Comparison of high-performance thin-layer with overpressured layer chromatography combined with direct bioautography and direct analysis in real time mass spectrometry for tansy root.

Direct analysis in real time – high resolution mass spectrometry Effect-directed analysis Overpressured layer chromatography Polyacetylenes Tansy (Tanacetum vulgare L.) root extract

Journal

Journal of chromatography. A
ISSN: 1873-3778
Titre abrégé: J Chromatogr A
Pays: Netherlands
ID NLM: 9318488

Informations de publication

Date de publication:
11 Oct 2019
Historique:
received: 14 01 2019
revised: 29 03 2019
accepted: 31 03 2019
pubmed: 13 4 2019
medline: 24 10 2019
entrez: 13 4 2019
Statut: ppublish

Résumé

Bioactive polyacetylenes in tansy (Tanacetum vulgare L.) root extract were separated by overpressured layer chromatography (OPLC) with better resolutions than achievable by capillary flow high-performance thin-layer chromatography (HPTLC). OPLC enabled a longer development distance in a shorter time (16 cm, 7 min) in comparison to conventional HPTLC (7 cm, 16 min). OPLC separations on HPTLC plates with spherical particles resulted in higher resolutions than on such with irregular particles. A slight distortion of zones sometimes occurred that could be eliminated by sonication of the mobile phase through removal of the dissolved air. However, zone distortion did not diminish the meaning of the qualitative outcome. The combination of OPLC with direct bioautography and direct analysis in real time-high resolution mass spectrometry (DART-HRMS) led to the determination of the individual polyacetylenes responsible for the diverse effects. In each recorded mass spectrum, the basepeak was the respective protonated molecule. The assignments confirmed the results of a previous study, however, compounds TR5a (tetradeca-2,4,6-triine-8-en-12-one) and TR5b (trans-2-(2,4-hexadiynylidene)-1,6-dioxaspiro[4,5]dec-3-ene) that were not separable by HPTLC were partially separated by OPLC. Thus, it was proven that TR5b was not an oxidation product of TR5a and thus not formed as artefact during the HPTLC-DART-HRMS analysis, but originally present in the sample.

Identifiants

pubmed: 30975527
pii: S0021-9673(19)30352-8
doi: 10.1016/j.chroma.2019.03.068
pii:
doi:

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

355-360

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Ágnes M Móricz (ÁM)

Plant Protection Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, Herman O. Str. 15, 1022, Budapest, Hungary. Electronic address: moricz.agnes@agrar.mta.hu.

Tim T Häbe (TT)

Justus Liebig University Giessen, Institute of Nutritional Science, Chair of Food Science, and Interdisciplinary Research Center (IFZ), Heinrich-Buff-Ring 26-32, 35392, Giessen, Germany.

Péter G Ott (PG)

Plant Protection Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, Herman O. Str. 15, 1022, Budapest, Hungary.

Gertrud E Morlock (GE)

Justus Liebig University Giessen, Institute of Nutritional Science, Chair of Food Science, and Interdisciplinary Research Center (IFZ), Heinrich-Buff-Ring 26-32, 35392, Giessen, Germany.

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Classifications MeSH