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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 />

Type:<br />

LD100<br />

Species:<br />

rat<br />

Strain:<br />

Wistar<br />

Sex:<br />

male<br />

Route of admin.: i.p.<br />

Test substance:<br />

other TS: ammonium sulfate, reagent grade<br />

Result:<br />

The effect of ammonia intoxication has been studied after<br />

intraperitoneal injection of various ammonium salts to rats<br />

including ammonium sulfate. A standardized dose of<br />

10.6 mmol NH4-N/kg (1,4 g/kg bw) was lethal within 8-13<br />

minutes for all 13 ammonium salts tested including ammonium<br />

sulfate.<br />

Reliability: (2) valid with restrictions<br />

limited documentation. No further information on purity.<br />

18-NOV-<strong>20</strong>03 (109)<br />

Type:<br />

other: pulmonary oedema<br />

Species:<br />

rat<br />

Strain:<br />

Wistar<br />

Sex:<br />

male/female<br />

No. of Animals: 19<br />

Doses:<br />

6 % (600 mg/kg bw)<br />

Route of admin.: i.p.<br />

Method:<br />

other<br />

Year: 1969<br />

GLP:<br />

no data<br />

Test substance: other TS: ammonium sulfate<br />

Result:<br />

Test condition:<br />

160<br />

The major lesion was the formation of large blebs in<br />

endothelial cells, associated with a variable degree of oedema<br />

of the interstitium and of epithelial lining cells. These<br />

changes were present in every animal exposed to ammonium<br />

sulfate, irrespective of the time-interval after injection,<br />

the only difference being that the changes prominent in those<br />

exposed for longer intervals.<br />

The ultrastructural changes, produced by ammonium sulphate are<br />

similar to the changes in pulmonary oedema induced by methods<br />

other than by altered haemodynamics. The absence of<br />

carbon-marker leakage through intercellular junctions in this<br />

experiment suggest that the increased vascular permeability<br />

necessary for the formation of pulmonary oedema differs from<br />

leakage occurring in acute inflammation, in quality if not in<br />

mechanism.<br />

19 rats were used. A colloidal carbon suspension was injected<br />

into the tailveins of the rats in a dosage of 0.1 ml per 100 g<br />

bw. immediately after, a 6 % solution of ammonium sulfate was<br />

injected i.p. in a dosage of 10 ml/kg bw. Rats were killed at<br />

varying intervals (1.5, 5, 7.5, 10, 15, <strong>20</strong>, 30, 90 min) after<br />

injection of ammonium sulfate. 9 control animals were used.<br />

The lungs were prepared and examined by electron microscopes.<br />

Other organs like liver, spleen, kidney, heart and skeletal<br />

muscle were prepared and stained as a routine with<br />

haematoxylin and eosin, and in some instances with Weigert´s<br />

elastic tissue stain or by the periodic acid-Schiff method and<br />

examined microscopically or stained with uranyl acetate and<br />

examined by electron microscopy.<br />

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