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Xenobiotica
the fate of foreign compounds in biological systems
Volume 12, 1982 - Issue 12
109
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Original Article

Disposition and metabolism of formoterol fumarate, a new bronchodilator, in rats and dogs

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Pages 803-812 | Received 23 Jun 1982, Published online: 30 Sep 2009
 

Abstract

1. The disposition and metabolism of formoterol fumarate, a highly potent β2-adrenoceptor stimulant, were studied in rats and dogs.

2. After oral administration of [3H]formoterol fumarate to dogs, unchanged formoterol accounted for > 60% of the plasma radioactivity immediately after dosage; > 20% was due to the unchanged drug until 12 h after dosage. In contrast, only 1-3% of the radioactivity was present as unchanged drug in rat plasma. After i.v. dosage, unchanged drug was much higher in both species. The elimination half-life of formoterol was 4-6 h in dogs and 1.7h in rats.

3. In both species, 36-45% of the dose was excreted in urine and 50-56% in faeces in 72 h, irrespective of the administration route. Biliary excretion after oral dosage amounted to 65 and 31% in rats and dogs, respectively.

4. T.l.c. before and after enzymic hydrolysis revealed that the drug was excreted in urine and bile of rats mostly as a conjugate. Dog urine also contained the conjugate but the unchanged drug was much higher than in rats. The conjugated metabolite was purified from rat urine and identified as the 2-O-glucuronide. The glucuronide was the only metabolite detected in the urine and bile of rats and in the urine of dogs.

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