Evidence map›Paper›PMID 37943345›Full record

ArticleAnalytical chemistry2023

High-Throughput Liquid Chromatographic Analysis Using a Segmented Flow Injector with a 1 s Cycle Time.

Devin M Makey, Roger C Diehl, Yue Xin, Bridget E Murray, Dwight R Stoll, Brandon T Ruotolo, James P Grinias, Alison R H Narayan, Veronica Lopez-Carillo, Michaela Stark and 2 more

Open access · greenAbstract read
In one paragraph

Article in Analytical chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

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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

12 authors at 4 institutions in 2 countries.

Devin M MakeyDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.ORCID 0000-0003-2991-6760
Roger C DiehlLife Sciences Institute, University of Michigan, Ann Arbor, Michigan 48109, United States.
Yue XinDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
Bridget E MurrayDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.ORCID 0000-0001-9865-9046
Dwight R StollDepartment of Chemistry, Gustavus Adolphus College, Saint Peter, Minnesota 56082, United States.ORCID 0000-0002-4070-9132
Brandon T RuotoloDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.ORCID 0000-0002-6084-2328
James P GriniasDepartment of Chemistry and Biochemistry, Rowan University, Glassboro, New Jersey 08028, United States.ORCID 0000-0001-9872-9630
Alison R H NarayanDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.ORCID 0000-0001-8290-0077
Veronica Lopez-CarilloBASF SE, 67063 Ludwigshafen am Rhein, Germany.
Michaela StarkBASF SE, 67063 Ludwigshafen am Rhein, Germany.
Philipp JohnenBASF SE, 67063 Ludwigshafen am Rhein, Germany.
Robert T KennedyDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.ORCID 0000-0003-2447-7471
University of Michigan · USBASF (Germany) · DEGustavus Adolphus College · USRowan University · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
Microfluidic Systems to Enable Enzyme Engineering for Chemical SynthesisR01GM150948 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROBERT T KENNEDY · 2023 to 2026
$1.3M
NIDDK NIH HHS P30 DK020572NIGMS NIH HHS R01 GM150948
6 · The paper itself

Abstract

High-throughput screening (HTS) workflows are revolutionizing many fields, including drug discovery, reaction discovery and optimization, diagnostics, sensing, and enzyme engineering. Liquid chromatography (LC) is commonly deployed during HTS to reduce matrix effects, distinguish isomers, and preconcentrate prior to detection, but LC separation time often limits throughput. Although subsecond LC separations have been demonstrated, they are rarely utilized during HTS due to limitations associated with the speed of common autosamplers. In this work, these limits are overcome by utilizing droplet microfluidics for sample introduction. In the method, a train of samples segmented by air are continuously pumped into the inlet of an LC injection valve that is actuated once each sample fills the sample loop. Coupled with 2.1 mm diameter × 5 mm long columns packed with 2.7 μm superficially porous C18 particles operated at 5 mL/min, the injector enabled separation of 3 components at 1 s/sample and analysis of a 96-well plate in 1.6 min with <2% peak area relative standard deviation. Analyte-dependent carryover was minimized by including wash droplets composed of organic solvent in between sample droplets. High-throughput LC coupled with mass spectrometric detection using the segmented flow injector was applied to a screen of inhibitors of a cytochrome P450-catalyzed hydroxylation reaction. Measurements of the reaction substrate and product concentrations made using fast LC with the segmented flow injector correlated well with measurements made using a more conventional, 3 min LC method. These results demonstrate the potential for droplet microfluidics to be used for sample introduction during high-throughput LC analysis.

Indexed as

MicrofluidicsChromatography, LiquidMass Spectrometry

Identifiers

PMID37943345
PMCPMC11027085
OpenAlexW4388523459

What OpenQuestion holds

Textmetadata
LicenceTDM
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.