Evidence map›Paper›PMID 38825160›Full record

ArticleAnalytical biochemistry2024

Development of sterile platform for quantification of extracellular analytes via single walled carbon nanotubes.

Ivon Acosta-Ramirez, Carley Conover, Jacob Larsen, Portia N A Plange, Ufuk Kilic, Becca Muller, Nicole M Iverson

Abstract read
In one paragraph

Article in Analytical biochemistry, 2024. 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. Article
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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

7 authors.

Ivon Acosta-RamirezDepartment of Biological Systems Engineering, College of Agricultural Sciences and Natural Resources, University of Nebraska-Lincoln, 4240 Fair St, Lincoln NE, 68504, United States. Electronic address: iacostaramirez2@huskers.unl.edu.
Carley ConoverDepartment of Biological Systems Engineering, College of Agricultural Sciences and Natural Resources, University of Nebraska-Lincoln, 4240 Fair St, Lincoln NE, 68504, United States. Electronic address: cconover4@huskers.unl.edu.
Jacob LarsenDepartment of Chemistry, College of Arts and Sciences, University of Nebraska-Lincoln, 639 N 12th Street, Lincoln NE, 68508, United States. Electronic address: jlarsen22@huskers.unl.edu.
Portia N A PlangeDepartment of Biological Systems Engineering, College of Agricultural Sciences and Natural Resources, University of Nebraska-Lincoln, 4240 Fair St, Lincoln NE, 68504, United States. Electronic address: pplange2@huskers.unl.edu.
Ufuk KilicDepartment of Electrical and Computer Engineering, University of Nebraska-Lincoln, 900 N 16th St, Lincoln NE, 68508, United States. Electronic address: ufukkilic@unl.edu.
Becca MullerDepartment of Biological Systems Engineering, College of Agricultural Sciences and Natural Resources, University of Nebraska-Lincoln, 4240 Fair St, Lincoln NE, 68504, United States.
Nicole M IversonDepartment of Biological Systems Engineering, College of Agricultural Sciences and Natural Resources, University of Nebraska-Lincoln, 4240 Fair St, Lincoln NE, 68504, United States. Electronic address: iverson@unl.edu.

Funding

Supplement for Equipment Purchase - Hyperspectral Near Infrared Confocal MicroscopeR35GM138245 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI IVERSON, NICOLE MARIE · 2020 to 2024
$2.0M
National Science Foundation OIA-2044049NIGMS NIH HHS R35 GM138245
6 · The paper itself

Abstract

Progress has been made studying cell-cell signaling communication processes. However, due to limitations of current sensors on time and spatial resolution, the role of many extracellular analytes is still unknown. A single walled carbon nanotube (SWNT) platform was previously developed based on the avidin-biotin immobilization of SWNT to a glass substrate. The SWNT platform provides real time feedback about analyte concentration and has a high concentration of evenly distributed sensors, both of which are essential for the study of extracellular analytes. Unfortunately, this initial SWNT platform is synthesized through unsterile conditions and cannot be sterilized post-production due to the delicate nature of the sensors, making it unsuitable for in vitro work. Herein the multiple-step process for SWNT immobilization is modified and the platform's biocompatibility is assessed in terms of sterility, cytotoxicity, cell proliferation, and cell morphology through comparison with non-sensors controls. The results demonstrate the SWNT platform's sterility and lack of toxicity over 72 h. The proliferation rate and morphology profiles for cells growing on the SWNT platform are similar to those grown on tissue culture substrates. This novel nano-sensor platform preserves cell health and cell functionality over time, offering opportunities to study extracellular analytes gradients in cellular communication.

Indexed as

Nanotubes, CarbonAvidinBiosensing TechniquesBiotinCell ProliferationHumansAvidinBiotinNanotubes, CarbonBiocompatibilityBiosensorsExtracellular analytesImmobilization methodNanoarraysSingle walled carbon nanotubes

Identifiers

PMID38825160
PMCPMC11251094

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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.