Evidence map›Paper›PMID 22662968›Full record

ArticleAnalytical chemistry2012

Production of isotopically labeled standards from a uniformly labeled precursor for quantitative volatile metabolomic studies.

Pilar Gómez-Cortés, J Thomas Brenna, Gavin L Sacks

Abstract read
In one paragraph

Article in Analytical chemistry, 2012. 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
0.3field-weighted citation impact, top 40% 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, 9 citations in OpenAlex.

  1. Article
  2. Article
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

3 authors at 2 institutions in 1 country.

Pilar Gómez-CortésDivision of Nutritional Sciences, Cornell University, Ithaca, New York 14853, USA.
J Thomas Brenna
Gavin L Sacks
Cornell University · USNew York State Department of Agriculture and Markets · US

Funding

GCx(py)GCC-IRMS for Isotope MetabolomicsR01GM103437 · NIGMS · CORNELL UNIVERSITY · PI BRENNA, JAMES T. · 2012 to 2014
$913k
GCx(py)GCC-IRMS for Isotope MetabolomicsR01RR031264 · NCRR · CORNELL UNIVERSITY · PI BRENNA, JAMES T. · 2010 to 2011
$702k
NCRR NIH HHS R01 RR031264NCRR NIH HHS RR031264NIGMS NIH HHS GM10343NIGMS NIH HHS R01 GM103437
6 · The paper itself

Abstract

Optimal accuracy and precision in small-molecule profiling by mass spectrometry generally requires isotopically labeled standards chemically representative of all compounds of interest. However, preparation of mixed standards from commercially available pure compounds is often prohibitively expensive and time-consuming, and many labeled compounds are not available in pure form. We used a single-prototype uniformly labeled [U-(13)C]compound to generate [U-(13)C]-labeled volatile standards for use in subsequent experimental profiling studies. [U-(13)C]-α-Linolenic acid (18:3n-3, ALA) was thermally oxidized to produce labeled lipid degradation volatiles which were subsequently characterized qualitatively and quantitatively. Twenty-five [U-(13)C]-labeled volatiles were identified by headspace solid-phase microextraction-gas chromatography/time-of-flight mass spectrometry (HS-SPME-GC/TOF-MS) by comparison of spectra with unlabeled volatiles. Labeled volatiles were quantified by a reverse isotope dilution procedure. Using the [U-(13)C]-labeled standards, limits of detection comparable to or better than those of previous HS-SPME reports were achieved, 0.010-1.04 ng/g. The performance of the [U-(13)C]-labeled volatile standards was evaluated using a commodity soybean oil (CSO) oxidized at 60 °C from 0 to 15 d. Relative responses of n-decane, an unlabeled internal standard otherwise absent from the mixture, and [U-(13)C]-labeled oxidation products changed by up to 8-fold as the CSO matrix was oxidized, demonstrating that reliance on a single standard in volatile profiling studies yields inaccurate results due to changing matrix effects. The [U-(13)C]-labeled standard mixture was used to quantify 25 volatiles in oxidized CSO and low-ALA soybean oil with an average relative standard deviation of 8.5%. Extension of this approach to other labeled substrates, e.g., [U-(13)C]-labeled sugars and amino acids, for profiling studies should be feasible and can dramatically improve quantitative results compared to use of a single standard.

Indexed as

Alkanesalpha-Linolenic AcidAnalytic Sample Preparation MethodsCalibrationGas Chromatography-Mass SpectrometryIsotope LabelingLimit of DetectionMetabolomicsOxidation-ReductionReference StandardsSolid Phase MicroextractionSoybean OilVolatile Organic CompoundsAlkanesalpha-Linolenic AciddecaneSoybean OilVolatile Organic Compounds

Identifiers

PMID22662968
PMCPMC3381853
OpenAlexW2318367269

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.