Most studies related to research on steroids in main edible tissues (muscle
, liver or kidney) have focused on measurement of parent or major metabolit
e residues. In order to evaluate the estradiol content in bovine edible tis
sues, a multi-step extraction procedure was developed in conjunction with p
arallel metabolism studies of [C-14]-17 beta -estradiol in cattle (1-2). Va
rious classes of free estradiol and conjugates were separated: estradiol -1
7 beta and -17 alpha, estradiol-17-fatty. acid esters, estradiol 17-glycosi
de, estradiol 3-glucuronide, estradiol-17-glycoside and 3- glucuronide (dic
onjugates) were separated. No sulphates conjugated forms have been found at
the detection level of the method. The quantification was realized by cali
bration with deuterated 17 beta -estradiol -d(3) standard and was validated
at the ng . kg(-1) (ppt) level. Muscle, liver, kidney and fat samples from
control or Revalor S (R) single (licensed implantation) or multi-implanted
steers have been assayed.
The results show a wide variation between animals, but both the highest val
ue and the mean of total estradiol content in each group proportionally inc
rease from untreated to multi-implanted animals. In accordance with interna
tional rules, a calculation of the daily food supply of estradiol by such e
dible tissues in comparison with the acceptable daily intake was performed.