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The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Genetic toxicity: in vitro

Currently viewing:

Administrative data

Endpoint:
in vitro gene mutation study in bacteria
Remarks:
Type of genotoxicity: gene mutation
Type of information:
experimental study
Adequacy of study:
key study
Study period:
17 Jul - 04 Aug 2003
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP Guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2003
Report date:
2003

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Version / remarks:
adopted July 21, 1997
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method B.13/14 (Mutagenicity - Reverse Mutation Test Using Bacteria)
Version / remarks:
published June 2000
Deviations:
no
GLP compliance:
yes
Type of assay:
bacterial reverse mutation assay

Test material

Reference
Name:
Unnamed
Type:
Constituent
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder
Details on test material:
- Name of test material (as cited in study report): UM-235
- Physical state: white powder
- Analytical purity: 98.8 %
- Purity test date: 22 Jul 2002
- Lot/batch No.: #SI-1
- Expiration date of the lot/batch: 01 Jan 2005
- Storage condition of test material: at room temperature in the dark

Method

Target gene:
his operon (S. typhimurium), trp operon (E. coli)
Species / strainopen allclose all
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Species / strain / cell type:
E. coli WP2 uvr A
Metabolic activation:
with and without
Metabolic activation system:
cofactor supplemented post-mitochondrial fraction (S9 mix), prepared from the livers of rats treated with Aroclor 1254
Test concentrations with justification for top dose:
first and second experiment: 3, 10, 33, 100 and 333 µg/plate (with and without metabolic activation)
Vehicle / solvent:
- Vehicle(s)/solvent(s) used: DMSO
Controls
Untreated negative controls:
yes
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
4-nitroquinoline-N-oxide
9-aminoacridine
sodium azide
methylmethanesulfonate
other: daunomycin, 2-aminoanthracene
Remarks:
without metabolic activation
Details on test system and experimental conditions:
METHOD OF APPLICATION: in agar (plate incorporation)

DURATION
- Exposure duration: 48 h

NUMBER OF REPLICATIONS: 3 replications each in 2 independent experiments

DETERMINATION OF CYTOTOXICITY
- Method: reduction of bacterial background lawn, increase in size of microcolonies, reduction of revertant colonies
Evaluation criteria:
A test is considered negative (not mutagenic) if
- the total number of revertants in any tester strain at any concentration is not greater than two times the solvent control value, with or without metabolic activation
- the negative response should be reproducible in at least one independently repeated experiment

A test substance is considered positive (mutagenic) if
- it induces a number of revertant colonies, dose related, greater than 2-times the number of revertants induced by solvent control in any of the tester strains, either with or without metabolic activation
- the positive response should be reproducible in at least one independently repeated experiment
For more criteria see tables under "Any other information on material and methods including tables"

Results and discussion

Test resultsopen allclose all
Species / strain:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity
Vehicle controls validity:
valid
Untreated negative controls validity:
not applicable
Positive controls validity:
valid
Species / strain:
E. coli WP2 uvr A
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity
Vehicle controls validity:
valid
Untreated negative controls validity:
not applicable
Positive controls validity:
valid
Additional information on results:
TEST-SPECIFIC CONFOUNDING FACTORS
- Precipitation was observed at concentrations of 100 µg/plate and above in the top agar and on the plates at 333 µg/plate at the start and the end of the experiment.

RANGE-FINDING/SCREENING STUDIES:
A dose-range finding test was performed with S. typhimurium TA100 and E. coli WP2 strains with concentrations of 3, 10, 33, 100, 333, 1000, 3330 and 5000 µg/plate. The highest concentration chosen for the main assay was the level at which the test substance showed limited solubility (333 µg/plate).

COMPARISON WITH HISTORICAL CONTROL DATA:
yes, see acceptability of the assay under any other information on materials and methods including tables
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Any other information on results incl. tables

Table 1: Results of Experiment I

 with or without S9 mix (5%)  test substance concentration  Mean number of revertant colonies per plate (average of 3 plates ± SD)            
   [µg/plate]  Base-pair substitution type     Frameshift type     
     TA100  TA1535  TA98  TA1537  WP2 uvrA
 -  DMSO 138 ± 6 8 ± 2 11 ± 2 4 ± 1 9 ± 2
 -  3 144 ± 4  7 ± 4  13 ± 2  5 ± 2  13 ± 5
 -  10  154 ± 20  11 ± 3  12 ± 4  4 ± 1  9 ± 1
 -  33  135 ± 11  9 ± 3  14 ± 2  3 ± 2  10 ± 3
 -  100  142 ± 13  11 ± 2  13 ± 4  4 ± 1  10 ± 2
 -  333SP  142 ± 9  8 ± 3 13 ± 1   5 ± 2  10 ± 4
  positive control, -S9  Name  SA  9AC  DM  MMS  4 -NQO
    Concentrations [µg/plate]  650  5  4  60  10

  Mean No. of colonies/plate (average of 3 ± SD)  962 ± 22  244 ± 16  516 ± 71  280 ± 46  812 ± 73
 +  DMSO  140 ± 21  10 ± 1  17 ± 1  4 ± 4  10 ± 1
 +  3  136 ± 15  7 ± 2  21 ± 2  5 ± 0  10 ± 2
 +  10  151 ± 1  6 ± 1  18 ± 2  5 ± 3  8 ± 1
 +  33  155 ± 7  7 ± 2  20 ± 2  5 ± 1  11 ± 1
+  100  138 ± 10 8 ± 3 19 ± 3  6 ± 2  10 ± 2
 +  333SP  137 ± 14  6 ± 3  18 ± 3  6 ± 4  9 ± 2
   positive control, +S9  Name  2 -AA  2 -AA  2 -AA  2 -AA  2 -AA
   Concentration [µg/plate]  2.5  2.5  2.5  5
    Mean No. of colonies/plate (average of 3 ± SD)  717 ± 50  100 ± 4  520 ± 7  75 ± 16  73 ± 11

SP = Slight Precipitate

Table 2: Results of Experiment II

 with or without S9 mix (10%)  test substance concentration  Mean number of revertant colonies per plate (average of 3 plates ± SD)            
   [µg/plate]  Base-pair substitution type     Frameshift type     
     TA100  TA1535  TA98  TA1537  WP2 uvrA
 -  DMSO  132 ± 8  9 ± 2  12 ± 3  8 ± 2  7 ± 2
 -  3  149 ± 22  16 ± 3  14 ± 3  7 ± 4  11 ± 4
 -  10  146 ± 17  10 ± 2  13 ± 1  8 ± 2  12 ± 0
 -  33  144 ± 5  9 ± 2  12 ± 4  7 ± 3  9 ± 4
 -  100  134 ± 11  10 ± 2  16 ± 2  9 ± 1  9 ± 1
 -  333SP  148 ± 19  11 ± 1 11 ± 4   5 ± 1  8 ± 3
  positive control, -S9  Name  SA  9AC  DM  MMS  4 -NQO
    Concentrations [µg/plate]  650  5  4  60  10
  Mean No. of colonies/plate (average of 3 ± SD)  965 ± 32  355 ± 75  326 ± 57  297 ± 6  1323 ± 72
 +  DMSO  135 ± 9  11 ± 4  19 ± 6  10 ± 4  8 ± 3
 +  3  123 ± 13  9 ± 2  19 ± 1  10 ± 4  9 ± 4
 +  10  131 ± 21  11 ± 1  22 ± 4  6 ± 2  11 ± 3
 +  33  131 ± 10  8 ± 1  17 ± 5  11 ± 3  7 ± 1
+  100  117 ± 26 13 ± 3 20 ± 2  14 ± 2  9 ± 4
 +  333SP  133 ± 3  8 ± 3  19 ± 1  9 ± 3  10 ± 3
   positive control, +S9  Name  2 -AA  2 -AA  2 -AA  2 -AA  2 -AA
 Concentration [µg/plate] 2.5  5  5  5  10
    Mean No. of colonies/plate (average of 3 ± SD)  829 ± 14  136 ± 6  196 ± 35  218 ± 31  120 ± 13

SP = Slight Precipitate

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative