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Safety evaluation of certain food additives - ipcs inchem

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46 ETHYL LAUROYL ARGINATE<br />

Figure 1. Biotransformation pathway <strong>of</strong> ethyl lauroyl arginate<br />

HO<br />

H 2N<br />

NH<br />

H<br />

N<br />

Lauric acid<br />

NH 2<br />

O<br />

L-Arginine ethyl ester<br />

Minor pathway<br />

Ethanol<br />

O<br />

NH 2<br />

H 2N<br />

NH<br />

L-Ornithine<br />

Carbon dioxide<br />

H<br />

N<br />

O<br />

L-Arginine<br />

NH 2<br />

+<br />

NH 2<br />

O<br />

O<br />

H<br />

N<br />

Ethyl lauroyl arginate<br />

OH<br />

H 2 N<br />

Urea<br />

NH 2<br />

O<br />

O O<br />

carcass, including 3.4 ± 0.4% in the liver. The low rate <strong>of</strong> excretion in the faeces<br />

indicated that ethyl lauroyl arginate–derived material was almost completely<br />

absorbed. Analysis <strong>of</strong> the urine (0–24 h) showed that the major metabolite cochromatographed<br />

with urea, although the identity <strong>of</strong> this metabolite was not<br />

confirmed. This metabolite represented a mean <strong>of</strong> 7.7% <strong>of</strong> the dose in urine. Six<br />

other radioactive components were detected in the urine, all <strong>of</strong> which represented<br />

0.2% <strong>of</strong> the dose.<br />

The authors concluded that ethyl lauroyl arginate was rapidly metabolized<br />

to the amino acid arginine, which then underwent normal amino acid catabolism,<br />

HO<br />

Lauric acid<br />

O<br />

N<br />

H<br />

NH<br />

N<br />

H<br />

Major pathway<br />

NH 2<br />

HN NH 2<br />

NH<br />

Ethanol<br />

O<br />

N α -Lauroyl-L-arginine

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