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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 />

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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