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 />
processes.<br />
Statistical analysis: two-way analysis of variance.<br />
Reliability: (4) not assignable<br />
no information on purity<br />
10-APR-<strong>20</strong>06 (128) (129)<br />
Type:<br />
Sub-acute<br />
Species: guinea pig Sex: male<br />
Strain:<br />
Hartley<br />
Route of administration: inhalation<br />
Exposure period:<br />
5 or <strong>20</strong> days<br />
Frequency of treatment: 6 hours/day, 5 days/week<br />
Post exposure period: no<br />
Doses: 1 mg/m3 (MMAD 0.4 um, geometric standard deviation 2.2)<br />
Control Group:<br />
other: filtered air<br />
Method:<br />
GLP:<br />
Test substance:<br />
Remark:<br />
Result:<br />
Test condition:<br />
182<br />
other: see Test Condition<br />
no data<br />
other TS: ammonium sulfate, reagent grade<br />
In this study, animals with elastase-induced pulmonary<br />
emphysema and saline-treated controls were used to determine<br />
if lung function changes related to ammonium sulfate exposure<br />
were greater (compared with controls) in animals with<br />
experimentally induced emphysema.<br />
Results from 29 treated and 27 control animals are reported.<br />
No information is provided on mortality.<br />
Body weight was not affected by ammonium sulfate exposure or<br />
elastase treatment. Ammonium sulfate exposures had no<br />
significant effect on any of the measured lung volumes, carbon<br />
monoxide diffusion capacity or on quasistatic compliance.<br />
There were no consistent differences observed between 5- and<br />
<strong>20</strong>-day exposed animals.<br />
The test animals (from Charles River Breeding Labs,<br />
Kingston, Mass.) were isolated for 3 weeks after delivery.<br />
Following isolation, animals were assigned to exposure<br />
groups such that preexposure body weight distributions were<br />
the same for all experimental groups exposed at the same<br />
time.<br />
Anesthetized Animals were instilled intratracheally with<br />
either sterile saline or porcine pancreatic elastase (EO127,<br />
Sigma Chemical Co.; 5 units/100 g bw). Elastase activity was<br />
determined immediately before daily instillations by the<br />
method of Sachar et al. (1955, Proc. Soc. Exp. Biol. Med. 90,<br />
323-326), using elastin-orcein as<br />
substrate. The doses of elastase were selected as the<br />
maximum doses tolerated that produced less than 10% acute<br />
mortality, based on results of previous studies (Busch et<br />
al., 1984, Environ. Res. 33, 473-496).<br />
Three weeks following intratracheal instillations, the then<br />
approximately 10 week old guinea pigs were exposed in<br />
Hazleton Systems Model 1000 stainless steel chambers for 5<br />
or <strong>20</strong> days to filtered room air, 1 mg/m3 ammonium sulfate or 1<br />
mg/m3 ammonium nitrate aerosols.<br />
Chamber aerosol concentration was monitored continuously and<br />
the variations throughout the chamber were less than 5% of the<br />
mean concentration. Aerosol concentrations were<br />
determined from four daily, 90-min, filter-pad samples;<br />
ammonium sulfate concentrations were determined by an<br />
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