The pharmacokinetics of ethifos and WR-1065 were investigated following iv administration to the rhesus monkey. Pharmacokinetic parameters were estimated by noncompartmental modeling of plasma concentration data from 10-min iv infusions. The results indicate the ethiofos and WR-1065 are cleared from the plasma at a rate of 40.4 and 67.8 ml/kg-min, respectively. The volumes of distribution at steady state were 0.28 L/kg for ethiofos and 1.5 L/kg for WR-1065. demonstrate a greater fraction of WR-1065 molecules reach the periphery compared with ethiofos and WR-1065 has a greater interaction with tissues.
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