Evidence map›Paper›PMID 34908400›Full record

ArticleACS sensors2022

Detection of Glial Fibrillary Acidic Protein in Patient Plasma Using On-Chip Graphene Field-Effect Biosensors, in Comparison with ELISA and Single-Molecule Array.

Lizhou Xu, Sami Ramadan, Oluwatomi E Akingbade, Yuanzhou Zhang, Sarah Alodan, Neil Graham, Karl A Zimmerman, Elias Torres, Amanda Heslegrave, Peter K Petrov and 4 more

Open access · hybridAbstract read
In one paragraph

Article in ACS sensors, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Ultrasensitive Detection of Neurofilament Light in Plasma Using F(Ab')Small (Weinheim an der Bergstrasse, Germany) · 2026
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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

14 authors at 5 institutions in 4 countries.

Lizhou XuDepartment of Materials, Imperial College London, London SW7 2AZ, U.K.
Sami RamadanDepartment of Materials, Imperial College London, London SW7 2AZ, U.K.ORCID 0000-0002-0013-731X
Oluwatomi E AkingbadeDepartment of Brain Sciences, Imperial College London, London W12 0BZ, U.K.
Yuanzhou ZhangDepartment of Materials, Imperial College London, London SW7 2AZ, U.K.
Sarah AlodanDepartment of Materials, Imperial College London, London SW7 2AZ, U.K.
Neil GrahamDepartment of Brain Sciences, Imperial College London, London W12 0BZ, U.K.
Karl A ZimmermanDepartment of Brain Sciences, Imperial College London, London W12 0BZ, U.K.
Elias TorresGraphenea Semiconductor, Paseo Mikeletegi 83, San Sebastián 20009, Spain.
Amanda HeslegraveUK Dementia Research Institute at UCL, University College London, London WC1E 6BT, U.K.
Peter K PetrovDepartment of Materials, Imperial College London, London SW7 2AZ, U.K.ORCID 0000-0003-3643-6685
Henrik ZetterbergUK Dementia Research Institute at UCL, University College London, London WC1E 6BT, U.K.
David J SharpDepartment of Brain Sciences, Imperial College London, London W12 0BZ, U.K.
Norbert KleinDepartment of Materials, Imperial College London, London SW7 2AZ, U.K.
Bing LiDepartment of Brain Sciences, Imperial College London, London W12 0BZ, U.K.ORCID 0000-0002-1737-3423
Imperial College London · GBUK Dementia Research Institute · GBGraphenea (Spain) · ESInstitute for Neurodegenerative Disorders · USSahlgrenska University Hospital · SE

Funding

Department of Health NIHR-RP-011-048Medical Research Council
6 · The paper itself

Abstract

Glial fibrillary acidic protein (GFAP) is a discriminative blood biomarker for many neurological diseases, such as traumatic brain injury. Detection of GFAP in buffer solutions using biosensors has been demonstrated, but accurate quantification of GFAP in patient samples has not been reported, yet in urgent need. Herein, we demonstrate a robust on-chip graphene field-effect transistor (GFET) biosensing method for sensitive and ultrafast detection of GFAP in patient plasma. Patients with moderate-severe traumatic brain injuries, defined by the Mayo classification, are recruited to provide plasma samples. The binding of target GFAP with the specific antibodies that are conjugated on a monolayer GFET device triggers the shift of its Dirac point, and this signal change is correlated with the GFAP concentration in the patient plasma. The limit of detection (LOD) values of 20 fg/mL (400 aM) in buffer solution and 231 fg/mL (4 fM) in patient plasma have been achieved using this approach. In parallel, for the first time, we compare our results to the state-of-the-art single-molecule array (Simoa) technology and the classic enzyme-linked immunosorbent assay (ELISA) for reference. The GFET biosensor shows competitive LOD to Simoa (1.18 pg/mL) and faster sample-to-result time (<15 min), and also it is cheaper and more user-friendly. In comparison to ELISA, GFET offers advantages of total detection time, detection sensitivity, and simplicity. This GFET biosensing platform holds high promise for the point-of-care diagnosis and monitoring of traumatic brain injury in GP surgeries and patient homes.

Indexed as

Biosensing TechniquesBrain Injuries, TraumaticGraphiteEnzyme-Linked Immunosorbent AssayGlial Fibrillary Acidic ProteinHumansGlial Fibrillary Acidic ProteinGraphitebiosensorglial fibrillary acidic proteinsingle-molecule array, graphene field-effect transistortraumatic brain injury blood biomarker

Identifiers

PMID34908400
PMCPMC8805154
OpenAlexW4200560206

What OpenQuestion holds

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LicenceCC BY
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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.