Evidence map›Paper›PMID 24182183›Full record

ArticleThe Review of scientific instruments2013

Note: Four-port microfluidic flow-cell with instant sample switching.

Christopher A MacGriff, Shaopeng Wang, Nongjian Tao

Erratum issuedAbstract read
In one paragraph

Article in The Review of scientific instruments, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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

  • Erratum issued
5 · Who and what money

Authors and funding

3 authors.

Christopher A MacGriffSchool of Electrical, Computer, and Energy Engineering, Arizona State University, Tempe, Arizona 85287, USA.
Shaopeng Wang
Nongjian Tao

Funding

Electrochemically-Enhanced Plasmonic Imaging for Quantitative ProteomicsR44GM106579 · NIGMS · BIOSENSING INSTRUMENT, INC. · PI LY, NGUYEN · 2013 to 2017
$1.9M
NIGMS NIH HHS R44 GM106579
6 · The paper itself

Abstract

A simple device for high-speed microfluidic delivery of liquid samples to a surface plasmon resonance sensor surface is presented. The delivery platform is comprised of a four-port microfluidic cell, two ports serve as inlets for buffer and sample solutions, respectively, and a high-speed selector valve to control the alternate opening and closing of the two outlet ports. The time scale of buffer/sample switching (or sample injection rise and fall time) is on the order of milliseconds, thereby minimizing the opportunity for sample plug dispersion. The high rates of mass transport to and from the central microfluidic sensing region allow for SPR-based kinetic analysis of binding events with dissociation rate constants (k(d)) up to 130 s(-1). The required sample volume is only 1 μL, allowing for minimal sample consumption during high-speed kinetic binding measurement.

Indexed as

LightMicrofluidic Analytical TechniquesSurface Plasmon Resonance

Identifiers

PMID24182183
PMCPMC4108724

What OpenQuestion holds

Textmetadata
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.