Evidence map›Paper›PMID 21111602›Full record

ArticleBiosensors & bioelectronics2011

Role of porosity in tuning the response range of microsphere-based glucose sensors.

Saurabh Singh, Mike McShane

Abstract read
In one paragraph

Article in Biosensors & bioelectronics, 2011. 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
2.1field-weighted citation impact, top 12% 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

3 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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

2 authors at 1 institution in 1 country.

Saurabh SinghDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Mike McShane
Texas A&M University · US

Funding

Fluorescent Glucose Sensors from Polyion MicroshellsR01EB000739 · NIBIB · TEXAS ENGINEERING EXPERIMENT STATION · PI MCSHANE, MIKE · 2002 to 2006
$1.3M
NIBIB NIH HHS R01 EB000739
6 · The paper itself

Abstract

Luminescent microspheres encapsulating glucose oxidase have recently been developed as implantable glucose sensors. Previous work has shown that the response range and sensitivity can be tuned by varying the thickness and composition of transport-controlling nanofilm coatings. Nevertheless, the linear response range of these sensors falls significantly below the desired clinical range for in vivo monitoring. We report here an alternative means of tuning the response range by adjusting microsphere porosity. A reaction-diffusion model was first used to evaluate whether increased porosity would be expected to extend the response range by decreasing the flux of glucose relative to oxygen. Sensors exhibiting linear response (R(2)>0.90) up to 600 mg/dL were then experimentally demonstrated by using amine-functionalized mesoporous silica microspheres and polyelectrolyte nanofilm coatings. The model was then used for sensor design, which led to the prediction that sensors constructed from ∼12 μm microspheres having an effective porosity between 0.005 and 0.01 and ∼65 nm transport-limiting coatings would respond over the entire physiological glucose range (up to 600 mg/dL) with maximized sensitivity.

Indexed as

Models, ChemicalBiosensing TechniquesComputer-Aided DesignComputer SimulationEquipment DesignEquipment Failure AnalysisGlucoseGlucose OxidaseLuminescent MeasurementsMicrospheresParticle SizeSensitivity and SpecificityGlucoseGlucose Oxidase

Identifiers

PMID21111602
PMCPMC3662048
OpenAlexW2075546919

What OpenQuestion holds

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LicenceTDM
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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.