Clinical pharmacology of IMPY by radioimmunoassay

Cancer Treat Rep. 1980;64(12):1253-60.

Abstract

A radioimmunoassay for IMPY has been developed using [3H]acetyl-IMPY and antibody induced by immunizing rabbits with succinyl-IMPY bovine serum albumin conjugates. The method was reproducible and sensitive at a dose of 0.2 microgram/ml. The cross-reactivities of IMPY and IMPY derivatives with the antibody were compared. Using this radioimmunoassay, clinical pharmacology was performed in cancer patients during phase I trials. Following 30-60-minute iv infusions of IMPY (450-1500 mg/m2/day for 5 days), the drug disappeared rapidly from plasma with an initial half-life of less than 10 minutes and second half-life of 4 hours. The half-lives are not affected by minimally abnormal hepatic function and are not dose-related. The apparent volume of distribution was approximately 125 ml/kg. The results obtained on Day 5 were essentially the same as those obtained on Day 1. IMPY was also detected in glioblastoma, brain, and temporalis muscle when the drug (500 mg/m2) was infused iv 4-5 hours before surgery. The tissue drug levels were comparable to or higher than those of plasma. The drug was also measurable in kidney and liver tissues obtained 4 hours after death in a patient who died 21 hours after iv infusion of IMPY at a dose of 1500 mg/m2/day for 3 days.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / analysis*
  • Cross Reactions
  • Drug Administration Schedule
  • Drug Evaluation
  • Female
  • Half-Life
  • Humans
  • Infusions, Parenteral
  • Male
  • Neoplasm Metastasis
  • Neoplasms / blood
  • Neoplasms / drug therapy*
  • Pyrazoles / administration & dosage
  • Pyrazoles / analysis*
  • Pyrazoles / metabolism
  • Radioimmunoassay / methods*
  • Reference Standards

Substances

  • Antineoplastic Agents
  • Pyrazoles
  • imidazopyrazole