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Published:
Journal of Analytical Toxicology,
ISSN 0146-4760,
Volume 27, Number 8, November/December,
pp. 574-580
Determination of Endogenous Levels of GHB in Human Hair.
Are there Possibilities for the Identification of GHB Administration through
Hair Analysis in Cases of Drug-Facilitated Sexual Assault?
Jean Pierre Goullé[1], Marjorie Chèze[2],
and Gilbert Pépin[2]
[1]Laboratoire de PharmacocInétique et de Toxicologie Cliniques, Hôpital
Jacques Monod, BP 24, 76083 Le Havre, France and [2]Laboratoire d’Expertises
TOXLAB, 7 rue Jacques Cartier, 75018 Paris, France
We have developed a GC–MS–MS assay for GHB in human
hair. Five milligrams of washed hair were hydrolyzed by 1M or 0.01M NaOH before
a liquid–liquid extraction with ethyl acetate under acidic conditions.
GHB-d6 was used as the internal standard. TMS derivatives were formed before
injection. TBDMS derivatives were used in cases of strong chromatographic interferences
or in a confirmatory procedure. Analysis of basal levels of GHB in 61 drug-free
donors gave the following results: the mean measured concentration for blond
hair was 0.60 ng/mg (n = 12), SD = 0.19 ng/mg, and extreme figures were in
the range 0.35–0.95 ng/mg. For brown hair, the mean measured concentration
was 0.90 ng/mg (n = 30), SD = 0.42 ng/mg, and extreme figures 0.41–1.86
ng/mg. For black hair, the mean measured concentration was 0.90 ng/mg (n =
19), SD = 0.37 ng/mg, and extreme figures 0.32–1.54 ng/mg, showing no
significant differences depending on hair color. Analysis of basal levels of
GHB of 12 or more specimens in segmented hair showed a mean concentration of
1.22 ng/mg (0.31–8.4 ng/mg) and a relative standard deviation for each
individual ranging from 6.75% to 37.98%. GHB was administered to a healthy
53-year-old white male (light brown hair) at oral dosages of 30, 45, and 60
mg/kg. Beard hair was collected just before administration and 24 h after (and
each day for one week for the last dose), and a 7.5-cm scalp hair lock was
collected 7 days after the last dose. A rise in GHB concentration was observed
in beard hair for the 45 and 60 mg/kg dosages with a maximum at 24 h, whereas
no change was observed for the 30 mg/kg dosage. Scalp hair was segmented into
3-mm long segments. The three proximal last segments showed significantly (0.0005 < p < 0.005)
different concentrations of GHB (1.22, 1.27, and 1.66 ng/mg, respectively)
when compared with the basal physiological level of GHB in this same person
(mean = 0.62 ng/mg, SD = 0.15 ng/mg). A case of daily GHB abuse during bodybuilding
allowed us to determine a concentration of GHB of 14 ng/mg, in a 2-cm long
segment (black hair). A case of rape under the influence of GHB was documented
through hair analysis (black hair) and positive analysis of the glass she used.
Sampled 7 days after the sexual assault, the three last 3-mm long proximal
segments tested for GHB exhibited concentrations of 3.1–5.3 and 4.3 ng/mg,
respectively, whereas the mean physiological level determined in this woman
was 0.71 ng/mg, SD = 0.17 ng/mg. The authors advise a two-step hair sampling
as evidence of GHB consumption: the first sample at the time of exposure to
show the contamination by sweat of the proximal segment in case of recent administration
with a significant rise of hair level at the root, and the second after at
least 3 or 4 weeks to avoid this contamination and determine the levels incorporated
in the hair matrix before, during, and after the exposure. Reproduction
of editorial content of this journal is prohibited without publishers
permission.
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