In exposure and risk evaluation, monitoring lead biologically has seve
ral advantages over technical exposure assessment. Traditionally, the
concentration in blood (B-Pb) has been widely used. However, the eryth
rocytes tend to become saturated, and this phenomenon causes a nonline
ar relationship between B-Pb and uptake and between metabolic and toxi
c effects and B-Pb. Recently, several techniques for determining lead
in finger bone, tibia, or calcaneus in vivo by X-ray fluorescence have
become available. Bone lead reflects long-term exposure and should pr
ove valuable in epidemiologic studies. Mobilization tests have been wi
dely used to monitor lead biologically. They mainly seem to reflect th
e lead in soft tissues and may not be an index of total body burden, m
ost of which is in the skeleton. It thus seems that, at least in adult
s, mobilization tests do not provide more information than traditional
lead determinations in blood and urine. A metabolic model for lead in
humans is presented.