controls validity:

not applicable

Negative controls validity:

valid

Positive controls validity:

valid

Remarks on result:

no indication of irritation

Other effects / acceptance of results:

- OTHER EFFECTS:
- Direct-MTT reduction: Yes
- Colour interference with MTT: No

DEMONSTRATION OF TECHNICAL PROFICIENCY: Historical data of negative and positive controls 2014-2017

ACCEPTANCE OF RESULTS:
- Acceptance criteria met for negative control: Yes
- Acceptance criteria met for positive control: Yes
- Acceptance criteria met for variability between replicate measurements: Yes
- Range of historical values:

Negative control
Average OD(mean CV %): 1.776
Average Viability [%]:100
Viability [%]: 87.4–110.8
CV [%]: 1.1–11.8
Irritant (I) /Non-irritant (NI): NI
Number of unqualified experiments: 0

Positive control
Average OD(mean CV %): 0.085
Average Viability [%]: 5.1
Viability [%]: 1.3–10.2
CV [%]: 1.8–15.1
Irritant (I) /Non-irritant (NI): I
Number of unqualified experiments: 0

Applicant's summary and conclusion

Interpretation of results:

other: skin Irritant

Remarks:

in accordance with Annex I of the CLP Regulation (1272/2008/EC).

Conclusions:

Based on the results of the in vitro skin irritation test for Ginger Hot Flavor CO2-TO extract, the test substance needs to be classified for skin irritation in accordance with the criteria outlined in Annex I of the CLP Regulation (1272/2008/EC).

Executive summary:

The skin irritant properties of Ginger Hot Flavor CO2-TO extract were examined in a study performed according to OECD Guideline 439 (EpiDermTM model), under GLP.

Three tissues were used for each treatment and control group. The optical density (OD) was determined by using the MTT reduction assay.  30 mL undiluted test material was applied to the model skin surface. D-PBS was used as the negative control. 5% aqueous sodium dodecyl sulphate (SDS) was used as the positive reference item. An exposure time of 60 minutes was employed followed by a 42-hour post-treatment incubation period in fresh medium.

The mean viability of cells exposed to the test material was 0.0% of the negative controls (viability was corrected for direct MTT reduction). The mean optical density (OD) of 3 negative and positive control tissues were respectively 1.699 and 5.2% of the negative control. All acceptance criteria were fulfilled.

Based on the cell viability being <50% of the cut-off value, Ginger Hot Flavor CO2-TO extract was considered to be cytotoxic and predicted to be irritant to skin.