Quaternary ammonium compounds, coco alkyltrimethyl, chlorides

Eye irritation

Administrative data

Endpoint:

eye irritation: in vivo

Type of information:

experimental study

Adequacy of study:

key study

Study period:

From 22 February 1988 to 14 March, 1988

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1988

Report date:

1988

Materials and methods

Test guideline

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 405 (Acute Eye Irritation / Corrosion)

GLP compliance:

yes (incl. QA statement)

Test material

Test material information

Constituent 1

Reference substance name:

Quaternary ammonium compounds, coco alkyltrimethyl, chlorides

EC Number:

263-038-9

EC Name:

Quaternary ammonium compounds, coco alkyltrimethyl, chlorides

Cas Number:

61789-18-2

Molecular formula:

C(n+3) H(2n+10) N Cl (n=8-18)

IUPAC Name:

Quaternary ammonium compounds, cocoalkyl trimethyl, chloride

Test material form:

liquid

Details on test material:

- Chemical name: Quaternary ammonium compounds, coco alkyltrimethyl, chlorides
- EC number: 263-038-9

To the best of knowledge, the sample used is representative to the boundary composition of the substance registered

Test animals / tissue source

Species:

rabbit

Strain:

New Zealand White

Details on test animals or tissues and environmental conditions:

TEST ANIMALS
- Source: Mohican Valley Rabbitry, Loudonville, Ohio
- Age at study initiation: Young adult
- Weight at study initiation: 2,634 to 3,104 g at study initiation
- Housing: Individual suspended wire-mesh cages. The animals were maintained in accordance with the recommendations contained in the "guide for care and use of laboratory animals" NIH publication, No. 8502
- Diet: Purina Certified Rabbit Chow #5322
- Water: Tap water
- Acclimation period: 7 d

ENVIRONMENTAL CONDITIONS
- Temperature : 67-74 °F
- Humidity (%): 40-74%
- Photoperiod (hrs dark / hrs light): 12 h/12 h

IN-LIFE DATES: From 23 February, 1988 to 8 March, 1988

Test system

Vehicle:

unchanged (no vehicle)

Controls:

not required

Amount / concentration applied:

0.1 mL

Duration of treatment / exposure:

Single treatment

Observation period (in vivo):

Both eyes were examined at approximately 1, 24, 48 and 72 h after dosing and at 96 h and 7, 14 and 21 d. In addition, both eyes of all rabbits were further examined at 72 h and 7, 14 and 21 d with sodium fluorescein and ultraviolet light.

Number of animals or in vitro replicates:

5 males and 4 females

Details on study design:

REMOVAL OF TEST SUBSTANCE
- Washing (if done): Out of the 9 animals, the eye of the three rabbits were washed with 120 mL of lukewarm tap water for approximately 1 min.
- Time after start of exposure: 30 sec after dosing

SCORING SYSTEM: Draize

TOOL USED TO ASSESS SCORE: Sodium fluorescein and ultraviolet light

Results and discussion

In vivo

Results

Results 1

Irritation parameter:

other: Maximum average score (M.A.S)

Basis:

mean

Time point:

other: 14 d

Score:

96.8

Max. score:

110

Reversibility:

not fully reversible within: 21 d

Remarks on result:

other: This value is for unwashed group

Results 2

Irritation parameter:

other: Maximum average score

Basis:

mean

Time point:

other: 72 h

Score:

69.7

Max. score:

110

Reversibility:

not fully reversible within: 21 d

Remarks on result:

other: This value is for washed group

Results 3

Irritation parameter:

other: Maximum average score

Basis:

mean

Time point:

other: 96 h

Score:

69.7

Max. score:

110

Reversibility:

not fully reversible within: 21 d

Remarks on result:

other: This value is for washed group

Results 4

Irritation parameter:

cornea opacity score

Basis:

mean

Time point:

24/48/72 h

Score:

ca. 2.5

Max. score:

4

Reversibility:

not fully reversible within: 21 d

Remarks on result:

positive indication of irritation

Results 5

Irritation parameter:

iris score

Basis:

mean

Time point:

24/48/72 h

Score:

ca. 1.03

Max. score:

4

Reversibility:

not fully reversible within: 21 d

Remarks on result:

positive indication of irritation

Results 6

Irritation parameter:

conjunctivae score

Remarks:

(redness)

Basis:

mean

Time point:

24/48/72 h

Score:

ca. 2.3

Max. score:

4

Reversibility:

not fully reversible within: 21 d

Remarks on result:

positive indication of irritation

Results 7

Irritation parameter:

conjunctivae score

Remarks:

(discharge)

Basis:

mean

Time point:

24/48/72 h

Score:

ca. 2.56

Max. score:

4

Reversibility:

not fully reversible within: 21 d

Remarks on result:

positive indication of irritation

Results 8

Irritation parameter:

chemosis score

Basis:

mean

Time point:

24/48/72 h

Score:

ca. 3.92

Max. score:

4

Reversibility:

not fully reversible within: 21 d

Remarks on result:

positive indication of irritation

Irritant / corrosive response data:

The test substance was maximally irritating for the unwashed group and extremely irritating for the washed group.

Other effects:

Purulent discharge, clear discharge, petite hemorrhage, blanching, corneal epithelial damage, corneal neovascularization, sodium fluorescein stain retention.

Any other information on results incl. tables

Table 1.                           Results of eye irritation study
	Cornea	Iris	Conjunctiva
			redness	chemosis
Score (average of animals investigated)	0 to 4	0 to 2	0 to 3	0 to4
60 min	3.0	1	1	4
24 h	2.8	1	1.7	4
48 h	2.8	1	2.3	4
72 h	2.8	1	2.8	4
21 days	4	0.3	1.8	2.5
Average 24h, 48h, 72h	2.8	1	2.3	4
Area effected	> 75%
Maximum average score (including area affected, max 110)	96.8 on day 14
Reversibility^*	n
Average time for reversion
Give method of calculation maximum average score. *          c :       completely reversible            n c :    not completely reversible            n :       not reversible	Cornea:   (opacity * area) * 5 Iris:          Iris * 5 Conjunct.: (redness+chemosis+discharge)*2 Max. score: 80 + 10 + 20 = 110

Applicant's summary and conclusion

Interpretation of results:

other: Category 1 (irreversible effects on the eye) based on CLP criteria

Conclusions:

Under the study conditions, the test substance is considered to cause irreversible effects on the eye.

Executive summary:

A study was conducted to determine the skin irritation potential of the test substance, Coco TMAC (33% active), in New Zealand White rabbits according to OECD 405 Guideline, in compliance with GLP. Nine rabbits received 0.1 mL of undiluted solution in one eye. The other eye remained untreated. The eyelids were held close for approximately 1 second after instillation. The eyes of three rabbits were washed for approximately 1 minute with 120 mL of lukewarm tap water commencing approximately 30 seconds after dosing. Both eyes were examined at for ocular irritation in accordance with the method of Draize approximately 1, 24, 48 and 72 h after dosing and at 96 h and 7, 14 and 21 d. In addition, both eyes of all rabbits were further examined at 72 h and 7, 14 and 21 d with sodium fluorescein and ultraviolet light. Body weights were obtained and recorded on study day 0 (initiation) and at termination (Day 21). Based on the data obtained, the Maximum Average Scores (according to Kay and Calandra) for the test substance were calculated to be 96.8 (extremely irritating) at 14 d for the unwashed group and 69.7 (severely irritating) at both 72 and 96 h for the washed group. Purulent discharge, clear discharge, petite haemorrhage, blanching, corneal epithelial damage and peeling, corneal neovascularisation, Sodium fluoresceinstain retention, and vascularised granulation scar tissue was observed in all 6 animals. Same effects were observed in the washed group, except for vascularised granulation scar tissue. There were no deaths or remarkable body weight changes during the study period. Under the study conditions, the test substance is considered to cause irreversible effects on the eye (Naas, 1988).