Publication October 2010, 31

FOR THE DETERMINATION OF HUMAN THYROGLOBULIN

Publication October 2010, 31

DEVELOPMENT OF ULTRA-SENSITIVE SOYBEAN PEROXIDASE-BASED CL-ELISA FOR THE DETERMINATION OF HUMAN THYROGLOBULIN
 
Abstract
Serum thyroglobulin (Tg) is a main marker of thyroid cancer relapses after total or near-total thyroidectomy of patients with differentiated thyroid carcinoma. In this study, we developed a chemiluminescent enzyme-linked immunosorbent assay (CL-ELISA) for detecting Tg in human serum. Soybean peroxidase (SbP) in combination with 3-(10′-phenothiazinyl)propane-1- sulfonate (SPTZ) and 4-morpholinopyridine (MORPH) and horseradish peroxidase (HRP) with p-iodophenol (PIP) were used as detection systems in the sandwich CL-ELISA. Comparison of these two systems showed that a lower detection limit (LOD) of CL-ELISA with SbP/SPTZ/ MORPH was 10 times lower than for the immunoassay with HRP/PIP. The LOD value for SbP based CL-ELISA of 0.2 ng/mL was identical to LOD value typical of CL-ELISA Immulite® kit produced with alkaline phosphatase. The sensitivity of Tg CL-ELISA using SbP/SPTZ/MORPH completely satisfies the requirements of modern endocrinology. Comparative study of clinical serum specimens assayed by the SbP-based CL-ELISA (x) and Immulite® kit (y) for detecting Tg showed a good correlation between these two immunoassays (y=1.15x−0.14, R=0.99). The obtained results open good perspectives for use of SbP/SPTZ/MORPH system in the development of ultra-sensitive immunoassays.

 
Figure:  Linear correlation analysis between thyroglobulin concentrations obtained using the SbP-based CL-ELISA (x) and Immulite® kit (y). Estimation of Tg levels by the SbP-based CL-ELISA was carried out in (A) undiluted (n=30) and (B) serum samples diluted (1:1) (n=11) using PBST with 1% BSA.

 
Link: http://www.sciencedirect.com/science/article/pii/S002217591000270X
Publication Date: October 2010, 31

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