Evidence map›Paper›PMID 35936867›Full record

ArticleFlow (Cambridge, England)2022

Fluidic operation of a polymer-based nanosensor chip for analysing single molecules.

Swarnagowri Vaidyanathan, Sachindra Gamage, Kavya Dathathreya, Renee Kryk, Anishkumar Manoharan, Zheng Zhao, Lulu Zhang, Junseo Choi, Daniel Park, Sunggook Park and 1 more

Abstract read
In one paragraph

Article in Flow (Cambridge, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Swarnagowri VaidyanathanBioengineering Program, The University of Kansas, Lawrence, KS 66045, USA.
Sachindra GamageDepartment of Chemistry, The University of Kansas, Lawrence, KS 66045, USA.
Kavya DathathreyaDepartment of Chemistry, The University of Kansas, Lawrence, KS 66045, USA.
Renee KrykDepartment of Mechanical Engineering, The University of Kansas, Lawrence, KS 66045, USA.
Anishkumar ManoharanDepartment of Chemistry, The University of Kansas, Lawrence, KS 66045, USA.
Zheng ZhaoBioengineering Program, The University of Kansas, Lawrence, KS 66045, USA.
Lulu ZhangDepartment of Chemistry, The University of Kansas, Lawrence, KS 66045, USA.
Junseo ChoiCenter of BioModular Multiscale Systems for Precision Medicine, Lawrence, KS 66047, USA.
Daniel ParkCenter of BioModular Multiscale Systems for Precision Medicine, Lawrence, KS 66047, USA.
Sunggook ParkCenter of BioModular Multiscale Systems for Precision Medicine, Lawrence, KS 66047, USA.
Steven A SoperBioengineering Program, The University of Kansas, Lawrence, KS 66045, USA.ORCID 0000-0002-8292-7058

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ROY A. JENSEN · 2012 to 2026
$40.1M
Understanding the mechanobiology of stem cells in a microengineered 3D cardiac tissue environment with cardiomyopathyP20GM103638 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI LUNTE, SUSAN M · 2012 to 2021
$22.1M
Using Integrated Omics to Identify Dysfunctional Genetic Mechanisms Influencing Schizophrenia and Sleep DisturbancesP20GM130423 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Kalyani Pyaram, Steven Allan Soper · 2019 to 2026
$21.5M
Single-Molecule Processing: Detection and Identification of Single DNAs, RNAs, and Proteins using Immobilized Nanoscale Enzymatic Reactors (INERs) and Nanoscale ElectrophoresisP41EB020594 · NIBIB · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Sunggook Park · 2015 to 2026
$15.2M
NCI NIH HHS P30 CA168524NIBIB NIH HHS P41 EB020594NIGMS NIH HHS P20 GM103638NIGMS NIH HHS P20 GM130423
6 · The paper itself

Abstract

Most medical diagnostic tests are expensive, involve slow turnaround times from centralized laboratories and require highly specialized equipment with seasoned technicians to carry out the assay. To facilitate realization of precision medicine at the point of care, we have developed a mixed-scale nanosensor chip featuring high surface area pillar arrays where solid-phase reactions can be performed to detect and identify nucleic acid targets found in diseased patients. Products formed can be identified and detected using a polymer nanofluidic channel. To guide delivery of this platform, we discuss the operation of various components of the device and simulations (COMSOL) used to guide the design by investigating parameters such as pillar array loading, and hydrodynamic and electrokinetic flows. The fabrication of the nanosensor is discussed, which was performed using a silicon (Si) master patterned with a combination of focused ion beam milling and photolithography with deep reactive ion etching. The mixed-scale patterns were transferred into a thermoplastic via thermal nanoimprint lithography, which facilitated fabrication of the nanosensor chip making it appropriate for

Indexed as

Electrokinetic flowHydrodynamic flowin vitro diagnosticsPlastic nanofluidics

Identifiers

PMID35936867
PMCPMC9356744

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.