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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 />

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

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