Shale oils

Eye irritation

Administrative data

Endpoint:

eye irritation: in vivo

Type of information:

experimental study

Adequacy of study:

key study

Study period:

10th May 2005 - 12th August 2005

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: Study conducted in compliance with agreed protocols, with no or minor deviations from standard test guidelines and/or minor methodological deficiencies, which do not affect the quality of the relevant results.

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2005

Report date:

2005

Materials and methods

Test guideline

Test guideline 1

Qualifier:

according to guideline

Guideline:

OECD Guideline 405 (Acute Eye Irritation / Corrosion)

Deviations:

no

Test guideline 2

Qualifier:

according to guideline

Guideline:

EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Test material

Test material information

Constituent 1

Reference substance name:

Shale oils

EC Number:

269-646-0

EC Name:

Shale oils

Cas Number:

68308-34-9

Molecular formula:

Not applicable (a generic molecular formula cannot be provided for this specific UVCB substance)

IUPAC Name:

Shale oil

Details on test material:

Identification: Shale oil, middle fraction
Description :Liquid
Batch number: 1
Purity min.: 99 %
Composition: Complex mixture of hydrocarbons and oxygen compounds
Stability of test item: Stable under storage conditions
Expiry date: 04-MAR-2006
Storage conditions: At room temperature (range of 20 ± 5 °C), light protected.
Safety precautions: Routine hygienic procedures were used to ensure the health and safety of the personnel.

Test animals / tissue source

Species:

rabbit

Strain:

New Zealand White

Details on test animals or tissues and environmental conditions:

TEST ANIMALS
- Source: Charles River Laboratories France, BP 0109, F-69592, L’Arbresle
- Age at study initiation: 14 weeks (male), 12-13 weeks (females)
- Weight at study initiation: NDA
- Housing: Individually in stainless steel cages equipped with feed hoppers and drinking water bowls.
- Diet (e.g. ad libitum): Pelleted standard Provimi Kliba 3418 rabbit maintenance diet ad libitum
- Water (e.g. ad libitum): Community tap water from Füllinsdorf, ad libitum.
- Acclimation period: 10th May - 17th May 2005

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 17 - 23 ºC
- Humidity (%): 30 - 70 %
- Air changes (per hr): 10 - 15
- Photoperiod (hrs dark / hrs light): 12/12
- Other: Music was played during the daytime light period.

IN-LIFE DATES: From: 10th May 2005 To: 8th June 2005

Test system

Vehicle:

unchanged (no vehicle)

Controls:

other: right eye served as control

Amount / concentration applied:

TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1 ml
- Concentration (if solution): N/A

VEHICLE
N/A

Duration of treatment / exposure:

The lids were then gently held together for about one second to prevent loss of test item.

Observation period (in vivo):

21 days

Number of animals or in vitro replicates:

1 male, 2 females

Details on study design:

REMOVAL OF TEST SUBSTANCE
- Washing (if done): not rinsed
- Time after start of exposure: N/A

SCORING SYSTEM:

The ocular reaction (i.e. corneal opacity, iridic effects, conjunctivae and chemosis) was assessed according to the numerical scoring system listed in the Commission Directive 67/548/EEC, at approximately 1, 24, 48 and 72 hours, as well as 7, 10, 14, 17 and 21 days after instillation.
Additionally, ocular discharge, reddening of the sclerae and staining of conjunctivae, sclerae and cornea by the test item was assessed according to the scheme given under the commission directive 67/548/EEC.
When present, corrosion was recorded and reported.

Results and discussion

In vivo

Results

Results 1

Irritation parameter:

cornea opacity score

Basis:

mean

Time point:

24/48/72 h

Score:

0.67

Max. score:

1

Reversibility:

fully reversible within: 14 days

Results 2

Irritation parameter:

iris score

Basis:

mean

Time point:

24/48/72 h

Score:

0.56

Max. score:

1

Reversibility:

fully reversible within: 7 days

Results 3

Irritation parameter:

conjunctivae score

Basis:

mean

Time point:

24/48/72 h

Score:

2

Max. score:

2

Reversibility:

fully reversible within: 21 days

Results 4

Irritation parameter:

chemosis score

Basis:

mean

Time point:

24/48/72 h

Score:

2.11

Max. score:

3

Reversibility:

fully reversible within: 14 days

Irritant / corrosive response data:

The mean score was calculated across 3 scoring times (24, 48 and 72 hours after instillation) for each animal for corneal opacity, iris, redness and chemosis of the conjunctivae, separately, insofar as numerical scores were assessable. The individual mean scores for corneal opacity were 1.00, 1.00 and 0.00 and for iris 1.00, 0.67 and 0.00 for all three animals. The individual mean scores for the conjunctivae was 2.00 for all three animals, for reddening and 3.00, 2.00 and 1.33 for chemosis, respectively.
Very slight corneal opacity affecting the whole area was noted in two animals from the 24-hour to the 72-hour reading and persisted in one animal up to the 10-day observation. Reduced light reflex was seen in two animals from the 24- or 48-hour to the 72-hour reading.
Slight to moderate reddening of the conjunctivae was noted in all animals form the 1-hour to the 10-day examination and slight reddening persisted in two animals up to the 17-day reading.
Slight to marked swelling (chemosis) with half-closed lids of the conjunctivae was observed in all animals from the 1-hour to the 72-hour examination and slight swelling persisted up to the 10-day reading in two animals.
Slight to moderate reddening of the sclerae was present in all animals from the 1-hour to the 72-hour observation and slight reddening persisted in two animals up to the 10-day examination, although symptoms of the sclera could not be assessed in one animal 24 hours after treatment due to swelling of the conjunctivae.
Slight to moderate ocular discharge was noted in all animals from 1-hour to the 48-hour reading and slight discharge was still present in two animals at the 72-hour observation and again in one animal at the 10-day reading.
Mucus was present in the eye from the 24- to the 72-hour reading in one animal, whereas this was only noted at the 48-hour observation in another animal.
No abnormal findings were observed in the treated eye of any animal 21 days after treatment, the end of the observation period for all animals.

Other effects:

No clinical signs of systemic toxicity were observed in the animals during the study and no mortality occurred.

No staining of the treated eyes produced by the test item was observed.

No corrosion of the cornea was observed at any of the reading times.

The body weights of all rabbits were considered to be within the normal range of variability.

Applicant's summary and conclusion

Interpretation of results:

other: Classified for eye irritation (category 2) according to EU criteria

Conclusions:

The mean chemosis score of the three animals at the mean of the 24, 48 and 72 hour time points was 2.11.
Based upon EU classification criteria, Shale oil, middle is considered to be “irritating” to eyes.

Executive summary:

The eye irritation potential of shale oils, middle was examined in an experiment which was conducted in accordance with the standardised guideline OECD 405 and under GLP conditions.

During the study Shale oils, middle fraction was applied by instillation into the left eye of 2 female and 1 male New Zealand white rabbits. Scoring of irritation effects was performed approximately 1, 24, 48 and 72 hours, as well as 7, 10, 14 and 21 days after instillation.

The mean chemosis score of the three animals at the mean of the 24, 48 and 72 hour time points was 2.11. Based upon EU classification criteria, Shale oil, middle is considered to be “irritating” to eyes.