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Diss Factsheets

Toxicological information

Genetic toxicity: in vitro

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Administrative data

Endpoint:
in vitro gene mutation study in bacteria
Remarks:
Type of genotoxicity: gene mutation
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
2000
Reference Type:
other: Authoritative data base
Title:
Study ID: 941907
Author:
NTP database
Year:
2012
Bibliographic source:
NTP (National Toxicological Program)by Mortelmans K, Zeiger E. The Ames Salmonella/microsome mutagenicity assay. Mutat Res. 2000 Nov 20;455(1-2):29-60

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other:
Principles of method if other than guideline:
In the standard protocol (preincubation) for conducting the Ames assay, a test tube containing a suspension of one strain of Salmonella typhimurium (or E. coli) plus S9 mix or plain buffer without S9, is incubated for 20 minutes at 37º C with the test chemical. Control cultures, with all the same ingredients except the test chemical, are also incubated. In addition, positive control cultures are prepared; these contain the particular bacterial tester strain under investigation, the various culture ingredients, and a known potent mutagen*. After 20 minutes, agar is added to the cultures and the contents of the tubes are thoroughly mixed and poured onto the surface of Petri dishes containing standard bacterial culture medium. The plates are incubated, and bacterial colonies that do not require an excess of supplemental histidine appear and grow. These colonies are comprised of bacteria that have undergone reverse mutation to restore function of the histidine-manufacturing gene. The number of colonies is usually counted after 2 days.
GLP compliance:
not specified
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
3-amino-4-hydroxybenzenesulphonic acid
EC Number:
202-662-8
EC Name:
3-amino-4-hydroxybenzenesulphonic acid
Cas Number:
98-37-3
Molecular formula:
C6H7NO4S
IUPAC Name:
3-amino-4-hydroxybenzenesulphonic acid
Test material form:
solid: crystalline
Details on test material:
- Name of test material : 3-amino-4-hydroxybenzenesulphonic acid
-Substance type-organic
-physical state-crystalline solid.

Method

Target gene:
Histidine manufacturing gene
Species / strain
Species / strain / cell type:
S. typhimurium TA 1535
Additional strain / cell type characteristics:
other: All the bacterial strains used in the Ames test carry a defective (mutant) gene that prevents them from synthesizing the essential amino acid histidine from the ingredients in standard bacterial culture medium
Metabolic activation:
with and without
Metabolic activation system:
S9
Test concentrations with justification for top dose:
0 - 2000 ug/Plate
Controlsopen allclose all
Untreated negative controls:
not specified
Negative solvent / vehicle controls:
yes
Remarks:
Dimethyl Sulfoxide
True negative controls:
not specified
Positive controls:
yes
Positive control substance:
sodium azide
Remarks:
with
Untreated negative controls:
not specified
Negative solvent / vehicle controls:
yes
Remarks:
Dimethyl Sulfoxide
True negative controls:
not specified
Positive controls:
yes
Positive control substance:
other: 2-aminoanthracene
Remarks:
without

Results and discussion

Test results
Species / strain:
S. typhimurium TA 1535
Metabolic activation:
with and without
Genotoxicity:
negative
Remarks:
10% RLI = induced male Sprague Dawley rat liver S9 ; 10% HLI = induced male Syrian hamster liver S9
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
not specified
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Any other information on results incl. tables

Strain: TA1535
Dose No Activation
(Negative)
No Activation
(Negative)
10% HLI
(Negative)
30% HLI
(Negative)
10% RLI
(Negative)
30% RLI
(Negative)
Protocol Preincubation Preincubation Preincubation Preincubation Preincubation Preincubation
ug/Plate Mean ± SEM Mean ± SEM Mean ± SEM Mean ± SEM Mean ± SEM Mean ± SEM
0     
13 2.1 26 4.1 6 1.7 15 0.3 8 0.7 13 2.6
33     
10 1.7 22 4.1 6 1.2 13 2.3 6 1.5 13 2.2
100     
11 1.2 29 3.2 8 0.6 8 1.7 5 1.2 15 1.5
333     
11 1.8 26 3.3 9 1.2 15 1.9 11 4.2 16 2.3
1000     
12 2.5 22 4.4 9 0.9 13 1.5 7 2.1 16 2.3
2000     
14 1.5 25 0.9 11 2.9 9 2.4 7 2.7 8 2.3
Positive Control 112 8.7 142 1.7 55 2.9 58 3.2 164 7.8 68 7.6

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative

Genetic toxicity in vitro for 3-amino-4-hydroxybenzenesulphonic acid in S. typhimurium TA 1535 is found to be negative at dose concentration of 0 - 2000 ug/Plate with and without metabolic activation
Executive summary:

Genetic toxicity in vitro for 3-amino-4-hydroxybenzenesulphonic acid in S. typhimurium TA 1535 is found to be negative at dose concentration of 0 - 2000 ug/Plate with and without metabolic activation