Registration Dossier
Registration Dossier
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EC number: 273-728-1 | CAS number: 69012-28-8 By-product of the manufacture of ferromanganese alloy containing primarily oxides of aluminum, manganese and silicon.
Endpoint summary
Administrative data
Key value for chemical safety assessment
Genetic toxicity in vitro
Description of key information
- Bacterial Reverse Mutation Assay (e.g. Ames test)
Negative (TA98, TA100, TA1535, TA1537, WP2uvrA), MnCl2, OECD 471,
Thompson & Bowles (2009)
- In Vitro Mammalian Chromosome Aberration Test
Negative (human lymphocyte cells), MnCl2, OECD 473, Morris & Durward
(2009)
- In Vitro Mammalian Cell Gene Mutation
Negative (L5178Y cells), MnCl2, OECD 476, Flanders (2009)
Link to relevant study records
- 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:
- 10 July 2009 to 4 August 2009
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Study conducted in compliance with agreed protocols, with no or minor deviations from standard test guidelines and/or minor methodological deficiencies, which do not affect the quality of the relevant results. The study report was conclusive, done to a valid guideline and the study was conducted under GLP conditions. Since the study was conducted with manganese chloride, which represents a more available form of manganese, rather than with the registered substance itself, the study was assigned a reliability score of 2. Use of data on manganese dichloride is considered to be suitable and more precautionary since manganese dichloride is highly soluble; findings from the study are therefore considered to represent a worst case scenario for inorganic Mn compounds.
- Reason / purpose for cross-reference:
- other: Target
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.13/14 (Mutagenicity - Reverse Mutation Test Using Bacteria)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of assay:
- bacterial reverse mutation assay
- Target gene:
- Histidine synthesis in the Salmonella typhimurium strains and tryptophan synthesis in the E. coli strain used.
- Species / strain / cell type:
- S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
- Details on mammalian cell type (if applicable):
- Not applicable
- Additional strain / cell type characteristics:
- other: GC base pairing at the primary reversion site.
- Species / strain / cell type:
- E. coli WP2 uvr A
- Additional strain / cell type characteristics:
- other: AT base pairing at the primary reversion site.
- Metabolic activation:
- with and without
- Metabolic activation system:
- S9 mix
- Test concentrations with justification for top dose:
- 50, 150, 500, 1500 and 5000 µg/plate
- Vehicle / solvent:
- - Vehicle(s)/solvent(s) used: Sterile distilled water
- Justification for choice of solvent/vehicle: The test material was found to be soluble in sterile distilled water and dimethyl sulphoxide at 50 mg/mL. Sterile distilled water was chosen as the solvent. - Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- other: 2-Aminoanthracene (2AA)
- Remarks:
- With S9 mix
- Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- benzo(a)pyrene
- Remarks:
- With S9 mix
- Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- N-ethyl-N-nitro-N-nitrosoguanidine
- Remarks:
- Without S9 mix
- Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- 4-nitroquinoline-N-oxide
- Remarks:
- Without S9 mix
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in medium; in agar (plate incorporation)
DURATION
- Preincubation period: 10 hours at 36 °C
- Exposure duration: 48 hours
- Expression time (cells in growth medium): Not reported - Evaluation criteria:
- Several criteria for determining a positive result. Dose-related increase in revertant frequency over the dose range tested and/or a reproducible increase at one or more concentrations in at least one bacterial strain with or without metabolic activation. Biological relevance of the results will be considered first, statistical methods, as recommended by the UKEMS can also be used as an aid to evaluation, however statistical significance will not be the only determining factor for a positive response.
- Statistics:
- The following was used to statistically evaluate the results from the mutagenicity test. Kirkland DJ (ED) (1989) Statistical Evaluation of Mutagenicity Test Data (UKEMS) sub-committee on Guidelines for Mutagenicity Testing. Report Part III - Cambridge University Press.
- 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:
- not specified
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Additional information on results:
- TEST-SPECIFIC CONFOUNDING FACTORS: Not reported
RANGE-FINDING/SCREENING STUDIES: The test substance was found to be non-toxic in the range-finding study.
COMPARISON WITH HISTORICAL CONTROL DATA: The historical control values were found to concur with the results from the study for both positive and vehicle controls.
ADDITIONAL INFORMATION ON CYTOTOXICITY: Not reported - Remarks on result:
- other: all strains/cell types tested
- Conclusions:
- Interpretation of results: negative with and without metabolic activation
The test material has been found to be non-mutagenic under the test conditions reported. - Executive summary:
The mutagenic potential of the test material was investigated in a study which was conducted under GLP conditions and in accordance with the standardised guidelines OECD 471 and EU Method B.13/14.
During the study test strains of Salmonella typhimurium (TA98, TA100, TA1535 and TA1537) and a tester strain of Escherichia coli (WP2uvrA) were exposed to the test material both in the presence and the absence of metabolic activation.Vehicle and positive controls were run concurrently. Two separate experiments were conducted, in the first five concentrations of test material (50, 150, 500, 1500 and 5000 µg/plate) were assayed in triplicate against each tester strain, using the direct plate incorporation method. In the second experiment the test material and vehicle control were dosed using a pre-incubation method.
The test material was found to cause no visible reduction in growth of the bacterial background lawn at any dose and was therefore tested up to the maximum dose level of 5000 µg/plate A particulate precipitate was at 1500 µg/plate and above. This was considered not to prevent the scoring of revertant colonies. No toxicologically significant increases in the frequency of revertant colonies were recorded for any of the bacterial strains, with any dose of the test substance, with or without metabolic activation. In the TA100 revertant colony, a small but statistically significant increase was observed on the 1500 µg/plate in Experiment 2 (increase of less than 1.5 times). However the increase was within the range specified by the Standard Test Method, and proved non-reproducible over two separate experiments. This was concluded to have no biological or toxicological relevance. All of the positive control substances induced marked increases in the frequency of revertant colonies, confirming the activity of the S9-mix and the sensitivity of the bacterial strains.
Therefore, under the conditions of the study the test material was concluded to be non-mutagenic.
Since the study was conducted with manganese chloride, which represents a more available form of manganese, rather than with the registered substance itself, the study was assigned a reliability score of 2. Use of data on manganese dichloride is considered to be suitable and more precautionary since manganese dichloride is highly soluble; findings from the study are therefore considered to represent a worst case scenario for inorganic Mn compounds.
- Endpoint:
- in vitro gene mutation study in bacteria
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study conducted on read-across material.
- Reason / purpose for cross-reference:
- read-across source
- Species / strain:
- other: S. Typhimurium TA 1535, TA 1537, TA 98 and TA 100
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not specified
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Endpoint:
- in vitro gene mutation study in bacteria
- Data waiving:
- study scientifically not necessary / other information available
- Justification for data waiving:
- other:
- Endpoint:
- in vitro gene mutation study in bacteria
- Remarks:
- Type of genotoxicity: gene mutation
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Documentation contains an insufficient level of information to enable a complete assessment on the reliability of the reported results. The study was conducted with silicomanganese slag, rather than with the registered substance itself. Use of data generated with silicomanganese slag, to address information requirements of ferromanganese slag, is considered to be justified on the basis of the similar compositions of the two substances. Both substances are UVCB substances, containing metallic oxides; each substance is obtained as a by-product in the manufacture of SiMn and FeMn alloy, respectively.
- Reason / purpose for cross-reference:
- other: Target
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The method was a standard Ames.
- GLP compliance:
- not specified
- Type of assay:
- bacterial reverse mutation assay
- Target gene:
- histidine locus
- Species / strain / cell type:
- S. typhimurium TA 98
- Additional strain / cell type characteristics:
- not applicable
- Species / strain / cell type:
- S. typhimurium TA 100
- Additional strain / cell type characteristics:
- not applicable
- Metabolic activation:
- with and without
- Species / strain:
- S. typhimurium TA 98
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not determined
- Species / strain:
- S. typhimurium TA 100
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not determined
- Conclusions:
- Interpretation of results: negative with and without metabolic activation
Under the conditions of the study the test material was concluded to be non-mutagenic to S. typhimurium TA 98 and S. typhimurium TA 100 with and without metabolic activation. - Executive summary:
An Ames test was conducted with the test material SiMn slag using the Salmonella typhimurium tester strains TA98 and TA100. The bacterial tester strains were exposed to the test material both in the presence and absence of metabolic activation.
Under the conditions of the study the test material was concluded to be non-mutagenic.
Use of data generated with silicomanganese slag, to address information requirements of ferromanganese slag, is considered to be justified on the basis of the similar compositions of the two substances. Both substances are UVCB substances, containing metallic oxides; each substance is obtained as a by-product in the manufacture of SiMn and FeMn alloy, respectively.
- Endpoint:
- in vitro gene mutation study in bacteria
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Study conducted on read-across material
- Reason / purpose for cross-reference:
- read-across source
- Species / strain:
- S. typhimurium TA 98
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not determined
- Species / strain:
- S. typhimurium TA 100
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not determined
- Endpoint:
- in vitro cytogenicity / chromosome aberration study in mammalian cells
- Remarks:
- Type of genotoxicity: chromosome aberration
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 3 July 2009 to 24 September 2009
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Study conducted in compliance with agreed protocols, with no or minor deviations from standard test guidelines and/or minor methodological deficiencies, which do not affect the quality of the relevant results. The study report was conclusive, done to a valid guideline and the study was conducted under GLP conditions. Since the study was conducted with manganese chloride, which represents a more available form of manganese, rather than with the registered substance itself, the study was assigned a reliability score of 2. Use of data on manganese dichloride is considered to be suitable and more precautionary since manganese dichloride is highly soluble; findings from the study are therefore considered to represent a worst case scenario for inorganic Mn compounds.
- Reason / purpose for cross-reference:
- other: Targat
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 473 (In Vitro Mammalian Chromosome Aberration Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of assay:
- in vitro mammalian chromosome aberration test
- Species / strain / cell type:
- lymphocytes: human, peripheral
- Details on mammalian cell type (if applicable):
- Not applicable
- Additional strain / cell type characteristics:
- not applicable
- Metabolic activation:
- with and without
- Metabolic activation system:
- S9-mix
- Test concentrations with justification for top dose:
- See table 1 under section Any other information on materials and methods incl. tables
- Vehicle / solvent:
- - Vehicle(s)/solvent(s) used: Minimal Essential Medium (MEM)
- Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- mitomycin C
- Remarks:
- In the absence of S9: 0.4 and 0.2 µg/mL for the 4(20)-hour and 24-hour exposures respectively in MEM
- Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- cyclophosphamide
- Remarks:
- In the presence of S9: 5 µg/mL dissolved in dimethyl sulphoxide
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in medium
DURATION
- Preincubation period: Approximately 48 hours incubation at 37 °C 5% CO2 in humidified air
- Exposure duration: 4 hour exposure (with a further 20 hour incubation once test material had been removed) and 24 hour exposure
- Expression time (cells in growth medium): Typically 17 hours average generation time under experimental exposure conditions
- Fixation: Mitosis was arrested two hours before the required harvest time. After incubation with demecolcine, the cells were centrifuged, the culture medium was drawn off and discarded, and the cells re-suspended in 0.075 M hypotonic KCl. After 14 minutes (including centrifugation), most of the hypotonic solution was drawn off and discarded. The cells were re-suspended and then fixed by dropping the KCl cell suspension into fresh methanol/glacial acetic acid (3:1 v/v). The fixative was changed at least three times and the cells stored at 4 °C for at least four hours to ensure complete fixation.
SPINDLE INHIBITOR (cytogenetic assays): Demecolcin (Colcemid 0.1 µg/mL) two hours before the required harvest time
STAIN (for cytogenetic assays): To prepare metaphase spreads, lymphocytes were suspended in several mL of fresh fixative before centrifugation and re-suspension in a small amount of fixative. Several drops of this suspension were dropped onto clean, wet microscope slides and left to air dry. Each slide was permanently labelled with the appropriate identification data. When the slides were dry they were stained in 5% Giemsa for 5 minutes, rinsed, dried and a cover slip applied using mounting medium.
NUMBER OF REPLICATIONS: Duplicate lymphocyte cultures (A and B) were prepared for each dose level
NUMBER OF CELLS EVALUATED: Where possible the first 100 consecutive well-spread metaphases
DETERMINATION OF CYTOTOXICITY
- Method: mitotic index
- Other: Slides were checked microscopically to determine the quality of the metaphases and also the toxicity and extent of precipitation of the test material. These observations were used to select the dose levels for mitotic index evaluation. - Evaluation criteria:
- - Coding: Slides were coded using a computerised random number generator and any supplementary slides were coded manually.
- Mitotic index: A total of 2000 lymphocyte cell nuclei were counted and the number of cells in metaphase recorded and expressed as the mitotic index and as a percentage of the vehicle control value.
- Scoring of chromosome damage: Where possible the first 100 consecutive well-spread metaphases from each culture were counted. Where there were approximately 30 to 50 % of cells with aberrations, slide evaluation was terminated at 50 cells. If the cell had 44-48 chromosomes, any gaps, breaks or rearrangements were noted according to the International System for Chromosome Nomenclature (1985) Scott et al and Savage (1976) in the UKEMS guidelines for mutagenicity testing. Cells with chromosome aberrations were reviewed as necessary by a senior cytogenticist prior to decoding the slides. - Statistics:
- The frequency of cells with aberrations excluding gaps and the frequency of polyploid cells was compared, where necessary, with the concurrent vehicle control value using Fisher's Exact test.
- Species / strain:
- lymphocytes: human, peripheral
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- cytotoxicity
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not specified
- Positive controls validity:
- valid
- Additional information on results:
- TEST-SPECIFIC CONFOUNDING FACTORS
- Precipitation: Test material was noted to precipitate at 315 µg/mL in the 4(20)-hour cultures without S9, and above 630 µg/mL in the 4(20)-hour cultures in the presence of S9. No precipitate was observed at the end of the exposure period in the 24-hour cultures.
RANGE-FINDING/SCREENING STUDIES: The preliminary toxicity test dose range was 4.92 to 1260 µg/mL. The maximum dose was based on the maximum recommended 10 mM concentration. A precipitate of the test material was observed in the cultures at the end of the exposure, at and above 157.5 µg/mL in the 4(20)-hour exposure in the absence of S9 at and above 78.75 µg/mL in the 4(20)-hour exposure in the presence of S9, and at above 315 µg/mL in the 24 hour continuous exposure group. Haemolysis was observed at and above 315 µg/mL at harvesting in all three exposure groups. Microscopic assessment of the slides prepared from the exposed cultures showed that metaphase cells were present up to 1260 µg/mL in the 4(20)-hour exposure in the presence of metabolic activation and up to 157.5 µg/mL in the 4(20)-hour exposure in the absence of S9. The maximum dose with metaphases present in the 24-hour continuous exposure was 39.38 µg/mL. The test material induced clear evidence of toxicity in all of the exposure groups. - Remarks on result:
- other: all strains/cell types tested
- Conclusions:
- Interpretation of results:
negative with or without metabolic activation
The test material did not induce any toxicologically significant increases in the frequency of cells with aberrations in either of the 4(20)-hour exposure groups in the absence or presence of a liver enzyme metabolising system or following 24 hours continuous exposure. The test material was therefore considered to be non-clastogenic to human lymphocytes in vitro. - Executive summary:
The potential of the test material to induce structural chromosomal aberrations in human lymphocyte cells in vitro was investigated in a study which was conducted under GLP conditions and in accordance with the standardised guideline OECD 473.
During the study duplicate cultures of human lymphocyte cells, treated with test material, were evaluated for chromosome aberrations over at least three dose levels. Vehicle and positive controls were run concurrently. Three treatment conditions were used for the study, as follows: firstly, cultures were exposed for 4 hours with a 20 hour expression time, both in the presence and absence of metabolic activation (S9 mix), secondly cultures were continuously exposed for 24 hours in the absence of metabolic activation. The frequencies of chromosome aberrations in both vehicle and positive controls were within the expected range and verified the sensitivity of the assay and the efficacy of the S9-mix.
The test material did not induce any toxicologically significant increases in the frequency of cells with aberrations in either of the 4(20)-hour exposure groups, in the absence or presence of a liver enzyme metabolising system, or following 24 hours continuous exposure. The test material was therefore considered to be non-clastogenic to human lymphocytes in vitro.
Since the study was conducted with manganese chloride, which represents a more available form of manganese, rather than with the registered substance itself, the study was assigned a reliability score of 2 in line with the criteria of Klimisch (1997). Use of data on manganese dichloride is considered to be suitable and more precautionary since manganese dichloride is highly soluble; findings from the study are therefore considered to represent a worst case scenario for inorganic Mn compounds.
- Endpoint:
- in vitro cytogenicity / chromosome aberration study in mammalian cells
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study conducted on read-across material
- Reason / purpose for cross-reference:
- read-across source
- Species / strain:
- lymphocytes: Human peripheral
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- cytotoxicity
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not specified
- Positive controls validity:
- valid
- Endpoint:
- in vitro cytogenicity / chromosome aberration study in mammalian cells
- Data waiving:
- study scientifically not necessary / other information available
- Justification for data waiving:
- other:
- Endpoint:
- in vitro gene mutation study in mammalian cells
- Remarks:
- Type of genotoxicity: gene mutation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 3 July 2009 to 20 October 2009
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Study conducted in compliance with agreed protocols, with no or minor deviations from standard test guidelines and/or minor methodological deficiencies, which do not affect the quality of the relevant results. The study report was conclusive, done to a valid guideline and the study was conducted under GLP conditions. Since the study was conducted with manganese chloride, which represents a more available form of manganese, rather than with the registered substance itself, the study was assigned a reliability score of 2. Use of data on manganese dichloride is considered to be suitable and more precautionary since manganese dichloride is highly soluble; findings from the study are therefore considered to represent a worst case scenario for inorganic Mn compounds.
- Reason / purpose for cross-reference:
- other: Target
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 476 (In Vitro Mammalian Cell Gene Mutation Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of assay:
- mammalian cell gene mutation assay
- Target gene:
- TK locus
- Species / strain / cell type:
- mouse lymphoma L5178Y cells
- Details on mammalian cell type (if applicable):
- - Periodically checked for Mycoplasma contamination: yes
- Periodically "cleansed" against high spontaneous background: yes - Additional strain / cell type characteristics:
- not applicable
- Metabolic activation:
- with and without
- Metabolic activation system:
- S9 mix
- Test concentrations with justification for top dose:
- Please see table 1 under section Any other information on materials and methods incl. tables for dosing regime
- Vehicle / solvent:
- - Vehicle(s)/solvent(s) used: R0 medium
- Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- ethylmethanesulphonate
- Remarks:
- In the absence of metabolic activation: 400 µg/mL and 150 µg/mL for the 4 hour and 24 hour exposures respectively.
- Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- cyclophosphamide
- Remarks:
- In the presence of activation: 2 µg/mL
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in medium
DURATION
- Exposure duration: 4 or 24 hours
- Generation time : 12 hours
- Selection time (if incubation with a selection agent): 2 days
NUMBER OF REPLICATIONS:Each dose level was performed in duplicate
SELECTION AGENT (mutation assays): 4 µg/mL 5-trifluorothymidine (TFT) selective medium
STAIN : MTT
Plate scoring: Microtitre plates were scored using a magnifying mirror box after 10-14 days incubation. The number of positive wells (wells with colonies) was recorded together with the total number of scorable wells (normally 96 per plate). The numbers of small and large colonies seen in the TFT mutation plates were also recorded. Colonies were scored manually by eye using qualitative judgement. Large colonies were defined as those that covered approximately 1/4 to 3/4 of the surface of the well and were generally no more than one or two cells thick. Generally all colonies less than 25% of the average area of the large colonies were scored as small colonies. 0.025 mL of MTT solution (2.5 mg/mL in PBS) was added to each well of the mutation plates to visualise the mutant colonies. The plates were incubated for two hours.
% Relative Suspension Growth (%RSG), Day 2 Viability (%V), Relative Total Growth (RTG) and Mutation Frequency (MF) were all calculated to assess the mutagenic potential. Please refer to section: Any other information on materials and methods incl. tables under the appropriate headings for full details.
DETERMINATION OF CYTOTOXICITY
- Method: relative total growth - Evaluation criteria:
- EVALUATION OF RESULTS
For a test substance to demonstrate a mutagenic response it must produce a statistically significant increase in the induced mutant frequency over the concurrent vehicle mutant frequency value.
For a response to be considered positive, the induced mutation frequency value must exceed the set Global Evaluation Factor (GEF) value at 126 x 10^-6 for the microwell method. Any test substance dose level that exhibits a mutation frequency value that is greater than the corresponding vehicle control by the GEF is considered positive. If a test substance produces a modest increase in mutant frequency, which only marginally exceeds the GEF value and is not reproducible or part of a dose-related response, then it may be considered to have no toxicological significance. When a test substance induces modest resproducible increases in the mutation frequencies that do not exceed the GEF value, then scientific judgement is applied. If the reproducible responses are significantly dose-related and include increases in the absolute numbers of mutant colonies then they may be considered to be toxicologically significant. - Statistics:
- Small significant increases designated by the UKEMS statistical package were reviewed using the criteria set out above and disregarded at the discretion of the Study Director.
- Species / strain:
- mouse lymphoma L5178Y cells
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- cytotoxicity
- Remarks:
- Test material-induced toxicity was noted at the highest dose level employed in the test.
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Additional information on results:
- TEST-SPECIFIC CONFOUNDING FACTORS
- Precipitation: Precipitate of the test material was observed at and above 10 µg/mL in the 4-hour exposure groups in the absence of metabolic activation and at and above 20 µg/mL in the 4-hour exposure group in the presence of metabolic activation.
RANGE-FINDING/SCREENING STUDIES: All three exposure groups employed in the screening test exhibited a marked reduction in the Relative Suspension Growth (%RSG) of cells treated with the test material when compared to the concurrent vehicle controls. A precipitate of the test material was observed at and above 78.75 µg/mL in the 4-hour exposure group in the absence of metabolic activation, at and above 39.98 µg/mL in the 4-hour exposure group in the presence of metabolic activation, and at and above 19.69 µg/mL in the 24-hour exposure group in the absence of metabolic activation. In the mutagenicity experiments the maximum dose level was limited by test-material-induced toxicity. - Remarks on result:
- other: all strains/cell types tested
- Conclusions:
- Interpretation of results:
negative With and without metabolic activation
The test material did not induce any toxicologically significant increases in the mutant frequency at the TK +/- locus in L5178Y cells and is therefore considered to be non-mutagenic under the conditions of the test. - Executive summary:
The mutagenic potential of the test material was determined in a study which was conducted under GLP conditions and in accordance with the standardised guideline OECD 476.
Based on the results from the preliminary toxicity test, the doses selected for treatment of the initial mutagenesis assay ranged from 2.5 to 120 µg/mL and 20 to 160 µg/mL for the S9 non-activated and activated cultures, respectively. Precipitate of the test material was observed at and above 10 µg/mL in the 4-hour exposure groups in the absence of metabolic activation and at and above 20 µg/mL in the 4-hour exposure group in the presence of metabolic activation. Toxicity in the cloned cultures was observed at doses at 120 and 160 µg/mL without and with S9 activation, respectively.
Based on the results of the preliminary toxicity test, the doses chosen for treatment of the extended treatment assay ranged from 0.31 to 15 µg/mL for non-activated cultures with a 24-hour exposure. Toxicity in the cloned cultures was observed at doses of 10 and 15 µg/mL.
Overall, the test material did not induce any toxicologically significant increases in the mutant frequency at the TK +/- locus in L5178Y cells and is therefore considered to be non-mutagenic under the conditions of the test.
Since the study was conducted with manganese chloride, which represents a more available form of manganese, rather than with the registered substance itself, the study was assigned a reliability score of 2.
Use of data on manganese dichloride is considered to be suitable and more precautionary since manganese dichloride is highly soluble; findings from the study are therefore considered to represent a worst case scenario for inorganic Mn compounds.
- Endpoint:
- in vitro gene mutation study in mammalian cells
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study conducted on read-across material
- Reason / purpose for cross-reference:
- read-across source
- Species / strain:
- mouse lymphoma L5178Y cells
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- cytotoxicity
- Remarks:
- Test material-induced toxicity was noted at the highest dose level employed in the test.
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Endpoint:
- in vitro gene mutation study in mammalian cells
- Data waiving:
- study scientifically not necessary / other information available
- Justification for data waiving:
- other:
Referenceopen allclose all
Table 2: Range finding study – toxicity assay
With (+) or Without (-) S9-mix |
Strain |
Dose (µg/plate) |
||||||||||
0 |
0.15 |
0.5 |
1.5 |
5 |
15 |
50 |
150 |
500 |
1500 |
5000 |
||
- |
TA100 |
75 |
81 |
78 |
96 |
89 |
77 |
85 |
74 |
70 |
86P |
84P |
+ |
TA100 |
77 |
96 |
84 |
85 |
74 |
75 |
91 |
88 |
74 |
70P |
73P |
- |
WP2uvrA- |
25 |
23 |
25 |
23 |
27 |
30 |
23 |
35 |
31 |
22P |
27P |
+ |
WP2uvrA- |
37 |
24 |
27 |
34 |
29 |
25 |
36 |
32 |
38 |
30P |
24P |
P - Precipitate |
||||||||||||
Table 3: Spontaneous Mutation Rates (Concurrent Negative Controls), Experiment 1
Number of Revertants (mean number of colonies per plate) |
||||
Base-pair substitution type |
Frameshift type |
|||
TA100 |
TA1535 |
WP2uvrA- |
TA98 |
TA1537 |
93 |
15 |
22 |
14 |
10 |
96 (95) |
19 (18) |
20 (22) |
16 (17) |
13 (12) |
97 |
21 |
24 |
20 |
13 |
Table 4: Spontaneous Mutation Rates (Concurrent Negative Controls), Experiment 2
Number of Revertants (mean number of colonies per plate) |
||||
Base-pair substitution type |
Frameshift type |
|||
TA100 |
TA1535 |
WP2uvrA- |
TA98 |
TA1537 |
123 |
22 |
33 |
22 |
12 |
123 (118) |
25 (23) |
25 (29) |
25 (24) |
12 (12) |
109 |
21 |
29 |
24 |
13 |
Table 5: Test Results, Experiment 1 – Without Metabolic Activation
Test Period |
From 19 July 2009 |
To 22 July 2009 |
|||
Test Material (µg/plate) |
Number of revertants (mean number of colonies per plate) |
||||
Base-pair substitution type |
Frameshift type |
||||
TA100 |
TA1535 |
WP2uvrA- |
TA98 |
TA1537 |
|
0 |
95 111 (102) 99 8.3# |
16 20 (18) 19 2.1 |
23 25 (23) 20 2.5 |
26 21 (23) 23 2.5 |
15 13 (14) 13 1.2 |
50 |
112 96 (104) 104 8.0 |
16 20 (19) 20 2.3 |
18 25 (22) 23 3.6 |
21 22 (22) 24 1.5 |
14 13 (12) 10 2.1 |
150 |
115 110 (109) 102 6.6 |
21 13 (18) 21 4.6 |
26 15 (20) 19 5.6 |
16 20 (21) 27 5.6 |
12 11 (12) 13 1.0 |
500 |
103 92 (95) 90 7.0 |
18 19 (17) 14 2.6 |
21 23 (25) 30 4.7 |
21 21 (21) 20 0.6 |
15 15 (12) 15 0.0 |
1500 |
110 P 95 P (103) 104P 7.5 |
19P 18P (18) 16P 1.5 |
22 24P (23) 22P 1.2 |
22P 23P (25) 26P 3.2 |
13P 15P (12) 9P 3.1 |
5000 |
88P 117P (105) 111P 15.3 |
18P 21P (19) 18P 1.7 |
26P 21P (24) 24P 2.5 |
25P 23P (25) 26P 1.5 |
9P 12P (12) 16P 3.5 |
Name Concentration No. colonies per plate |
ENNG |
ENG |
ENNG |
4NQO |
9AA |
3 |
5 |
2 |
0.2 |
80 |
|
475 526 (492) 476 29.2 |
99 150 (115) 95 30.7 |
145 145 (145) 145 0.0 |
123 118 (119) 115 4.0 |
345 462 (400) 394 58.8 |
|
ENNG – N-ethyl-N’-nitro-N-nitrosoguanidine 4NQO – 4-Nitroquinoline-1-oxide 9AA – 9-Aminoacridine P – Precipitate # - Standard deviation |
|||||
Table 6: Test Results, Experiment 1 – With Metabolic Activation
Test Period |
From 19 July 2009 |
To 22 July 2009 |
|||
Test Material (µg/plate) |
Number of revertants (mean number of colonies per plate) |
||||
Base-pair substitution type |
Frameshift type |
||||
TA100 |
TA1535 |
WP2uvrA- |
TA98 |
TA1537 |
|
0 |
97 96 (98) 100 8.3# |
12 12 (11) 9 1.7 |
23 29 (28) 32 4.6 |
25 24 (23) 20 2.6 |
14 9 (12) 14 2.9 |
50 |
117 101 (106) 100 9.5 |
11 9 (10) 10 1.0 |
31 25 (25) 19 6.0 |
20 21 (20) 18 1.5 |
12 12 (12) 12 0.0 |
150 |
97 102 (101) 103 3.2 |
10 9 (9) 9 0.6 |
25 23 (25) 27 2.0 |
26 22 (24) 24 2.0 |
15 10 (12) 11 12.6 |
500 |
115 74 (94) 92 20.6 |
13 8 (10) 9 2.6 |
29 19 (23) 21 5.3 |
31 20 (24) 20 6.4 |
16 15 (15) 13 1.5 |
1500 |
90 P 82 P (88) 91P 4.9 |
12P 9P (11) 13P 2.1 |
26P 24P (23) 20P 3.1 |
19P 18P (24) 20P 6.4 |
11P 15P (12) 9P 3.1 |
5000 |
92P 104P (95) 90P 7.6 |
12P 9P (11) 11P 1.5 |
24P 24P (23) 20P 2.3 |
20P 24P (22) 22P 2.0 |
12P 9P (11) 13P 2.1 |
Name Concentration No. colonies per plate |
2AA |
2AA |
2AA |
BP |
2AA |
1 |
2 |
10 |
5 |
2 |
|
2248 2526 (2506) 2743 248.1 |
209 151 (179) 177 29.1 |
172 225 (184) 154 36.9 |
206 184 (197) 202 11.7 |
278 217 (247) 247 30.5 |
|
2AA – 2-Aminoanthracene BP – Benzo(a)pyrene P – Precipitate # - Standard deviation |
|||||
Table 7: Test Results, Experiment 2 – Without Metabolic Activation
Test Period |
From 19 July 2009 |
To 22 July 2009 |
|||
Test Material (µg/plate) |
Number of revertants (mean number of colonies per plate) |
||||
Base-pair substitution type |
Frameshift type |
||||
TA100 |
TA1535 |
WP2uvrA- |
TA98 |
TA1537 |
|
0 |
101 95 (104) 115 10.3# |
20 16 (19) 20 2.3 |
21 24 (23) 25 2.1 |
26 26 (25) 23 1.7 |
11 16 (14) 15 2.6 |
50 |
106 97 (104) 106 5.2 |
21 21 (21) 21 0.0 |
18 26 (24) 29 5.7 |
20 26 (25) 2 9 4.6 |
8 15 (12) 13 3.6 |
150 |
113 107 (111) 114 3.8 |
24 20 (21) 20 2.3 |
22 29 (25) 23 3.8 |
20 19 (22) 27 4.4 |
10 8 (9) 10 1.2 |
500 |
96 104 (102) 106 5.3 |
16 22 (17) 14 4.2 |
23 24 (24) 25 1.0 |
23 25 (26) 30 3.6 |
15 8 (9) 10 1.2 |
1500 |
118P (118) 119P 1.0 117 * |
24P 20P (23) 26P 3.1 |
21P 24P (22) 22P 1.5 |
29P 21P (25) 26P 4.0 |
10P 11P (10) 9P 1.0 |
5000 |
101P 104P (105) 110P 4.6 |
22P 23P (22) 21P 1.0 |
27P 24P (24) 21P 3.0 |
26P 25P (25) 24P 1.0 |
12P 13P (11) 9P 2.1 |
Name Concentration No. colonies per plate |
ENNG |
ENG |
ENNG |
4NQO |
9AA |
3 |
5 |
2 |
0.2 |
80 |
|
295 312 (309) 320 12.8 |
209 222 (212) 206 8.5 |
416 492 (462) 477 40.3 |
246 217 (228) 220 15.9 |
1078 2042 (1426) 1157 535.2 |
|
ENNG – N-ethyl-N’-nitro-N-nitrosoguanidine 4NQO – 4-Nitroquinoline-1-oxide 9AA – 9-Aminoacridine P – Precipitate # - Standard deviation * p≤0.05 |
|||||
Table 8: Test Results, Experiment 2 – With Metabolic Activation
Test Period |
From 19 July 2009 |
To 22 July 2009 |
|||
Test Material (µg/plate) |
Number of revertants (mean number of colonies per plate) |
||||
Base-pair substitution type |
Frameshift type |
||||
TA100 |
TA1535 |
WP2uvrA- |
TA98 |
TA1537 |
|
0 |
108 106 (108) 109 1.5# |
10 9 (11) 13 2.1 |
25 27 (26) 26 1.0 |
22 21 (22) 22 0.6 |
16 16 (15) 12 2.3 |
50 |
93 91 (106) 107 8.7 |
15 9 (12) 13 3.1 |
22 22 (25) 31 5.2 |
21 26 (22) 22 0.6 |
13 15 (15) 16 1.5 |
150 |
98 89 (99) 110 10.5 |
13 8 (10) 13 3.1 |
22 23 (22) 31 0.6 |
19 24 (22) 22 2.5 |
14 14 (12) 7 4.0 |
500 |
91 106 (102) 110 10.0 |
12 14 (12) 9 2.5 |
30 29 (30) 30 0.6 |
26 21 (23) 22 2.6 |
16 14 (14) 12 2.0 |
1500 |
81P 100P (96) 110P 10.0 |
9P 13P (10) 9P 2.3 |
25P 31P (27) 25P 3.5 |
25P 25P (24) 22P 1.7 |
9P 16P (14) 16P 4.0 |
5000 |
90P 84P (92) 102P 9.2 |
11P 10P (10) 8P 1.5 |
26P 23P (25) 27P 2.1 |
24P 21P (22) 22P 1.5 |
12P 15P (12) 10P 2.5 |
Name Concentration No. colonies per plate |
2AA |
2AA |
2AA |
BP |
2AA |
1 |
2 |
10 |
5 |
2 |
|
2474 2427 (2510) 2629 105.7 |
374 332 (332) 291 41.5 |
342 264 (313) 333 42.7 |
261 620 (457) 490 181.8 |
497 494 (498) 504 5.1 |
|
2AA – 2-Aminoanthracene BP – Benzo(a)pyrene P – Precipitate # - Standard deviation |
|||||
The test material was found to cause no visible reduction in growth of the bacterial background lawn at any dose and was therefore tested up to the maximum dose level of 5000 µg/plate A particulate precipitate was at 1500 µg/plate and above. This was considered not to prevent the scoring of revertant colonies. No toxicologically significant increases in the frequency of revertant colonies were recorded for and of the bacterial strains, with any dose of the test material, with or without metabolic activation. In the TA100 revertant colony, a small but statistically significant increase was observed on the 1500 µg/plate in Experiment 2 (increase of less than 1.5 times). However these were within the range specified by the Standard Test Method, this increase proved non-reproducible over two separate experiments. This was concluded to have no biological or toxicological relevance. All of the positive control substances induced marked increases in the frequency of revertant colonies, confirming the activity of the S9-mix and the sensitivity of the bacterial strains.
All vehicle (solvent) controls had frequencies of cells with aberrations within the range expected for normal human lymphocytes. All the positive control materials induced statistically significant increases in the frequency of cells with aberrations indicating the satisfactory performance of test and of the activity of the metabolising system. The test material was found to be toxic to lymphocytes, and did not induce any toxicologically significant increases in the frequency of cells with aberrations, in any of the exposure conditions, using a dose range that included dose levels that induced approximately 50% mitotic inhibition.
Please refer to attached document, Appendix 1 for full tabulated results
Table 2: Results from the preliminary toxicity test
Dose (µg/mL) |
%RSG (-S9) 4-Hour Exposure |
%RSG (+S9) 4-Hour Exposure |
%RSG (-S9) 24-Hour Exposure |
0 |
100 |
100 |
100 |
4.92 |
102 |
89 |
33 |
9.84 |
96 |
100 |
11 |
19.69 |
89 |
89 |
1 |
39.38 |
72 |
75 |
0 |
78.75 |
2 |
57 |
0 |
157.5 |
9 |
1 |
0 |
315 |
1 |
0 |
0 |
630 |
0 |
0 |
0 |
1260 |
0 |
0 |
0 |
Table 3: Summary of results for main experiment, 4 hour exposure
Treatment (µg/mL) |
4-Hours –S9 |
Treatment (µg/mL) |
4-Hours +S9 |
||||
%RSG |
RTG |
MF§ |
%RSG |
RTG |
MF§ |
||
0 |
100 |
1.00 |
81.37 |
0 |
100 |
1.00 |
74.20 |
2.5† |
97 |
|
|
20 |
91 |
1.04 |
64.08 |
5 |
95 |
1.06 |
73.26 |
40 |
68 |
0.86 |
78.58 |
10 |
91 |
0.94 |
96.72 |
60 |
43 |
0.41 |
116.75 |
20 |
101 |
1.24 |
90.28 |
80 |
37 |
0.32 |
96.12 |
40 |
44 |
0.46 |
104.53 |
100 |
32 |
0.22 |
104.65 |
60 |
19 |
0.08 |
128.81 |
120 |
26 |
0.15 |
104.12 |
80 |
17 |
0.13 |
91.23 |
140 |
25 |
0.18 |
100.39 |
120† |
14 |
|
|
160‡ |
13 |
0.04 |
42.87 |
Linear trend |
NS |
Linear trend |
|||||
EMS |
|
|
|
CP |
|
|
|
400 |
71 |
0.62 |
656.51 |
2 |
55 |
0.22 |
1662.80 |
† Not plated for viability or 4-TFT resistance MF§ 5-TFT resistant mutants/106viable cells 2 days after treatment NS Not significant ‡ Treatment excluded from test statistics due to toxicity |
|||||||
Table 4: Summary of results for main experiment, 24 hour exposure
Treatment (µg/mL) |
4-Hours –S9 |
||
%RSG |
RTG |
MF§ |
|
0 |
100 |
1.00 |
103.16 |
0.31 |
97 |
0.99 |
91.33 |
0.63 |
105 |
0.97 |
79.60 |
1.25 |
95 |
1.07 |
50.22 |
2.5 |
76 |
0.81 |
100.92 |
5 |
41 |
0.38 |
173.75* |
7.5 |
14 |
0.11 |
372.63* |
10† |
7 |
|
|
15† |
4 |
|
|
Linear trend |
*** |
||
EMS |
|
|
|
150 |
54 |
0.32 |
1211.25 |
† Not plated for viability or 4-TFT resistance * p<0.05 *** p<0.001 |
|||
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Genetic toxicity in vivo
Description of key information
- In Vivo Micronucleus Assay
Negative (mouse erythrocytes), MnCl2, OECD 474, Streicker (2009)
Link to relevant study records
- Endpoint:
- in vivo mammalian somatic cell study: cytogenicity / erythrocyte micronucleus
- Remarks:
- Type of genotoxicity: chromosome aberration
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 15 April 2009 to 4 September 2009
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Study conducted in compliance with agreed protocols, with no or minor deviations from standard test guidelines and/or minor methodological deficiencies, which do not affect the quality of the relevant results. The study report was conclusive, done to a valid guideline and the study was conducted under GLP conditions. Since the study was conducted with manganese chloride, which represents a more available form of manganese, rather than with the registered substance itself, the study was assigned a reliability score of 2. Use of data on manganese dichloride is considered to be suitable and more precautionary since manganese dichloride is highly soluble; findings from the study are therefore considered to represent a worst case scenario for inorganic Mn compounds.
- Reason / purpose for cross-reference:
- other: Target
- 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
- Species:
- mouse
- Strain:
- B6C3F1
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River Laboratories, Raleigh, NC USA
- Age at study initiation: Approximately 8 weeks
- Weight at study initiation: 18.9-22.2 g
- Assigned to test groups randomly: yes under following basis: Animals were stratified by body weight and assigned to a dose group such that mean animal weights across dose groups were approximately equal
- Housing: Animals were housed individually housed in polycarbonate cages with absorbent hardwood bedding (Betachip, Northeastern products Corp., Warrensbury, NY USA). Animals were transferred to clean cages weekly
- Diet : Purina Certified Rodent Chow 5002 (Ralston Purina, St. Louis, MO, USA) available ad libitum
- Water : Reverse-osmosis water was provided ad libitum using plastic water bottles with stainless steel sipper tubes. Fresh water was supplied weekly.
- Acclimation period: All animals were examined by a veterinarian or other appropriate persons during the acclimation period to assess the health status. All animals were re-examined at the end of the acclimation period.
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18-26 °C
- Humidity (%): 30-70 %
- Photoperiod (hrs dark / hrs light): 12 hour light/12 hour dark - Route of administration:
- oral: gavage
- Vehicle:
- - Vehicle used: physiol. saline
- Amount of vehicle : 10 mL/kg bw - Details on exposure:
- PREPARATION OF DOSING SOLUTIONS:
The dosing solutions were made from manganese chloride tetrahydrate and concentrations calculated as manganese (Mn2+). The manganese chloride dosing solutions were freshly prepared in 0.9 % saline on each day of treatment.
DOSE ADMINISTRATION
The animals were dosed on days 1 and 2 via oral gavage in a single dose using a stainless steel or disposable gavage needle. Each dose was administered 24 ± 0.5 hours after the first dose.
JUSTIFICATION OF DOSING ROUTE
An appropriate route of human exposure is oral. - Duration of treatment / exposure:
- Single oral exposures
- Frequency of treatment:
- Animals were dosed twice within 24 hours
- Post exposure period:
- 46 hours
- Remarks:
- Doses / Concentrations:
25 mg/kg
Basis:
nominal conc. - Remarks:
- Doses / Concentrations:
50 mg/kg
Basis:
nominal conc. - Remarks:
- Doses / Concentrations:
100 mg/kg
Basis:
nominal conc. - Remarks:
- Doses / Concentrations:
200 mg/kg
Basis:
nominal conc. - No. of animals per sex per dose:
- 5 animals were included in each dosing group
- Control animals:
- yes, concurrent vehicle
- Positive control(s):
- - Positive control : cyclophosphamide
- Route of administration: oral gavage
- Doses / concentrations: 25 mg/kg/day in 0.9 % saline - Tissues and cell types examined:
- Blood was collected from each mouse for analysis. 350 µL of MicroFlowPLUS kit Solution B (anticoagulant) was aliquoted into an appropriately labelled sterile microcentrifuge tube for each animal. One day prior to collection of blood, 2 mL of MicroFlowPLUS Solution A (fixative) was aliquoted into two appropriately labelled 15 mL polypropylene conical tubes for each study animal. Immediately prior to use, each tube containing Solution B was shaken immediately before bleeding each animal to coat the inside of the tube. Following anaesthesia by isofluorane, blood was collected from the retro-orbital sinus by heparinized hemocrit. 120 (± 20) µL of blood was dispensed into the corresponding microcentrifuge tube containing Solution B and mixed by inverting several times. The stabilised blood samples were maintained at room temperature and fixed within 5 hours of collection.
- Details of tissue and slide preparation:
- CRITERIA FOR DOSE SELECTION:
Results from a range finding study.
METHOD OF ANALYSIS: Blood samples were fixed by 180 µL of each blood-Solution B sample was withdrawn from the tube. All tubes of fixed cells were quickly transferred back to the freezer and stored at -75 ± 10 °C for at least 24 hours prior to processing for flow cytometry analysis of reticulocytes. Flow cytometry of MN was performed using MicroFlowPLUS (Mouse) kit reagents (Litron Laboratories, Rochester NY) according to the kit’s instructional manual with minimal modification, 1) 1 mL of fixed cells for each experimental sample was transferred to a tube containing 12 mL of Solution C and washed in preparation for labelling and 2) volumes of labelling solution I, labelling solution II and DNA stain were adjusted as appropriate each day to minimise the use of excess reagents. The MicroFlowPLUS method utilises CD71 and CD61 antibodies as well as a fixed malaria biostandard that contains DNA in the same size range as MN to properly configure the flow cytometer to exclude platelets (CD61+) and only count micronucleus events in erythrocytes. For each peripheral blood sample, 20,000 immature (CD71+) reticulocytes were analysed to determine the frequency of both MN-RET and micronucleated mature (CD41-) normochromatic erythrocytes (NCE). A BD FACSCalibur™, a four-colour, dual laser benchtop system, was used for MN-RET and MN-NCE analysis. - Evaluation criteria:
- - Validity criteria
For a negative result, the highest test substance concentration evaluated for MN induction must, unless precluded by the use of the limit dose of 2000 mg/kg, induce bone marrow or animal toxicity or be a dose only slightly lower than that which would be expected to induce mortality.
- Evaluation of results
Positive control:
The reference control (positive control) cyclophosphamide, is expected to induce an increase in the frequency of MN-RET at p < 0.05.
Test substance:
A test substance is considered to induce a positive response if a dose-related increase in micronucleated polychromatic erythrocytes is observed and one or more doses are statistically elevated relative to the vehicle control.
A test substance is judged negative if no statistically significant increase in micronucleated polychromatic erythrocytes above the concurrent vehicle control values and no evidence of dose response was observed at any sampling time. - Statistics:
- Statistical analysis was conducted on the frequency of MN-RET, MN-NCE and RET. Using individual animal data, the analysis involved the use of the Shapiro-Wilk test with a confidence level of 95 % to determine the normality of the MN-RET data in the vehicle control group.
Normally distributed MN-RET frequency data were then analysed for linearity and variance between treatment groups using linear regression and one-way ANOVA analyses, respectively. The Dunnett multiple comparison test was used to determine if a treatment groups was significantly different (p < 0.05) from vehicle controls. A one-tailed independent t-test was used to verify a positive response to the control compound, cyclophosphamide. - Sex:
- female
- Genotoxicity:
- negative
- Toxicity:
- no effects
- Remarks:
- Animal number 23 which showed hunched posture at the 1 hour post dose observation on Day 1 of the study. All other animals were found to be normal throughout the study
- Vehicle controls validity:
- valid
- Negative controls validity:
- not examined
- Positive controls validity:
- valid
- Additional information on results:
- RESULTS OF RANGE-FINDING STUDY
- Dose range: 125-1000 mg/kg bw
RESULTS OF DEFINITIVE STUDY
- Micronucleus Assay Results (incl. statistical analysis): The percent of micronucleated cells among 20,000 RET and ≥900,000 NCE from the peripheral blood of B6C3F1 mice treated with the vehicle, reference chemical, and test material as analysed by flow cytometry. Based on a one-way ANOVA (p = 0.415) test and Dunnett pair wise comparison of each dose group against the concurrent control, the group %MN-RET means comparison of each dose group against the concurrent control, the group %MN-RET means were not significantly increased by treatment with manganese at dose levels 25, 50, 100 or 200 mg/kg bw. No dose response was indicated by linear regression analysis (p = 0.509). There was also no impact on treatment with manganese on %MN-NCE (p = 0.3939) or %RET (p = 0.7375). Treatment with 25 mg/kg/day of the reference control, cyclophosphamide, induced a statistically significant increase in MN-RET (p < 0.0001) as well as MN-NCE (p = 0.0012) and resulted in a 40.6% decrease in %RET.
- Clinical signs of toxicity in test animals: Cage side observations were conducted prior to dosing and at 1 and 4 hours post-dose each day. All animals in the definitive study were considered normal throughout with the exception of animal number 23 which showed hunched posture at the 1 hour post dose observation on Day 1 of the study. - Conclusions:
- Interpretation of results: negative
Manganese administered twice at 24 ± 0.5 hour intervals to female B6C3F1 mice by oral gavage at 25, 50, 100 or 200 mg/kg bw did not induce chromosomal damage. - Executive summary:
The potential of the test material (manganese chloride) to induce chromosomal damage in vivo was investigated in a study which was conducted under GLP conditions and in accordance with the standardised guideline OECD 476.
The assay was performed in two phases. The first phase (dose range-finding phase), designed to assess the toxicity of the test material and set dose levels for the definitive study consisted of a toxicity study followed supplemental toxicity study. The second phase was the definitive micronucleus study.
In the range finding phase, male and female mice were treated with Mn2 + at 1000, 500, 250 and 125 mg/kg bw. However, based on the high levels of toxicity observed on the first day of treatment, the study was discontinued and restarted using doses of 175, 200 and 225 mg/kg bw. At the 1-hour post-treatment observation, the female mice in the 225 mg/kg group exhibited a hunched posture, decreased movement and piloerection. These mice were immediately euthanised. All other animals were considered normal throughout the study. Therefore, based on the range-finding study, the selected doses for the definitive study were 25, 50, 100 and 200 mg/kg manganese. Female mice only were dosed in the definitive test.
In the definitive micronucleus study there were no significant increases in micronucleated polychromatic erythrocytes in test material-treated groups relative to the respective vehicle control groups was observed in the female mice at any treatment level.
The results of the assay indicate that under the conditions of the study, administration of the test material at doses up to 200 mg/kg bw did not induce a significant increase in micronucleated polychromatic erythrocytes in female mice. Therefore, the test material was considered to be negative in this mouse micronucleus assay.
Since the study was conducted with manganese chloride, which represents a more available form of manganese, rather than with the registered substance itself, the study was assigned a reliability score of 2.
Use of data on manganese dichloride is considered to be suitable and more precautionary since manganese dichloride is highly soluble; findings from the study are therefore considered to represent a worst case scenario for inorganic Mn compounds.
- Endpoint:
- in vivo mammalian somatic cell study: cytogenicity / erythrocyte micronucleus
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study conducted on read-across material
- Reason / purpose for cross-reference:
- read-across source
- Sex:
- female
- Genotoxicity:
- negative
- Toxicity:
- no effects
- Remarks:
- Animal number 23 which showed hunched posture at the 1 hour post dose observation on Day 1 of the study. All other animals were found to be normal throughout the study
- Vehicle controls validity:
- valid
- Negative controls validity:
- not examined
- Positive controls validity:
- valid
- Endpoint:
- genetic toxicity in vivo
- Data waiving:
- study scientifically not necessary / other information available
- Justification for data waiving:
- other:
Referenceopen allclose all
Range finding study:
Male and female mice were treated with Mn2 + at 1000, 500, 250 and 125 mg/kg bw. A few minutes after dosing, the fist animal (male) in the 1000 mg/kg treatment group exhibited seizures and convulsions. This animal was euthanised and no further mice were treated in this dose group. At the 1-hour post-treatment observation period, male and female mice in the 500 mg/kg treatment groups exhibited lethargy, unco-ordinated movement, and abnormal breathing. These mice were euthanised after the 1-hour observation period. Also at the 1-hour post-treatment observation period, the mice in the 250 mg/kg treatment group exhibited hunched posture, decreased movement and piloerection. At the 4-hour post-treatment observation, the mice in the 250 mg/kg group continued to exhibit a hunched posture, decreased movement and lethargy, with one animal found dead. These mice were immediately euthanised. The control mice and the mice in the 125 mg/kg treatment group were normal throughout both days of treatment.
Based on the results of the first day of treatment, the study was discontinued and restarted using treatment levels of 175, 200 and 225 mg/kg bw. At the 1-hour post-treatment observation, the female mice in the 225 mg/kg group exhibited a hunched posture, decreased movement and piloerection. These mice were immediately euthanised. All other animals were considered normal throughout the study.
Based on the range-finding study, the selected doses for the definitive study were 25, 50, 100 and 200 mg/kg manganese. Female mice were dosed chosen for the definitive test.
Definitive test:
Table 2: Frequency of RET, MN-RET and MN-NCE in peripheral blood reticulocytes of female B6C3F1 mice administered manganese and cyclophosphamide by oral gavage
Dose (mg/kg) |
% MN-RET |
SEM |
% MN-NCE |
SEM |
% RET |
SEM |
Vehicle |
||||||
0 |
0.202 |
0.006 |
0.118 |
0.001 |
1.725 |
0.172 |
Manganese |
||||||
25 50 100 200 |
0.173 0.202 0.197 0.180 |
0.012 0.017 0.019 0.008 |
0.120 0.113 0.122 0.112 |
0.007 0.005 0.003 0.004 |
1.527 1.565 1.697 1.675 |
0.087 0.191 0.067 0.105 |
Cyclophosphamide |
||||||
25 |
1.057 |
0.020 |
0.144 |
0.004 |
1.025 |
0.077 |
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Additional information
Use of data on manganese dichloride is considered to be suitable and more precautionary since manganese dichloride is highly soluble; the compound therefore represents a more bioavailable form of manganese. The below data are therefore considered to represent the worst case scenario in terms of exposure to manganese.
IN VITRO
- Bacterial Reverse Mutation Assay (e.g. Ames test)
The mutagenic potential of the test material, manganese dichloride, was investigated in a study which was conducted under GLP conditions and in accordance with the standardised guidelines OECD 471 and EU Method B.13/14.
During the study test strains of Salmonella typhimurium (TA98, TA100, TA1535 and TA1537) and a tester strain of Escherichia coli (WP2uvrA) were exposed to the test material both in the presence and the absence of metabolic activation. Vehicle and positive controls were run concurrently. Two separate experiments were conducted, in the first five concentrations of test material (50, 150, 500, 1500 and 5000 µg/plate) were assayed in triplicate against each tester strain, using the direct plate incorporation method. In the second experiment the test materials and vehicle control were dosed using a pre-incubation method.
The test material was found to cause no visible reduction in growth of the bacterial background lawn at any dose and was therefore tested up to the maximum dose level of 5000 µg/plate A particulate precipitate was at 1500 µg/plate and above. This was considered not to prevent the scoring of revertant colonies. No toxicologically significant increases in the frequency of revertant colonies were recorded for and of the bacterial strains, with any dose of the test material, with or without metabolic activation. In the TA100 revertant colony, a small but statistically significant increase was observed on the 1500 µg/plate in Experiment 2 (increase of less than 1.5 times). However the increase was within the range specified by the Standard Test Method, and proved non-reproducible over two separate experiments. This was concluded to have no biological or toxicological relevance. All of the positive control substances induced marked increases in the frequency of revertant colonies, confirming the activity of the S9-mix and the sensitivity of the bacterial strains.
Therefore, under the conditions of the study the test material was concluded to be non-mutagenic.
An Ames test, has also been conducted with silicomanganese slag using the Salmonella typhimurium tester strains TA98 and TA100. The bacterial tester strains were exposed to the test material both in the presence and absence of metabolic activation.
Under the conditions of the study the test material was concluded to be non-mutagenic.
Use of data generated with silicomanganese slag, to address information requirements of ferromanganese slag, is considered to be justified on the basis of the similar compositions of the two substances. Both substances are UVCB substances, containing metallic oxides; each substance is obtained as a by-product in the manufacture of SiMn and FeMn alloy, respectively. The finding from this study supports findings from the study with manganese chloride and further substantiates the argument for not repeating the studies with the registered substance itself.
- In Vitro Mammalian Chromosome Aberration Test
The potential of the test material, manganese dichloride, to induce structural chromosomal aberrations in human lymphocyte cells in vitro was investigated in a study which was conducted under GLP conditions and in accordance with the standardised guideline OECD 473.
During the study duplicate cultures of human lymphocyte cells, treated with test material, were evaluated for chromosome aberrations over at least three dose levels. Vehicle and positive controls were run concurrently. Three treatment conditions were used for the study, as follows: firstly, cultures were exposed for 4 hours with a 20 hour expression time, both in the presence and absence of metabolic activation (S9 mix), secondly cultures were continuously exposed for 24 hours in the absence of metabolic activation. The frequencies of chromosome aberrations in both vehicle and positive controls were within the expected range and verified the sensitivity of the assay and the efficacy of the S9-mix.
The test material did not induce any toxicologically significant increases in the frequency of cells with aberrations in either of the 4(20)-hour exposure groups, in the absence or presence of a liver enzyme metabolising system, or following 24 hours continuous exposure. The test material was therefore considered to be non-clastogenic to human lymphocytes in vitro.
- In Vitro Mammalian Cell Gene Mutation
The mutagenic potential of the test material, manganese dichloride, was determined in a study which was conducted under GLP conditions and in accordance with the standardised guideline OECD 476.
Based on the results from the preliminary toxicity test, the doses selected for treatment of the initial mutagenesis assay ranged from 2.5 to 120 µg/mL and 20 to 160 µg/mL for the S9 non-activated and activated cultures, respectively. Precipitate of the test material was observed at and above 10 µg/mL in the 4-hour exposure groups in the absence of metabolic activation and at and above 20 µg/mL in the 4-hour exposure group in the presence of metabolic activation. Toxicity in the cloned cultures was observed at doses at 120 and 160 µg/mL without and with S9 activation, respectively.
Based on the results of the preliminary toxicity test, the doses chosen for treatment of the extended treatment assay ranged from 0.31 to 15 µg/mL for non-activated cultures with a 24-hour exposure. Toxicity in the cloned cultures was observed at doses of 10 and 15 µg/mL.
Overall, the test material did not induce any toxicologically significant increases in the mutant frequency at the TK +/- locus in L5178Y cells and is therefore considered to be non-mutagenic under the conditions of the test.
IN VIVO
- In Vivo Micronucleus Assay
The potential of the test material, manganese dichloride, to induce chromosomal damage in vivo was investigated in a study which was conducted under GLP conditions and in accordance with the standardised guideline OECD 476.
The assay was performed in two phases. The first phase (dose range-finding phase), designed to assess the toxicity of the test material and set dose levels for the definitive study consisted of a toxicity study followed supplemental toxicity study. The second phase was the definitive micronucleus study.
In the range finding phase, male and female mice were treated with Mn2 +at 1000, 500, 250 and 125 mg/kg bw. However, based on the high levels of toxicity observed on the first day of treatment, the study was discontinued and restarted using doses of 175, 200 and 225 mg/kg bw. At the 1-hour post-treatment observation, the female mice in the 225 mg/kg group exhibited a hunched posture, decreased movement and piloerection. These mice were immediately euthanised. All other animals were considered normal throughout the study. Therefore, based on the range-finding study, the selected doses for the definitive study were 25, 50, 100 and 200 mg/kg manganese. Female mice only were dosed in the definitive test.
In the definitive micronucleus study there were no significant increases in micronucleated polychromatic erythrocytes in test material-treated groups relative to the respective vehicle control groups was observed in the female mice at any treatment level.
The results of the assay indicate that under the conditions of the study, a administration of the test material at doses up to 200 mg/kg bw did not induce a significant increase in micronucleated polychromatic erythrocytes in female mice. Therefore, the test material was considered to be negative in this mouse micronucleus assay.
All studies with manganese dichloride were conducted under GLP conditions and in accordance with standardised guidelines. Since the studies were conducted on a more bioavailable form of manganese, rather than on the registration substance itself, they have been assigned a reliability score of 2 in line with the criteria of Klimisch (1997). Use of data on manganese dichloride is considered to be suitable and more precautionary since manganese dichloride is highly soluble; findings from these studies are therefore considered to represent a worst case scenario for inorganic Mn compounds.
Justification for selection of genetic toxicity endpoint
Multiple studies have been provided to address the different
endpoint of genetic toxicity, each addressing different types of genetic
toxicity. Since all the studies showed negative results, a single study
could not be selected as key over the others.
In accordance with Annex XI of REACH, Section 1.1 (use of existing
data), a further study is not required. A comprehensive literature
review, which is attached to this endpoint summary (Jenkinson P (2009),
Manganese and its inorganic compounds: 2. Genotoxicity Aspects), showed
no evidence of genetic toxicity for inorganic managnese. To support
this, in-vitro and in-vivo genetic toxicity studies conducted on a more
bioavailable substance (manganese chloride) were negative; these studies
are therefore representative of a worst case following exposure to
inorganic manganese.
Justification for classification or non-classification
In accordance with the criteria for classification as defined in Annex I, Regulation (EC) No. 1272/2008, the substance does not require classification with respect to mutagenicity.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
