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Articles |
1
National Diagnostics CentreBioresearch Ireland, University College, Galway, Ireland.
2
Department of Obstetrics & Gynecology, Asahikawa Medical
College, Japan.
3
Department of Biochemistry, University College, Galway,
Ireland.
4
Fertility Unit, Department of Obstetrics & Gynecology,
University College Hospital, Galway, Ireland.
a Author for correspondence. Fax 353 91 586570; e-mail: marian. kane{at}ucg.ie
We developed a direct microtiter plate enzyme immunoassay to measure estradiol-17ß in saliva. The assay has a commercially available monoclonal antibody, raised against estradiol-17ß6-carboxymethyloximebovine serum albumin, and a homologous horseradish peroxidase conjugate measured colorimetrically. The detection limit (equivalent to B0 - 3 SD) is 365 amol/well or 7.3 pmol/L when 50-µL samples are assayed. Cross-reactivity with estrone and estriol, testosterone, or progesterone is <0.2%. Estradiol-17ß was measured in daily samples over five natural menstrual cycles and eight cycles stimulated as a preliminary to in vitro fertilization, and the concentrations and fluctuations found agreed with previously published data. This method gives results in ~3 h and may be useful for fertility monitoring and management.
Key Words: indexing terms: menstrual cycle in vitro fertilization
The following articles in journals at HighWire Press have cited this article:
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G Wycherley, D Downey, M T Kane, and A C Hynes A novel follicle culture system markedly increases follicle volume, cell number and oestradiol secretion Reproduction, June 1, 2004; 127(6): 669 - 677. [Abstract] [Full Text] [PDF] |
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