Determination of Salvinorin A in body fluids by high performance liquid chromatography-atmospheric pressure chemical ionization

J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Apr 25;818(2):221-5. doi: 10.1016/j.jchromb.2004.12.041.

Abstract

Salvinorin A was quantitated in human and rhesus monkey plasma, rhesus monkey cerebrospinal fluid, and human urine by negative ion LC-MS/APCI. The method for Salvinorin A has been fully validated, the LLOQ using FDA guidelines is 2 ng/mL for 0.5 mL plasma samples. The linear range was from 2 to 1000 ng/mL. Several derivatives in the Salvinorin family can also be analyzed by this method; d(3)-Salvinorin A was prepared and used as internal standard. The metabolite Salvinorin B can be semi quantitatively determined. The method has been used to establish that Salvinorin B is the principal metabolite of Salvinorin A ex vivo and to establish the analytical method to study in vivo samples.

Publication types

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

MeSH terms

  • Animals
  • Chromatography, High Pressure Liquid / methods*
  • Diterpenes / analysis*
  • Diterpenes / blood
  • Diterpenes / cerebrospinal fluid
  • Diterpenes / urine
  • Diterpenes, Clerodane
  • Hallucinogens / analysis
  • Humans
  • Macaca mulatta
  • Receptors, Opioid, kappa / agonists
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Diterpenes
  • Diterpenes, Clerodane
  • Hallucinogens
  • Receptors, Opioid, kappa
  • salvinorin A