Evidence map›Paper›PMID 31174353›Full record

ArticleSensors (Basel, Switzerland)2019

Adaptable Xerogel-Layered Amperometric Biosensor Platforms on Wire Electrodes for Clinically Relevant Measurements.

Lillian B Hughes, Najwa Labban, Grace E Conway, Julie A Pollock, Michael C Leopold

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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

5 authors.

Lillian B HughesDepartment of Chemistry, Gottwald Science Center, University of Richmond, Richmond, VA 23173, USA. lillian.hughes@richmond.edu.
Najwa LabbanDepartment of Chemistry, Gottwald Science Center, University of Richmond, Richmond, VA 23173, USA. najwa.labban@richmond.edu.ORCID 0000-0003-0021-2591
Grace E ConwayDepartment of Chemistry, Gottwald Science Center, University of Richmond, Richmond, VA 23173, USA. grace.conway@richmond.edu.ORCID 0000-0003-4594-2934
Julie A PollockDepartment of Chemistry, Gottwald Science Center, University of Richmond, Richmond, VA 23173, USA. jpollock@richmond.edu.ORCID 0000-0003-0153-9991
Michael C LeopoldDepartment of Chemistry, Gottwald Science Center, University of Richmond, Richmond, VA 23173, USA. mleopold@richmond.edu.

Funding

Arnold and Mabel Beckman Foundation NoneCamille and Henry Dreyfus Foundation NoneCommonwealth Health Research Board 307-01-13Floyd D. and Elisabeth S. Gottwald Endowed Chair of Chemistry Not applicableNational Science Foundation CHE-1401593
6 · The paper itself

Abstract

Biosensing strategies that employ readily adaptable materials for different analytes, can be miniaturized into needle electrode form, and function in bodily fluids represent a significant step toward the development of clinically relevant in vitro and in vivo sensors. In this work, a general scheme for 1st generation amperometric biosensors involving layer-by-layer electrode modification with enzyme-doped xerogels, electrochemically-deposited polymer, and polyurethane semi-permeable membranes is shown to achieve these goals. With minor modifications to these materials, sensors representing potential point-of-care medical tools are demonstrated to be sensitive and selective for a number of conditions. The potential for bedside measurements or continuous monitoring of analytes may offer faster and more accurate clinical diagnoses for diseases such as diabetes (glucose), preeclampsia (uric acid), galactosemia (galactose), xanthinuria (xanthine), and sepsis (lactate). For the specific diagnostic application, the sensing schemes have been miniaturized to wire electrodes and/or demonstrated as functional in synthetic urine or blood serum. Signal enhancement through the incorporation of platinum nanoparticle film in the scheme offers additional design control within the sensing scheme. The presented sensing strategy has the potential to be applied to any disease that has a related biomolecule and corresponding oxidase enzyme and represents rare, adaptable, sensing capabilities.

Indexed as

biomedicalbiosensorsbodily fluidselectrochemicalenzymein vitroin vivoneedle electrodeplatinum blacksepsiswire

Identifiers

PMID31174353
PMCPMC6603663

What OpenQuestion holds

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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.