Development and validation of a liquid chromatography-mass spectrometry method for the quantitation of naltrexone and 6beta-naltrexol in guinea pig plasma

J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Oct 25;810(2):259-67. doi: 10.1016/j.jchromb.2004.08.016.

Abstract

A quantitative liquid chromatographic-electrospray ionization mass spectrometry method for the determination of naltrexone and 6beta-naltrexol in guinea pig plasma has been developed and validated using naloxone as an internal standard. A single step precipitation-extraction technique was carried out to extract the plasma samples using acetonitrile:ethyl acetate (1:1, v/v). The chromatographic separation was performed on a C(18) column using a mobile phase consisting of 35:65 (v/v) acetonitrile:2 mM ammonium acetate with 0.01 mM ammonium citrate at a flow rate of 0.25 mL/min. The analyte was detected after positive electrospray ionization using selected ion monitoring (SIM) mode. The mean recoveries for naltrexone, naltrexol, and naloxone were 91.7, 89.3, and 99.0%, respectively. The lower limit of quantification (LLOQ) for naltrexone and 6beta-naltrexol was 1.25 ng/mL, and the limit of detection (LOD) was 0.75 ng/mL. The method was applied to a pharmacokinetic study in order to assess the drug disposition of naltrexone in guinea pigs.

Publication types

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

MeSH terms

  • Animals
  • Calibration
  • Chromatography, High Pressure Liquid
  • Guinea Pigs
  • Naltrexone / analogs & derivatives*
  • Naltrexone / blood*
  • Naltrexone / pharmacokinetics
  • Narcotic Antagonists / blood*
  • Narcotic Antagonists / pharmacokinetics
  • Quality Control
  • Reference Standards
  • Reproducibility of Results
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Narcotic Antagonists
  • 6 beta-hydroxynaltrexone
  • Naltrexone