A sensitive chemiluminescence based immunoassay for the detection of cortisol and cortisone as stress biomarkers

被引:11
|
作者
Abdulsattar, Jwan O. [1 ]
Greenway, Gillian M. [2 ]
机构
[1] Mustansiriyah Univ, Coll Sci, Dept Chem, Baghdad, Iraq
[2] Univ Hull, Dept Chem & Biochem, Kingston Upon Hull, N Humberside, England
关键词
Stress hormones; Biosensors; Immunoassays; Chemiluminescence; ENDOGENOUS STEROID-HORMONES; NIGHT SALIVARY CORTISOL; LC-MS/MS; ENHANCED CHEMILUMINESCENCE; CUSHINGS-SYNDROME; PERFORMANCE; ASSAYS; FECES; OXIDE;
D O I
10.1186/s40543-019-0196-y
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An electrochemically based antibody immobilization was used to perform environmentally and clinically relevant immunoassays for stress hormones biomarkers (cortisol and cortisone) using chemiluminescence (CL) detection. To achieve CL detection, the ferrocene tag on the antibodies was first oxidised, and this then acted as a catalyst for the luminol and hydrogen peroxide CL reaction. The conditions were optimised and measurements were made with an incubation time of 30 min. Using this approach limits of detection were obtained of 0.47 pg ml(-1) and 0.34 pg ml(-1) also R-2 0.9912 and 0.9902 for cortisol and cortisone respectively with a linear concentration from 0 to 50 ng ml(-1). The method was then applied to Zebrafish whole body and artificial saliva samples. For the Zebrafish sample recoveries of 91.0% and 90.0% were obtained with samples spiked with cortisol and cortisone, for artificial saliva the recoveries were 92.59% and 90.73% respectively. Interference studies showed only minor effects on the measurement of the analyte. A comparison between this procedure and the standard enzyme-linked immunosorbent assay (ELISA) procedure gave approximately the same R-2 values.
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页数:13
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