Nonamethylenediamine

Endpoint summary

Key value for chemical safety assessment

Genetic toxicity in vitro

Description of key information

All required in vitro tests showed negative results of genetic toxicity. According to Column 2 in Annex VIII (Section 8.4), an in vivo test is not necessary given the consistently negative results in multiple in vitro studies.

Link to relevant study records

Reference

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:

2012-08-17 to 2012-09-10

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

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:

Thymidine Kinase (TK+/-)

Species / strain / cell type:

mouse lymphoma L5178Y cells

Details on mammalian cell type (if applicable):

- Type and identity of media: complete growth medium F10P [Dulbecco’s modified Eagle’s Medium (DMEM) with 4 mM L-glutamine adjusted to contain 1.5 g/L sodium bicarbonate and 4.5 g/L glucose supplied with 0.1 % Pluronic, 90 % and Fetal bovine serum, 1 0%]. Treatment medium F5P [Dulbecco’s modified Eagle’s Medium (DMEM) with 4 mM Lglutamine adjusted to contain 1.5 g/L sodium bicarbonate and 4.5 g/L glucose supplied with 0.1 % Pluronic, 95 % and Fetal bovine serum, 5 %].

Metabolic activation:

with and without

Metabolic activation system:

A co-factor supplemented postmitochondrial fraction (S9) from the liver of Aroclor 1254 induced Sprague- Dawley rats.

Test concentrations with justification for top dose:

0.40 mg/ml, 0.20 mg/ml, 0.10 mg/ml and 0.05 mg/ml

Vehicle / solvent:

distilled water

Untreated negative controls:

yes

Remarks:

sterile distilled water

Positive controls:

yes

Positive control substance:

benzo(a)pyrene

methylmethanesulfonate

Details on test system and experimental conditions:

METHOD OF APPLICATION: in medium

DURATION
- Exposure duration: 4 hours
- Expression time (cells in growth medium): 48 hours
- Selection time (if incubation with a selection agent): 13 days

SELECTION AGENT (mutation assays): Trifluorothymidine (TFT)

NUMBER OF REPLICATIONS: 3

NUMBER OF CELLS EVALUATED: 3 x 10e6

DETERMINATION OF CYTOTOXICITY
- Method: relative total growth

Evaluation criteria:

The total number of colonies per TFT plate were determined for those cultures with > = 10 % total growth.

Species / strain:

mouse lymphoma L5178Y cells

Metabolic activation:

with and without

Genotoxicity:

negative

Cytotoxicity / choice of top concentrations:

no cytotoxicity nor precipitates, but tested up to recommended limit concentrations

Remarks:

Cytotoxic effect of cell growth inhibition was observed at 2.5 µg/ml and above.

Untreated negative controls validity:

valid

Positive controls validity:

valid

Additional information on results:

TEST-SPECIFIC CONFOUNDING FACTORS
- Precipitation: none

RANGE-FINDING/SCREENING STUDIES: The concentrations of the test substances for the study were selected based on the results of preliminary range-finding test using L5178Y/TK+/- mouse lymphoma cells. In the range-finding test, cytotoxic effect of cell growth inhibition was observed at 0.4 mg/ml and above.

Remarks on result:

other: all strains/cell types tested

Conclusions:

From the above study, the test item nonamethylenediamine (NMDA) is non-mutagenic to the L5178Y TK+/- clone, both in the absence and presence of S9 metabolic activation system.

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed (negative)

Genetic toxicity in vivo

Endpoint conclusion

Endpoint conclusion:

no study available

Additional information

Additional information from genetic toxicity in vitro:

Information is available from reliable studies for all required in vitro endpoints. The results of the studies are in agreement. 1,9-nonanediamine has been tested in a bacterial reverse mutation assay according to OECD 471, in a mammalian cell gene mutation assay according to OECD 476 and in an in vitro mammalian chromosome aberration test according to OECD 473 to determine the genetic toxicity of the substance. The results show that the substance does not induce mutations in bacterial or mammalian cells, nor chromosome aberrations in mammalian cells.

Justification for selection of genetic toxicity endpoint
Data are available from reliable studies for all the required in vitro endpoints. No mutagenic effects were observed in all of the tests.

Justification for classification or non-classification

The available information for the substance indicates that 1,9 -nonanediamine does not induce mutations in bacterial or mammalian cells, nor chromosome aberrations in mammalian cells. Therefore it is considered that classification for mutagenicity is not required.