Evidence map›Paper›PMID 36875634›Full record

ArticleMicrosystems & nanoengineering2023

Microfabricated polymer-metal biosensors for multifarious data collection from electrogenic cellular models.

Charles M Didier, Julia F Orrico, Omar S Cepeda Torres, Jorge Manrique Castro, Aliyah Baksh, Swaminathan Rajaraman

Open access · goldAbstract read
In one paragraph

Article in Microsystems & nanoengineering, 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
1.4field-weighted citation impact, top 21% 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, 13 citations in OpenAlex.

  1. Review
  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

6 authors at 1 institution in 2 countries.

Charles M Didier *NanoScience Technology Center, University of Central Florida, 4353 Scorpius Street, Research I, Suite 231, FL 32816 Orlando, USA.ORCID 0000-0002-5556-8694
Julia F Orrico *NanoScience Technology Center, University of Central Florida, 4353 Scorpius Street, Research I, Suite 231, FL 32816 Orlando, USA.ORCID 0000-0002-5247-7949
Omar S Cepeda Torres *NanoScience Technology Center, University of Central Florida, 4353 Scorpius Street, Research I, Suite 231, FL 32816 Orlando, USA.ORCID 0000-0002-6338-9928
Jorge Manrique CastroNanoScience Technology Center, University of Central Florida, 4353 Scorpius Street, Research I, Suite 231, FL 32816 Orlando, USA.ORCID 0000-0002-9248-3120
Aliyah BakshNanoScience Technology Center, University of Central Florida, 4353 Scorpius Street, Research I, Suite 231, FL 32816 Orlando, USA.ORCID 0000-0002-6980-4432
Swaminathan RajaramanNanoScience Technology Center, University of Central Florida, 4353 Scorpius Street, Research I, Suite 231, FL 32816 Orlando, USA.ORCID 0000-0003-2279-2013
University of Central Florida · US

Funding

Human Microphysiological Model of Afferent Nociceptive SignalingUG3TR003150 · NCATS · TULANE UNIVERSITY OF LOUISIANA · PI ASHTON, RANDOLPH S, MOORE, MICHAEL J · 2019 to 2019
$1.2M
NCATS NIH HHS UG3 TR003150
6 · The paper itself

Abstract

Benchtop tissue cultures have become increasingly complex in recent years, as more on-a-chip biological technologies, such as microphysiological systems (MPS), are developed to incorporate cellular constructs that more accurately represent their respective biological systems. Such MPS have begun facilitating major breakthroughs in biological research and are poised to shape the field in the coming decades. These biological systems require integrated sensing modalities to procure complex, multiplexed datasets with unprecedented combinatorial biological detail. In this work, we expanded upon our polymer-metal biosensor approach by demonstrating a facile technology for compound biosensing that was characterized through custom modeling approaches. As reported herein, we developed a compound chip with 3D microelectrodes, 3D microfluidics, interdigitated electrodes (IDEs) and a microheater. The chip was subsequently tested using the electrical/electrochemical characterization of 3D microelectrodes with 1 kHz impedance and phase recordings and IDE-based high-frequency (~1 MHz frequencies) impedimetric analysis of differential localized temperature recordings, both of which were modeled through equivalent electrical circuits for process parameter extraction. Additionally, a simplified antibody-conjugation strategy was employed for a similar IDE-based analysis of the implications of a key analyte (l-glutamine) binding to the equivalent electrical circuit. Finally, acute microfluidic perfusion modeling was performed to demonstrate the ease of microfluidics integration into such a polymer-metal biosensor platform for potential complimentary localized chemical stimulation. Overall, our work demonstrates the design, development, and characterization of an accessibly designed polymer-metal compound biosensor for electrogenic cellular constructs to facilitate comprehensive MPS data collection.

Indexed as

BionanoelectronicsBiosensorsElectrical and electronic engineering

Identifiers

PMID36875634
PMCPMC9974480
OpenAlexW4322621411

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.