(1S-endo)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

Endpoint summary

Description of key information

Eye irritation (in vitro): Key study. Test method according to the OECD 438 Guideline with GLP. The test item L-borneol is not classified for eye irritation

Skin irritation (in vitro): Key study. Test method according to the OECD 439 Guideline with GLP study. The mean percent viability of the SkinEthic® RHE treated tissues was 5.6% versus 1.2% in the positive control. Therefore, the test item L-borneol must be considered as skin irritant (cat 2) or skin corrosive (Cat 1).

Skin corrosion (in vitro): Key study. Test method according to the OECD 431 Guideline with GLP study.Under RHE test method performed in EpiCS® model the test item does not have to be classified as skin corrosive (cat. 1).

Key value for chemical safety assessment

Skin irritation / corrosion

Link to relevant study records

Reference

Reference 1

Endpoint:

skin irritation: in vitro / ex vivo

Type of information:

experimental study

Adequacy of study:

key study

Study period:

13 March 2017 - 06 April 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)

Deviations:

no

Qualifier:

according to guideline

Guideline:

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

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Test system:

human skin model

Remarks:

SkinEthic RHE® model

Source species:

human

Cell type:

non-transformed keratinocytes

Cell source:

other: foreskin (number of donors not specified)

Source strain:

not specified

Justification for test system used:

The SkinEthic RHE® model has been validated for irritation testing (Validation study based on the original ECVAM Performance Standards (21) in 2008) and its use is recommended by the relevant OECD guideline for irritation testing (OECD No. 439); therefore, it was considered to be suitable for this study.

Vehicle:

unchanged (no vehicle)

Details on test system:

RECONSTRUCTED HUMAN EPIDERMIS (RHE) TISSUE
- Model used: SkinEthic RHE® model
- Tissue batch number(s): 17-RHE-039
- Delivery date: 04/04/2017
- Expiration date: 10/04/2017
- Date of initiation of testing: 04/04/2017

TEMPERATURE USED FOR TEST SYSTEM
- Temperature used during treatment / exposure: room temperature
- Temperature of post-treatment incubation (if applicable): 37ºC

REMOVAL OF TEST MATERIAL AND CONTROLS
-Volume and number of washing steps: 25 x 1 mL of DPBS
- Observable damage in the tissue due to washing: no
- Modifications to validated SOP: no

MTT DYE USED TO MEASURE TISSUE VIABILITY AFTER TREATMENT / EXPOSURE
- MTT concentration: 300 µL of a MTT solution at 1.0 mg/mL
- Incubation time: 3 hours at 37°C, 5% CO2
- Spectrophotometer: ELx800 absorbance microplate reader (BioTek)
- Wavelength: 570 nm
- Linear OD range of spectrophotometer: The linearity range of optical density measured is validated for an optical density between 0 and 2.0.

FUNCTIONAL MODEL CONDITIONS WITH REFERENCE TO HISTORICAL DATA
- Viability: 1.4 (CV = 2.8%) specification OD > 0.7. Historical negative control mean OD range = 0.834-1.574.
- Barrier function: 4.8 h (Specification 0h < ET50< 10h)
- Morphology: 5.5 Cell layers, absence of significant histological abnormalities, well differentiated epidermis, specification > 4
- Contamination: no

NUMBER OF REPLICATE TISSUES: 3

CONTROL TISSUES USED IN CASE OF MTT DIRECT INTERFERENCE: no interference.

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

PREDICTION MODEL / DECISION CRITERIA
- The test substance is considered to be irritant to skin if the viability after 42 minutes exposure is less than or equal to 50%.
- The test substance is considered to be non-irritant to skin if the viability after 42 minutes exposure is greater than 50%.

Control samples:

yes, concurrent negative control

yes, concurrent positive control

Amount/concentration applied:

TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 16 mg (32mg/cm2)

NEGATIVE CONTROL
- Amount(s) applied (volume or weight): 16 µL

POSITIVE CONTROL
- Amount(s) applied (volume or weight): 16 µL
- Concentration (if solution): 5% SDS

Duration of treatment / exposure:

42 minutes

Duration of post-treatment incubation (if applicable):

41 hours and 47 minutes.

Number of replicates:

3

Irritation / corrosion parameter:

% tissue viability

Run / experiment:

mean

Value:

5.6

Vehicle controls validity:

not applicable

Negative controls validity:

valid

Remarks:

(DPBS)

Positive controls validity:

valid

Remarks:

1.2% viability (5% SDS)

Remarks on result:

positive indication of irritation

Other effects / acceptance of results:

The mean percent viability of the treated tissues was 5.6% versus 1.2% in the positive control (5% Sodium Dodecyl Sulfate). Therefore, the test item must be considered as skin irritant (cat 2) or skin corrosive (Cat 1).

- OTHER EFFECTS:
- Visible damage on test system: no
- Direct-MTT reduction: no
- Colour interference with MTT: no

DEMONSTRATION OF TECHNICAL PROFICIENCY: yes. A full demonstration of proficiency was performed for the EpiSkin-SM model, plus a reduced validation with the SkinEthic RHE model. Adequate results were obtained for the evaluated chemicals.

ACCEPTANCE OF RESULTS:
- Acceptance criteria met for negative control: yes, SD of the negative control group was 4.3% (acceptablility criteria, SD ≤ 18%) and OD mean is 1.077 (acceptability criteria, 0.8≤OD≤3).
- Acceptance criteria met for positive control: yes
- Acceptance criteria met for variability between replicate measurements: yes. SD of test item was 5% (acceptablility criteria, SD ≤ 18%).

Table 1. Summary of results.

	Skin	OD	Mean OD /disc (#)	Mean OD / product	Viability %	Mean viability %	SD Viability	Conclusion
Negative Control	1	0.965	1.026	1.077	95.2	100.0	4.3
		1.052
		1.060
	2	1.109	1.117		103.7
		1.222
		1.121
	3	1.090	1.089		101.1
		1.076
		1.102
Positive Control	4	0.012	0.012	0.013	1.1	1.2	0.1	Irritant
		0.012
		0.012
	5	0.013	0.013		1.2
		0.013
		0.013
	6	0.013	0.013		1.2
		0.012
		0.013
Test item	13	0.114	0.121	0.060	11.2	5.6	5.0	Corrosive or irritant
		0.124
		0.124
	14	0.016	0.018		1.7
		0.019
		0.018
	15	0.039	0.042		3.9
		0.043
		0.044

# mean of 3 values (triplicate of the same extract)

OD: optical density

*The optical density was measured after a 1:2 dilution of the formazan extracts in isopropanol.

Acceptability criteria: SD≤18%.

Interpretation of results:

other: classified as corrosive (Cat 1) or irritant (Cat 2) (CLP Regulation EC no. 1272/2008)

Conclusions:

The mean percent viability of the treated tissues was 5.6% versus 1.2% in the positive control (5% Sodium Dodecyl Sulfate). Therefore, the test item must be considered as skin irritant (cat 2) or skin corrosive (Cat 1).

Executive summary:

An in vitro skin irritation test of the test item was performed in a reconstructed human SkinEthic RHE® model, according to OECD TG 439 (GLP study). Three epidermis units were treated with 16 mg test item for 42 minutes at room temperature. Exposure of the test item was terminated by rinsing with25 x 1 mL of DPBS.The epidermis units were then incubated at 37°C for 41 hours 47 minutes in an incubator with 5% CO2. The viability of each disk was assessed by incubating the tissues with MTT, extracting the precipitated formazan crystals using isopropanol during 2 hours under gentle agitation in the dark, and measuring the concentration of formazan by determining the OD at 570 nm, just after dilution of the extracts 1:2 in isopropanol. Under test conditions, the mean percent viability of the treated tissues was 5.6%, versus 1.2% in the positive control (5% Sodium Dodecyl Sulfate). Therefore, the test item must be considered as skin irritant (cat 2) or skin corrosive (Cat 1).

Reference 2

Endpoint:

skin corrosion: in vitro / ex vivo

Type of information:

experimental study

Adequacy of study:

key study

Study period:

13 June 2017 - 14 June 2017

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Qualifier:

according to guideline

Guideline:

OECD Guideline 431 (In Vitro Skin Corrosion: Reconstructed Human Epidermis (RHE) Test Method)

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Test system:

human skin model

Remarks:

EpiCS® model

Source species:

human

Cell type:

non-transformed keratinocytes

Cell source:

other: not specified

Source strain:

not specified

Justification for test system used:

The EpiCS® model (previously named EST-1000) has been validated for corrosion testing (Validation study based on the statement issued by the ECVAM Scientific Advisory Committee (ESAC30) on 12 June 2009) and its use is recommended by the relevant OECD guideline for corrosion testing (OECD No. 431); therefore, it was considered to be suitable for this study.

Vehicle:

unchanged (no vehicle)

Details on test system:

RECONSTRUCTED HUMAN EPIDERMIS (RHE) TISSUE
- Model used: EpiSC® model
- Tissue batch number(s): 100-AG1038-1
- Production date: 12/06/2017
- Shipping date: 13/06/2017
- Delivery date: 13/06/2017
- Date of initiation of testing: 13/06/2017

TEMPERATURE USED FOR TEST SYSTEM
- Temperature used during treatment / exposure: room temperature for 3 min exposure and 37°C ± 1°C for 1 hour exposure.
- Temperature of post-treatment incubation (if applicable): 37ºC

REMOVAL OF TEST MATERIAL AND CONTROLS
-Volume and number of washing steps: 20 x 1 mL of DPBS
- Observable damage in the tissue due to washing: no
- Modifications to validated SOP: no

MTT DYE USED TO MEASURE TISSUE VIABILITY AFTER TREATMENT / EXPOSURE
- MTT concentration: 300 µL of a MTT solution at 1.0 mg/mL
- Incubation time: 3 hours at 37°C, 5% CO2
- Spectrophotometer: ELx800 absorbance microplate reader (BioTek)
- Wavelength: 570 nm
- Linear OD range of spectrophotometer: The linearity range of optical density measured is validated for an optical density between 0 and 2.0.

FUNCTIONAL MODEL CONDITIONS WITH REFERENCE TO HISTORICAL DATA
- Viability: Not specified. Historical negative control mean OD range = 0.946-1.511 (3 min exposure) and 0.917-1.379 (1 hour exposure).
- Barrier function: 59.8% (test method: MTT, 2 hrs Triton X-100), specification = 50%.
- Morphology: sufficient nº of cornified layers (specification =5) and sufficient nº of vital cell layers (specification =4)
- Contamination: no

NUMBER OF REPLICATE TISSUES: 2

CONTROL TISSUES USED IN CASE OF MTT DIRECT INTERFERENCE: no interference.

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): 25 mg (41.7mg/cm2)

NEGATIVE CONTROL
- Amount(s) applied (volume or weight): 50 µL

POSITIVE CONTROL
- Amount(s) applied (volume or weight): 50 µL
- Concentration (if solution): N/A

Duration of treatment / exposure:

3 minutes and 60 minutes

Duration of post-treatment incubation (if applicable):

2 hours and 55 minutes (incubation in MTT solution)

Number of replicates:

3

Irritation / corrosion parameter:

% tissue viability

Run / experiment:

mean after 3 min exposure

Value:

93.79

Vehicle controls validity:

not applicable

Negative controls validity:

valid

Remarks:

(distilled water)

Positive controls validity:

valid

Remarks:

7.44% viability (8N KOH)

Irritation / corrosion parameter:

% tissue viability

Run / experiment:

mean after 1 hour exposure

Value:

88.99

Vehicle controls validity:

not applicable

Negative controls validity:

valid

Remarks:

(distilled water)

Positive controls validity:

valid

Remarks:

0.93% viability (8N KOH)

Other effects / acceptance of results:

The mean percent viabilities of the epidermis skins treated with the test item were 93.79% (for 3 min exposure) and 88.99% (for 60 min exposure) versus 7.44% and 0.93%, respectively, with the positive control item (potassium hydroxide 8N). Therefore, the test item must be considered as non-corrosive.

- OTHER EFFECTS:
- Visible damage on test system: no
- Direct-MTT reduction: no
- Colour interference with MTT: no

DEMONSTRATION OF TECHNICAL PROFICIENCY: yes. A demonstration of proficiency was performed for the EpiCS® model. Adequate results were obtained for the evaluated chemicals.

ACCEPTANCE OF RESULTS:
- Acceptance criteria met for negative control: yes. The mean OD of negative control tissues for treatment time 3 min and 1 hour were 1.063 and 1.186 (acceptability criteria, 0.8≤OD≤2.8 for the EpiCS® model). The extract was diluted at 1:3 isoborneol just before the OD measure, thus the acceptability criteria should be in the range ≥ 0.3 and ≤ 0.9. However, even for values 1.063 or 1.186 the test item remains clearly classified as non-corrosive. This deviation is considered as without any impact on the conclusion and the validity of the study.
- Acceptance criteria met for positive control: yes. Mean viability of the tissue replicates exposed for 1 hour, expressed as % of the negative control, is 0.93% < 20%.
- Acceptance criteria met for variability between replicate measurements: yes. 9.3% (for 3 min exposure) and 5.9% (for 60 min exposure) < 30%.

Table 1. Individual and average values after 3 minutes exposure

	Skin	OD	Mean OD/disc (#)	Mean OD/product	Viability %	Mean viability %	Viability difference between replicates %
Negative control	1	1.095	1.094	1.063	102.96	100.00	5.9
		1.073
		1.114
	2	1.030	1.031		97.04
		1.012
		1.049
Positive control	3	0.076	0.074	0.079	6.96	7.44	0.9
		0.073
		0.072
	4	0.082	0.084		7.91
		0.085
		0.083
Test item PH-17/0129	7	1.014	1.046	0.997	98.45	93.79	9.3
		1.057
		1.067
	8	0.950	0.947		89.13
		0.974
		0.917

Table 2. Individual and average values after 1 hour exposure

	Skin	OD	Mean OD/disc (#)	Mean OD/product	Viability %	Mean viability %	Viability difference between replicates %
Negative control	1	1.117	1.156	1.186	97.51	100.00	5.0
		1.182
		1.168
	2	1.278	1.215		102.49
		1.076
		1.290
Positive control	3	0.009	0.014	0.011	1.18	0.93	0.5
		0.024
		0.010
	4	0.009	0.008		0.67
		0.008
		0.008
Test item PH-17/0129	7	1.117	1.020	1.055	86.04	88.99	5.9
		1.006
		0.937
	8	1.169	1.090		91.94
		1.063
		1.038

Note:

#: mean of 3 values

OD: optical density

As the extract was diluted at 1:3 just before the OD measure, the acceptability criteria should be in the range ≥ 0.3 and ≤ 0.9 for the negative control.

Interpretation of results:

other: non classified as corrosive (Cat 1) (CLP Regulation EC no. 1272/2008)

Conclusions:

Under RHE test method performed in EpiCS® model the test item does not have to be classified as skin corrosive (cat. 1).

Executive summary:

An in vitro skin corrosion test for the test item was performed in a reconstructed human epidermis EpiCS® model, according to OECD TG 431 (GLP study). Two epidermis units were treated with 25 mg test item for 3 minutes at room temperature and for 1 hour, at 37°C, 5% CO2. Exposure of the test item was terminated by rinsing with 20 x 1 mL of DPBS. The viability of each disk was assessed by incubating the tissues with MTT, extracting the precipitated formazan crystals using isopropanol during 2 hours under agitation in the dark, and measuring the concentration of formazan by determining the OD at 570 nm, just after dilution of the extracts 1:3 in isopropanol. Under test conditions, the mean percent viabilities of the treated tissues were 93.79% (for 3 min exposure) and 88.99% (for 60 min exposure) versus 7.44% and 0.93%, respectively, with the positive control item (potassium hydroxide 8N). Therefore, the test item must be considered as non-corrosive.

Endpoint conclusion

Endpoint conclusion:

adverse effect observed (irritating)

Eye irritation

Link to relevant study records

Reference

Endpoint:

eye irritation: in vitro / ex vivo

Type of information:

experimental study

Adequacy of study:

key study

Study period:

March 27, 2017

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Qualifier:

according to guideline

Guideline:

OECD Guideline 438 (Isolated Chicken Eye Test Method for Identifying i) Chemicals Inducing Serious Eye Damage and ii) Chemicals Not Requiring Classification for Eye Irritation or Serious Eye Damage)

Deviations:

no

Qualifier:

according to guideline

Guideline:

EU method B.48 (Isolated chicken eye test method for identifying occular corrosives and severe irritants)

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Species:

chicken

Strain:

not specified

Details on test animals or tissues and environmental conditions:

SOURCE OF COLLECTED EYES
- Source: eyes collected from chickens obtained from a slaughterhouse (Etablissement Brun, 33820 Etauliers, France) where they are killed for human consumption.
- Characteristics of donor animals (e.g. age, sex, weight): 7 weeks old. 1.5 - 2.5 kg.
- Storage, temperature and transport conditions of ocular tissue (e.g. transport time, transport media and temperature, and other conditions):Because eyes were dissected in the laboratory, the intact heads were transported from the slaughterhouse at ambient temperature in plastic boxes humidified with towels moistened with physiological saline.
- Time interval prior to initiating testing: The heads have been collected on 27 March 2017 at 8: 20 am.The eyes were enucleated at Phycher on 27 March 2017 at 10:00 am.
- indication of any existing defects or lesions in ocular tissue samples: no
- Indication of any antibiotics used: no

Vehicle:

unchanged (no vehicle)

Controls:

yes, concurrent positive control

yes, concurrent negative control

Amount / concentration applied:

TEST MATERIAL
- Amount(s) applied (volume or weight with unit):30 mg of test item

Duration of treatment / exposure:

10 second

Duration of post- treatment incubation (in vitro):

No post-treatment incubation is performed.

Number of animals or in vitro replicates:

3

Details on study design:

SELECTION AND PREPARATION OF ISOLATED EYES
The eyelids were carefully excised, taking care not to damage the cornea. Then, the eye was further dissected from the skull, taking care not to damage the cornea. The eyeball was pulled from the orbit by holding the nictitating membrane firmly with surgical forceps, and the eye muscles were cut with a bent, blunt-tipped scissor. When the eye is removed from the orbit, a visible portion of the optic nerve should be left attached. Once removed from the orbit, the eye was placed on an absorbent pad and the nictitating membrane and other connective tissue were cut away.
The enucleated eye was mounted in a stainless steel clamp with the cornea positioned vertically. The clamp was then transferred to a chamber of the superfusion apparatus. The clamps were positioned in the superfusion apparatus such that the entire cornea was supplied with the physiological saline drip (in the range 0.1 to 0.15 mL/min). The chambers of the superfusion apparatus was temperature controlled between 32.0°C and 32.5°C.
After being placed in the superfusion apparatus, the eyes were examined with a slit-lamp microscope to ensure that they have not been damaged during the dissection procedure using sodium fluorescein. Corneal thickness was also measured at this time at the corneal apex using the depth measuring device on the slit-lamp microscope.
Eyes with; (i), a fluorescein retention score of > 0.5; (ii) corneal opacity > 0.5; or, (iii), any additional signs of damage were replaced. For eyes that are not rejected based on any of these criteria, individual eyes with a corneal thickness deviating more than 10% from the mean value for all eyes are to be rejected. (see table appendix No.4 on "Any other information on results incl. tables")
Once all eyes had been examined and approved, the eyes were incubated between 45 and 56 minutes to equilibrate them to the test system prior to dosing.

EQUILIBRATION AND BASELINE RECORDINGS:
Eyes were incubated between 45 and 56 minutes to equilibrate them to the test system prior to dosing
Following the equilibration period, a zero reference measurement was recorded for corneal thickness and opacity to serve as a baseline (i.e., time = 0). The fluorescein score determined at dissection was used as the baseline measurement for that endpoint.

NUMBER OF REPLICATES:3

NEGATIVE CONTROL USED
30 μL physiological saline - Dutscher Batch No. 3012316 (one eye)

SOLVENT CONTROL USED: not applicable.

POSITIVE CONTROL USED
Sodium hydroxide – Sigma, Batch No. MKBP7805V - 30 mg (three eyes)

APPLICATION DOSE AND EXPOSURE TIME
30 mg of the test item was applied for 10 seconds.

OBSERVATION PERIOD:Treated corneas were evaluated pretreatment and starting at 30, 75, 120, 180, and 240 minutes (± 5 minutes) after the post-treatment rinse.

REMOVAL OF TEST SUBSTANCE
- Volume and washing procedure after exposure period: The test item was rinsed from the eye after 10 seconds of observation with 20 mL of physiological saline at ambient temperature.
- Indicate any deviation from test procedure in the Guideline: NO

METHODS FOR MEASURED ENDPOINTS:
- Corneal opacity: It was calculated by using the area of the cornea that was most densely opacified for scoring. The mean corneal opacity value for all test eyes was calculated for all observation time points (see table 4)
- Damage to epithelium based on fluorescein retention: Fluorescein retention value for all test eyes was calculated for the 30-minute observation time point only, which was used for the overall category score given for each test or control item (Table No.5)
- Swelling: optical pachymeter on a slit-lamp microscope ((HaagStreit BP900 slit-lamp microscope with depth-measuring device no. I). The slit-width was set at 9 1/2 equalling 0.095 mm. The mean percentage of corneal swelling for all test eyes was calculated for all observation time points. Based on the highest mean score for corneal swelling, as observed at any time point, an overall category score was then given for each test item (see table 3).
- Macroscopic morphological damage to the surface: The aim of this evaluation was to determine whether any “pitting” of corneal epithelial cells, “loosening” of epithelium, “roughening” of the corneal surface and “sticking” of the test item to the cornea were visible.These findings can vary in severity and may occur simultaneously.

SCORING SYSTEM:
- Mean corneal swelling: It was expressed as a percentage and was calculated from corneal thickness measurements according to the following formula:
(corneal thickness measurement at time t - corneal thickness at time=0 / corneal thickness at ime=0 )*100

- Mean maximum opacity score:
0 - No opacity,
0.5 -Very faint opacity
1- Scattered or diffuse areas; details of the iris clearly visible
2- Easily discernible translucent area; details of the ris are slightly obscured,
3-Severe corneal opacity; no specific details of the iris are visible; size of the pupil is barely discernible
4-Complete corneal opacity; iris invisible

- Mean fluorescein retention score at 30 minutes post-treatment :
0-No fluorescein retention,
0.5-Very minor single cell staining,
1-Single cell staining scattered throughout the treated area of the cornea,
2-Focal or confluent dense single cell staining,
3-Confluent large areas of the cornea retaining fluorescein

DECISION CRITERIA: Decision criteria was used as indicated in the TG.

Irritation parameter:

cornea opacity score

Run / experiment:

Mean

Value:

0

Vehicle controls validity:

not applicable

Negative controls validity:

valid

Positive controls validity:

valid

Remarks on result:

other:

Remarks:

ICE Class I

Irritation parameter:

fluorescein retention score

Run / experiment:

Mean

Value:

0.5

Vehicle controls validity:

not applicable

Negative controls validity:

valid

Positive controls validity:

valid

Remarks on result:

other:

Remarks:

ICE class I

Irritation parameter:

percent corneal swelling

Run / experiment:

Mean

Value:

ca. 1

Vehicle controls validity:

not applicable

Negative controls validity:

valid

Positive controls validity:

valid

Remarks on result:

other:

Remarks:

ICE class I

Irritation parameter:

morphological effects

Vehicle controls validity:

not applicable

Negative controls validity:

valid

Positive controls validity:

valid

Remarks on result:

other: No effects

Other effects / acceptance of results:

OTHER EFFECTS:
- Visible damage on test system: NO, No morphological effects were noted, whatever the examination time.

DEMONSTRATION OF TECHNICAL PROFICIENCY:Yes.

ACCEPTANCE OF RESULTS:
- Acceptance criteria met for negative control:YES, the combination of the three endpoints for the negative control, physiological saline, was 3xI classified as “No Category”
- Acceptance criteria met for positive control: YES, the combination of the three endpoints for the positive control, sodium hydroxide, was 3 x IV,classified as “Corrosive/Severe Irritant ”

Appendix No. 4: Selected eyes for the performance of the ICE test

Chamber	Fluorescein retention	Corneal opacity	Morphological effects	Corneal thickness (e)
1	0.5	0	N.t.R.	0.58
2	0.5	0	N.t.R.	0.59
3	0.5	0	N.t.R.	0.54
4	0.5	0	N.t.R.	0.60
5	0.5	0	N.t.R.	0.60
6	0.5	0	N.t.R.	0.59
7	0.5	0	N.t.R.	0.62
8	0.5	0	N.t.R.	0.60
9	0.5	0	N.t.R.	0.59
10	0.5	0	N.t.R.	0.59

Table 9: INDIVIDUAL AND AVERAGE VALUES FOR EVALUATION OF CORNEAL LESIONS AFTER TREATMENT

Test item

Endpoint measured	Eye No.	0	30	75	120	180	240
Corneal opacity	7	0	0	0	0	0	0
	8	0	0	0	0	0	0
	9	0	0	0	0	0	0
Mean		0.0	0.0	0.0	0.0	0.0	0.0
ICE class					I
Fluorescein retention	7	0.5	0.5
	8	0.5	0.5
	9	0.5	0.5
Mean		0.5	0.5
ICE class			I
Corneal thickness	7	0.62	0.63	0.63	0.63	0.63	0.63
	8	0.60	0.60	0.60	0.60	0.60	0.60
	9	0.59	0.59	0.59	0.59	0.59	0.59
Corneal swelling (%)	7	-	2	2	2	2	2
	8	-	0	0	0	0	0
	9	-	0	0	0	0	0
Mean			1	1	1	1	1
ICE class					I
Combination of the 3 Endpoints	3 x I
CLASSIFICATION	No category

Note: No morphological effects were noted, whatever the examination time.

Table 8: INDIVIDUAL AND AVERAGE VALUES FOR EVALUATION OF CORNEAL LESIONS AFTER TREATMENT

Positive control

Endpoint measured	Eye No.	0	30	75	120	180	240
Corneal opacity	1	0	4	4	4	4	4
	2	0	4	4	4	4	4
	3	0	4	4	4	4	4
Mean		0.0	4.0	4.0	4.0	4.0	4.0
ICE class					IV
Fluorescein retention	1	0.5	3
	2	0.5	3
	3	0.5	3
Mean		0.5	3.0
ICE class			IV
Corneal thickness	1	0.58	-	-	-	-	-
	2	0.59	-	-	-	-	-
	3	0.54	-	-	-	-	-
Corneal swelling (%)	1	-	(-)	(-)	(-)	(-)	(-)
	2	-	(-)	(-)	(-)	(-)	(-)
	3	-	(-)	(-)	(-)	(-)	(-)
Mean		-	-	-	-	-	-
ICE class					IV
Combination of the 3 Endpoints	3 x IV
CLASSIFICATION	Category 1 : Corrosive/Severe irritant

Note:

(-): evaluation of corneal swelling not possible (Corneal opacity = 4 at each examination time, leading to a marked refraction

of the light preventing from the evaluation of the corneal swelling with the biomicroscope).

Table 7: INDIVIDUAL AND AVERAGE VALUES FOR EVALUATION OF CORNEAL LESIONS AFTER TREATMENT

Negative control

Endpoint measured	Eye No.	0	30	75	120	180	240
Corneal opacity	10	0.0	0.0	0.0	0.0	0.0	0.0
ICE class					I
Fluorescein retention	10	0.5	0.5	-	-	-	-
ICE class			I
Corneal thickness	10	0.59	0.60	0.60	0.60	0.60	0.60
Corneal swelling (%)	10	-	2	2	2	2	2
ICE class					I
Combination of the 3 Endpoints	3 x I
CLASSIFICATION	No Category

Note: No morphological effects were noted, whatever the examination time.

Interpretation of results:

other: Not classified (CLP Regulation EC no. 1272/2008)

Conclusions:

The test item L-borneol was determined to not cause severe damage or irrritation for eyes in the ICE test.

Executive summary:

An in vitro (ex vivo) study was conducted in order to determine the potential severe eye damaging effects of the test item according to the OECD guideline 438 under GLP conditions. Eyeballs were isolated from chickens killed for human consumption and after the appropriate preparation were exposed to either 30 mg of the test item, 30 mg of sodium hydroxide (positive control) or 30μL of physiological saline (negative control). Three eyeballs were used in test item and positive groups, and one for the negative control group. Fluorescein retention, corneal opacity and corneal swelling were evaluated, then the results of each endpoint were assigned to ICE classes according to OECD guideline 438. According to CLP Regulation EC no. 1272/2008 the test item L-borneol does not require classification for eye irritation and serious eye damage as defined by the UN GHS (No category), since the combinations of the 3 endpoints for the test item were 3x I.

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed (not irritating)

Additional information

Eye irritation (in vitro): Key study. An in vitro (ex vivo) study was conducted in order to determine the potential severe eye damaging effects of the test item according to the OECD guideline 438 under GLP conditions. Eyeballs were isolated from chickens killed for human consumption and after the appropriate preparation were exposed to either 30 mg of the test item, 30 mg of sodium hydroxide (positive control) or 30μL of physiological saline (negative control). Three eyeballs were used in test item and positive groups, and one for the negative control group. Fluorescein retention, corneal opacity and corneal swelling were evaluated, then the results of each endpoint were assigned to ICE classes according to OECD guideline 438. According to CLP Regulation EC no. 1272/2008 the test item L-borneol does not require classification for eye irritation and serious eye damage as defined by the UN GHS (No category), since the combinations of the 3 endpoints for the test item were 3x I.

Skin irritation (in vitro): Key study. An in vitro skin irritation test of the test item was performed in a reconstructed human SkinEthic RHE®model, according to OECD TG 439 (GLP study). Three epidermis units were treated with 16 mg test item for 42 minutes at room temperature. After 42h post-incubation, the viability of each tissue was assessed by incubating the solution with MTT, extracting the precipitated formazan crystals, and determing the OD spectrophotometrically. Under test conditions, the mean percent viability of the treated tissues was 5.6%, versus 1.2% in the positive control. The test item L-borneol must be considered as skin irritant (cat 2) or skin corrosive (Cat 1).

Skin corrosion (in vitro): Key study. An in vitro skin corrosion test for the test item was performed in a reconstructed human epidermis EpiCS® model, according to OECD TG 431 (GLP study). Two epidermis units were treated with 25 mg test item for 3 minutes at room temperature and for 1 hour, at 37°C, 5% CO2. Exposure of the test item was terminated by rinsing with 20 x 1 mL of DPBS. The viability of each disk was assessed by incubating the tissues with MTT, extracting the precipitated formazan crystals using isopropanol during 2 hours under agitation in the dark, and measuring the concentration of formazan by determining the OD at 570 nm, just after dilution of the extracts 1:3 in isopropanol. Under test conditions, the mean percent viabilities of the treated tissues were 93.79% (for 3 min exposure) and 88.99% (for 60 min exposure) versus 7.44% and 0.93%, respectively, with the positive control item (potassium hydroxide 8N). Therefore, the test item must be considered as non-corrosive.

Justification for classification or non-classification

Eye irritation: Based on the available data, the substance is not classified for eye irritation according to CLP Regulation no. 1272/2008.

Skin irritation/corrision: Based on the available data, the substance is classified as skin irritant (Cat 2) according to CLP Regulation no. 1272/2008.