Evidence map›Paper›PMID 27083258›Full record

ArticleJournal of chromatography. A2016

Benzoyl chloride derivatization with liquid chromatography-mass spectrometry for targeted metabolomics of neurochemicals in biological samples.

Jenny-Marie T Wong, Paige A Malec, Omar S Mabrouk, Jennifer Ro, Monica Dus, Robert T Kennedy

Open access · greenAbstract read
In one paragraph

Article in Journal of chromatography. A, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed
12.0field-weighted citation impact, top 1% 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

119 citing papers in PubMed, 249 citations in OpenAlex.

  1. Vitamin BNature communications · 2026
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  6. Vitamin BResearch square · 2025
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59 more citing papers are in PubMed but not listed here.

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 1 country.

Jenny-Marie T WongDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, United States.
Paige A MalecDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, United States.
Omar S MabroukDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, United States; Department of Pharmacology, University of Michigan, Ann Arbor, MI 48109, United States.
Jennifer RoDepartment of Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, MI 48109, United States.
Monica DusDeparment of Molecular, Cellular, Developmental Biology, University of Michigan, Ann Arbor, MI 48109, United States.
Robert T KennedyDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, United States; Department of Pharmacology, University of Michigan, Ann Arbor, MI 48109, United States. Electronic address: rtkenn@umich.edu.
University of Michigan–Ann Arbor · 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
In vivo chemical monitoring using capillary separationsR37EB003320 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KENNEDY, ROBERT T · 2008 to 2017
$3.6M
MICROELECTRODE AND MICRODIALYSIS-BASED INSULIN SENSORSR01DK046960 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KENNEDY, ROBERT T · 1993 to 2020
$3.3M
Design and Use of Methods for Peptide Secretion Studies - Diversity SupplementR37DK046960 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KENNEDY, ROBERT T · 2006 to 2015
$3.0M
Mechanisms of Dietary Restriction in DrosophilaR01AG023166 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PLETCHER, SCOTT · 2004 to 2014
$2.9M
In vivo chemical monitoring using capillary separationsR01EB003320 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KENNEDY, ROBERT T · 2003 to 2020
$2.7M
Modulation of aging through mechanisms of nutrient demand and rewardR37AG051649 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCOTT PLETCHER · 2021 to 2026
$2.3M
The role of neuroepigenetics in bidirectional behavioral statesDP2DK113750 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DUS, MONICA · 2016 to 2016
$2.0M
Modulation of aging through mechanisms of nutrient demand and rewardR01AG051649 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PLETCHER, SCOTT · 2016 to 2020
$1.6M
Neural and molecular mechanisms of glucosensation mediating food choice behaviorR00DK097141 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DUS, MONICA · 2015 to 2017
$700k
The role of serotonin in dietary protein perception and diet-dependent longevityF31AG047696 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RO, JENNIFER · 2014 to 2015
$62k
NIA NIH HHS F31 AG047696NIA NIH HHS R01 AG023166NIA NIH HHS R37 AG051649NIBIB NIH HHS R01 EB003320NIBIB NIH HHS R37 EB003320NIDDK NIH HHS DP2 DK113750NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R00 DK097141NIDDK NIH HHS R01 DK046960NIDDK NIH HHS R37 DK046960
6 · The paper itself

Abstract

Widely targeted metabolomic assays are useful because they provide quantitative data on large groups of related compounds. We report a high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method that utilizes benzoyl chloride labeling for 70 neurologically relevant compounds, including catecholamines, indoleamines, amino acids, polyamines, trace amines, antioxidants, energy compounds, and their metabolites. The method includes neurotransmitters and metabolites found in both vertebrates and insects. This method was applied to analyze microdialysate from rats, human cerebrospinal fluid, human serum, fly tissue homogenate, and fly hemolymph, demonstrating its broad versatility for multiple physiological contexts and model systems. Limits of detection for most assayed compounds were below 10nM, relative standard deviations were below 10%, and carryover was less than 5% for 70 compounds separated in 20min, with a total analysis time of 33min. This broadly applicable method provides robust monitoring of multiple analytes, utilizes small sample sizes, and can be applied to diverse matrices. The assay will be of value for evaluating normal physiological changes in metabolism in neurochemical systems. The results demonstrate the utility of benzoyl chloride labeling with HPLC-MS/MS for widely targeted metabolomics assays.

Indexed as

MetabolomeAmino AcidsAnimalsBenzoatesCatecholaminesChromatography, High Pressure LiquidDrosophilaHemolymphHumansMetabolomicsNeurotransmitter AgentsRatsRats, Sprague-DawleySpecies SpecificityTandem Mass SpectrometryAmino AcidsBenzoatesbenzoyl chlorideCatecholaminesNeurotransmitter AgentsBrainDerivatizationDrosophilaHPLCMass spectrometryNeurochemistry

Identifiers

PMID27083258
PMCPMC4845038
OpenAlexW2336829371

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.