AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate

Stable isotope labeling of pollutants is a valuable tool to investigate their environmental transport and degradation. For the globally most frequently used herbicide glyphosate, such studies have, so far, been hampered by the absence of an analytical standard for its labeled metabolite AMPA-15N, wh...

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Main Authors: Marisa A. Wirth, Lars Longwitz, Marion Kanwischer, Peter Gros, Peter Leinweber, Thomas Werner
Format: Article
Language:English
Published: Elsevier 2021-12-01
Series:Ecotoxicology and Environmental Safety
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0147651321008800
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spelling doaj-875001472c6a4827ae7eff0f5e1ab3d02021-10-01T04:44:02ZengElsevierEcotoxicology and Environmental Safety0147-65132021-12-01225112768AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosateMarisa A. Wirth0Lars Longwitz1Marion Kanwischer2Peter Gros3Peter Leinweber4Thomas Werner5Leibniz-Institute for Baltic Sea Research Warnemünde, Department of Marine Chemistry, Seestraße 15, 18119 Rostock, GermanyLeibniz-Institute for Catalysis, Catalysis with renewable resources, Albert-Einstein-Str. 29a, 18059 Rostock, Germany; University of Antwerp, Organic Synthesis (ORSY), Groenenborgerlaan 171, 2020 Antwerpen, BelgiumLeibniz-Institute for Baltic Sea Research Warnemünde, Department of Marine Chemistry, Seestraße 15, 18119 Rostock, Germany; Corresponding author.University of Rostock, Faculty of Agriculture and Environmental Sciences, Soil Science, Justus-von-Liebig-Weg 6, 18059 Rostock, Germany; State Office for Agriculture and Rural Area Thüringen, Department for Soil and Fertilizer Investigations, Naumburger Straße 98, 07743 Jena, GermanyUniversity of Rostock, Faculty of Agriculture and Environmental Sciences, Soil Science, Justus-von-Liebig-Weg 6, 18059 Rostock, GermanyLeibniz-Institute for Catalysis, Catalysis with renewable resources, Albert-Einstein-Str. 29a, 18059 Rostock, Germany; Paderborn University, Department of Chemistry and Center for Sustainable Systems Design (CSSD), Warburger Straße 100, 33098 Paderborn, GermanyStable isotope labeling of pollutants is a valuable tool to investigate their environmental transport and degradation. For the globally most frequently used herbicide glyphosate, such studies have, so far, been hampered by the absence of an analytical standard for its labeled metabolite AMPA-15N, which is formed during the degradation of all commercially available glyphosate isotopologues. Without such a standard, detection and quantitation of AMPA-15N, e.g. with LC-MS/MS, is not possible. Therefore, a synthetic pathway to AMPA-15N from benzamide-15N via the hemiaminal was developed. AMPA-15N was obtained in sufficient yield and purity to be used as a standard compound for LC-MS/MS analysis. Suitable MS-detection settings as well as a calibration using the internal standard (IS) approach were established for Fmoc-derivatized AMPA-15N. The use of different AMPA isotopologues as IS was complicated by the parallel formation of [M+H]+ and [M]+• AMPA-Fmoc precursor ions in ESI-positive mode, causing signal interferences between analyte and IS. We recommend the use of either AMPA-13C–15N, AMPA-13C–15N-D2 or a glyphosate isotopologue as IS, as they do not affect the linearity of the calibration curve. As a proof of concept, the developed analysis procedure for AMPA-15N was used to refine the results from a field lysimeter experiment investigating leaching and degradation of glyphosate-2-13C–15N. The newly enabled quantitation of AMPA-15N in soil extracts showed that similar amounts (0.05 – 0.22 mg·kg–1) of the parent herbicide glyphosate and its primary metabolite AMPA persisted in the topsoil over the study period of one year, while vertical transport through the soil column did not occur for either of the compounds. The herein developed analysis concepts will facilitate future design and execution of experiments on the environmental fate of the herbicide glyphosate.http://www.sciencedirect.com/science/article/pii/S0147651321008800Aminomethylphosphonic acidPesticide degradationIsotope labelingTandem mass spectrometryLysimeter
collection DOAJ
language English
format Article
sources DOAJ
author Marisa A. Wirth
Lars Longwitz
Marion Kanwischer
Peter Gros
Peter Leinweber
Thomas Werner
spellingShingle Marisa A. Wirth
Lars Longwitz
Marion Kanwischer
Peter Gros
Peter Leinweber
Thomas Werner
AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate
Ecotoxicology and Environmental Safety
Aminomethylphosphonic acid
Pesticide degradation
Isotope labeling
Tandem mass spectrometry
Lysimeter
author_facet Marisa A. Wirth
Lars Longwitz
Marion Kanwischer
Peter Gros
Peter Leinweber
Thomas Werner
author_sort Marisa A. Wirth
title AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate
title_short AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate
title_full AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate
title_fullStr AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate
title_full_unstemmed AMPA-15N – Synthesis and application as standard compound in traceable degradation studies of glyphosate
title_sort ampa-15n – synthesis and application as standard compound in traceable degradation studies of glyphosate
publisher Elsevier
series Ecotoxicology and Environmental Safety
issn 0147-6513
publishDate 2021-12-01
description Stable isotope labeling of pollutants is a valuable tool to investigate their environmental transport and degradation. For the globally most frequently used herbicide glyphosate, such studies have, so far, been hampered by the absence of an analytical standard for its labeled metabolite AMPA-15N, which is formed during the degradation of all commercially available glyphosate isotopologues. Without such a standard, detection and quantitation of AMPA-15N, e.g. with LC-MS/MS, is not possible. Therefore, a synthetic pathway to AMPA-15N from benzamide-15N via the hemiaminal was developed. AMPA-15N was obtained in sufficient yield and purity to be used as a standard compound for LC-MS/MS analysis. Suitable MS-detection settings as well as a calibration using the internal standard (IS) approach were established for Fmoc-derivatized AMPA-15N. The use of different AMPA isotopologues as IS was complicated by the parallel formation of [M+H]+ and [M]+• AMPA-Fmoc precursor ions in ESI-positive mode, causing signal interferences between analyte and IS. We recommend the use of either AMPA-13C–15N, AMPA-13C–15N-D2 or a glyphosate isotopologue as IS, as they do not affect the linearity of the calibration curve. As a proof of concept, the developed analysis procedure for AMPA-15N was used to refine the results from a field lysimeter experiment investigating leaching and degradation of glyphosate-2-13C–15N. The newly enabled quantitation of AMPA-15N in soil extracts showed that similar amounts (0.05 – 0.22 mg·kg–1) of the parent herbicide glyphosate and its primary metabolite AMPA persisted in the topsoil over the study period of one year, while vertical transport through the soil column did not occur for either of the compounds. The herein developed analysis concepts will facilitate future design and execution of experiments on the environmental fate of the herbicide glyphosate.
topic Aminomethylphosphonic acid
Pesticide degradation
Isotope labeling
Tandem mass spectrometry
Lysimeter
url http://www.sciencedirect.com/science/article/pii/S0147651321008800
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