Evidence map›Paper›PMID 25006996›Full record

ArticleSensors (Basel, Switzerland)2014

In vitro evaluation of fluorescence glucose biosensor response.

Mamdouh Aloraefy, T Joshua Pfefer, Jessica C Ramella-Roman, Kim E Sapsford

Open access · goldAbstract readComparative StudyEvaluation StudyValidation Study
In one paragraph

Article in Sensors (Basel, Switzerland), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 30 citations in OpenAlex.

  1. Biosensors Based on Inorganic Composite Fluorescent Hydrogels.Nanomaterials (Basel, Switzerland) · 2023
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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.

Mamdouh AloraefyCenter for Devices and Radiological Health, Food and Drug Administration, Silver Spring, MD 20993, USA. Mamdouh.Aloraefy@fda.hhs.gov.
T Joshua PfeferCenter for Devices and Radiological Health, Food and Drug Administration, Silver Spring, MD 20993, USA. Joshua.Pfefer@fda.hhs.gov.
Jessica C Ramella-RomanDepartment of Biomedical Engineering and Herbert Wertheim College of Medicine, Florida International University, Miami, FL 33174, USA. jramella@fiu.edu.
Kim E SapsfordCenter for Devices and Radiological Health, Food and Drug Administration, Silver Spring, MD 20993, USA. Kim.Sapsford@fda.hhs.gov.
Center for Devices and Radiological Health · USCatholic University of America · USFlorida International University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rapid, accurate, and minimally-invasive glucose biosensors based on Förster Resonance Energy Transfer (FRET) for glucose measurement have the potential to enhance diabetes control. However, a standard set of in vitro approaches for evaluating optical glucose biosensor response under controlled conditions would facilitate technological innovation and clinical translation. Towards this end, we have identified key characteristics and response test methods, fabricated FRET-based glucose biosensors, and characterized biosensor performance using these test methods. The biosensors were based on competitive binding between dextran and glucose to concanavalin A and incorporated long-wavelength fluorescence dye pairs. Testing characteristics included spectral response, linearity, sensitivity, limit of detection, kinetic response, reversibility, stability, precision, and accuracy. The biosensor demonstrated a fluorescence change of 45% in the presence of 400 mg/dL glucose, a mean absolute relative difference of less than 11%, a limit of detection of 25 mg/dL, a response time of 15 min, and a decay in fluorescence intensity of 72% over 30 days. The battery of tests presented here for objective, quantitative in vitro evaluation of FRET glucose biosensors performance have the potential to form the basis of future consensus standards. By implementing these test methods for a long-visible-wavelength biosensor, we were able to demonstrate strengths and weaknesses with a new level of thoroughness and rigor.

Indexed as

Biosensing TechniquesConcanavalin AEquipment DesignEquipment Failure AnalysisFluorescence Resonance Energy TransferGlucoseIn Vitro TechniquesReproducibility of ResultsSensitivity and SpecificityConcanavalin AGlucose

Identifiers

PMID25006996
PMCPMC4168472
OpenAlexW2009601921

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.