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Safety evaluation of certain food additives - ipcs inchem

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510 FURAN-SUBSTITUTED ALIPHATIC HYDROCARBONS<br />

(f) 4-(2-Furyl)-3-buten-2-one (No. 1511)<br />

Groups <strong>of</strong> five male and five female Fischer 344 rats were maintained on<br />

diets that provided 4-(2-furyl)-3-buten-2-one at doses <strong>of</strong> 0 (control) or an estimated<br />

30 mg/kg bw per day for 14 days. Animals were examined for viability twice daily.<br />

Body weights were recorded on days 1, 6 and 14 <strong>of</strong> the study, and <strong>food</strong> consumption<br />

was measured on days 7 and 14. Necropsy was performed on each <strong>of</strong> the animals<br />

at the end <strong>of</strong> the study. Kidney and liver weights were recorded prior to fixation in<br />

10% buffered formalin for histological examination. All macroscopic lesions were<br />

also fixed for histological examination.<br />

Treatment with 4-(2-furyl)-3-buten-2-one resulted in no adverse clinical<br />

effects. A slight increase in <strong>food</strong> consumption was noted in females; however, no<br />

such increase was observed with the males, and there was no corresponding<br />

increase in weight gain. Absolute and relative liver weights for females and relative<br />

liver weights for males fed a diet containing 4-(2-furyl)-3-buten-2-one were<br />

increased compared with controls by 13%, 15% and 8%, respectively; however, no<br />

histological findings accompanied these increases. The authors stated that, when<br />

compared with control animals <strong>of</strong> the same strain from the same vendor used in<br />

other studies under identical conditions, the absolute liver weights <strong>of</strong> the control<br />

animals in this study were lower than usual. The authors concluded that dietary<br />

administration <strong>of</strong> 4-(2-furyl)-3-buten-2-one produced no evidence <strong>of</strong> toxic effects<br />

under the conditions <strong>of</strong> this study (Gill & Van Miller, 1987).<br />

(g) 3-Acetyl-2,5-dimethylfuran (No. 1506) and furfuryl methyl ether<br />

(No. 1520)<br />

Groups <strong>of</strong> five male and five female Fischer 344 rats were maintained on<br />

diets estimated to provide 3-acetyl-2,5-dimethylfuran at 0 (control) or 10 mg/kg bw<br />

per day or furfuryl methyl ether at 0 (control) or 27 mg/kg bw per day for 14 days.<br />

Animals were examined for viability twice daily. Body weights were recorded on<br />

days 1, 6 and 14 <strong>of</strong> the study, and <strong>food</strong> consumption was measured on days 7 and<br />

14. Necropsy was performed on each <strong>of</strong> the animals at the end <strong>of</strong> the study. Kidney<br />

and liver weights were recorded prior to fixation in 10% buffered formalin for<br />

histological examination. All macroscopic lesions were also fixed for histological<br />

examination. No statistically significant differences in any <strong>of</strong> the parameters tested<br />

were noted between treated and control animals. The authors concluded that dietary<br />

administration <strong>of</strong> 3-acetyl-2,5-dimethylfuran or furfuryl methyl ether produced no<br />

evidence <strong>of</strong> toxic effects under the conditions <strong>of</strong> this study (Van Miller & Weaver,<br />

1987).<br />

(h) O-Ethyl S-(2-furylmethyl)thiocarbonate (No. 1526)<br />

Wistar rats (three per sex per dose) were administered doses <strong>of</strong> 0 (control),<br />

2, 8 or 32 mg O-ethyl S-(2-furylmethyl)thiocarbonate (99% pure)/kg bw per day by<br />

gavage for 28 days in a study conducted according to Organisation for Economic<br />

Co-operation and Development (OECD) guidelines. Observations for mortality were<br />

made twice daily, and clinical signs were recorded once daily. Body weights and<br />

<strong>food</strong> consumption were recorded weekly. All animals surviving to the end <strong>of</strong> the

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