Tetrasodium 4-[[3,5-bis[[4-[(4-nitro-2-sulphonatophenyl)amino]phenyl]azo]-2,4(or 2,6)-dihydroxyphenyl]azo]-5-hydroxynaphthalene-2,7-disulphonate

Genetic toxicity: in vivo

Administrative data

Endpoint:

in vivo mammalian germ cell study: cytogenicity / chromosome aberration

Type of information:

other: read across from analogue substance

Adequacy of study:

key study

Study period:

Since april 21, 1988 to june 01, 1988

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: GLP compliant with international guideline

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1988

Report date:

1992

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

OECD Guideline 474 (Mammalian Erythrocyte Micronucleus Test)

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Type of assay:

micronucleus assay

Test material

Test material information

1

Reference substance name:

-

EC Number:

405-071-5

EC Name:

-

Cas Number:

-

Molecular formula:

C28H15N8Na3O17S3

IUPAC Name:

Trisodium 5-[[dihydroxy[(2-hydroxynitrosulfophenyl)azo]phenyl]azo]4-hydroxy-3-[(4-nitrophenyl)azo-2,7-naphthalenedisulfonate

Test animals

Species:

rat

Strain:

Wistar

Sex:

male/female

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: SAVO med. Versuchstierzuchten GmbH
- Weight at study initiation: ~ 120 g
- Assigned to test groups randomly: yes
- Fasting period before study:Approximately 18 hours before treatment with the test article the animals received no food but water ad libitum.
- Housing: single housed in Makrolon Type II, with wire mesh top , granulated soft wood bedding
- Diet: pelleted standard diet, ad libitum
- Water: tap water, ad libitum
- Acclimation period: 5 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C):21 ± 3°C
- Humidity(%): 30-70%
- Photoperiod : 12 hours cycle dark/light from artificial light at 6.00 a.m. to 6.00 p.m.

Administration / exposure

Route of administration:

oral: gavage

Vehicle:

- Vehicle(s)/solvent(s) used: deionized water

Duration of treatment / exposure:

28 days

Frequency of treatment:

24 +/- 2 hours for 28 days

Post exposure period:

24 hours after the last application the bone marrow cells were collected for micronuclei analysis.

Doses / concentrations

Remarks:

Doses / Concentrations:
1000 mg/kg bw
Basis:
nominal conc.

No. of animals per sex per dose:

6 animals x sex x dose (test item)
6 animals x sex x dose (positive control)
6 animals x sex x dose (negative control)

Control animals:

no

Positive control(s):

- Name: Cyclophosphamide
- Route of administration: oral
- Doses / concentrations: 10 ml/kg bw

Examinations

Tissues and cell types examined:

bone marrow cells were collected for micronuclei analysis.

Details of tissue and slide preparation:

The animals were sacrificed by cervical dislocation. The femora were removed, the epiphyses were cut off and the marrow was flushed out with fetal calf serum, using a 5 ml syringe. The cell suspension was centrifuged at 1,500 rpm for 10 minutes and the supernatant was discarded. A small drop of the resuspended cell pellet was spread on a slide. The smear was air-dried and then stained with May-Grünwald (MERCK, D-6100 Darmstadt)/Giemsa (Gurr, BDH Limited Poole, Great Britain). Cover slips were mounted with EUKITT (KINDLER, D-7800 Freiburg). At least one slide was made from each bone marrow sample.

Evaluation criteria:

A test article is classified as mutagenic if it induces either a statistically significant dose-related increase in the number of micronucleated polychromatic erythrocytes or a reproducible statistically significant positive response for at least one of the test points.
A test article producing neither a statistically significant dose-relat-ed increase in the number of micronucleated polychromatic erythrocytes nor a statistically significant and reproducible positive response at any one of the test points is considered non-mutagenic in this system.
This can be confirmed by means of the nonparametric Mann-Whitney test.
However, both biological and statistical significance should be considered together.

Statistics:

Statistical significance at the five per cent level (p < 0.05) was evaluated by means of the non-parametric Mann-Whitney test.

Results and discussion

Test results

Sex:

male/female

Genotoxicity:

negative

Toxicity:

no effects

Vehicle controls validity:

valid

Negative controls validity:

valid

Positive controls validity:

valid

Any other information on results incl. tables

A dose of 1000 mg/kg b.w. was administered. 1000 mg/kg b.w. of the test article was close to the maximum tolerated dose. 3 out of 12 treated animals died during the 28 days period (1 male, 2 females).

Applicant's summary and conclusion

Conclusions:

The analogue substance was tested for in vivo micronucleus following OECD 474. Under the experiemtnal conditions test article did not induce micronuclei as determined by the micronucleus test with bone marrow cells of the rat.

Executive summary:

The analogue substance was tested for in vivo micronucleus following OECD 474. This study was performed to investigate the potential of the substance to induce micronuclei in polychromatic erythrocytes (PCE) in the bone marrow of the rat.

The test article was dissolved in deionized water. This solvent was used as negative control. The volume administered orally was 10 ml/kg b.w. The animals received the test article or negative control once per 24 +/- 2 h for 28 days. 24 hours after the last application the bone marrow cells were collected for micronuclei analysis.

Ten animals (5 males, 5 females) per test group with the exception of the test article group in which only 9 animals survived (5 males and 4 females) were evaluated for the occurrence of micronuclei. 1000 polychromatic erythrocytes (PCE) per animal were scored for micronuclei.

To describe a cytotoxic effect due to the treatment with the test article the ratio between polychromatic and normochromatic erythrocytes (NCE) was determined in the same sample and reported as the number of NCE per 1000 PCE.

A dose of 1000 mg/kg b.w. was administered. 1000 mg/kg b.w. of the test article was close to the maximum tolerated dose. 3 out of 12 treated animals died during the 28 days period (1 male, 2 females).

After treatment with the test article the ratio between PCEs and NCEs was affected as compared to the corresponding negative control thus indicating a test article-dependent effect on the target cells.

In comparison to the corresponding negative controls there was neither for the females nor for the total collective of FAT 40'317/B treated animals a statistically significant enhancement in the frequency of the detected micronuclei.

An appropriate reference mutagen was administered once and used as positive control which showed a distinct increase of induced micronucleus frequency.