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Gold Excretion and Retention During Auranofin Treatment: a Preliminary Report

Overview
Specialty Rheumatology
Date 1979 Jan 1
PMID 385875
Citations 2
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Abstract

Auranofin, an oral gold compound, was administered to 12 patients with rheumatoid arthritis using 2 dosage schedules (3 mg or 1 mg twice daily for 8 weeks, and then once daily for 18 weeks). In addition to outpatient clinic monitoring, all patients were admitted to a metabolic ward for 3 days for collection of 24 hr daily urine and feces. Gold content of excreta was determined by atomic absorption spectroscopy. Seventy-three per cent of the administered gold was recovered in the urine and feces of patients receiving 3 mg b.i.d., and all the gold was recovered in those taking 1 mg b.i.d. Ninety-five per cent of the recovered gold was in the feces and 5% was in the urine. These findings contrast with those observed during intramuscular (gold sodium thiomalate) chrysotherapy: 40% of the injected dose was recovered, 70% in urine, 30% in feces. Less tissue gold retention occurred with oral gold than with parenteral therapy. Following 20 weeks of auranofin (6 mg/day) chrysotherapy approximately 66 mg of gold was retained. By comparison, 300 mg of gold was retained after injectable gold sodium thiomalate treatment. The significance of these findings is discussed.

Citing Articles

Auranofin. A preliminary review of its pharmacological properties and therapeutic use in rheumatoid arthritis.

Chaffman M, Brogden R, Heel R, Speight T, Avery G Drugs. 1984; 27(5):378-424.

PMID: 6426923 DOI: 10.2165/00003495-198427050-00002.


Clinical pharmacokinetics of oral and injectable gold compounds.

Blocka K, Paulus H, Furst D Clin Pharmacokinet. 1986; 11(2):133-43.

PMID: 3082559 DOI: 10.2165/00003088-198611020-00003.