Exp Clin Endocrinol Diabetes 1994; 102(1): 39-43
DOI: 10.1055/s-0029-1211263
Original

© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Time-resolved fluoroimmunoassay (TR-FIA) of gonadotropins

A. Iwasawa, K. Tomizawa, T. Kato, K. Wakabayashi, Y. Kato
  • Hormone Assay Center, Institute of Endocrinology, Gunma University, Maebashi, Japan
Further Information

Publication History

Publication Date:
15 July 2009 (online)

Summary

Time-resolved fluoroimmunoassay (TR-FIA), which has recently been developed as a non-isotopic immunoassay, was intended for assay of gonadotropins (LH and FSH). Ovine LH or FSH was labeled with N1-(p-isothiocyanatobenzyl)-diethylenetriamine-N1, N2, N3, N3-tetraacetic acid Eu-chelate (DTTA), and competitive binding assay was performed using a 96-weel titer plate previously coated with a second antibody, followed by measurement using time-resolved fluorometry. TR-FIA for standard ovine LH (NIDDK, LH-I-3) or FSH (NIDDK, FSH-I-1) had a sensitivity of about 25 pg/50 μl sample. The assay system was applied to heterologous assay of porcine gonadotropins. Linearity was obtained by the dilution test using medium from primary culture of porcine anterior pituitary cells. Intra- and inter-assay coefficients of variation of LH and FSH determination in 31 different porcine samples were satisfactorily low, between 3.5 and 8.1% (intra-assay) and between 1.7 and 13.1% (inter-assay). Correlation coefficients between radioimmunoassay and TR-FIA were calculated to be 0.945 for LH and 0.978 for FSH. Stimulation of LH and FSH release with GnRH was observed by TR-FIA. This non-isotopic TR-FIA thus provides as good sensitivity, reproducibility and accuracy as conventional RIAs.

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