Contact Info
Stuart Chalk, Ph.D.
Department of Chemistry
University of North Florida
Phone: 1-904-620-1938
Fax: 1-904-620-3535
Email: schalk@unf.edu
Website: @unf
Corticosterone
- IUPAC Name: (8S,9S,10R,11S,13S,14S,17S)-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
- Molecular Formula: C21H30O4
- CAS Registry Number: 50-22-6
- InChI: InChI=1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-17,19,22,24H,3-8,10-11H2,1-2H3/t14-,15-,16+,17-,19+,20-,21-/m0/s1
- InChI Key: OMFXVFTZEKFJBZ-HJTSIMOOSA-N
Citations 1
"Flow Injection Chemiluminometric Analysis Of Some Steroids By Their Sensitizing Effect On The Bromate-sulfite Reaction"
Anal. Chim. Acta
1990 Volume 239, Issue 2 Pages 195-202
Aristotelis B. Syropoulos, Evangelos G. Sarantonis and Antony C. Calorkerinos
Abstract:
The solution of cortisone (I), hydrocortisone, corticosterone, testosterone (II) or progesterone (III) were injected into 2 mM NaBrO3 in 20 mM H2SO4 at 1.5 mL min-1. After mixing with 0.5 mM SO32- the luminescence was measured with a photomultiplier. The responses were rectilinear between 0.5 and 5 to 6 µg mL-1 except for I which was from 0.5 to 20.0 µg mL-1, with limits of detection between 0.1 and 0.4 µg mL-1. The coefficient of variation (n = 6) for 0.5 and 4.0 µg mL-1 of III were 2.3 and 0.5%, respectively, which were typical for all the steroids. Recoveries of II from various excipients were between 95.8 and 104.0%.
Chemiluminescence
Sensitivity
Detection limit
Indirect