Evidence map›Paper›PMID 26311037›Full record

ArticleJournal of nanobiotechnology2015

Surface plasmon resonance based on molecularly imprinted nanoparticles for the picomolar detection of the iron regulating hormone Hepcidin-25.

Lucia Cenci, Erika Andreetto, Ambra Vestri, Michele Bovi, Mario Barozzi, Erica Iacob, Mirko Busato, Annalisa Castagna, Domenico Girelli, Alessandra Maria Bossi

Abstract readEvaluation Study
In one paragraph

Article in Journal of nanobiotechnology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

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  15. MIRATE: MIps RATional dEsign Science Gateway.Journal of integrative bioinformatics · 2018
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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

10 authors.

Lucia CenciDepartment of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy. lucia.cenci@univr.it.
Erika AndreettoDepartment of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy. erika.andreetto@univr.it.
Ambra VestriDepartment of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy. ambra.vestri@univr.it.
Michele BoviDepartment of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy. michele.bovi@univr.it.
Mario BarozziCenter for Materials and Microsystems CMM-MNF, FBK Fondazione Bruno Kessler, Via Sommarive 18, 38123, Povo-Trento, Italy. barozzi@fbk.eu.
Erica IacobCenter for Materials and Microsystems CMM-MNF, FBK Fondazione Bruno Kessler, Via Sommarive 18, 38123, Povo-Trento, Italy. iacob@fbk.eu.
Mirko BusatoDepartment of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy. mirko.busato@univr.it.
Annalisa CastagnaDepartment of Medicine, University of Verona, Section of Internal Medicine B, 37134, Verona, Italy. annalisa.castagna@univr.it.
Domenico GirelliDepartment of Medicine, University of Verona, Section of Internal Medicine B, 37134, Verona, Italy. domenico.girelli@univr.it.
Alessandra Maria BossiDepartment of Biotechnology, University of Verona, Strada Le Grazie 15, 37134, Verona, Italy. alessandramaria.bossi@univr.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMolecularly imprinted polymer (MIP) technique is a powerful mean to produce tailor made synthetic recognition sites. Here precipitation polymerization was exploited to produce a library of MIP nanoparticles (NPs) targeting the N terminus of the hormone Hepcidin-25, whose serum levels correlate with iron dis-metabolisms and doping. Biotinylated MIP NPs were immobilized to NeutrAvidin™ SPR sensor chip. The response of the MIP NP sensor to Hepcidin-25 was studied.

findingsMorphological analysis showed MIP NPs of 20-50 nm; MIP NP exhibited high affinity and selectivity for the target analyte: low nanomolar Kds for the interaction NP/Hepcidin-25, but none for the NP/non regulative Hepcidin-20. The MIP NP were integrated as recognition element in SPR allowing the detection of Hepcidin-25 in 3 min. Linearity was observed with the logarithm of Hepcidin-25 concentration in the range 7.2-720 pM. LOD was 5 pM. The response for Hepcidin-20 was limited. Hepcidin-25 determination in real serum samples spiked with known analyte concentrations was also attempted.

conclusionThe integration of MIP NP to SPR allowed the determination of Hepcidin-25 at picomolar concentrations in short times outperforming the actual state of art. Optimization is still needed for real sample measurements in view of future clinical applications.

Indexed as

Molecular ImprintingHepcidinsHumansIronLimit of DetectionNanoparticlesSurface Plasmon Resonancehepcidin 25, humanHepcidinsIron

Identifiers

PMID26311037
PMCPMC4549936

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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.