Petroleum kerosene fraction, co-processed with renewable hydrocarbons of plant and/or animal origin

Genetic toxicity: in vitro

Administrative data

Endpoint:

in vitro cytogenicity / chromosome aberration study in mammalian cells

Remarks:

Type of genotoxicity: DNA damage and/or repair

Type of information:

read-across from supporting substance (structural analogue or surrogate)

Adequacy of study:

key study

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: This study is classified as reliable without restrictions because it was carried out in a method equivalent/similar to OECD TG 479.

Justification for type of information:

Read across justification included in Section 13

Cross-reference

Reason / purpose for cross-reference:

read-across source

Reference

Endpoint:

in vitro cytogenicity / chromosome aberration study in mammalian cells

Remarks:

Type of genotoxicity: DNA damage and/or repair

Type of information:

read-across from supporting substance (structural analogue or surrogate)

Adequacy of study:

key study

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: This study is classified as reliable without restrictions because it was carried out in a method equivalent/similar to OECD TG 479.

Justification for type of information:

Read across justification included in Section 13

Reason / purpose for cross-reference:

read-across: supporting information

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 479 (Genetic Toxicology: In Vitro Sister Chromatid Exchange Assay in Mammalian Cells)

GLP compliance:

yes

Type of assay:

sister chromatid exchange assay in mammalian cells

Species / strain / cell type:

Chinese hamster Ovary (CHO)

Details on mammalian cell type (if applicable):

- Type and identity of media: Ham’s F-12 or McCoy’s 5A medium supplemented with 10% foetal bovine serum (FBS)
- Properly maintained: no data
- Periodically checked for Mycoplasma contamination: no data
- Periodically checked for karyotype stability: no data
- Periodically "cleansed" against high spontaneous background: no data

Metabolic activation:

with and without

Metabolic activation system:

S9

Test concentrations with justification for top dose:

Without metabolic activation: 0.007, 0.013, 0.025, and 0.05 µl/ml
With metabolic activation: 0.05, 0.1, 0.2, and 0.4 µl/ml

Vehicle / solvent:

- Vehicle(s)/solvent(s) used: acetone
- Justification for choice of solvent/vehicle: None reported

Untreated negative controls:

yes

Negative solvent / vehicle controls:

yes

Positive controls:

yes

Positive control substance:

other: without activation: triethylenemelamine; with activation: cyclophosphamide

Details on test system and experimental conditions:

METHOD OF APPLICATION: in medium

DURATION
- Preincubation period: 16 to 24 hours
- Exposure duration: Without activation: 25 hours; with activation: 2 hours


NUMBER OF REPLICATIONS: Two


NUMBER OF CELLS EVALUATED:Twenty-five cells from each replicate flask


DETERMINATION OF CYTOTOXICITY
- Method: mitotic index; relative total growth

Evaluation criteria:

The test material was considered positive if it induced a doubling in SCE frequency over the solvent control at a minimum of three consecutive dose levels or if a dose responsive and statistically significant increase was observed over a minimum of three dose levels.

Statistics:

Student's t-test

Species / strain:

Chinese hamster Ovary (CHO)

Metabolic activation:

with and without

Genotoxicity:

negative

Vehicle controls validity:

valid

Untreated negative controls validity:

valid

Positive controls validity:

valid

Additional information on results:

RANGE-FINDING/SCREENING STUDIES: Preliminary studies tested for the cytotoxicity of the test compound in acetone. In the absence of metabolic activation, concentrations greater than 0.1 µl/ml inhibited the relative growth and mitotic indices. In the presence of metabolic activation, a concentration of 1 µl/ml was needed to inhibit the relative growth by 50% or more.

Remarks on result:

other: other: Chinese Hamster Ovary cells

Remarks:

Migrated from field 'Test system'.

The test material was soluble at all concentrations tested. The study in both the presence and absence of S9 was repeated since there was a poor metaphase cell yield. Only the results of the second study with and without S9 are summarized in the following table.

Replicate flask	SCEs/ chromosome	Flask mean SCEs/cell	Group mean SCEs/cell
Assay in absence of exogenous activation
		(±SD)	(±SD)
Untreated cells
A	0.42	8.4±3.16
B	0.42	8.28±2.57	8.34±2.85
Acetone
A	0.48	9.44±3
B	0.45	8.96±2.35	9.20±2.68
API 81-07 0.007 µl/ml
A	0.44	8.80±2.87
B	0.43	8.68±2.54	8.74±2.69
API 81-07 0.013 µl/ml
A	0.47	9.4±2.96
B	0.42	8.32±2.58	8.86±2.80
API 81-07 0.025 µl/ml
A	0.47	9.36±2.96
B	0.48	9.64±3.12	9.50±3.01
API 81-07 0.05 µl/ml
A	NE (a)
B	NE
TEM
A	1.53	30.6±6.81
B	1.75	34.92±7.60	32.76±7.47**
Assay in presence of exogenous activation
Untreated cells
A	0.5	10.16±2.98
B	0.55	11.04±2.76	10.6±2.88
Acetone
A	0.47	9.36±3.94
B	0.45	8.96±2.99	9.16±3.47
API 81-07 0.05 µl/ml
A	0.63	12.52±4.09
B	0.58	11.64±3.38	12.08±3.74**
API 81-07 0.1 µl/ml
A	0.48	9.56±3.8
B	0.51	10.36±4.27	9.96±4.02
API 81-07 0.2 µl/ml
A	0.5	10.04±3.23
B	0.44	8.84±3.5	9.44±3.39
API 81-07 0.4 µl/ml
A	0.5	9.96±3.25
B	0.58	11.56±3.57	10.76±3.47*
CP
A	1.91	38.2±7.06
B	2.01	40.2±12.18	39.2±9.91**
(a)      Not evaluated due to absence of second-division metaphase cells
*      P</=0.05
**      P</=0.01

 

The responses to the positive and negative control materials fulfilled the requirements for the assays. The test material did not cause an increase in SCEs in the absence of exogenous activation. API 81-07 did cause a significant increase in SCEs at two non adjacent doses in the activation assay. However, the increased activity was only seen in one of two treatment flasks. These increases appeared to be random and of no biological significance. It was concluded that API 81-07 was negative in the SCE assay.

Conclusions:

Interpretation of results (migrated information):
negative

The test compound was not genotoxic.

Executive summary:

Hydrodesulfurised kerosine was tested in the sister chromatid exchange assay using Chinese hamster ovary cells. The assay was conducted with Aroclor-induced rat liver S-9 activation system at concentrations of 0.05, 0.1, 0.2, or 0.4 µl/mL or without at concentrations of 0.007, 0.013, 0.025, and 0.05 µl/mL. The high doses were selected based on the cytotoxicity of the test compound, which was tested in a preliminary study. A small but statistically significant increase in the frequency of sister chromatid exchanges was observed at the high and low concentrations with metabolic activation. These increases appeared to be random and of no biological significance. There were no significant increases observed at any concentration in the absence of metabolic activation. Under the conditions of the study, hydrodesulfurised kerosine is considered to be negative in the sister chromatid exchange assay with Chinese hamster ovary cells.

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1988

Materials and methods

Test guideline

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 479 (Genetic Toxicology: In Vitro Sister Chromatid Exchange Assay in Mammalian Cells)

GLP compliance:

yes

Type of assay:

sister chromatid exchange assay in mammalian cells

Test material

Test material information

Constituent 1

Reference substance name:

Petroleum kerosine fraction, co-processed (hydrotreatment) with renewable hydrocarbons of plant or animal origin

EC Number:

941-379-0

Molecular formula:

It is not possible to provide molecular and structural information for a UVCB substance

IUPAC Name:

Petroleum kerosine fraction, co-processed (hydrotreatment) with renewable hydrocarbons of plant or animal origin

Test material form:

liquid

Details on test material:

EC 941-379-0
Reference substance for target in read-across analogue approach

Method

Species / strain

Species / strain / cell type:

Chinese hamster Ovary (CHO)

Details on mammalian cell type (if applicable):

- Type and identity of media: Ham’s F-12 or McCoy’s 5A medium supplemented with 10% foetal bovine serum (FBS)
- Properly maintained: no data
- Periodically checked for Mycoplasma contamination: no data
- Periodically checked for karyotype stability: no data
- Periodically "cleansed" against high spontaneous background: no data

Metabolic activation:

with and without

Metabolic activation system:

S9

Test concentrations with justification for top dose:

Without metabolic activation: 0.007, 0.013, 0.025, and 0.05 µl/ml
With metabolic activation: 0.05, 0.1, 0.2, and 0.4 µl/ml

Vehicle / solvent:

- Vehicle(s)/solvent(s) used: acetone
- Justification for choice of solvent/vehicle: None reported

Controls

Untreated negative controls:

yes

Negative solvent / vehicle controls:

yes

Positive controls:

yes

Positive control substance:

other: without activation: triethylenemelamine; with activation: cyclophosphamide

Details on test system and experimental conditions:

METHOD OF APPLICATION: in medium

DURATION
- Preincubation period: 16 to 24 hours
- Exposure duration: Without activation: 25 hours; with activation: 2 hours


NUMBER OF REPLICATIONS: Two


NUMBER OF CELLS EVALUATED:Twenty-five cells from each replicate flask


DETERMINATION OF CYTOTOXICITY
- Method: mitotic index; relative total growth

Evaluation criteria:

The test material was considered positive if it induced a doubling in SCE frequency over the solvent control at a minimum of three consecutive dose levels or if a dose responsive and statistically significant increase was observed over a minimum of three dose levels.

Statistics:

Student's t-test

Results and discussion

Test results

Species / strain:

Chinese hamster Ovary (CHO)

Metabolic activation:

with and without

Genotoxicity:

negative

Vehicle controls validity:

valid

Untreated negative controls validity:

valid

Positive controls validity:

valid

Additional information on results:

RANGE-FINDING/SCREENING STUDIES: Preliminary studies tested for the cytotoxicity of the test compound in acetone. In the absence of metabolic activation, concentrations greater than 0.1 µl/ml inhibited the relative growth and mitotic indices. In the presence of metabolic activation, a concentration of 1 µl/ml was needed to inhibit the relative growth by 50% or more.

Remarks on result:

other: other: Chinese Hamster Ovary cells

Remarks:

Migrated from field 'Test system'.

Any other information on results incl. tables

The test material was soluble at all concentrations tested. The study in both the presence and absence of S9 was repeated since there was a poor metaphase cell yield. Only the results of the second study with and without S9 are summarized in the following table.

Replicate flask	SCEs/ chromosome	Flask mean SCEs/cell	Group mean SCEs/cell
Assay in absence of exogenous activation
		(±SD)	(±SD)
Untreated cells
A	0.42	8.4±3.16
B	0.42	8.28±2.57	8.34±2.85
Acetone
A	0.48	9.44±3
B	0.45	8.96±2.35	9.20±2.68
API 81-07 0.007 µl/ml
A	0.44	8.80±2.87
B	0.43	8.68±2.54	8.74±2.69
API 81-07 0.013 µl/ml
A	0.47	9.4±2.96
B	0.42	8.32±2.58	8.86±2.80
API 81-07 0.025 µl/ml
A	0.47	9.36±2.96
B	0.48	9.64±3.12	9.50±3.01
API 81-07 0.05 µl/ml
A	NE (a)
B	NE
TEM
A	1.53	30.6±6.81
B	1.75	34.92±7.60	32.76±7.47**
Assay in presence of exogenous activation
Untreated cells
A	0.5	10.16±2.98
B	0.55	11.04±2.76	10.6±2.88
Acetone
A	0.47	9.36±3.94
B	0.45	8.96±2.99	9.16±3.47
API 81-07 0.05 µl/ml
A	0.63	12.52±4.09
B	0.58	11.64±3.38	12.08±3.74**
API 81-07 0.1 µl/ml
A	0.48	9.56±3.8
B	0.51	10.36±4.27	9.96±4.02
API 81-07 0.2 µl/ml
A	0.5	10.04±3.23
B	0.44	8.84±3.5	9.44±3.39
API 81-07 0.4 µl/ml
A	0.5	9.96±3.25
B	0.58	11.56±3.57	10.76±3.47*
CP
A	1.91	38.2±7.06
B	2.01	40.2±12.18	39.2±9.91**
(a)      Not evaluated due to absence of second-division metaphase cells
*      P</=0.05
**      P</=0.01

 

The responses to the positive and negative control materials fulfilled the requirements for the assays. The test material did not cause an increase in SCEs in the absence of exogenous activation. API 81-07 did cause a significant increase in SCEs at two non adjacent doses in the activation assay. However, the increased activity was only seen in one of two treatment flasks. These increases appeared to be random and of no biological significance. It was concluded that API 81-07 was negative in the SCE assay.

Applicant's summary and conclusion

Conclusions:

Interpretation of results (migrated information):
negative

The test compound was not genotoxic.

Executive summary:

Hydrodesulfurised kerosine was tested in the sister chromatid exchange assay using Chinese hamster ovary cells. The assay was conducted with Aroclor-induced rat liver S-9 activation system at concentrations of 0.05, 0.1, 0.2, or 0.4 µl/mL or without at concentrations of 0.007, 0.013, 0.025, and 0.05 µl/mL. The high doses were selected based on the cytotoxicity of the test compound, which was tested in a preliminary study. A small but statistically significant increase in the frequency of sister chromatid exchanges was observed at the high and low concentrations with metabolic activation. These increases appeared to be random and of no biological significance. There were no significant increases observed at any concentration in the absence of metabolic activation. Under the conditions of the study, hydrodesulfurised kerosine is considered to be negative in the sister chromatid exchange assay with Chinese hamster ovary cells.