W
hile i
mmunoassays
have been extensively applied toevaluate environ
mental conta
mination, to date t
hey
haverarely been used for t
he analysis of biological fluids outsideof
hu
man
medicine. T
hese
media are i
mportant becausepollutants suc
h as polycyclic aro
matic
hydrocarbons (PAHs)and t
heir
metabolites beco
me concentrated in tissues,body fluids, and excreta, t
hereby offering a
measure ofexposure to biologically available conta
minants. Suc
hanalyses also provide a nondestructive tool for
monitoringexposure. Crabs (
Carcinus maenas) were exposed top
henant
hrene and pyrene (separately) at concentrationsranging fro
m 0 to 200
![](/i<font color=)
mages/entities/
mgr.gif">g L
-1. After 48
h, urine sa
mples weretaken and analyzed by i
mmunoassay and UV-fluorescencespectrop
hoto
metry. Urinary levels (calibrated against
hydroxylated
metabolites) proved to be dose dependentfor bot
h co
mpounds, and good agree
ment was de
monstratedbetween t
he i
mmunoassay and t
he fluorescence tec
hniques.T
he cross reactivity of t
he i
mmunoc
he
mical tec
hnique(ELISA) for pyrene and
hydroxy-
metabolites was lower t
hanfor p
henant
hrene. HPLC analyses de
monstrated t
haturine fro
m t
he crabs exposed to pyrene contained
mainlyconjugate PAH
metabolites w
hose concentrations (t
hesu
m of t
he four
main pyrene
metabolites/conjugates) s
howedvery good agree
ment wit
h t
he ELISA (
r2 > 0.94) andfluorescence (
r2 > 0.91) data. Environ
mental sa
mples werealso analyzed by ELISA and UV-fluorescence, and bot
htec
hniques detected PAH (
mainly petrogenic) conta
minationin t
he urine sa
mples fro
m a polluted
harbor. T
hese datade
monstrate t
he potential of urine analyses by ELISA and UV-fluorescence to
measure exposure of crabs to PAH.