Strontium bis[2-chloro-5-[(2-hydroxy-1-naphthyl)azo]toluene-4-sulphonate]

Eye irritation

Administrative data

Endpoint:

eye irritation: in vivo

Type of information:

migrated information: read-across based on grouping of substances (category approach)

Adequacy of study:

key study

Study period:

november 1993

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: well documented, GLP conform, according then in force OECD guideline (7 days post observation period only), acclimatization period not mentioned, in life data not given

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1993

Report date:

1993

Materials and methods

Test guideline

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 405 (Acute Eye Irritation / Corrosion)

GLP compliance:

yes

Test material

Test material information

Constituent 1

Reference substance name:

Barium bis[2-chloro-5-[(2-hydroxy-1-naphthyl)azo]toluene-4-sulphonate]

EC Number:

225-935-3

EC Name:

Barium bis[2-chloro-5-[(2-hydroxy-1-naphthyl)azo]toluene-4-sulphonate]

Cas Number:

5160-02-1

IUPAC Name:

barium bis{5-chloro-2-[(2-hydroxy-1-naphthyl)diazenyl]-4-methylbenzenesulfonate}

Test animals / tissue source

Species:

rabbit

Strain:

New Zealand White

Details on test animals or tissues and environmental conditions:

TEST ANIMALS
- Source: Chemisch pharmazeutische Fabrik Dr. K. Thomae, 88400 Biberach
- Age at study initiation: about 3 - 5 months
- Weight at study initiation: 2.3 - 3 kg
- Housing: singly
- Diet: ad libitum
- Water: ad libitum
- Acclimation period: /

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18 ± 3 °C
- Humidity (%): 55 ± 20 %
- Photoperiod (hrs dark / hrs light): 12 hours per day

Test system

Vehicle:

unchanged (no vehicle)

Controls:

not required

Amount / concentration applied:

TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 100 mg

Observation period (in vivo):

1, 24, 48 and 72 hours after application

Number of animals or in vitro replicates:

3

Details on study design:

REMOVAL OF TEST SUBSTANCE
- Washing (if done): 24 hours after application and at all other designated examination times at which the tr ated eyes still showed discharge or at which a corneal examination with fluorescein-sodium solution took place, the treated eyes were washed out thoroughly with physiological saline at approx. 37 °C.

SCORING SYSTEM:

CORNEA

Degree of opacity (most dense area used)

No opacity................................................................ 0
SCattered or diffuse areas, details of iris clearly visible............... 1
Easily discernible translucent areas, details of iris slightly obscured... 2
Op&lescent areas, no details of iris visible, size of pupilbarely di scernib1e. . . . . . . .3
Opaque, iris invisible ...........4

IRIS

Normal ................0
Folds above normal, congestion, swelling, circumcorneal injection
(any of all 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 (refers to palpebral and bulbar coniunctivae)

Blood vessels nomal......... 0
Blood vessels definitely injected above normal............................ 1
More diffuse, deeper crimson red, individual blood vessels not easily discernible..........................2
Diffuse beefy red............................3

Chemosis (refers to palpebral and bylbar conjunctivae)

no swelling..............0
Any swelling bove normal (includes nictitating membran).................. 1
Obvious swelling with partial eversion of lids............................ 2
Swell ing with lids about half closed...................................... 3
Swelling with lids half closed to completely closed....................... 4

Discharge

No discharge............................................................... 0
Any a.ount different from normal (does not include small amounts normally observed in inner canthus) ..........1
Discharge with moistening of the lids and hairs just adjacent to the lids...................2
Discharge with moistening of the lids and hairs, and considerable area around the eye........................................... 3

TOOL USED TO ASSESS SCORE: fluorescein

Results and discussion

In vivo

Results

Results 1

Irritation parameter:

cornea opacity score

Basis:

mean

Time point:

other: all time points

Score:

0

Max. score:

4

Results 2

Irritation parameter:

iris score

Basis:

mean

Time point:

other: all time points

Score:

0

Max. score:

2

Results 3

Irritation parameter:

conjunctivae score

Basis:

mean

Time point:

other: all time points

Score:

0.1

Max. score:

3

Reversibility:

fully reversible within: 2d

Results 4

Irritation parameter:

chemosis score

Basis:

mean

Time point:

other: all time points

Score:

0

Max. score:

4

Irritant / corrosive response data:

One hour up to 24 hours after application of the test substance the conjunctiva of the animals showed definitely injected blood vessels and slight swellings. Additionally clear from substance coloured discharge was observed up to one hour after application. Two days after application all signs of irritationes were reversible.

Applicant's summary and conclusion

Interpretation of results:

not irritating

Remarks:

Migrated information Criteria used for interpretation of results: EU