(2,4,6-trioxotriazine-1,3,5(2H,4H,6H)-triyl)tris(hexamethylene) isocyanate

Eye irritation

Administrative data

Endpoint:

eye irritation: in vivo

Type of information:

migrated information: read-across from supporting substance (structural analogue or surrogate)

Adequacy of study:

key study

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: Klimisch reliability of study is 1 (GLP guideline study); according to ECHA Practical Guide 6 rel. 2 is selected from the IUCLID pick-list as this should be the maximum score for read-across.

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1996

Report date:

1996

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

OECD Guideline 405 (Acute Eye Irritation / Corrosion)

Version / remarks:

(1987)

GLP compliance:

yes (incl. QA statement)

Test material

Test material information

Constituent 1

Reference substance name:

HDI oligomers, isocyanurate

IUPAC Name:

HDI oligomers, isocyanurate

Test animals / tissue source

Species:

rabbit

Strain:

New Zealand White

Details on test animals or tissues and environmental conditions:

TEST ANIMALS
- Source: Regal Group UK, Great Bookham, Surrey, UK.
- Age at study initiation: approx. 14 to 17 weeks
- Weight at study initiation: weight range of 3.4 - 3.8 kg
- Housing: individually in metal cages with perforated floors
- Diet and water: ad libitum
- Acclimation period: All rabbits were acclimatised to the experimental environment. No information concerning period of time.

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18-19.5
- Humidity (%): 44-76
- Air changes (per hr): approx. 19
- Photoperiod (hrs dark / hrs light): 12/12

Test system

Vehicle:

unchanged (no vehicle)

Controls:

other: the contralateral eye remained untreated and served as control

Amount / concentration applied:

0.1 mL

Duration of treatment / exposure:

The eyelids were gently held together for one second before releasing.

Observation period (in vivo):

Examinations were terminated after 7 days, since all changes had completely subsided then.

Number of animals or in vitro replicates:

3 (two males, one female)

Details on study design:

PROCEDURE: The eyes of each animal were examined prior to instillation of the test substance to ensure that there was no pre-existing corneal damage, iridial or conjunctival inflammation.
One animal was treated in advance of the others, to ensure that if a severe response was produced, no further animals would be exposed. Approximately 0.1 mL of the test substance was placed into the lower everted lid of one eye of each animal. The eyelids were gently held together for one second before releasing.

SCORING SYSTEM:
Cornea opacity - degree of density: No ulceration or opacity 0; Scattered or diffuse areas of opacity (other than slight dulling of normal lustre), details of iris clearly visible 1; Easily discernible translucent areas, details of iris slightly obscured 2; Nacreous areas, no details of iris visible, size of pupil barely discernible 3; Opaque cornea, iris not discernible through the opacity 4
Iris: Normal 0; Markedly deepened rugae, congestion, swelling, moderate circumcorneal hyperaemia or injection, any of these or combination of any thereof, iris still reacting to light (sluggish reaction is positive) 1; No reaction to light, haemorrhage, gross destruction (any or all of these) 2
Conjunctivae redness: Blood vessels normal 0; Some blood vessels definitely hyperaemic (injected) 1; Diffuse, crimson colour, individual vessels not easily discernible 2; Diffuse beefy red 3
Chemosis: No swelling 0; Any swelling above normal (includes nictating membranes) 1; Obvious swelling with partial eversion of lids 2; Swelling with lids about half-closed 3; Swelling with lids more than half-closed 4

TOOL USED TO ASSESS SCORE: Observation of the eyes was aided by the use of a handheld light.

Results and discussion

In vivo

Results

Results 1

Irritation parameter:

cornea opacity score

Basis:

animal: #1, #2, #3

Time point:

other: 24, 48, 72 hours

Score:

0

Max. score:

4

Results 2

Irritation parameter:

iris score

Basis:

animal: #1, #2, #3

Time point:

other: 24, 48, 72 hours

Score:

0

Max. score:

2

Results 3

Irritation parameter:

conjunctivae score

Remarks:

(redness)

Basis:

animal #1

Time point:

other: 24, 48, 72 hours

Score:

1

Max. score:

3

Reversibility:

fully reversible within: 7 days

Results 4

Irritation parameter:

conjunctivae score

Remarks:

(redness)

Basis:

animal: #2, #3

Time point:

other: 24, 48, 72 hours

Score:

1

Max. score:

3

Reversibility:

fully reversible within: 4 days

Results 5

Irritation parameter:

chemosis score

Basis:

animal: #1, #3

Time point:

other: 24, 48, 72 hours

Score:

0

Max. score:

4

Results 6

Irritation parameter:

chemosis score

Basis:

animal #2

Time point:

other: 24, 48, 72 hours

Score:

0 - 1

Max. score:

4

Reversibility:

fully reversible within: 3 days

Remarks on result:

other: mean score: 0.7

Irritant / corrosive response data:

No corneal damage or iridial inflammation was observed. Hyperaemia of blood vessels with slight swelling was seen in all animals. These reactions had resolved in all instances by four or seven days after instillation.

Other effects:

There were no signs of toxicity or ill health in any rabbit during the observation period.

Any other information on results incl. tables

For (2,4,6-trioxotriazine-1,3,5(2H,4H,6H)-triyl)tris(hexamethylene) isocyanate (EC 223-242-0, CAS 3779-63-3, mono constituent substance), in the following referred to as "HDI Trimer pure", a read across from the close structural analogue HDI oligomers, isocyanurate type (EC 931-274-8, CAS 28182-81-2, UVCB) is applied. A justification for the read-across with special focus on inhalation toxicity was elaborated and is attached to the chapter endpoint summary. Based on this justification all available toxicological data for HDI oligomers, isocyanurate type can be used for the toxicological evaluation of HDI Trimer pure. This approach is in accordance with Annex XI, section 1.5 of the REACH Regulation (EC) No 1907/2006.

Applicant's summary and conclusion

Executive summary:

An Acute Eye Irritation/Corrosion test was conducted according to OECD TG 405. In this study no corneal damage or iridial inflammation was observed (all scores zero). Hyperaemia of blood vessels with slight swelling was seen in all animals (Mean scores for time points 24, 48, and 72 h: 1 for conjuntiva/redness, 0.2 for chemosis). These reactions had resolved in all instances by four or seven days after instillation. No signs of toxicity or ill health were observed.