Isodecyl diphenyl phosphate

Genetic toxicity: in vitro

Administrative data

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:

28 February 2006 - 30 March 2006

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: Test was conducted according to OECD Test Guideline No. 473, under GLP Standards, and QA.

Cross-reference

Reason / purpose for cross-reference:

reference to same study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2006

Report date:

2006

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

OECD Guideline 473 (In Vitro Mammalian Chromosome Aberration Test)

Deviations:

no

Principles of method if other than guideline:

Not applicable

GLP compliance:

yes

Remarks:

Statement of Compliance

Type of assay:

in vitro mammalian chromosome aberration test

Test material

Test material information

Constituent 1

Reference substance name:

Isodecyl diphenyl phosphate

EC Number:

249-828-6

EC Name:

Isodecyl diphenyl phosphate

Cas Number:

29761-21-5

Molecular formula:

C22H31O4P

IUPAC Name:

isodecyl diphenyl phosphate

Details on test material:

- Name of test material (as cited in study report): Isodecyl diphenyl phosphate
- Physical state: liquid
- Analytical purity: confidential
- Composition of test material, percentage of components: confidential
- Lot/batch No.: confidential
- Stability under test conditions: stable
- Storage condition of test material: Room temperature, stored in the dark

Method

Target gene:

Not relevant

Species / strain

Species / strain / cell type:

Chinese hamster Ovary (CHO)

Details on mammalian cell type (if applicable):

- Type and identity of media: Complete medium (McCoy's 5A medium)
- Properly maintained: yes
- Periodically checked for Mycoplasma contamination: yes
- Periodically checked for karyotype stability: yes

Additional strain / cell type characteristics:

not applicable

Metabolic activation:

with and without

Metabolic activation system:

Aroclor 1254-induced rat liver S9

Test concentrations with justification for top dose:

- Preliminary Toxicity Test: 50, 350, 750, 1000, 1500, 2000, 2500, 3000, and 3905 ug/ml.
- Concurrent Toxicity Test: 15, 30.5, 61, 488, 1952.5 , 3905 ug/ml.
- Chromosome Aberration Assay: 30.5, 61, and 3905 ug/ml.

Vehicle / solvent:

- Vehicle(s)/solvent(s) used: Dimethyl sulfoxide (DMSO)
- Justification for choice of solvent/vehicle: DMSO was the solvent of choice based on the solubility of the test article and compatibility with the target cells. The test article was soluble in DMSO at a concentration of approximately 500 mg/ml, the maximum concentration tested for solubility.

Controls

Untreated negative controls:

no

Negative solvent / vehicle controls:

yes

Remarks:

DMSO

True negative controls:

no

Positive controls:

yes

Positive control substance:

other: Without S9 mix: Mitomycin C (direct-acting mutagen); with S9 mix: Cyclophosphamide (promutagen)

Details on test system and experimental conditions:

METHOD OF APPLICATION: in medium

DURATION
- Exposure duration: with S9-mix: 4 hours; without S9-mix: 4 hours or 20 hours continuous exposure
- Fixation time (start of exposure up to fixation or harvest of cells): approx. 20 hours

SPINDLE INHIBITOR (cytogenetic assays): Colcemid, 0.1 μg/ml medium, last 2 hours of incubation
STAIN (for cytogenetic assays): Giemsa solution, 5 %

NUMBER OF REPLICATIONS: duplicate cultures for each treatment

NUMBER OF CELLS EVALUATED: 100 metaphase chromosome spreads from each culture

DETERMINATION OF CYTOTOXICITY
- Method: mitotic index

OTHER EXAMINATIONS:
- Determination of polyploidy: yes
- Determination of endoreplication: yes

OTHER: A preliminary toxicity assay was performed for the purpose of selecting dose levels for the chromosome aberration assay and consisted of an evaluation of test article effect on cell growth. The osmolality of the solvent and of the highest and lowest concentration of dosing solution in the treatment medium was measured. The pH of the highest concentration of dosing solution in the treatment medium was measured. The presence of test article precipitate was assessed using the unaided eye. Cell viability was determined. The cell counts and percent viability were used to determine cell growth inhibition relative to the solvent control.

Evaluation criteria:

The test article was considered to induce a positive response when the percentage of cells with aberrations is increased in a dose-responsive manner with one or more concentrations being statistically significant (p ≤ 0.05). However, values that are statistically significant but do not exceed the range of historic solvent controls may be judged as not biologically significant. Test articles not demonstrating a statistically significant increase in aberrations will be concluded to be negative.

Statistics:

Statistical analysis of the percent aberrant cells was performed using the Fisher's exact test. In the event of a positive Fisher's exact test at any test article dose level, the Cochran-Armitage test was used to measure dose-responsiveness.

Results and discussion

Test results

Species / strain:

Chinese hamster Ovary (CHO)

Metabolic activation:

with and without

Genotoxicity:

negative

Cytotoxicity / choice of top concentrations:

no cytotoxicity

Vehicle controls validity:

valid

Untreated negative controls validity:

not applicable

Positive controls validity:

valid

Additional information on results:

RANGE-FINDING/SCREENING STUDIES: In the preliminary toxicity assay, the maximum dose tested was 3905 µg/ml (10 mM). The test article was soluble in DMSO at all 9 dose levels (50, 350, 750, 1000, 1500, 2000, 2500, 3000, and 3905 ug/ml) tested. Visible precipitate was observed in treatment medium at all dose levels tested at the beginning of the treatment period. At the conclusion of the treatment period, visible precipitate was observed in treatment medium at dose levels ≥ 350 µg/ml, and dose level 50 µg/ml was soluble in treatment medium.

COMPARISON WITH HISTORICAL CONTROL DATA: The number of cells with chromosome aberrations found in the solvent control cultures was within the laboratory historical control data range. The number of polyploid cells and cells with endoreduplicated chromosomes in the solvent control cultures was within the laboratory historical control data range. The percentage of cells with numerical aberrations observed in the non-activated 20-hour exposure group (4.0%) was within the historical solvent control range of 0.0% to 7.5%.

ADDITIONAL INFORMATION ON CYTOTOXICITY: Selection of dose levels for the chromosome aberration assay was based upon a dose-responsive increase in cell growth (cell growth inhibition) relative to the solvent control. Substantial toxicity (i.e., at least 50% cell growth inhibition, relative to the solvent control) was not observed at any dose level in all 3 exposure groups. Based on these findings, the doses chosen for the chromosome aberration assay ranged from 15 to 3905 µg/ml for all 3 exposure groups.

Remarks on result:

other: all strains/cell types tested

Remarks:

Migrated from field 'Test system'.

Applicant's summary and conclusion

Conclusions:

Interpretation of results:
negative with metabolic activation
negative without metabolic activation

The percentage of cells with structural or numerical aberrations in the non-activated and the S9-activated 4-hour exposure groups was not significantly increased above that of the solvent control at any dose level. The percentage of cells with structural aberrations in the non-activated 20-hour exposure group was not significantly increased above that of the solvent control at any dose level. The percentage of cells with numerical aberrations in the test article-treated group was significantly increased above that of the solvent control at 3905 µg/ml (p ≤ 0.05, Fisher's exact test). The Cochran-Armitage test was negative for a dose response (p>0.05). However, the percentage of cells with numerical aberrations in the test article-treated group (4.0%) was within the historical solvent control range of 0.0% to 7.5%. Therefore, it is not considered to be biologically significant. Based on the findings of this study, Isodecyl diphenyl phosphate was concluded to be negative for the induction of structural and numerical chromosome aberrations in CHO cells in both the non-activated and the S9-activated test systems.

Executive summary:

The test article, Isodecyl diphenyl phosphate, was tested in the chromosome aberration assay using Chinese hamster ovary (CHO) cells in both the absence and presence of an Aroclor-induced S9 activation system. The test was performed according to OECD Guideline 473. A preliminary toxicity test was performed to establish the dose range for the chromosome aberration assay. The chromosome aberration assay was used to evaluate the clastogenic potential of the test article. DMSO was the solvent of choice based on the solubility of the test article and compatibility with the target cells. The test article was soluble in DMSO at a concentration of approximately 500 mg/ml, the maximum concentration tested for solubility. In the preliminary toxicity assay, the maximum dose tested was 3905 µg/ml (10 mM). The test article was soluble in DMSO at all 9 dose levels (50, 350, 750, 1000, 1500, 2000, 2500, 3000, and 3905 ug/ml) tested. Visible precipitate was observed in treatment medium at all dose levels tested at the beginning of the treatment period. At the conclusion of the treatment period, visible precipitate was observed in treatment medium at dose levels ≥ 350 µg/ml, and dose level 50 µg/ml was soluble in treatment medium. Selection of dose levels for the chromosome aberration assay was based upon a dose-responsive increase in cell growth (cell growth inhibition) relative to the solvent control. Substantial toxicity (i.e., at least 50% cell growth inhibition, relative to the solvent control) was not observed at any dose level in all 3 exposure groups. Based on these findings, the doses chosen for the chromosome aberration assay ranged from 15 to 3905 µg/ml for all 3 exposure groups. In the chromosome aberration assay, the cells were treated for 4 and 20 hours in the non-activated test system, and for 4 hours in the S9-activated test system. All cells were harvested 20 hours after treatment initiation. The test article was soluble in DMSO at all dose levels tested. Visible precipitate was observed in treatment medium at dose levels ≥ 61 µg/ml, and dose levels ≤ 30.5 µg/ml were soluble in treatment medium at the beginning and conclusion of the treatment period. The top dose (3905 ug/ml) selected for microscopic analysis was based on dose dependent increase in toxicity observed consistently in the preliminary toxicity and the definitive assays. The mid-dose (61 ug/ml) was selected based on the lowest precipitating dose. The low dose (30.5 ug/ml) was the highest soluble dose. The percentage of cells with structural or numerical aberrations in the non-activated and the S9-activated 4-hour exposure groups was not significantly increased above that of the solvent control at any dose level. The percentage of cells with structural aberrations in the non-activated 20-hour exposure group was not significantly increased above that of the solvent control at any dose level. The percentage of cells with numerical aberrations in the test article-treated group was significantly increased above that of the solvent control at 3905 µg/ml (p ≤ 0.05, Fisher's exact test). The Cochran-Armitage test was negative for a dose response (p>0.05). However, the percentage of cells with numerical aberrations in the test article-treated group (4.0%) was within the historical solvent control range of 0.0% to 7.5%. Therefore, it is not considered to be biologically significant. Based on the findings of this study, Isodecyl diphenyl phosphate was concluded to be negative for the induction of structural and numerical chromosome aberrations in CHO cells in both the non-activated and the S9-activated test systems.