Evidence map›Paper›PMID 37622875›Full record

ArticleBiosensors2023

A Polarity-Sensitive Far-Red Fluorescent Probe for Glucose Sensing through Skin.

Lydia Colvin, Dandan Tu, Darin Dunlap, Alberto Rios, Gerard Coté

Open access · goldAbstract read
In one paragraph

Article in Biosensors, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 1 country.

Lydia ColvinDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Dandan TuDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0003-3827-6486
Darin DunlapDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Alberto RiosDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Gerard CotéDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0002-3164-9625
Texas A&M University · USTexas A&M Engineering Experiment Station

Funding

National Science Foundation 1648541Robert J. Kleberg, Jr. and Helen C. Kleberg Foundation N/A
6 · The paper itself

Abstract

The field of glucose biosensors for diabetes management has been of great interest over the past 60 years. Continuous glucose monitoring (CGM) is important to continuously track the glucose level to provide better management of the disease. Concanavalin A (ConA) can reversibly bind to glucose and mannose molecules and form a glucose biosensor via competitive binding. Here, we developed a glucose biosensor using ConA and a fluorescent probe, which generated a fluorescent intensity change based on solvatochromism, the reversible change in the emission spectrum dependent on the polarity of the solvent. The direction in which the wavelength shifts as the solvent polarity increases can be defined as positive (red-shift), negative (blue-shift), or a combination of the two, referred to as reverse. To translate this biosensor to a subcutaneously implanted format, Cyanine 5.5 (Cy5.5)-labeled small mannose molecules were used, which allows for the far-red excitation wavelength range to increase the skin penetration depth of the light source and returned emission. Three Cy5.5-labeled small mannose molecules were synthesized and compared when used as the competing ligand in the competitive binding biosensor. We explored the polarity-sensitive nature of the competing ligands and examined the biosensor's glucose response. Cy5.5-mannotetraose performed best as a biosensor, allowing for the detection of glucose from 25 to 400 mg/dL. Thus, this assay is responsive to glucose within the physiologic range when its concentration is increased to levels needed for an implantable design. The biosensor response is not statistically different when placed under different skin pigmentations when comparing the percent increase in fluorescence intensity. This shows the ability of the biosensor to produce a repeatable signal across the physiologic range for subcutaneous glucose monitoring under various skin tones.

Indexed as

Fluorescent DyesQuinolinesBlood GlucoseBlood Glucose Self-MonitoringCarbocyaninesConcanavalin AGlucoseMannoseBlood GlucoseCarbocyaninesConcanavalin ACY5.5 cyanine dyeFluorescent DyesGlucoseMannoseQuinolinescompetitive bindingConcanavalin ACyanine 5.5far-redfluorescenceglucose sensorNIRpolaritysolvatochromism

Identifiers

PMID37622875
PMCPMC10452146
OpenAlexW4385576489

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.