Evidence map›Paper›PMID 30453519›Full record

ArticleMolecules (Basel, Switzerland)2018

Derivatization of Methylglyoxal for LC-ESI-MS Analysis-Stability and Relative Sensitivity of Different Derivatives.

Stefan Fritzsche, Susan Billig, Robby Rynek, Ramarao Abburi, Elena Tarakhovskaya, Olga Leuner, Andrej Frolov, Claudia Birkemeyer

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. 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
0.6field-weighted citation impact, top 32% 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, 14 citations in OpenAlex.

  1. Article
  2. Review
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

8 authors at 5 institutions in 4 countries.

Stefan FritzscheInstitute of Analytical Chemistry, Faculty of Chemistry and Mineralogy, University of Leipzig, 04103 Leipzig, Germany. stefan.fritzsche@uni-leipzig.de.
Susan BilligInstitute of Analytical Chemistry, Faculty of Chemistry and Mineralogy, University of Leipzig, 04103 Leipzig, Germany. billig@uni-leipzig.de.
Robby RynekInstitute of Analytical Chemistry, Faculty of Chemistry and Mineralogy, University of Leipzig, 04103 Leipzig, Germany. r.rynek@live.de.ORCID 0000-0001-8929-7135
Ramarao AbburiInstitute of Analytical Chemistry, Faculty of Chemistry and Mineralogy, University of Leipzig, 04103 Leipzig, Germany. rams.abburi@gmail.com.
Elena TarakhovskayaInstitute of Analytical Chemistry, Faculty of Chemistry and Mineralogy, University of Leipzig, 04103 Leipzig, Germany. elena.tarakhovskaya@gmail.com.ORCID 0000-0002-5341-2813
Olga LeunerInstitute of Analytical Chemistry, Faculty of Chemistry and Mineralogy, University of Leipzig, 04103 Leipzig, Germany. leuner@ftz.czu.cz.
Andrej FrolovDepartment of Bioorganic Chemistry, Leibniz Institute of Plant Biochemistry, 06120 Halle (Saale), Germany. andrej.frolov@ipb-halle.de.
Claudia BirkemeyerInstitute of Analytical Chemistry, Faculty of Chemistry and Mineralogy, University of Leipzig, 04103 Leipzig, Germany. birkemeyer@chemie.uni-leipzig.de.ORCID 0000-0002-8538-8838
Leipzig University · DECzech University of Life Sciences Prague · CZKrishna University · INLeibniz Institute of Plant Biochemistry · DESt Petersburg University · RU

Funding

Deutsche Forschungsgemeinschaft BI 1340/4-1Deutscher Akademischer Austauschdienst Dmitrij-Mendeleev-ProgrammeErasmus+ Training Mobility Programme
6 · The paper itself

Abstract

The great research interest in the quantification of reactive carbonyl compounds (RCCs), such as methylglyoxal (MGO) in biological and environmental samples, is reflected by the fact that several publications have described specific strategies to perform this task. Thus, many reagents have also been reported for the derivatization of RCCs to effectively detect and quantify the resulting compounds using sensitive techniques such as liquid chromatography coupled with mass spectrometry (LC-MS). However, the choice of the derivatization protocol is not always clear, and a comparative evaluation is not feasible because detection limits from separate reports and determined with different instruments are hardly comparable. Consequently, for a systematic comparison, we tested 21 agents in one experimental setup for derivatization of RCCs prior to LC-MS analysis. This consisted of seven commonly employed reagents and 14 similar reagents, three of which were designed and synthesized by us. All reagents were probed for analytical responsiveness of the derivatives and stability of the reaction mixtures. The results showed that derivatives of 4-methoxyphenylenediamine and 3-methoxyphenylhydrazine-reported here for the first time for derivatization of RCCs-provided a particularly high responsiveness with ESI-MS detection. We applied the protocol to investigate MGO contamination of laboratory water and show successful quantification in a lipoxidation experiment. In summary, our results provide valuable information for scientists in establishing accurate analysis of RCCs.

Indexed as

Chromatography, LiquidLaboratoriesLimit of DetectionPyruvaldehydeSpectrometry, Mass, Electrospray IonizationWater Pollutants, ChemicalPyruvaldehydeWater Pollutants, Chemicalcarbonyl derivatizationhydroxylaminelipoxidationphenylenediaminephenylhydrazinewater analysis

Identifiers

PMID30453519
PMCPMC6278547
OpenAlexW2900708289

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.