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EC number: 484-440-2 | CAS number: 502157-74-6
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
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- Particle size distribution (Granulometry)
- Vapour pressure
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- Additional physico-chemical properties of nanomaterials
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- Endpoint summary
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- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
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- Toxicological Summary
- Toxicokinetics, metabolism and distribution
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Endpoint summary
Administrative data
Key value for chemical safety assessment
Genetic toxicity in vitro
Description of key information
The test material was considered to be non-mutagenic under the conditions of this
test.
Link to relevant study records
- Endpoint:
- in vitro gene mutation study in bacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- The experimental phase of this study was performed between 15 October 2003 and
03 November 2003. - Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- Deviations:
- not specified
- GLP compliance:
- yes (incl. QA statement)
- Type of assay:
- bacterial reverse mutation assay
- Specific details on test material used for the study:
- Sponsor's identification SBCAT-03
Description White powder
Batch number UK030622B
Date received 09 October 2003
Storage conditions Room temperature in the dark
Data relating to the identity, purity and stability of the test material are the responsibility of the
Sponsor.
The test material was accurately weighed and approximate half-log dilutions prepared in dimethyl
formamide by mixing on a vortex mixer on the day of each experiment. Dimethyl formamide is
considered an acceptable vehicle for use in this test system. Analysis for concentration,
homogeneity and stability of the test material formulations is not a requirement of the test
guidelines and was, therefore, not determined. Prior to use, the solvent was dried using molecular
sieves (sodium alumino-silicate) ie 2 mm pellets with a nominal pore diameter of 4 x 10-4
microns. - Target gene:
- Histidine auxotrophs of Salmonella typhimurium
Tryptophan auxotrophs of Escherichia coli - Species / strain / cell type:
- S. typhimurium TA 1535, TA 1537, TA 98, TA 100 and E. coli WP2
- Additional strain / cell type characteristics:
- not specified
- Metabolic activation:
- with and without
- Metabolic activation system:
- S9 was prepared in-house on 19 July 2003 from the livers of male Sprague-Dawley rats weighing
~ 250g. These had each orally received three consecutive daily doses of
phenobarbitone/β-naphthoflavone (80/100 mg per kg per day) prior to S9 preparation on Day 4.
Before use, each batch of S9 was assayed for its ability to metabolise appropriate indirect
mutagens used in the Ames Test. The S9 was stored at -196°C.
The S9-mix was prepared immediately before use using sterilised co-factors and maintained on
ice for the duration of the test.
S9 5.0ml
1.65 M KCl/0.4 M MgCh 1.0 ml
0.1 M Glucose-6-phosphate 2.5ml
0.lMNADPH 2.0ml
0.lMNADH 2.0 ml
0.2 M Sodium phosphate buffer (pH 7.4) 25.0 ml
Sterile distilled water 12.5 ml
A 0.5 ml aliquot of S9-mix and 2 ml of molten, trace histidine or tryptophan supplemented, top
agar was overlaid onto a sterile Vogel-Bonner Minimal agar plate in order to assess the sterility of
the S9-mix. This procedure was repeated, in triplicate, on the day of each experiment.
Top agar was prepared using 0.6% Difeo Bacto agar and 0.5% sodium chloride with 5 ml of
1.0 mM histidine and 1.0 mM biotin or 1.0 mM tryptophan solution added to each 100 ml of top
agar. Vogel-Bonner Minimal agar plates were purchased from ILS Ltd. - Test concentrations with justification for top dose:
- In order to select appropriate dose levels for use in the main test, a preliminary assay was carried
out to determine the toxicity of the test material. The concentrations tested were 0, 0.15, 0.5, 1.5,
5, 15, 50, 150, 500, 1500 and 5000 μg/plate. The assay was performed by mixing 0.1 ml of
bacterial culture (TAlO0 or WP2uvrA"), 0.1 ml of test material formulation, 0.5 ml of S9-mix or
phosphate buffer and 2 ml of molten, trace histidine or tryptophan supplemented, top agar and
overlaying onto sterile plates of Vogel-Bonner Minimal agar (30 ml/plate). Ten concentrations of
the test material and a vehicle control (dimethyl formamide) were tested. In addition, 0.1 ml of
the maximum concentration of the test material and 2 ml of molten, trace histidine or tryptophan
supplemented, top agar was overlaid onto a sterile Nutrient agar plate in order to assess the
sterility of the test material. After approximately 48 hours incubation at 37°C the plates were
assessed for numbers of revertant colonies using a Domino colony counter and examined for
effects on the growth of the bacterial background lawn. - Vehicle / solvent:
- The test material was insoluble in sterile distilled water, acetone, and ethanol at 50mg/ml (the most concentrated stock solution) but was soluble in dimethyl formamide at the same concentration in solubility checks performed in house. Dimethyl formamide was, therefore, selected as the vehicle of choice. The test material was poorly soluble in dimethyl sulphoxide and was, therefore, not selected.
The test material was accurately weighed and approximate half-log dilutions prepared in dimethyl
formamide by mixing on a vortex mixer on the day of each experiment. Dimethyl formamide is
considered an acceptable vehicle for use in this test system (Maron D et al (1981) Mutation Research, 88, 343-350).
Analysis for concentration, homogeneity and stability of the test material formulations is not a requirement of the test guidelines and was, therefore, not determined. Prior to use, the solvent was dried using molecular sieves (sodium alumino-silicate) ie 2 mm pellets with a nominal pore diameter of 4 x 10-4 microns.
Vehicle and positive controls were used in parallel with the test material. A solvent treatment
group was used as the vehicle control and the positive control materials were as follows:
N-ethyl-N'-nitro-N-nitrosoguanidine (ENNG): 2 μg/plate for WP2uvrA-, 3 μg/plate for TA100
and 5 μg/plate for TA1535
9-Aminoacridine (9AA): 80 μg/plate for TA1537
4-Nitroquinoline-1-oxide ( 4NQO): 0.2 μg/plate for TA98
In addition, 2-Aminoanthracene (2AA) and Benzo(a)pyrene (BP), which are non-mutagenic in the
absence of metabolising enzymes, were used in the series of plates with S9-mix at the following
concentrations:
2AA at 1 μg/plate for TA100
2AA at 2 μg/plate for TA1535 and TA1537
2AA at 10 μg/plate for WP2uvrABP
at 5 μg/plate for T A98 - 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
- N-ethyl-N-nitro-N-nitrosoguanidine
- Details on test system and experimental conditions:
- Seven concentrations of the test material (5, 15, 50, 150, 500, 1500 and 5000 μg/plate) were
assayed in triplicate against each tester strain, using the direct plate incorporation method.
Additional dose levels were included to allow for test material induced toxicity, ensuring that a
minimum of four non-toxic doses were achieved.
Measured aliquots (0.1 ml) of one of the bacterial cultures were dispensed into sets of test tubes
followed by 2.0 ml of molten, trace histidine or tryptophan supplemented, top agar, 0.1 ml of the
test material formulation, vehicle or positive control and either 0.5 ml of S9-mix or phosphate
buffer. The contents of each test tube were mixed and equally distributed onto the surface of
Vogel-Bonner Minimal agar plates (one tube per plate). This procedure was repeated, in
triplicate, for each bacterial strain and for each concentration of test material both with and
without S9-mix.
All of the plates were incubated at 37°C for approximately 48 hours and the frequency of revertant
colonies assessed using a Domino colony counter.
Mutation Test - Experiment 2 (Main Test)
The second experiment was performed using methodology as described for the range-finding test, using fresh bacterial cultures, test material and control solutions. The test material dose range was the same as the range-finding test (5 to 5000 μg/plate ). - Rationale for test conditions:
- In accordance with test guidelines
- Evaluation criteria:
- The test material may be considered positive in this test system if the following criteria are met:
The test material should have induced a reproducible, dose-related and statistically (Dunnett's
method of linear regression significant increase in the revertant count in at least one strain of
bacteria. - Statistics:
- Dunnett's method of linear regression
- Key result
- Species / strain:
- E. coli WP2 uvr A
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not determined
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- True negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 1537
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not determined
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- True negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 1535
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not determined
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- True negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 100
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not determined
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- True negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 98
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not determined
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- True negative controls validity:
- not examined
- Positive controls validity:
- valid
- Additional information on results:
- Preliminary Toxicity Test
The test material was initially toxic at 500 μg/plate to the strains of bacteria used (TAlO0 and
WP2uvrA). The test material formulation and S9-mix used in this experiment were both shown
to be effectively sterile.
The number of revertant colonies for the toxicity assay were: see "Any other information on results"
Prior to use, the master strains were checked for characteristics, viability and spontaneous
reversion rate (all were found to be satisfactory). These data are not given in the report. The
S9-mix used in both experiments of the main test was shown to be sterile.
Results for the negative controls (spontaneous mutation rates) are presented in "Any other information on results" and were
considered to be acceptable. These data are for concurrent untreated control plates performed on
the same day as the Mutation Test.
The individual plate counts, the mean number of revertant colonies and the standard deviations for the test material, vehicle and positive controls both with and without metabolic activation, are
presented in "Any other information on results" with the results also expressed graphically in "Illustrations".
Information regarding the equipment and methods used in these experiments as required by the
Japanese Ministry of Economy, Trade and Industry and Japanese Ministry of Health, Labour and
Welfare are presented in "Any other information on materials".
A history profile of vehicle and positive control values is presented in "Any other information on materials".
The test material caused a visible reduction in the growth of the bacterial background lawn to all
of the tester strains, both in the presence and absence of S9, from 1500 μgiplate. The test material was tested up to the maximum recommended dose level of 5000 μgiplate. No test material precipitate was observed on the plates at any of the doses tested in either the presence or absence
of S9-mix.
No significant increases in the frequency of revertant colonies were recorded for any of the
bacterial strains, at any dose level either with or without metabolic activation.
All of the positive control chemicals used in the test induced marked increases in the frequency of
revertant colonies thus confirming the activity of the S9-mix and the sensitivity of the bacterial
strains. - Conclusions:
- The test material was considered to be non-mutagenic under the conditions of this test.
- Executive summary:
Introduction.
The method was designed to conform to the guidelines for bacterial mutagenicity testing published by the major Japanese Regulatory Authorities including METI, MHLW and MAFF. It also meets the requirements of the OECD Guidelines for Testing of Chemicals No. 471 "Bacterial Reverse Mutation Test", Method Bl3/14 of Commission Directive 2000/32/EC and the USA, EPA (TSCA) OPPTS harmonised guidelines.
Methods.Salmonella typhimurium strains TA1535, TA1537, TA98 and TA100 and Escherichia coli strain WP2uvrA· were treated with the test material using the Ames plate incorporation method at seven dose levels, in triplicate, both with and without the addition of a rat liver homogenate metabolising system (10% liver S9 in standard co-factors). The dose range for the range-finding test was determined in a preliminary toxicity assay and was 5 to 5000 μg/plate. The experiment was repeated on a separate day using the same dose range as the range-finding test, fresh cultures of the bacterial strains and fresh test material formulations.
Additional dose levels were included to allow for test material induced toxicity, ensuring that a minimum of four non-toxic dose levels were achieved.
Results. The vehicle ( dimethyl formamide) control plates gave counts of revertant colonies within the normal range. All of the positive control chemicals used in the test induced marked increases in the frequency of revertant colonies, both with or without metabolic activation. Thus, the sensitivity of the assay and the efficacy of the S9-mix were validated.
The test material caused a visible reduction in the growth of the bacterial background lawn to all of the tester strains, both in the presence and absence of S9, from 1500 μg/plate.The test material was tested up to the maximum recommended dose level of 5000 μg/plate. No test material precipitate was observed on the plates at any of the doses tested in either the presence or absence
of S9-mix.
No significant increases in the frequency of revertant colonies were recorded for any of the bacterial strains, with any dose of the test material, either with or without metabolic activation.Conclusion.
The test material was considered to be non-mutagenic under the conditions of this
test.
Reference
The number of revertant colonies for the toxicity assay were:
With (+) or without (-) S9-mix | Strain | Dose (µg/plate) | ||||||||||
0 | 0.15 | 0.5 | 1.5 | 5 | 15 | 50 | 150 | 500 | 1500 | 5000 | ||
- | TA100 | 101 | 87 | 93 | 81 | 98 | 72 | 98 | 88 | 63* | 0* | 0* |
+ | TA100 | 121 | 85 | 93 | 95 | 90 | 101 | 73 | 75 | 69 | 0* | 0* |
- | WP2urvA- | 26 | 23 | 23 | 31 | 20 | 24 | 19 | 24 | 21 | 0* | 0* |
+ | WP2urvA- | 25 | 43 | 25 | 26 | 32 | 22 | 25 | 24 | 25 | 9* | 0* |
*- Partial or complete absence of bacterial background lawn
Spontaneous Mutation Rates (Concurrent Negative Controls)
Range-finding Test
Number of revertants (mean number of colonies per plate) | ||||
Base-pair substitution type | Frameshift type | |||
TA100 | TA1535 | WP2uvrA- | TA98 | TA1537 |
118 | 36 | 22 | 21 | 5 |
120 (124) | 34 (33) | 35 (26) | 18 (20) | 5 (7) |
134 | 30 | 22 | 20 | 12 |
Main Test
Number of revertants (mean number of colonies per plate) | ||||
Base-pair substitution type | Frameshift type | |||
TA100 | TA1535 | WP2uvrA- | TA98 | TA1537 |
96 | 33 | 30 | C | 21 |
119 (103) | 37 (34) | 25 (29) | 19 (17) | 12 (15) |
93 | 33 | 32 | 15 | 11 |
C=Contaminated
Test Results: Range-Finding Test- Without Metabolic Activation
Test Period | From: 27 October 2003 | To: 30 October 2003 | ||||
With or without S9 mix | Test substance concentration (µg/plate) | Number of revertants (mean number of colonies per plate) | ||||
Base-pair substitution type | Frameshift type | |||||
TA100 | TA1535 | WP2uvrA- | TA98 | TA1537 | ||
- | 0 | 83 | 33 | 15 | 25 | 6 |
95 (89) | 23 (28) | 22 (18) | 18 (22) | 20 (11) | ||
90 6.0# | 28 5.0 | 18 3.5 | 22 3.5 | 6 8.1 | ||
- | 5 | 67 | 33 | 22 | 25 | 9 |
85 (84) | 34 (32) | 28 (22) | 24 (29) | 10 (9) | ||
101 17.0 | 30 2.1 | 15 6.5 | 38 7.8 | 9 0.6 | ||
- | 15 | 96 | 33 | 11 | 16 | 4 |
116 (107) | 33 (34) | 26 (19) | 20 (20) | 9 (6) | ||
108 10.1 | 36 1.7 | 21 7.6 | 24 4.0 | 5 2.6 | ||
- | 50 | 89 | 27 | 27 | 21 | 6 |
121 (107) | 27 (29) | 20 (23) | 26 (27) | 12 (9) | ||
111 16.4 | 33 3.5 | 21 3.8 | 34 6.6 | 8 3.1 | ||
- | 150 | 106 | 33 | 12 | 16 | 16 |
109 (113) | 28 (32) | 24 (18) | 19 (15) | 8 (11) | ||
123 9.1 | 36 4.0 | 18 6.0 | 11 4.0 | 8 4.6 | ||
- | 500 | 83 | 30 | 17 | 18 | 8 |
62 (78) | 23 (27) | 20 (15) | 18 (23) | 8 (8) | ||
88 13.8 | 29 3.8 | 8 6.2 | 33 8.7 | 7 0.6 | ||
- | 1500 | 0* | 0* | 8* | 8* | 0* |
0* (0) | 0* (0) | 5* (15) | 5* (6) | 0* (0) | ||
0* 0.0 | 0* 0.0 | 4* 6.4 | 4* 2.1 | 0* 0.0 | ||
- | 5000 | 0* | 0* | 0* | 0* | 0* |
0* (0) | 0* (0) | 0* (0) | 0* (0) | 0* (0) | ||
0* 0.0 | 0* 0.0 | 0* 0.0 | 0* 0.0 | 0* 0.0 | ||
Positive controls
S9 mix
-
| Name Concentration (µg/plate)
No. colonies per plate
| ENNG | ENNG | ENNG | 4NQO | 9AA |
3 | 5 | 2 | 0.2 | 80 | ||
460 | 247 | 608 | 103 | 730 | ||
453 (515) | 249 (239) | 624 (694) | 125 (137) | 732 (730) | ||
631 100.8 | 222 15.0 | 851 135.9 | 183 41.3 | 727 2.5 |
ENNG = N-ethyl-N'-nitro-N-nitrosoguanidine
4NQO = 4-Nitroquinoline-1-oxide
9AA = 9-Aminoacridine
* = Partial or complete absence of bacterial background lawn
# = Standard deviation
Test Results: Range-Finding Test- With Metabolic Activation
Test Period | From: 27 October 2003 | To: 30 October 2003 | ||||
With or without S9 mix | Test substance concentration (µg/plate) | Number of revertants (mean number of colonies per plate) | ||||
Base-pair substitution type | Frameshift type | |||||
TA100 | TA1535 | WP2uvrA- | TA98 | TA1537 | ||
+ | 0 | 117 | 12 | 24 | 22 | 16 |
114 (107) | 8 (15) | 27 (28) | 20 (21) | 11 (14) | ||
89 15.4# | 25 8.9 | 34 5.1 | 21 1.0 | 15 2.6 | ||
+ | 5 | 106 | 12 | 34 | 27 | 10 |
101 (107) | 12 (11) | 22 (29) | 27 (30) | 10 (11) | ||
113 6.0 | 8 2.3 | 32 6.4 | 36 5.2 | 12 1.2 | ||
+ | 15 | 112 | 16 | 34 | 22 | 9 |
90 (97) | 15 (14) | 22 (30) | 35 (29) | 15 (14) | ||
90 12.7 | 12 2.1 | 35 7.2 | 30 6.6 | 18 4.6 | ||
+ | 50 | 98 | 11 | 23 | 35 | 9 |
98 (98) | 13 (12) | 17 (26) | 23 (27) | 8 (10) | ||
98 0.0 | 11 1.2 | 39 11.4 | 22 7.2 | 13 2.6 | ||
+ | 150 | 95 | 23 | 15 | 28 | 7 |
115 (105) | 15 (19) | 28 (23) | 27 (27) | 9 (9) | ||
104 10.0 | 19 4.0 | 26 7.0 | 25 1.5 | 10 1.5 | ||
+ | 500 | 82 | 10 | 21 | 35 | 15 |
85 (89) | 18 (12) | 17 (20) | 25 (27) | 11 (16) | ||
100 9.6 | 7 5.7 | 23 3.1 | 20 7.6 | 22 5.6 | ||
+ | 1500 | 0* | 0* | 18* | 12* | 0* |
0* (0) | 0* (0) | 10* (12) | 13* (11) | 0* (0) | ||
0* 0.0 | 0* 0.0 | 8* 5.3 | 9* 2.1 | 0* 0.0 | ||
+ | 5000 | 0* | 0* | 0* | 0* | 0* |
0* (0) | 0* (0) | 0* (0) | 0* (0) | 0* (0) | ||
0* 0.0 | 0* 0.0 | 0* 0.0 | 0* 0.0 | 0* 0.0 | ||
Positive controls
S9 mix
+
| Name Concentration (µg/plate)
No. colonies per plate
| 2AA | 2AA | 2AA | BP | 2AA |
1 | 2 | 10 | 5 | 2 | ||
1876 | 459 | 983 | 188 | 351 | ||
2035 | 360 | 948 | 188 | 361 | ||
1850 | 421 | 765 | 211 | 512 |
BP = Benzo( a )pyrene
2AA = 2-Aminoanthracene
* = Partial or complete absence of bacterial background lawn
# = Standard deviation
Test Results: Main Test- Without Metabolic Activation
Test Period | From: 31 October 2003 | To: 03 November 2003 | ||||
With or without S9 mix | Test substance concentration (µg/plate) | Number of revertants (mean number of colonies per plate) | ||||
Base-pair substitution type | Frameshift type | |||||
TA100 | TA1535 | WP2uvrA- | TA98 | TA1537 | ||
- | 0 | 100 | 43 | 18 | 17 | 21 |
121 (105) | 43 (40) | 21 (20) | 20 (18) | 9 (14) | ||
94 14.2# | 34 5.2 | 20 1.5 | 18 1.5 | 11 6.4 | ||
- | 5 | 101 | 38 | 19 | 19 | 17 |
112 (109) | 39 (39) | 16 (18) | 17 (15) | 10 (14) | ||
115 7.4 | 40 1.0 | 19 1.7 | 10 4.7 | 16 3.8 | ||
- | 15 | 93 | 40 | 20 | 15 | 10 |
109 (105) | 41 (40) | 29 (21) | 12 (12) | 8 (9) | ||
113 10.6 | 40 0.6 | 13 8.0 | 10 2.5 | 8 1.2 | ||
- | 50 | 106 | 39 | 16 | 13 | 22 |
105 (108) | 38 (36) | 15 (18) | 23 (15) | 19 (17) | ||
113 4.4 | 30 4.9 | 24 4.9 | 9 7.2 | 9 6.8 | ||
- | 150 | 136 | 32 | 26 | 19 | 8 |
119 (125) | 32 (34) | 18 (20) | 16 (15) | 10 (9) | ||
119 9.8 | 39 4.0 | 17 4.9 | 9 5.1 | 10 1.2 | ||
- | 500 | 91 | 25 | 8 | 8 | 4 |
109 (9.2) | 28 (26) | 12 (10) | 6 (8) | 2 (4) | ||
75 17.0 | 25 1.7 | 10 2.0 | 10 2.0 | 6 2.0 | ||
- | 1500 | 0* | 0* | 3* | 6* | 0* |
0* (0) | 0* (0) | 10* (6) | 6* (5) | 0* (0) | ||
0* 0.0 | 0* 0.0 | 6* 3.5 | 3* 1.7 | 0* 0.0 | ||
- | 5000 | 0* | 0* | 0* | 0* | 0* |
0* (0) | 0* (0) | 0* (0) | 0* (0) | 0* (0) | ||
0* 0.0 | 0* 0.0 | 0* 0.0 | 0* 0.0 | 0* 0.0 | ||
Positive controls
S9 mix
-
| Name Concentration (µg/plate)
No. colonies per plate
| ENNG | ENNG | ENNG | 4NQO | 9AA |
3 | 5 | 2 | 0.2 | 80 | ||
467 | 267 | 578 | 113 | 632 | ||
479 (468) | 263 (265) | 605 (606) | 147 (139) | 512 (592) | ||
458 10.5 | 266 2.1 | 635 28.5 | 158 23.5 | 633 69.6 |
ENNG = N-ethyl-N'-nitro-N-nitrosoguanidine
4NQO = 4-Nitroquinoline-1-oxide
9AA = 9-Aminoacridine
* = Partial or complete absence of bacterial background lawn
# = Standard deviation
Test Results: Main Test- With Metabolic Activation
Test Period | From: 31 October 2003 | To: 03 November 2003 | ||||
With or without S9 mix | Test substance concentration (µg/plate) | Number of revertants (mean number of colonies per plate) | ||||
Base-pair substitution type | Frameshift type | |||||
TA100 | TA1535 | WP2uvrA- | TA98 | TA1537 | ||
+ | 0 | 112 | 16 | 19 | 37 | 16 |
93 (101) | 16 (15) | 20 (23) | 38 (37) | 12 (14) | ||
98 9.8# | 12 2.3 | 31 6.7 | 35 1.5 | 15 2.1 | ||
+ | 5 | 103 | 13 | 28 | 35 | 21 |
101 (104) | 17 (13) | 24 (23) | 37 (35) | 17 (20) | ||
109 4.2 | 9 4.0 | 17 5.6 | 32 2.5 | 21 2.3 | ||
+ | 15 | 108 | 10 | 22 | 35 | 12 |
107 (111) | 19 (16) | 16 (20) | 36 (38) | 12 (12) | ||
119 6.7 | 20 5.5 | 23 3.8 | 43 4.4 | 13 0.6 | ||
+ | 50 | 90 | 13 | 16 | 34 | 12 |
91 (91) | 19 (16) | 27 (20) | 30 (33) | 17 (13) | ||
93 1.5 | 17 3.1 | 17 6.1 | 34 2.3 | 10 3.6 | ||
+ | 150 | 104 | 16 | 29 | 35 | 11 |
90 (105) | 10 (14) | 18 (22) | 29 (33) | 12 (9) | ||
122 16.0 | 15 3.2 | 20 5.9 | 29 3.5 | 5 3.8 | ||
+ | 500 | 100 | 4 | 10 | 29 | 8 |
103 (99) | 11 (8) | 17 (17) | 28 (29) | 6 (7) | ||
94 4.6 | 8 3.5 | 23 6.5 | 30 1.0 | 8 1.2 | ||
+ | 1500 | 0* | 0* | 7* | 19 | 0* |
0* (0) | 0* (0) | 8* (8) | 20 (17) | 0* (0) | ||
0* 0.0 | 0* 0.0 | 9* 1.0 | 12 4.4 | 0* 0.0 | ||
+ | 5000 | 0* | 0* | 0* | 0* | 0* |
0* (0) | 0* (0) | 0* (0) | 0* (0) | 0* (0) | ||
0* 0.0 | 0* 0.0 | 0* 0.0 | 0* 0.0 | 0* 0.0 | ||
Positive controls
S9 mix
+
| Name Concentration (µg/plate)
No. colonies per plate
| 2AA | 2AA | 2AA | BP | 2AA |
1 | 2 | 10 | 5 | 2 | ||
1845 | 283 | 1051 | 108 | 429 | ||
2000 (1939) | 269 (280) | 1204 (1135) | 117 (121) | 425 (389) | ||
1971 82.4 | 288 9.8 | 1151 77.7 | 139 15.9 | 314 65.3 |
BP = Benzo( a )pyrene
2AA = 2-Aminoanthracene
* = Partial or complete absence of bacterial background lawn
# = Standard deviation
COMBINED VEHICLE AND UNTREATED CONTROL VALUES 2001
Strain S9-mix | TA100 | TA1535 | WP2urvA- | TA102 | TA98 | TA1537 | TA1538 | WP2uvrA- pKM101 | TA97a | TA104 | ||||||||||
-S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | |
Mean | 106 | 116 | 16 | 15 | 22 | 26 | 278 | 305 | 23 | 32 | 11 | 13 | 14 | nd | 144 | 147 | 116 | 131 | 512 | nd |
SD | 23 | 23 | 4 | 4 | 5 | 6 | 45 | 39 | 7 | 8 | 4 | 4 | 5 | nd | 61 | 14 | 21 | 24 | 93 | nd |
Min | 58 | 62 | 8 | 7 | 11 | 13 | 195 | 201 | 10 | 13 | 2 | 4 | 6 | nd | 74 | 131 | 84 | 114 | 389 | nd |
Max | 178 | 178 | 37 | 37 | 41 | 52 | 405 | 421 | 56 | 58 | 23 | 29 | 20 | nd | 292 | 164 | 134 | 134 | 616 | nd |
Values | 817 | 658 | 790 | 621 | 656 | 501 | 244 | 157 | 814 | 662 | 793 | 630 | 5 | nd | 10 | 4 | 5 | 2 | 5 | nd |
nd = no data available
POSITIVE CONTROL VALUES 2001
Strain S9-mix | TA100 | TA1535 | WP2urvA- | TA102 | TA98 | TA1537 | TA1538 | WP2uvrA- pKM101 | TA97a | TA104 | ||||||||||
-S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | |
Mean | 505 | 1582 | 431 | 336 | 685 | 756 | 849 | 830 | 140 | 303 | 1415 | 428 | 153 | 501 | 1946 | 2102 | 618 | 750 | 825 | 1445 |
SD | 190 | 541 | 412 | 110 | 323 | 243 | 179 | 159 | 43 | 96 | 713 | 146 | 60 | 246 | 794 | 844 | 62 | 142 | 209 | 202 |
Min | 259 | 454 | 98 | 113 | 248 | 242 | 461 | 485 | 72 | 136 | 197 | 139 | 113 | 322 | 672 | 956 | 547 | 649 | 644 | 1224 |
Max | 1829 | 2738 | 2039 | 990 | 1960 | 1340 | 1541 | 1303 | 362 | 679 | 3616 | 792 | 133 | 413 | 2790 | 3100 | 655 | 850 | 1125 | 1621 |
Values | 165 | 163 | 163 | 161 | 156 | 155 | 92 | 93 | 166 | 164 | 162 | 160 | 4 | 4 | 7 | 7 | 3 | 2 | 4 | 3 |
COMBINED VEHICLE AND UNTREATED CONTROL VALUES 2002
Strain S9-mix | TA100 | TA1535 | WP2urvA- | TA102 | TA98 | TA1537 | WP2uvrA- pKM101 | |||||||
-S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | |
Mean | 91 | 100 | 20 | 17 | 23 | 27 | 322 | 349 | 22 | 35 | 12 | 17 | 169 | 215 |
SD | 16.6 | 18.0 | 5.5 | 4.3 | 4.8 | 5.3 | 47.7 | 34.6 | 5.2 | 6.8 | 4 | 4.7 | 42.8 | 50.2 |
Min | 61 | 68 | 8 | 8 | 10 | 14 | 183 | 255 | 11 | 13 | 4 | 5 | 92 | 131 |
Max | 160 | 162 | 38 | 37 | 47 | 45 | 414 | 449 | 44 | 66 | 29 | 38 | 234 | 277 |
Values | 939 | 742 | 912 | 718 | 685 | 521 | 329 | 210 | 946 | 749 | 918 | 718 | 25 | 11 |
POSITIVE CONTROL VALUES 2002
Strain S9-mix | TA100 | TA1535 | WP2urvA- | TA102 | TA98 | TA1537 | WP2uvrA- pKM101 | |||||||
-S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | -S9 | +S9 | |
Mean | 460 | 1880 | 347 | 310 | 621 | 866 | 1126 | 858 | 136 | 239 | 1953 | 453 | 1384 | 2608 |
SD | 118.2 | 594.3 | 204.0 | 119.7 | 235.5 | 350.5 | 289.4 | 169.5 | 38.2 | 803.1 | 803.1 | 145.9 | 333.7 | 1109.6 |
Min | 235 | 499 | 80 | 91 | 185 | 210 | 686 | 568 | 66 | 486 | 486 | 140 | 960 | 186 |
Max | 952 | 3397 | 1385 | 810 | 1295 | 3406 | 2456 | 2009 | 323 | 4622 | 4622 | 1365 | 2073 | 3900 |
Values | 190 | 190 | 188 | 186 | 169 | 168 | 117 | 118 | 192 | 192 | 188 | 184 | 14 | 14 |
SD = Standard deviation
Min = Minimum value
Max = Maximum value
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Additional information
Justification for classification or non-classification
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