Liquid chromatographic-tandem mass spectrometric method for the quantitation of huperzine A in dog plasma

J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Apr 25;803(2):375-8. doi: 10.1016/j.jchromb.2004.01.013.

Abstract

A rapid and sensitive LC-MS-MS method for the determination of huperzine A in dog plasma using huperzine B as internal standard has been developed and validated. The analyte and internal standard were extracted from plasma using n-hexane-dichloromethane-2-propanol (300:150:15, v/v/v), chromatographed on a C(18) column (5 microm, 50 mm x 4.6 mm i.d.) with a mobile phase consisting of acetonitrile-methanol-10mM ammonium acetate (35:40:25, v/v/v), and detected using a tandem mass spectrometer with a TurboIonSpray ionization interface. The run time was only 2 min. The assay was linear over the concentration range 0.05-20 ng/ml and intra- and inter-day precision over this range were <5.3% with good accuracy. The limit of detection in plasma was 0.01 ng/ml. The method was successfully applied to define plasma concentration-time curves of huperzine A in dogs after the last dose of an intramuscular injection (10 microg/kg per day for 15 days) of a sustained-release formulation of huperzine A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids
  • Animals
  • Dogs
  • Mass Spectrometry
  • Neuroprotective Agents / blood*
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Sesquiterpenes / blood*

Substances

  • Alkaloids
  • Neuroprotective Agents
  • Sesquiterpenes
  • huperzine A