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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Genetic toxicity: in vitro

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Administrative data

Endpoint:
in vitro cytogenicity / chromosome aberration study in mammalian cells
Remarks:
Type of genotoxicity: chromosome aberration
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The reliability and summary were made based on the HPV program adopted during OECD SIAM 25 (October 2007). Only limited information is available on methods and results; the article is a review article of more than 200 investigated substances.

Data source

Reference
Reference Type:
publication
Title:
Primary mutagenicity screening of food additives currently used in Japan
Author:
Ishidate Jr M, Sofuni T, Yoshikawa K, Hasashi M, Nohmi T, Sawada M and Matsuoka A
Year:
1984
Bibliographic source:
Fd Chem Toxic 22: 623-636

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
no metabolic activation used, cytotoxicity not measured, exposure durations of 24 and 48 hours, 100 metaphases investigated
GLP compliance:
no
Type of assay:
in vitro mammalian chromosome aberration test

Test material

Constituent 1
Reference substance name:
Sodium nitrate
EC Number:
231-554-3
EC Name:
Sodium nitrate
Cas Number:
7631-99-4
IUPAC Name:
sodium nitrate
Details on test material:
- Name of test material: Sodium nitrate
- Analytical purity: 99.3 %

Method

Species / strain
Species / strain / cell type:
other: Chinese hamster fibroblast cell line, CHL
Details on mammalian cell type (if applicable):
- Type and identity of media: minimum essential medium (MEM), supplemented by 10 % calf serum
- Other: The cell line was originally established from the lung of a newborn female at the Cancer Research Institute, Tokyo (Koyama, Utakoji and Ono, 1970). The modal chromosome number was 25 and the doubling time was approximately 15 hours.

Reference
- Koyama H, Utakoji T and Ono T (1970). A new cell line derived from newborn Chinese hamster lung tissue. Gann 61: 161-167.
Metabolic activation:
without
Test concentrations with justification for top dose:
5 mg/mL (highest dose tested), maximum dose selected in a preliminary test (not reported), 3 different concentrations (not given)
Vehicle / solvent:
- Vehicle/solvent used: physiological saline
Controls
Untreated negative controls:
yes
Negative solvent / vehicle controls:
yes
True negative controls:
not specified
Positive controls:
not specified
Positive control substance:
not specified
Details on test system and experimental conditions:
DURATION
- Exposure duration: 24 and 48 hours

SPINDLE INHIBITOR
- Colcemid (added 2 hours prior to cell harvesting)

FIXATION
- Cells were fixed with acetic acid-methanol (1:3 v/v)

STAIN
- Giemsa

NUMBER OF CELLS EVALUATED
- 100 well-spread metaphases were observed
Evaluation criteria:
The result was considered to be negative if the incidence of aberrations was less than 4.9 %, equivocal if it was between 5.0 and 9.9 % and positive if it was more than 10 %.
Statistics:
For a quantitative evaluation of the clastogenic potential, the D20 was calculated, which is the dose (mg/mL) at which structural aberrations (including gaps) were detected in 20 % of the metaphases observed.
In addition, the TR value was calculated, which indicates the frequency of cells with exchange-type aberrations per unit dose (mg/mL).

Results and discussion

Test results
Species / strain:
other: Chinese hamster fibroblast cell line, CHL
Metabolic activation:
without
Genotoxicity:
positive
Remarks:
24 % structural aberration at 48 hours
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
other: incidence of aberrations usually less than 3.0 %
Untreated negative controls validity:
other: incidence of aberrations usually less than 3.0 %
Positive controls validity:
not specified
Additional information on results:
D20: 5.73 mg/mL
TR: 0.8
Also positive at 4 mg/mL at both 24 hours (10.0 %) and 48 hours (10.0 %).
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'.

Applicant's summary and conclusion