THE ANALYSIS OF LYSERGIDE (LSD) - THE DEVELOPMENT OF NOVEL ENZYME-IMMUNOASSAY AND IMMUNOAFFINITY EXTRACTION PROCEDURES TOGETHER WITH AN HPLC-MS CONFIRMATION PROCEDURE
Ks. Webb et al., THE ANALYSIS OF LYSERGIDE (LSD) - THE DEVELOPMENT OF NOVEL ENZYME-IMMUNOASSAY AND IMMUNOAFFINITY EXTRACTION PROCEDURES TOGETHER WITH AN HPLC-MS CONFIRMATION PROCEDURE, Journal of forensic sciences, 41(6), 1996, pp. 938-946
A forensic procedure for the screening and confirmation of the presenc
e of lysergide (lysergic acid diethylamide, LSD) in urine is described
together with the evaluation of a novel enzyme immunoassay (EIA) and
immunoaffinity extraction procedure. Following initial screening using
either an established radioimmunoassay (RIA) or a novel EIA procedure
, a quantitative estimate is established using a conventional high per
formance liquid chromatography-fluorescence (HPLC) technique following
solid phase extraction. Final confirmation and quantitation, without
derivatization, is established using HPLC in combination with electros
pray ionization (ESI) mass spectrometry using methysergide as an inter
nal standard. The detection limit of LSD in urine is 0.5 ng/mL. A blin
d trial confirmed the validity of the results. The choice of internal
standard is discussed. Consideration is given to the photosensitivity
of LSD solutions. A study of potential interferants in the HPLC-MS con
firmation of LSD is presented and shows that for the wide range of com
pounds studied, there are none that would interfere with this confirma
tion technique. A comparison is shown between solid phase and immunoaf
finity extraction/clean up procedures, and between RIA and EIA screeni
ng procedures.