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Articles & Issues

3. Pharmacokinetics of Anti-SARS-CoV Agent Niclosamide and Its Analogs in Rats

【Update Date:2006-04-03】 unit:
Pharmacokinetics of Anti-SARS-CoV Agent Niclosamide and Its Analogs in Rats

YI-WEI CHANG1, TENG-KUANG YEH1, KE-TA LIN1, WEI-CHENG CHEN1, HSIEN-TSUNG YAO1,
SHIH-JUNG LAN1, YU-SHAN WU1, HSING-PANG HSIEH1, CHI-MIN CHEN2 AND CHIUNG-TONG CHEN1*

1. Division of Biotechnology and Pharmaceutical Research,
National Health Research Institutes, 35, Keyan Rd., Zhunan, Miaoli 35053, Taiwan, R.O.C.
2. Division of Animal Medicine, Animal Technology Institute Taiwan, 52, Kedong 2nd Rd., Zhunan, Miaoli 35053, Taiwan, R.O.C.

(Received: March 10, 2006; Accepted: June 16, 2006)

ABSTRACT

   Niclosamide has been demonstrated with inhibitory activity on the replication of SARS-CoV in Vero E6 cells.  This study examined the pharmacokinetics and oral bioavailability of niclosamide and its two analogs, BPR1H366 and BPR1H369, in male Sprague-Dawley rats.  After a single 2-mg/kg intravenous dose, the total body clearance (CL) of niclosamide, BPR1H366 and BPR1H369 was 20.0 ± 2.9, 26.7 ± 4.4 and 39.4 ± 6.7 mL/kg/min, and the volume of distribution at steady state (VSS) was 0.9 ± 0.4, 0.3 ± 0.1 and 1.1 ± 0.2 L/kg, respectively.  The half-life (t1/2) of BPR1H366 and BPR1H369 was 2.6 ± 0.3 and 3.7 ± 1.1 hr, respectively, shorter than 6.7 ± 2.0 hr of niclosamide.  The AUC was 1413 ± 118, 1019 ± 203 and 750 ± 113 ng/mL × hr for niclosamide, BPR1H366 and BPR1H369, respectively.  After a single 5-mg/kg oral dose, all three compounds were rapidly absorbed.  Niclosamide showed the highest Cmax of 354 ± 152 ng/mL within 30 min after oral gavage.  The oral bioavailability of niclosamide, BPR1H366 and BPR1H369 was 10%, 12% and 15%, respectively.  Our results demonstrated that the extents of drug exposure of the three compounds were comparable in rats.  The pharmacokinetic properties of the compounds in humans are needed to be determined before their potential uses in SARS-CoV infected patients.

Key words: SARS, Coronavirus, Niclosamide, Pharmacokinetics, Bioavailability.