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AMMONIUM SULFATE CAS N°: 7783-20-2

AMMONIUM SULFATE CAS N°: 7783-20-2

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OECD SIDS<br />

<strong>AMMONIUM</strong> <strong>SULFATE</strong><br />

5. TOXICITY ID: <strong>7783</strong>-<strong>20</strong>-2<br />

DATE: 18.04.<strong>20</strong>06<br />

The chromosomal aberration rates in cells treated with<br />

ammonium sulfate alone were not increased:<br />

% ABERRANT METAPHASES (<strong>20</strong>0 metaphases analyzed, including<br />

achromatic lesions):<br />

5.5, 6, 6, 3, 3 for controls without treatment, with <strong>20</strong> h<br />

buffer treatment, with buffer plus ammonium sulfate<br />

treatment (<strong>20</strong> h), with 46 h buffer treatment, and with<br />

buffer plus ammonium sulfate treatment (46h), respectively.<br />

Test condition: Lymphocytes were isolated from whole blood in a Ficoll<br />

gradient. 1x10e6 lymphocytes were incubated in 5 mL plastic<br />

tubes in 2.5 mL McCoy`s 5A medium supplemented with <strong>20</strong>%<br />

fetal calf serum, 0.06 mL phytohemagglutinin M, 100 U/mL<br />

penicillin and 0.1 mg/mL dihydrostreptomycin sulfate. The<br />

cultures were incubated for 50 hrs, including a treatment<br />

with colcemid (0.08 ug/mL) for 3 hrs. Treatment for 15 min<br />

with Alu I, ammonium sulfate or Alu I shipping buffer was done<br />

at culture times of <strong>20</strong> and 46 hrs, principally as described<br />

previously (Obe and Winkel, 1985, Mut Res. 152, 25-29).<br />

Shipping buffer consisted of: KPO4, <strong>20</strong> mM; KCl, 50 mM; EDTA,<br />

0.1 mM; dithioerythritol, 10 mM; glycerin, 50% (v/v), pH 7.5.<br />

Up to 7 independent experiments were performed with blood<br />

from 5 different donors. Preparations were made following a<br />

routine protocol and were stained with Giemsa stain.<br />

The following aberrations were analysed: achromatic lesions,<br />

chromatid breaks, isochromatid/chromosome breaks, chromatid<br />

intrachanges, chromatid interchanges, triradials,<br />

polycentric chromosomes, ring chromosomes and minutes.<br />

YEAR OF STUDY: not reported.<br />

Reliability: (2) valid with restrictions<br />

limited documentation; only one dose level, no standard test<br />

system for chromosomal aberrations<br />

Flag:<br />

Critical study for SIDS endpoint<br />

07-NOV-<strong>20</strong>03 (140)<br />

Type:<br />

Cytogenetic assay<br />

System of testing: CHO cells<br />

Concentration:<br />

0; 0.8; 1.6; 3.2 M (0; 106; 211; 423 mg/mL)<br />

Cytotoxic Concentration: not reported<br />

Metabolic activation: without<br />

Result:<br />

negative<br />

Method:<br />

GLP:<br />

Test substance:<br />

Result:<br />

other: see Test Condition<br />

no data<br />

other TS: ammonium sulfate, not specified further<br />

3.2M Ammonium sulfate did not induce chromosomal aberrations<br />

in Chinese hamster ovary (CHO) cells. However, high<br />

concentrations of ammonium sulfate, magnesium chloride,<br />

calcium chloride or sodium chloride increased the frequency<br />

of chromosome-type aberrations in CHO cells induced by the<br />

restriction endonuclease Alu 1.<br />

The results for cultures treated with Alu I, Alu I +<br />

ammonium sulfate and control cultures were as follows:<br />

Treatment / Percent aberrant metaphases / DIC*<br />

Alu I / 40.7 / 34.3<br />

UNEP PUBLICATIONS 187

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