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Updated: Aug 9, 2026

Reproductive Techniques for Ovarian Monitoring and Control in Amphibians
Published on: May 12, 2019
Pregnancy serum contains the beta-core fragment of human choriogonadotropin
1Department of Obstetrics and Gynecology, Helsinki University Central Hospital, Finland.
Insights
We developed a sensitive assay to measure the core fragment of human chorionic gonadotropin (c beta hCG) in serum. This finding confirms c beta hCG is present during pregnancy, not solely formed in the kidneys.
Area of Science:
- Biochemistry
- Immunology
- Reproductive Biology
Background:
- Human chorionic gonadotropin (hCG) plays a vital role in pregnancy.
- The core fragment of the beta-subunit of hCG (c beta hCG) is a marker of hCG degradation.
- Understanding c beta hCG formation is crucial for reproductive health research.
Purpose of the Study:
- To develop and validate a sensitive time-resolved immunofluorometric assay (IFMA) for quantifying c beta hCG.
- To investigate the presence and origin of c beta hCG in serum during pregnancy.
Main Methods:
- Development of a two-monoclonal antibody-based IFMA utilizing a europium chelate label.
- Separation of hCG, beta hCG, and c beta hCG using gel chromatography.
- Quantification of separated components via specific IFMAs.
Main Results:
- The developed IFMA demonstrated high sensitivity (0.44 pmol/L).
- Cross-reactivity with free beta hCG necessitated chromatographic separation for accurate c beta hCG measurement in serum.
- c beta hCG was detected in serum from pregnant women, eluting identically to purified c beta hCG.
Conclusions:
- The presence of c beta hCG in pregnancy serum is confirmed.
- Proteolytic degradation in the kidneys may not be the sole source of c beta hCG.
- The developed IFMA provides a sensitive tool for studying c beta hCG in reproductive contexts.
Abstract:
We have developed a time-resolved immunofluorometric assay (IFMA) for quantification of the core fragment of the beta-subunit (c beta hCG) of hCG. The assay uses two monoclonal antibodies. One antibody is immobilized onto the wall of a microtiter strip well, and the other one is labeled with a europium chelate. The assay is sensitive (0.44 pmol/L = 4.6 ng/L), but cross-reaction with free beta-subunits of hCG (beta hCG) prevents direct determination of c beta hCG in serum. To circumvent this limitation we separated hCG and beta hCG from c beta hCG by gel chromatography and quantified each component in the fractions by specific IFMAs. The high sensitivity of the newly developed IFMA enabled us to demonstrate that serum from pregnant women contains c beta hCG and elutes at the same position in gel chromatography as c beta hCG purified from urine. The proportion of c beta hCG to hCG in pregnancy serum was 0.012-0.045% (mean +/- SD, 0.028 +/- 0.01) on a molar basis. Our finding of c beta hCG in serum confirms earlier reports suggesting that proteolytic degradation of beta hCG in the kidneys may not be the only pathway by which c beta hCG is formed.
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