Evidence map›Paper›PMID 31426452›Full record

ArticleInternational journal of molecular sciences2019

A Zinpyr-1-based Fluorimetric Microassay for Free Zinc in Human Serum.

Wiebke Alker, Tanja Schwerdtle, Lutz Schomburg, Hajo Haase

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.1field-weighted citation impact, top 9% of its field
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

28 citing papers in PubMed, 51 citations in OpenAlex.

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  2. ZnbioRxiv : the preprint server for biology · 2026
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  17. Albumin-mediated extracellular zinc speciation drives cellular zinc uptake.Chemical communications (Cambridge, England) · 2022
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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 at 3 institutions in 1 country.

Wiebke AlkerDepartment of Food Chemistry and Toxicology, Berlin Institute of Technology, 13355 Berlin, Germany.
Tanja SchwerdtleTraceAge-DFG Research Unit on Interactions of essential trace elements in healthy and diseased elderly, Potsdam-Berlin-Jena, Germany.
Lutz SchomburgTraceAge-DFG Research Unit on Interactions of essential trace elements in healthy and diseased elderly, Potsdam-Berlin-Jena, Germany.
Hajo HaaseDepartment of Food Chemistry and Toxicology, Berlin Institute of Technology, 13355 Berlin, Germany. Haase@tu-berlin.de.
Fraunhofer Institute for Production Systems and Design Technology · DEHumboldt-Universität zu Berlin · DEUniversity of Potsdam · DE

Funding

Deutsche Forschungsgemeinschaft FOR 2558/1, HA 4318/4-1, SCH 903/16-1, SCHO 849/6-1
6 · The paper itself

Abstract

Zinc is an essential trace element, making it crucial to have a reliable biomarker for evaluating an individual's zinc status. The total serum zinc concentration, which is presently the most commonly used biomarker, is not ideal for this purpose, but a superior alternative is still missing. The free zinc concentration, which describes the fraction of zinc that is only loosely bound and easily exchangeable, has been proposed for this purpose, as it reflects the highly bioavailable part of serum zinc. This report presents a fluorescence-based method for determining the free zinc concentration in human serum samples, using the fluorescent probe Zinpyr-1. The assay has been applied on 154 commercially obtained human serum samples. Measured free zinc concentrations ranged from 0.09 to 0.42 nM with a mean of 0.22 ± 0.05 nM. It did not correlate with age or the total serum concentrations of zinc, manganese, iron or selenium. A negative correlation between the concentration of free zinc and total copper has been seen for sera from females. In addition, the free zinc concentration in sera from females (0.21 ± 0.05 nM) was significantly lower than in males (0.23 ± 0.06 nM). The assay uses a sample volume of less than 10 µL, is rapid and cost-effective and allows us to address questions regarding factors influencing the free serum zinc concentration, its connection with the body's zinc status, and its suitability as a future biomarker for an individual's zinc status.

Indexed as

BiomarkersFemaleFluoresceinsFluorescent DyesHumansLimit of DetectionMaleSpectrometry, FluorescenceZincBiomarkersFluoresceinsFluorescent DyesZinczinpyr-1biomarkerfluorescent probefree zincserumzincZinypr-1

Identifiers

PMID31426452
PMCPMC6720863
OpenAlexW2969134051

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.