Evidence map›Paper›PMID 41575582›Full record

ArticleMikrochimica acta2026

Ultra-sensitive nanostructured electrochemical immunosensor for selective monitoring of L-phenylalanine in phenylketonuria patients.

Rebecca L Houston, Eric C Y Law, Emad L Izake

Abstract read
In one paragraph

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

0numbers the graph read from it
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

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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

3 authors.

Rebecca L HoustonSchool of Chemistry and Physics, Queensland University of Technology, Brisbane, QLD, Australia. rebeccca.houston@hdr.qut.edu.au.
Eric C Y LawThe Children's Hospital at Westmead, Sydney, NSW, 2145, Australia.
Emad L IzakeSchool of Chemistry and Physics, Queensland University of Technology, Brisbane, QLD, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A low cost and rapid electrochemical immunosensor for direct screening of L-phenylalanine (L-Phe) using square wave voltammetry (SWV) is presented. Fern-like gold nanostructures were electro-deposited onto a screen-printed electrode (SPE) using chronoamperometry (CA), to enhance sensitivity and surface area. A novel light-driven surface functionalisation process was used to decorate the gold nanostructured SPE with target-specific antibody fragments and develop the L-Phe-specific immunosensor. The selectivity of the sensor was confirmed against tyrosine, tryptophan and D-phenylalanine, thus indicating the sensor's potential for use at points of care (POC) without interference from structurally related biomolecules. The sensor demonstrated high sensitivity across the full clinical range (120 µM-1200 µM) and excellent linearity within the concentration range 1 µM to 2000 µM (R²= 0.99, LOD = 0.3 µM, LOQ = 1 µM). Quantification of L-Phe in human blood dry spots (DBS) by the new sensor and SWV were in excellent agreement with mass spectroscopy (MS) measurements by 2 independent pathology labs. The sensor was successfully integrated with an ultra-compact potentiostat in a Lab-on-a-Phone assembly for L-Phe screening in DBS, thus demonstrating its potential for use at POC and at home by phenylketonuria (PKU) patients in both remote and rural areas.

Indexed as

Biosensing TechniquesElectrochemical TechniquesNanostructuresPhenylalaninePhenylketonuriasElectrodesGoldHumansImmunoassayLimit of DetectionMetal NanoparticlesGoldPhenylalanineElectrochemical immunosensorFern-like gold nanostructuresLight-driven surface modificationPhenylalaninePhenylketonuria

Identifiers

PMID41575582
PMCPMC12830426

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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.