AMMONIUM SULFATE CAS N°: 7783-20-2
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