Steroids 1995-09-01

Radioimmunoassay of three deoxycorticoids in human plasma following HPLC separation.

M Hill, O Lapcík, R Hampl, L Stárka, Z Putz

Index: Steroids 60(9) , 615-20, (1995)

Full Text: HTML

Abstract

A radioimmunoassay of three deoxycorticoids, namely 11 beta,17 alpha-dihydroxy-4-pregnene-3,20-dione (21-deoxycortisol), 17 alpha,21-dihydroxy-4-pregnene-3,20-dione (11-deoxycortisol), and 21-hydroxy-4-pregnene-3,20-dione (11-deoxycorticosterone) which are important for differential diagnosis of congenital adrenal disorders, is described and evaluated. Antisera against 3-(O-carboxymethyl)oximes conjugated to bovine serum albumin were raised in rabbits. The radioligands were prepared by radioiodination of previously synthesized homologous tyrosine methyl ester derivatives. Following diethyl ether extraction, the steroids were separated from each other and from cross-reactants by HPLC using a Nucleosil C8 reverse-phase column and a methanol-water mixture (7:5, v/v) as an eluent. Normal levels of analyzed steroids ranged from 0.02 to 0.348, 0.185 to 3.80, and 0.013 to 0.299 nmol/l, for 21-deoxycortisol, 11-deoxycortisol and 11-deoxycorticosterone, respectively. The levels of both deoxycortisols rose significantly after ACTH treatment. Data are given with respect to the concentrations of these steroids in some pathological situations such as 21-hydroxylase and 11 beta-hydroxylase block, hyperaldosteronism, and polycystic ovary syndrome.


Related Compounds

Related Articles:

An LC-MS/MS method for steroid profiling during adrenal venous sampling for investigation of primary aldosteronism.

2015-01-01

[J. Steroid Biochem. Mol. Biol. 145 , 75-84, (2015)]

Hirsutism and acne in women: coordinated radioimmunoassays for eight relevant plasma steroids.

1994-12-01

[Clin. Chem. 40(12) , 2296-305, (1994)]

Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency.

2010-12-01

[Clin. Endocrinol. (Oxf.) 73(6) , 700-6, (2010)]

Neonatal screening: identification of children with 11β-hydroxylase deficiency by second-tier testing.

2012-01-01

[Horm. Res. Paediatr. 77(3) , 195-9, (2012)]

Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriers.

2010-05-01

[Gynecol. Endocrinol. 26(5) , 319-24, (2010)]

More Articles...