Tetrasodium tripotassium (.my.-((2,2'-((3-imino-6-sulfonatophenyl-(N-methyl)-imino)bis((6-chloro-1,3,5-triazin-4,2-diyl)imino(2-hydroxy-5-sulfonato-3,1-phenylen)azo(phenylmethylen)azo))bis(4-sulfonatobenzoato))-dicuprate(7-)

Skin sensitisation

Administrative data

Endpoint:

skin sensitisation: in vivo (non-LLNA)

Type of information:

experimental study

Adequacy of study:

key study

Study period:

1990

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1990

Report date:

1990

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

OECD Guideline 406 (Skin Sensitisation)

GLP compliance:

yes

Type of study:

guinea pig maximisation test

Justification for non-LLNA method:

Method was not available

Test material

Test material information

Constituent 1

Reference substance name:

-

EC Number:

406-077-0

EC Name:

-

Molecular formula:

Hill formula: C53H29Cl2Cu2K3N18Na4O21S5

IUPAC Name:

dicopper(2+) tripotassium tetrasodium 2-{[({2-[3-({4-[(3-{[4-({3-[({[2-(2-carboxylato-5-sulfonatophenyl)diazen-1-yl](phenyl)methylidene}amino)azanidyl]-2-oxido-5-sulfonatophenyl}amino)-6-chloro-1,3,5-triazin-2-yl](methyl)amino}-4-sulfonatophenyl)amino]-6-chloro-1,3,5-triazin-2-yl}amino)-2-oxido-5-sulfonatophenyl]hydrazin-2-id-1-ylidene}(phenyl)methyl)imino]amino}-4-sulfonatobenzoate

Test material form:

solid: particulate/powder

In vivo test system

Test animals

Species:

guinea pig

Strain:

Pirbright-Hartley

Remarks:

Pirbright White, Dunkin Hartley HOE DHPK [SPF-LAC] BÖ

Sex:

female

Details on test animals and environmental conditions:

TEST ANIMALS
- Source: Lippische Versuchstierzucht, Hagemann GmbH & Co. KG, Extertal 1, Germany
- Females (if applicable) nulliparous and non-pregnant: yes
- Microbiological status of animals, when known: SPF
- Age at study initiation: young adults
- Weight at study initiation: 273 - 337 g
- Housing: 5/cage
- Diet (e.g. ad libitum): Kliba Labordiät 341 (Kaninchen-Meerschweinchen-Haltungsdiät) ad libitum
- Water (e.g. ad libitum): Water ad libitum (tap water; about 2 g of ascorbic acid per 10 L water was added to the drinking water twice a week)
- Acclimation period: at least 7 days
- Indication of any skin lesions: no

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20-24
- Humidity (%): 30-70
- Air changes (per hr):
- Photoperiod (hrs dark / hrs light): 12/12
- In-life dates: From March 27, 1990 To April 27, 1990.

Study design: in vivo (non-LLNA)

Induction

Induction 1

Route:

intradermal

Vehicle:

water

Concentration / amount:

5%: four injections a 0.1 mL

Day(s)/duration:

Day 1

Adequacy of induction:

highest concentration used causing mild-to-moderate skin irritation and well-tolerated systemically

Induction 2

Route:

epicutaneous, occlusive

Vehicle:

water

Concentration / amount:

50%

Day(s)/duration:

on Day 8 - 48 hours

Adequacy of induction:

highest concentration used causing mild-to-moderate skin irritation and well-tolerated systemically

Challenge

Challenge 1

No.:

#1

Route:

epicutaneous, occlusive

Vehicle:

water

Concentration / amount:

25%

Day(s)/duration:

on Day 15 - for 24 hours

Adequacy of challenge:

highest non-irritant concentration

Challenge 2

No.:

#2

Route:

epicutaneous, occlusive

Vehicle:

water

Concentration / amount:

25%

Day(s)/duration:

on Day 22 - for 24 hours

Adequacy of challenge:

highest non-irritant concentration

No. of animals per dose:

Main test
Number of animals per control group: 10
Number of animals of the test group: 20

Details on study design:

RANGE FINDING TESTS:
Determination of the primary non-irritant concentration
Determination of the tolerance of the intradermal injections

MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: 1 intradermal + 1 epicutaneous
- Exposure period: intradermal: 24 hours; epicutaneous: 48 hours
- Test groups: 1
- Control group: 2
- Site: shoulder
- Frequency of applications: Day 1; Day 8
- Duration: 24 and 48 hours
- Concentrations: 5 and 50%

B. CHALLENGE EXPOSURE
- No. of exposures: 2
- Day(s) of challenge: Day 22 and Day 29
- Exposure period: 24 hours
- Test groups: 1
- Control group: 1 + 1
- Site: flank
- Concentrations: 25%
- Evaluation (hr after challenge): 24, 48 and 72 h after the beginning of application

1st challenge:
- treatment of the test group and of control group 1 with the test substance formulation (control group 2 remained untreated)
2nd challenge:
- treatment of the test group and of control groups 1 and 2 with the test substance formulation


OTHER:
Weight check of the individual animals: before intradermal induction and before the end of the study.
Clipping of the test animals: if required, about 3 to 5 hours before each reading and before each test substance application at the appropriate application sites.
Clinical examinations: no detailed examinations; check for sick animals and for those showing a deteriorated general state each workday.

Challenge controls:

yes

Positive control substance(s):

yes

Remarks:

a separate study is performed twice a year

Results and discussion

In vivo (non-LLNA)

Results

Results 1

Reading:

1st reading

Hours after challenge:

24

Group:

negative control

Dose level:

25%

No. with + reactions:

0

Total no. in group:

10

Results 2

Reading:

2nd reading

Hours after challenge:

48

Group:

negative control

Dose level:

25%

No. with + reactions:

0

Total no. in group:

10

Results 3

Reading:

1st reading

Hours after challenge:

24

Group:

test chemical

Dose level:

25%

No. with + reactions:

1

Total no. in group:

18

Remarks on result:

no indication of skin sensitisation

Results 4

Reading:

2nd reading

Hours after challenge:

48

Group:

test chemical

Dose level:

25%

No. with + reactions:

1

Total no. in group:

18

Remarks on result:

no indication of skin sensitisation

Results 5

Reading:

rechallenge

Hours after challenge:

24

Group:

negative control

Dose level:

25%

No. with + reactions:

0

Total no. in group:

19

Results 6

Reading:

rechallenge

Hours after challenge:

48

Group:

negative control

Dose level:

25%

No. with + reactions:

0

Total no. in group:

19

Results 7

Key result

Reading:

rechallenge

Hours after challenge:

24

Group:

test chemical

Dose level:

25%

No. with + reactions:

1

Total no. in group:

18

Remarks on result:

no indication of skin sensitisation

Results 8

Key result

Reading:

rechallenge

Hours after challenge:

48

Group:

test chemical

Dose level:

25%

No. with + reactions:

0

Total no. in group:

18

Remarks on result:

no indication of skin sensitisation

Any other information on results incl. tables

Body weights: The expected body weight gain has generally been observed in the course of the study.

Mortality: One animal of control group 1 and 2 animals of the test group died 9, 10 or 12 days after the beginning of the study. Macroscopic examination revealed that the animals suffered from pneumonia.

Applicant's summary and conclusion

Interpretation of results:

GHS criteria not met

Conclusions:

The test substance does not have a sensitizing effect on the skin of the guinea pig in the Maximization Test under the test conditions chosen

Executive summary:

The substance Reaktivblau 1463 was tested for its sensitizing effect on the skin of the guinea pig in the maximization test based on the method of Magnusson and Kligman.

After intradermal induction distinct erythema and oedema were observed at the injection sites of the control and the test animals at which only Freund's adjuvant/0.9% aqueous NaCl-solution (1 : 1) was applied. Injection of the test substance preparation in 0.9% aqueous NaCl-solution or in Freund's adjuvant/0.9% aqueous NaCl-solution (1 : 1) caused distinct oedema in the test animals. The irritation index for erythema could not be determined because of staining due to the colour of the test substance. The control animals injected with 0.9% aqueous NaCl-solution (vehicle) did not show any skin reactions.

The percutaneous induction was only carried out in the test group, because with aqua dest. a vehicle was used that was not expected to influence the result of the study. Incrustation, partially open (caused by the intra-dermal induction) could be observed in addition to distinct oedema. The index for erythema could not be determined because of staining due to the colour of the test substance.

The number of animals with skin findings after the 1st challenge (20 days after intradermal induction) and after the 2nd challenge (27 days after intradermal induction) is summarized in the following table:

 

		1^stchallenge	2^ndchallenge
		25% in aqua dest.	25% in aqua dest.
Control group	1	0/10	0/10
Control group	2*	no application of test substance	0/9
Test group**		1/18	1/18

x/y:  number of positive reactions/number of animals tested; readings 48 h after the beginning of application

*      one animal died 9 days after intradermal induction cause of death: pneumonia

**    two animals died 10 and 12 days after intradermal induction; cause of death: pneumonia

 

After the first challenge with the 25% test substance preparation in aqua dest. one test animal exhibited distinct erythema. Control group animals did not show any skin reactions.

The second challenge with the 25% test substance preparation in aqua dest. caused slight erythema in one animal of the test group. Animals of control groups one and two did not show any skin reactions.

Under these test conditions and following the results described above Reaktivblau 1483 does not have a sensitizing effect on the skin of the guinea pig.