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Measuring Sulforaphane and Its Metabolites in Human Plasma: A High Throughput Method

(1) Background: There is increasing understanding of the potential health benefits of cruciferous vegetables. In particular sulforaphane (SFN), found in broccoli, and its metabolites sulforaphane-glutathione (SFN-GSH), sulforaphane-cysteine (SFN-Cys), sulforaphane cysteine-glycine (SFN-CG) and sulfo...

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Autores principales: Langston-Cox, Annie, Anderson, Dovile, Creek, Darren J., Palmer, Kirsten, Wallace, Euan M., Marshall, Sarah A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070302/
https://www.ncbi.nlm.nih.gov/pubmed/32070059
http://dx.doi.org/10.3390/molecules25040829
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author Langston-Cox, Annie
Anderson, Dovile
Creek, Darren J.
Palmer, Kirsten
Wallace, Euan M.
Marshall, Sarah A.
author_facet Langston-Cox, Annie
Anderson, Dovile
Creek, Darren J.
Palmer, Kirsten
Wallace, Euan M.
Marshall, Sarah A.
author_sort Langston-Cox, Annie
collection PubMed
description (1) Background: There is increasing understanding of the potential health benefits of cruciferous vegetables. In particular sulforaphane (SFN), found in broccoli, and its metabolites sulforaphane-glutathione (SFN-GSH), sulforaphane-cysteine (SFN-Cys), sulforaphane cysteine-glycine (SFN-CG) and sulforaphane-N-acetyl-cysteine (SFN-NAC) have potent antioxidant effects that may offer therapeutic value. Clinical investigation of sulforaphane as a therapeutic antioxidant requires a sensitive and high throughput process for quantification of sulforaphane and metabolites; (2) Methods: We collected plasma samples from healthy human volunteers before and for eight hours after consumption of a commercial broccoli extract supplement rich in sulforaphane. A rapid and sensitive method for quantification of sulforaphane and its metabolites in human plasma using Liquid Chromatography–Mass Spectrometry (LC–MS) has been developed; (3) Results: The LC–MS analytical method was validated at concentrations ranging between 3.9 nM and 1000 nM for SFN-GSH, SFN-CG, SFN-Cys and SFN-NAC and between 7.8 nM and 1000 nM in human plasma for SFN. The method displayed good accuracy (1.85%–14.8% bias) and reproducibility (below 9.53 %RSD) including low concentrations 3.9 nM and 7.8 nM. Four SFN metabolites quantitation was achieved using external standard calibration and in SFN quantitation, SFN-d(8) internal standardization was used. The reported method can accurately quantify sulforaphane and its metabolites at low concentrations in plasma; (4) Conclusions: We have established a time- and cost-efficient method of measuring sulforaphane and its metabolites in human plasma suitable for high throughput application to clinical trials.
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spelling pubmed-70703022020-03-19 Measuring Sulforaphane and Its Metabolites in Human Plasma: A High Throughput Method Langston-Cox, Annie Anderson, Dovile Creek, Darren J. Palmer, Kirsten Wallace, Euan M. Marshall, Sarah A. Molecules Article (1) Background: There is increasing understanding of the potential health benefits of cruciferous vegetables. In particular sulforaphane (SFN), found in broccoli, and its metabolites sulforaphane-glutathione (SFN-GSH), sulforaphane-cysteine (SFN-Cys), sulforaphane cysteine-glycine (SFN-CG) and sulforaphane-N-acetyl-cysteine (SFN-NAC) have potent antioxidant effects that may offer therapeutic value. Clinical investigation of sulforaphane as a therapeutic antioxidant requires a sensitive and high throughput process for quantification of sulforaphane and metabolites; (2) Methods: We collected plasma samples from healthy human volunteers before and for eight hours after consumption of a commercial broccoli extract supplement rich in sulforaphane. A rapid and sensitive method for quantification of sulforaphane and its metabolites in human plasma using Liquid Chromatography–Mass Spectrometry (LC–MS) has been developed; (3) Results: The LC–MS analytical method was validated at concentrations ranging between 3.9 nM and 1000 nM for SFN-GSH, SFN-CG, SFN-Cys and SFN-NAC and between 7.8 nM and 1000 nM in human plasma for SFN. The method displayed good accuracy (1.85%–14.8% bias) and reproducibility (below 9.53 %RSD) including low concentrations 3.9 nM and 7.8 nM. Four SFN metabolites quantitation was achieved using external standard calibration and in SFN quantitation, SFN-d(8) internal standardization was used. The reported method can accurately quantify sulforaphane and its metabolites at low concentrations in plasma; (4) Conclusions: We have established a time- and cost-efficient method of measuring sulforaphane and its metabolites in human plasma suitable for high throughput application to clinical trials. MDPI 2020-02-13 /pmc/articles/PMC7070302/ /pubmed/32070059 http://dx.doi.org/10.3390/molecules25040829 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Langston-Cox, Annie
Anderson, Dovile
Creek, Darren J.
Palmer, Kirsten
Wallace, Euan M.
Marshall, Sarah A.
Measuring Sulforaphane and Its Metabolites in Human Plasma: A High Throughput Method
title Measuring Sulforaphane and Its Metabolites in Human Plasma: A High Throughput Method
title_full Measuring Sulforaphane and Its Metabolites in Human Plasma: A High Throughput Method
title_fullStr Measuring Sulforaphane and Its Metabolites in Human Plasma: A High Throughput Method
title_full_unstemmed Measuring Sulforaphane and Its Metabolites in Human Plasma: A High Throughput Method
title_short Measuring Sulforaphane and Its Metabolites in Human Plasma: A High Throughput Method
title_sort measuring sulforaphane and its metabolites in human plasma: a high throughput method
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070302/
https://www.ncbi.nlm.nih.gov/pubmed/32070059
http://dx.doi.org/10.3390/molecules25040829
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