Evidence map›Paper›PMID 41748485›Full record

ArticleAnalytical chemistry2026

Development of an Anti-Immunocomplex Antibody and Non-competitive Immunoassay for the Detection of Testosterone.

Ida Bäckström, Urpo Lamminmäki, Etvi Juntunen, Janne Leivo

Abstract read
In one paragraph

Article in Analytical chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Ida BäckströmDepartment of Life Technologies and InFLAMES Flagship, University of Turku, Turku 20014, Finland.ORCID 0009-0007-8003-417X
Urpo LamminmäkiDepartment of Life Technologies and InFLAMES Flagship, University of Turku, Turku 20014, Finland.
Etvi JuntunenOlo Health Oy, Turku 20100, Finland.
Janne LeivoDepartment of Life Technologies and InFLAMES Flagship, University of Turku, Turku 20014, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate and sensitive quantification of testosterone using simple, high-throughput, and low-cost methods has remained a longstanding analytical challenge, despite the issue being highlighted by the endocrinology community more than a decade ago. Existing competitive immunoassays lack sensitivity and specificity, while reference methods based on mass spectrometry are complex, costly, and unsuitable for routine large-scale testing. Alternative approaches are needed to aid in the diagnosis of androgen deficiency and excess in men, women, and children. In this study, we report a novel anti-immunocomplex (anti-IC) antibody that recognizes a monoclonal anti-testosterone antibody bound to testosterone. The anti-IC antibody was generated using phage display, and the antibody pair was utilized in the development of a non-competitive time-resolved fluorescence immunoassay for the detection of testosterone. The assay demonstrated reliable detection within the physiological range of testosterone in men, women, and children and compatibility with plasma as a sample matrix. These findings emphasize the potential of novel anti-IC antibodies in the development of more sensitive immunoassays, offering accessible alternatives to existing methods for testosterone analysis.

Indexed as

Antibodies, MonoclonalTestosteroneAnimalsFemaleHumansImmunoassayMaleAntibodies, MonoclonalTestosterone

Identifiers

PMID41748485
PMCPMC12980484

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.