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 />
Conclusion:<br />
preparations was determined by the selective incorporation<br />
of tritium-uridine. Four T- and B-cell specific mitogens<br />
were utilized for the mitogen-induced activation test<br />
(concanavalin A (Con A), phytohemagglutinin (PHA), pokeweed<br />
mitogen (PWM), lipopolysaccharide (LPS)).<br />
STATISTICAL ANALYSES. two-way analysis of variance, analysis<br />
of covariance, Fisher´s exact test. Immunologic studies did<br />
not involve comparisons of lung condition, and only the<br />
differences among the four exposure groups were tested by<br />
analysis of variance.<br />
A series of studies in which rats and guinea pigs were exposed<br />
to 1 or 0.5 mg/m3 for up to 8 month describes<br />
histomorphometrically determined increases in emphysema<br />
formation, hyperplasia of non-ciliated cells in the<br />
bronchiolar epithelium and increased interstitial<br />
birefringence indicating increased collagen content. The<br />
findings showed a high variation within the control animals<br />
and no consistent time-response pattern. There was no close<br />
correlation between the morphological findings and lung<br />
function tests, most of which did not show differences between<br />
control and treated groups. Therefore these findings cannot<br />
definitively be attributed to the test substance treatment.<br />
This conclusion is supported by the fact that ammonium sulfate<br />
is a highly soluble material with a moderately acidic pH<br />
(around 5), which is rapidly neutralized and absorbed when<br />
deposited in the respiratory tract. It is thus not expected to<br />
show cytotoxicity.<br />
Reliability: (4) not assignable<br />
no information on purity, only one dose tested.<br />
11-APR-<strong>20</strong>06 (128) (130)<br />
Type:<br />
Sub-acute<br />
Species: rat Sex: male<br />
Strain:<br />
Sprague-Dawley<br />
Route of administration: inhalation<br />
Exposure period:<br />
23.5 h up to 7 days<br />
Doses:<br />
5 mg/m3 as aerosol<br />
Result:<br />
The apparent lung collagen synthesis rate, assayed by the<br />
incorporation of tritium labeled proline into hydroxyproline<br />
of lung collagen, was increased to 35 nmol/g at 0.64 ppm<br />
ozone, which was about <strong>20</strong>0% above the control values. Total<br />
protein content of bronchoalveolar lavage reached a maximum of<br />
about 10 mg, a 590% increase over the control levels after a 1<br />
day (23.5h) exposure to 0.64 ppm of ozone. The level declined<br />
to near base amounts after 7 days. Lower ozone doses elicited<br />
proportionally smaller increases in the total protein. The<br />
lung protein content increased to about 140 mg at the high<br />
ozone level after 7 days. The lung DNA content was elevated to<br />
125% over the base amount at 0.64 ppm, the 0.12 and 0.<strong>20</strong> ppm<br />
doses showed no increase. The exposure to 0.<strong>20</strong> ppm of ozone<br />
and about 5 mg/m3 of ammonium sulfate resulted in a 125%<br />
increase in collagen synthesis. Exposures to 5 mg/m3 of<br />
Ammonium sulfate alone have been shown previously not to cause<br />
changes in collagen synthesis rate as compared with control.<br />
Seven day exposure to the high level of ozone increased the<br />
UNEP PUBLICATIONS 169