Development of enantioselective gas chromatographic quantitation assay for dl-threo-methylphenidate in biological fluids

J Chromatogr. 1986 May 28;378(1):109-23. doi: 10.1016/s0378-4347(00)80704-5.

Abstract

An enantioselective gas chromatographic quantitation assay was developed for the enantiomers of dl-threo-methylphenidate in plasma and urine. dl-threo-Methylphenidate and the internal standard were acylated with N-heptafluorobutyryl-1-prolylchloride under Schotten-Baumann conditions prior to gas chromatographic separation on achiral mixed stationary phases. The derivatives were detected by means of a nitrogen-phosphorus detector. Linear and reproducible calibration curves were obtained over the concentration ranges 0.43-43.25 and 2.16-216.25 ng/ml enantiomer in plasma or urine, respectively. This enantioselective gas chromatographic quantitation assay was applied in a single oral dose disposition study of dl-threo-methylphenidate in a healthy adult volunteer. Stereoselective differences were observed in the plasma concentration-time profiles and cumulative urinary excretion profiles following oral doses of 20 and 40 mg of dl-threo-methylphenidate hydrochloride. Only d-threo-methylphenidate was detectable in plasma after 4 h.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Chromatography, Gas
  • Drug Stability
  • Humans
  • Indicators and Reagents
  • Kinetics
  • Male
  • Methylphenidate / analysis*
  • Methylphenidate / blood
  • Methylphenidate / urine
  • Stereoisomerism
  • Temperature

Substances

  • Indicators and Reagents
  • Methylphenidate