POUR-AMIR M, RASAEE M, DJALALI M, MALEKANEH M. DETERMINATION OF SERUM CORTISOL LEVEL BY A DIREC T ENZYME IMMUNOASSAY USING PENICILLINASE AS LABEL. Med J Islam Repub Iran 1998; 11 (4) :335-340
URL:
http://mjiri.iums.ac.ir/article-1-1078-en.html
From the Biochemistry Department, Tarbiat Modarres University, School of Medical Sciences, Tehran, I.R.lran
Abstract: (4607 Views)
Serum cortisol level was measured by an enzyme immunoassay (EIA) using
the enzyme penicillinase as a label without prior extraction and purification.
Polyclonal antibodies were raised against cortisol-3-ortho-carboxymethyl-oxime
(cortisol-3-0-CMO) conjugated to bovine serum albumin (BSA). This antibody
showed a very low cross-reactivity with structurally related steroids (3.7% for
corticosterone and 4% for II-deoxycorticosterone).
Standard doses were prepared in a serum sample stripped from endogenous
cortisol. Danazol, 8-anilinonaphtalosulphonic acid (8-ANS) and salicylic acid
were used as blocking reagents. However these reagents were not suitable in this
assay. Samples were heat treated (60° C for 30 min) in order to denature the binding
proteins. The assay was sensitive from 250 pg per tube covering up to 50 ng with
each point having a coefficient of variation (CV) of less then 15% throughout ten
successive assays. CortisoI3-0-CM 0 was conjugated to the penicillinase following
a carbodiimide procedure.
The formed conjugate retained almost 90% of the enzyme activity. Recoveries
of exogenously added cortisol from charcoal-stripped plasma in three different
ranges varied between 90-100%.
Inter and intra-assay variations showed a CV of less than 12 %. The correlation
coefficient was calculated as r=0.99 using our method and the results reported by
a local hospital for 20 samples.