Sulisobenzone

Skin sensitisation

Administrative data

Endpoint:

skin sensitisation: in vivo (non-LLNA)

Type of information:

experimental study

Adequacy of study:

key study

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Justification for type of information:

data is from experimental reports

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1998

Report date:

1998

Materials and methods

Test guideline

Test guideline 1

Qualifier:

according to guideline

Guideline:

OECD Guideline 406 (Skin Sensitisation)

Test guideline 2

Qualifier:

according to guideline

Guideline:

EU Method B.6 (Skin Sensitisation)

Principles of method if other than guideline:

The Guinea Pig Maximization Test (GPMT) was performed to identify the sensitizing effect of the test chemical on the skin of the guinea pigs

GLP compliance:

yes

Type of study:

guinea pig maximisation test

Justification for non-LLNA method:

The Guinea Pig Maximization Test (GPMT) has been carried out as an animal test to predict human sensitization for over a decade and is recommended by international test guidelines such as OECD .

Test material

Test material information

Constituent 1

Reference substance name:

Sulisobenzone

EC Number:

223-772-2

EC Name:

Sulisobenzone

Cas Number:

4065-45-6

Molecular formula:

C14H12O6S

IUPAC Name:

5-benzoyl-4-hydroxy-2-methoxybenzenesulfonic acid

Test material form:

solid

Details on test material:

- Name of test material: Benzenesulfonic acid, 5-benzoyl-4-hydroxy-2-methoxy-
- Molecular formula: C14-H12-O6-S
- Molecular weight: 308.3088 g/mol
- Smiles notation: c1(cc(c(cc1O)OC)S(=O)(=O)O)C(=O)c1ccccc1
- InChl: 1S/C14H12O6S/c1-20-12-8-11(15)10(7-13(12)21(17,18)19)14(16)9-5-3-2-4-6-9/h2-8,15H,1H3,(H,17,18,19)
- Substance type: Organic
- Physical state: Solid

In vivo test system

Test animals

Species:

guinea pig

Strain:

other: Pirbright White, Dunkin Hartley Crl : (HA) BR [SPF ]

Sex:

female

Details on test animals and environmental conditions:

TEST ANIMALS
- Source: Charles River GmbH - Wiga,Kisslegg, FRG
- Age at study initiation: Young adult animals
- Weight at study initiation: 331 - 378 g
- Housing: Stainless steel wire mesh cages with plastic-coated grating, floor area 40 cm x 51 cm
- Bedding : bedding in the cages ; sawdust in the waste trays .
- Diet (e.g. ad libitum): Kliba Labordiät (Kaninchen-Meerschweinchen-Haltungsdiät), ad libitum
- Water (e.g. ad libitum): Water ad libitum (tap water ; about 2 g of ascorbic acid per10 l water was added to the drinking water twice a week)
- Identification of the animals : Ear tattoo
- Acclimation period: 7 days before the beginning of the study in the laboratory for dermal toxicity


ENVIRONMENTAL CONDITIONS
- Temperature (°C): temperature in the range of 21 - 25°C
- Humidity (%): relative humidity in the range of 30 -70 % .
- Air changes (per hr): The animals were housed in fully air-conditioned rooms in which a central air-conditioning system
- Photoperiod: 12 h light ( 6 .00 am - 6 .00 pm); 12 h darkness ( 6 .00 pm - 6 .00 am)

Study design: in vivo (non-LLNA)

No. of animals per dose:

The study was performed on 10 guinea pigs in the test group and 5 animals in each of control groups 1 and 2 .
Additionally all control group animals have been treated with the vehicle .

Details on study design:

RANGE FINDING TESTS: The pretest was performed with 4 female animals for percutaneous and with 4 female animals for intradermal application.
For the dermal induction treatment the highest concentration of the test substance that causes slight to moderate irritation and for the challenge the maximum non-irritant concentration was determined with the pretest . For detecting a possible influence on irritating effects of previous intradermal treatment with Freund's adjuvant, animals pretreated with Freund's
adjuvant / 0 .9% aqueous NaCl-solution (1 : 1) each, in the same manner as intradermal pretest referring front row (A) and back row (C) without test substance about 3 or 4 weeks prior to the
application of the test substance were used . The test substance or the vehicle (empty formulation) was applied to the skin of the flanks for 2 x 24 hours under occlusive dressing .The minimum irritant concentration was found to be a 10% test substance formulation in a oil/water emulsion (mixture of the test substance in aqua bidest . (neutralized with 10 M NaOH), paraffin oil DAB 10 and Cremophor A 25) . The maximum non-irritant concentration was found to be a 5% test substance formulation in a oil/water emulsion (mixture of the test substance in distilled water (neutralized with 10 M NaOH), paraffin oil DAB 10 and Cremophor A 25) .



MAIN STUDY
A. INDUCTION EXPOSURE
Intradermal exposure
- No. of exposures: 6 intradermal injections in groups of two per animal were given .
- Exposure period:
- Test groups: 10
- Control group: 10
- Site: shoulder
- Frequency of applications: 2 injections per concentration
- Duration: single
- Concentrations: test substance formulation 5% in a oil/water emulsion or in Freund' s adjuvant / 0 .9% aqueous NaCl-solution (1 : 1) (test group) and empty formulation (oil/water emulsion without test substance) or 50 % preparation of the empty formulation with Freund's adjuvant / 0 .9% aqueous NaCl-solution (1 : 1) (control groups) with test substance at the selected concentration .

Epicutaneous Exposure
- No. of exposures: 6 intradermal injections in groups of two per animal were given .
- Exposure period: 48 hours
- Test groups:test substance formulation 10% in a oil/water emulsion (test group)
- Control group: empty formulation (oil/water emulsion without test substance) (control groups )
- Site:shoulder, same area as in the case of the previous intradermal application
- Frequency of applications: single
- Duration: 48 hours
- Concentrations: test substance formulation 10% in a oil/water emulsion (test group)

B. CHALLENGE EXPOSURE
- No. of exposures: single
- Day(s) of challenge: The first challenge was performed 14 days after the percutaneous induction . A second challenge was carried out one week after the first one .
- Exposure period: 24 hours
- Test groups: 10
- Control group: 10
- Site: flank
- Concentrations: First challenge : The test group and control group 1 were treated with the test substance formulation 5% in an oil/water emulsion or empty formulation (oil/water emulsio n
without test substance). Control group'2 only received the empty formulation. 2nd challenge : test substance formulation 5% in a oil/water emulsion or empty formulation (oil/water emulsio n without test substance)
- Evaluation (hr after challenge): 24 hours and 48 hours after the removal of the patch

OTHER: Assessment of the skin reactions
The evaluation of the skin reactions was performed according to the following grading scale of Magnusson and Kligman :
0 = no visible change
1= discrete or patchy erythema
2 = moderate and confluent erythema
3 = intense erythema and swelling
Descriptions of any dermal findings not covered by this scale were recorded .

Positive control substance(s):

yes

Remarks:

Alpha-Hexylcinnamaldehyde techn . was used as positiv control

Results and discussion

Positive control results:

The positive control with Alpha-Hexylcinnamaldehyde techn . 85 % showed that the chosen guinea pig strain was able to detect sensitizing compounds under the laboratory conditions chosen .

In vivo (non-LLNA)

Results

Results 1

Key result

Reading:

1st reading

Hours after challenge:

48

Group:

test chemical

Dose level:

5% test substance formulation

No. with + reactions:

10

Total no. in group:

10

Clinical observations:

5% test substance formulation, moderate and confluent or intense erythema and swelling could be observed in test group animals .

Remarks on result:

positive indication of skin sensitisation

Results 2

Key result

Reading:

rechallenge

Hours after challenge:

48

Group:

test chemical

Dose level:

5% test substance formulation

No. with + reactions:

9

Total no. in group:

10

Clinical observations:

5% test substance formulation, moderate and confluent or intense erythema and swelling could be observed in test group animals .

Remarks on result:

positive indication of skin sensitisation

Any other information on results incl. tables

The number of animals with skin findings after the lst challenge and after the 2nd challenge is summarized in the following table :

	1^stchallenge		2^ndchallenge
	5% test formulation in a oil/water emulsion*	Vehicle control- empty formulation oil/water emulsion	5% test formulation in a oil/water emulsion*	Vehicle control- empty formulation oil/water emulsion
Control group 1	0/5	0/5	0/5	0/5
Control group 2	No application of test chemical	0/5	0/5	0/5
Test group	10/10	0/10	9/10	0/10

x/y : number of positive reactions/number of animals tested ( reading at 24 h and/or 48 h after the removal of the patch )

mixture of 5 g test substance + 83 g aqua bidest . (including the necessary amount of 10 M NaOH for neutralization of the acid solution) + 12 g mixture of paraffin oil/Cremophor A 25 (10 paraffin oil viscous DAB 10 + 2 g Cremophor A 25) .

** : mixture of 88 g aqua bidest . + 12 g mixture of paraffin oil/Cremophor A 25 (10 g paraffin oil viscous DAB 10 + 2 g Cremophor A 25) .

Applicant's summary and conclusion

Interpretation of results:

Category 1 (skin sensitising) based on GHS criteria

Conclusions:

The intradermal induction with 5% test substance formulations caused moderate and confluent erythema and swelling in all test group animals . After the percutaneous induction with a 10% test
substance formulation incrustation, partially open (caused by the intradermal induction) could be observed in addition to moderate and confluent erythema and swelling in all test group animals .
Two challenges were performed 14 and 21 days after the percutaneous induction . After the challenge(s) with a 5% test substance formulation, moderate and confluent or intense
erythema and swelling could be observed in test group animals .Based on the results of this study and applying the evaluation criteria, it was concluded that the test chemical has a sensitizing effect on the skin of the guinea pig in the Maximization Test under the test conditions chosen .

Executive summary:

The Guinea Pig Maximization Test (GPMT) was performed to identify the sensitizing effect of the test chemical on the skin of the guinea pigs following the procedures mentioned in OECD 406 Guidelines. Young adult FemalePirbright White, Dunkin Hartley Crl : (HA) BR [SPF] guinea pigs were chosen for the study.

The pretest was performed with 4 female animals for percutaneous and with 4 female animals for intradermal application.

For the dermal induction treatment the highest concentration of the test substance that causes slight to moderate irritation and for the challenge the maximum non-irritant concentration was determined with the pretest . For detecting a possible influence on irritating effects of previous intradermal treatment with Freund's adjuvant, animals pretreated with Freund's adjuvant / 0 .9% aqueous NaCl-solution (1 : 1) each, in the same manner as intradermal pretest referring front row (A) and back row (C) without test substance about 3 or 4 weeks prior to the application of the test substance were used . The test substance or the vehicle (empty formulation) was applied to the skin of the flanks for 2 x 24 hours under occlusive dressing .The minimum irritant concentration was found to be a 10% test substance formulation in a oil/water emulsion (mixture of the test substance in aqua bidest . (neutralized with 10 M NaOH), paraffin oil DAB 10 and Cremophor A 25) . The maximum non-irritant concentration was found to be a 5% test substance formulation in a oil/water emulsion (mixture of the test substance in distilled water (neutralized with 10 M NaOH), paraffin oil DAB 10 and Cremophor A 25) .

The main study was performed on 10 guinea pigs in the test group and 5 animals in each of control groups 1 and 2 .

The intradermal induction with 5% test substance  formulations caused moderate and confluent erythema and swelling in all test group animals . After the percutaneous induction with a 10% test substance formulation incrustation, partially open (caused by the intradermal induction) could be observed in addition to moderate and confluent erythema and swelling in all test group animals .Two challenges were performed 14 and 21 days after the percutaneous induction . After the challenge(s) with a 5% test substance formulation, moderate and confluent or intense erythema and swelling could be observed in test group animals .Based on the results of this study and applying the evaluation criteria, it was concluded that the test chemical has a sensitizing effect on the skin of the guinea pig in the Maximization Test under the test conditions chosen .