A. Marsh et Mb. Evans, RADIOIMMUNOASSAY OF DRUGS OF ABUSE IN HAIR .1. METHADONE IN HUMAN HAIR, METHOD ADAPTATION AND THE EVALUATION OF DECONTAMINATION PROCEDURES, Journal of pharmaceutical and biomedical analysis, 12(9), 1994, pp. 1123-1130
A method suitable for the determination of methadone in human hair is
presented. Adaptation and evaluation of a solid-phase I-125 radioimmun
oassay, designed for the quantitative measurement of methadone in urin
e, and development of a pre-analytical wash procedure has enabled a sp
ecific, sensitive and accurate analytical procedure to be developed. T
he specificity of the antiserum towards other drugs or biologically ac
tive compounds is evaluated up to a concentration of 100,000 ng ml(-1)
and accuracy covering a range of 0-450 ng ml(-1) is found to be withi
n 6% of expected methadone concentrations prepared in both drug free h
air extract and urine. Inter-assay relative standard deviation (RSD) a
t concentrations of 5.1, 76.0 and 247 ng ml(-1) methadone art 5.5, 2.5
and 3.6% respectively (n = 10) and intraassay RSD at concentrations 2
.3, 25.2 and 217 ng ml(-1) are 5.3, 3.6 and 6.8% (n = 5). The limit of
detection is 0.5 ng ml(-1). Extraction of control drug free hair samp
les spiked with methadone at concentrations of 100, 250 and 400 ng ml(
-1) achieved recoveries of 86, 80 and 89%, respectively. Control hair
samples contaminated with methadone an examined under differing wash p
rocedures to assess their effectiveness in the removal of methadone co
ntaminant. A suitable preanalytical wash regime is proposed for remova
l of contaminant derived from external or environmental sources. The m
echanics of the wash action and contaminant application to the hair is
discussed. It is concluded that the adapted radioimmunoassay and deve
loped pre-analytical decontamination procedure is a suitable technique
to employ for the measurement of methadone in human hair, be it presc
ribed or abused, with concentrations expressed as ng methadone per mg
hair.