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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 />

weighed between 6 and 14 mg (mean value 9.2 mg). Similar or<br />

higher increases in parathyroid weight were also found with<br />

all other chemicals tested in this study (ammonium<br />

hydroxide, carbonate, chloride, hydrophosphate, acetate,<br />

lactate, calcium chloride, hydrochloric acid, lactic and<br />

acetic acids, sodium ammonium phosphate, and sodium<br />

dihydrogen phosphate). The author considers this effect to<br />

be caused by metabolic acidosis that was induced by the<br />

various chemicals (though no experimental data relating to<br />

the latter were provided in the publication).<br />

Test condition: 10 females were treated with 100-<strong>20</strong>0 mg ammonium sulfate /<br />

kg bw, dissolved in 100-150 cm3 drinking water every second<br />

day. The dose was gradually increased over the experimental<br />

period of 5-16 months (no further details given). Each 4th<br />

week was scheduled as a recovery period without treatment.<br />

Reliability: (4) not assignable<br />

documentation insufficient for assessment<br />

19-JUL-<strong>20</strong>04 (136)<br />

Type:<br />

Sub-chronic<br />

Species: Syrian hamster Sex: male<br />

Route of administration: inhalation<br />

Exposure period:<br />

15 weeks<br />

Frequency of treatment: 6 hours/day, 5 days/week<br />

Doses:<br />

186.6 ug/m3 (analytical) (<strong>20</strong>0 ug/m3 , nominal)<br />

Control Group:<br />

other: BaP<br />

Method:<br />

other: see Test Condition<br />

Year: 1978<br />

GLP:<br />

no<br />

Test substance: other TS: ammonium sulfate, no further specified<br />

Remark:<br />

Result:<br />

The study evaluated the influence of ammonium sulfate as a<br />

cofactor in carcinogenesis studies employing benzo(a)pyrene as<br />

the prime agent. Additional information concerning influence<br />

on a metabolic enzyme (arylhydroxylase) and the body`s<br />

absorption and excretion of sulfate was also included (cf<br />

IUCLID section on toxicokinetics). NOTE: wrong units (mg<br />

instead of ug) were used in some parts of the publication by<br />

Godleski et al., 1984.<br />

Inhaled ammonium sulfate did not increase the incidence or<br />

severity of pneumonitis or pulmonary fibrosis in the hamster.<br />

This inhalation did increase the incidence of emphysema as<br />

examined microscopically but not the severity. The increase in<br />

emphysema incidence was not statistically significant (9.0 vs<br />

15.2%, EPA 1978). Another publication of this study described<br />

an increase in emphysema incidence, which is however of<br />

doubtful statistical significance. It was based on only 80<br />

animals per group (8.6 vs 16.1%, Godleski, 1984). Due to the<br />

higher number of animals used the EPA results are more<br />

reliable and 0.2 mg/ammonium sulfate/m3 cannot be regarded as<br />

a LOAEL. However it seems not acceptable to take 0.2 mg/m3 as<br />

the NOAEL from this study because the animals were not<br />

examined immediately after exposure but only after 2 years.<br />

Test condition: 80 approximately 10-week old animals were exposed for 6<br />

hours/day, 5 days/week for 15 weeks at an average<br />

concentration of 186.6 ug/m3 (nominal concentration <strong>20</strong>0<br />

ug/m3).<br />

After 2 years, histological sections of the respiratory tract<br />

UNEP PUBLICATIONS 179

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