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Diss Factsheets

Administrative data

Endpoint:
in vitro gene mutation study in bacteria
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study without detailed documentation

Data source

Reference
Reference Type:
other company data
Title:
Unnamed
Year:
2002

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
GLP compliance:
not specified
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Reference substance name:
Acid Blue 278
IUPAC Name:
Acid Blue 278

Method

Species / strain
Species / strain / cell type:
S. typhimurium, other: TA 98, TA 100, TA 1535, TA 1537 and TA 1538
Metabolic activation:
with and without
Metabolic activation system:
S9
Test concentrations with justification for top dose:
Range Finder Experiment and Experiment l: 1.6, 8, 40, 200, 1000 and 5000 µg/plate
Vehicle / solvent:
- Vhicle: sterile purified water.
Controls
Untreated negative controls:
yes
Remarks:
water
Positive controls:
yes
Positive control substance:
9-aminoacridine
2-nitrofluorene
sodium azide
benzo(a)pyrene
other: 2-Aminoanthracene
Details on test system and experimental conditions:
Maximum solubility of the test article was achieved at 25 mg/ml in sterile purified water, therefore volume additions were increased to 200 µl in order to achieve the required treatment doses.
The top dose treatment plates in the Range-Finder Experiment and Experiment I were counted manually due to the dark colour of the test article affecting automated counting.

Results and discussion

Test results
Species / strain:
S. typhimurium, other: TA 98, TA 100, TA 1535, TA 1537 and TA 1538
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Remarks:
a slight thinning of the background bacterial at two highest doses in TA 98, without S9
Vehicle controls validity:
valid
Untreated negative controls validity:
valid
Positive controls validity:
valid
Additional information on results:
When the data from the Range-Finder Experiment were analysed at the 1 % level using Dunnett's test a statistically significant increase in revertant numbers was observed following TA 100 treatments in the presence of S9. TA 100 treatments were therefore repeated in Experiment I in order to investigate the reproducibility of this response. Following Experiment I treatments, no increases in revertant number were observed following test item treatments of TA 100 in the presence of S9. As the increase in revertant numbers observed in the Range-Finder Experiment was small in magnitude, and showed little evidence of a dose-response it was considered to be due to a chance event.
A statistically significant increase in revertant numbers was also observed following TA 98 treatments in the absence of S9 in Experiment I, but this was observed at one of the lowest treatment doses and was not considered to be indicative of test item mutagenic activity in this strain under this treatment condition. No other treatments in this study induced statistically significant increases in revertant numbers, when the data were analvsed at the 1 % level usins Dunnett's test.

PRECIPITATION
No precipitation of test agent was observed following any of the treatments in either the presence or absence of S9.

TOXICITY
Evidence of toxicity, as manifest by a slight thinning of the background bacterial lawn was observed following the top two dose treatments of strain TA98 in the absence of S9 only.

Any other information on results incl. tables

Summary of mean revertant colonies (-S9) - Experiment I

Subsance Dose Level µg/plate Mean ± SD
TA 98 TA 100 TA 1535 TA 1537  TA 1538
Water 200 43 ± 3 87 ± 6 17 ± 4 16 ± 5 19 ± 7
Test item 16 49 ± 5 77 ± 14 17 ± 5 12 ± 3 14 ± 3
Test item 8 59 ± 3 91 ± 6 12 ± 3 7 ± 2 19 ± 2
Test item 40 46 ± 11 86 ± 4 17 ± 4 13 ± 5 19 ± 1
Test item 200 48 ± 8 83 ± 12 16 ± 3 9 ± 3 23 ± 6
Test item 100 30 ± 3 (S) 87 ± 10 10 ± 1 9 ± 2 18 ± 6
Test item 5000 33 ± 4 (S+M) 72 ± 7 (M) 10 ± 1 (M) 8 ± 1 (M) 19 ± 2 (M)
2-Nitrofluorene 5 535 ± 26 - - - 101 ± 17
Sodium azide 2 - 392 ± 23 531 ± 8 - -
9-Aminoacridine 50 - - - 300 ± 26 -

(S) Slight thinning of background lawn

(M) Plates counted manually

Summary of mean revertant colonies (+S9) - Experiment I

Subsance Dose Level µg/plate Mean ± SD
TA 98 TA 100 TA 1535 TA 1537  TA 1538
Water 200 38 ± 9 88 ± 12 19 ± 5 15 ± 4 21 ± 2
Test item 16 35 ± 4 91 ± 9 16 ± 2 11 ± 2 23 ± 5
Test item 8 40 ± 10 88 ± 1 18 ± 4 12 ± 4 19 ± 5
Test item 40 42 ± 2 88 ± 10 20 ± 2 11 ± 5 19 ± 1
Test item 200 43 ± 4 99 ± 8 14 ± 2 18 ± 4 17 ± 4
Test item 100 38 ± 7 111 ± 33 13 ± 2 13 ± 5 21 ± 2
Test item 5000 39 ± 10 (M) 89 ± 2 (M) 13 ± 4 (M) 12 ± 1 (M) 14 ± 3 (M)
Benzo[a]pyrene 10 252 ± 10 - - - -
2-Aminoanthracene 5 - 1903 ± 62 127 ± 20 431 ± 98 1335 ± 93

(M) Plates counted manually

Summary of mean revertant colonies - Range Finder Experiment

Subsance Dose Level µg/plate Mean ± SD
TA 100 -S9 TA 100 +S9
Water

200

100 ± 8

102 ± 12

Test item

16

100 ± 8

112 ± 11

Test item

8

107 ± 14

106 ± 3

Test item

40

105 ± 5

110 ± 8

Test item

200

103 ± 7

127 ± 7

Test item

100

91 ± 10

116 ± 11

Test item

5000

75 ± 6 (M)

83 ± 3 (M)

Sodium azide

2

849 ± 17

-

2-Aminoanthracene

5 - 2230 ± 110

(M) plates counted manually

Applicant's summary and conclusion

Conclusions:
Non-mutagenic
Executive summary:

The study was performed to investigate the potential of test item to induce gene mutations using the Salmonella typhimurium strains TA 3538, TA 1535, TA 1537, TA 98 and TA 100. The assay was performed in a range finding test, involving only strain TA 100, and in a complete main Experiment I. The test article was assessed at the following concentrations: 1.6, 8, 40, 200, 1000 and 5000 µg/plate

When the data from the Range-Finder Experiment were analysed significant increase in revertant numbers was observed following TA 100 treatments in the presence of S9. TA 100 treatments were therefore repeated in Experiment I in order to investigate the reproducibility of this response. Following Experiment I treatments, no increases in revertant number were observed following test item treatments of TA 100 in the presence of S9. As the increase in revertant numbers observed in the Range-Finder Experiment was small in magnitude, and showed little evidence of a dose-response it was considered to be due to a chance event.

A statistically significant increase in revertant numbers was also observed following TA 98 treatments in the absence of S9 in Experiment I, but this was observed at one of the lowest treatment doses and was not considered to be indicative of test item mutagenic activity in this strain under this treatment condition. No other treatments in this study induced statistically significant increases in revertant numbers

No precipitation of test agent was observed following any of the treatments in either the presence or absence of S9.

Evidence of toxicity, as manifest by a slight thinning of the background bacterial lawn was observed following the top two dose treatments of strain TA98 in the absence of S9 only.

Conclusion

In conclusion, under the experimental conditions reported, the test article did not induce gene mutations by base pair changes or frameshifts in the genome of the strains used.

Therefore, test item is considered to be non-mutagenic in Salmonella typhimurium reverse mutation assay.