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>Radioimmunoassay of AntarelixTM, a Luteinizing Hormone Releasing-Hormone Antagonist, in Plasma and Its Application for Pharmacokinetic Study in Dogs
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Radioimmunoassay of AntarelixTM, a Luteinizing Hormone Releasing-Hormone Antagonist, in Plasma and Its Application for Pharmacokinetic Study in Dogs
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机译：Radioimmunoassay of AntarelixTM, a Luteinizing Hormone Releasing-Hormone Antagonist, in Plasma and Its Application for Pharmacokinetic Study in Dogs
A procedure for the radioimmunoassay (RIA) of AntarelixTM(teverelix) in plasma has been developed for the pharmacokinetic study of this potent LHRH antagonist in dogs. Antiserum was produced by coupling the deamidated Antarelix analog to bovine serum albumin by a carbodiimide reaction and immunizing rabbits with the conjugate. The crossreactivity of the antiserum with LHRH, LHRH agonist Metereline and LHRH antagonists tested was negligible, except for Antide which displayed a crossreactivity of 33. No crossreactivity with Antarelix metabolites could be detected. The RIA is suitable for the direct determination of Antarelix in plasma, with a minimum detectable level of 1.12 fmol/assay. The accuracy and precision of the method were assessed with plasma samples spiked with Antarelix at concentrations ranging from 0.4 to 6.4 pmol/ml. The recovery was 104.8 with intra- and interassay CV between 1 and 3.7. Pharmacokinetic profiles of Antarelix in dogs were established following an IV or a SC dose of 10 #x3BC;g/kg.
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