Cargando…
Analysis of Pyrrolizidine Alkaloids in Queensland Honey: Using Low Temperature Chromatography to Resolve Stereoisomers and Identify Botanical Sources by UHPLC-MS/MS
Pyrrolizidine alkaloids (PAs) are a diverse group of plant secondary metabolites with known varied toxicity. Consumption of 1,2-unsaturated PAs has been linked to acute and chronic liver damage, carcinogenicity and death, in livestock and humans, making their presence in food of concern to food regu...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6950414/ https://www.ncbi.nlm.nih.gov/pubmed/31835836 http://dx.doi.org/10.3390/toxins11120726 |
_version_ | 1783486066168168448 |
---|---|
author | Hungerford, Natasha L. Carter, Steve J. Anuj, Shalona R. Tan, Benjamin L. L. Hnatko, Darina Martin, Christopher L. Sharma, Elipsha Yin, Mukan Nguyen, Thao T. P. Melksham, Kevin J. Fletcher, Mary T. |
author_facet | Hungerford, Natasha L. Carter, Steve J. Anuj, Shalona R. Tan, Benjamin L. L. Hnatko, Darina Martin, Christopher L. Sharma, Elipsha Yin, Mukan Nguyen, Thao T. P. Melksham, Kevin J. Fletcher, Mary T. |
author_sort | Hungerford, Natasha L. |
collection | PubMed |
description | Pyrrolizidine alkaloids (PAs) are a diverse group of plant secondary metabolites with known varied toxicity. Consumption of 1,2-unsaturated PAs has been linked to acute and chronic liver damage, carcinogenicity and death, in livestock and humans, making their presence in food of concern to food regulators in Australia and internationally. In this survey, honey samples sourced from markets and shops in Queensland (Australia), were analysed by high-resolution Orbitrap UHPLC-MS/MS for 30 common PAs. Relationships between the occurrence of pyrrolizidine alkaloids and the botanical origin of the honey are essential as pyrrolizidine alkaloid contamination at up to 3300 ng/g were detected. In this study, the predominant alkaloids detected were isomeric PAs, lycopsamine, indicine and intermedine, exhibiting identical MS/MS spectra, along with lesser amounts of each of their N-oxides. Crucially, chromatographic UHPLC conditions were optimised by operation at low temperature (5 °C) to resolve these key isomeric PAs. Such separation of these isomers by UHPLC, enabled the relative proportions of these PAs present in honey to be compared to alkaloid levels in suspect source plants. Overall plant pyrrolizidine alkaloid profiles were compared to those found in honey samples to help identify the most important plants responsible for honey contamination. The native Australian vines of Parsonsia spp. are proposed as a likely contributor to high levels of lycopsamine in many of the honeys surveyed. Botanical origin information such as this, gained via low temperature chromatographic resolution of isomeric PAs, will be very valuable in identifying region of origin for honey samples. |
format | Online Article Text |
id | pubmed-6950414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69504142020-01-16 Analysis of Pyrrolizidine Alkaloids in Queensland Honey: Using Low Temperature Chromatography to Resolve Stereoisomers and Identify Botanical Sources by UHPLC-MS/MS Hungerford, Natasha L. Carter, Steve J. Anuj, Shalona R. Tan, Benjamin L. L. Hnatko, Darina Martin, Christopher L. Sharma, Elipsha Yin, Mukan Nguyen, Thao T. P. Melksham, Kevin J. Fletcher, Mary T. Toxins (Basel) Article Pyrrolizidine alkaloids (PAs) are a diverse group of plant secondary metabolites with known varied toxicity. Consumption of 1,2-unsaturated PAs has been linked to acute and chronic liver damage, carcinogenicity and death, in livestock and humans, making their presence in food of concern to food regulators in Australia and internationally. In this survey, honey samples sourced from markets and shops in Queensland (Australia), were analysed by high-resolution Orbitrap UHPLC-MS/MS for 30 common PAs. Relationships between the occurrence of pyrrolizidine alkaloids and the botanical origin of the honey are essential as pyrrolizidine alkaloid contamination at up to 3300 ng/g were detected. In this study, the predominant alkaloids detected were isomeric PAs, lycopsamine, indicine and intermedine, exhibiting identical MS/MS spectra, along with lesser amounts of each of their N-oxides. Crucially, chromatographic UHPLC conditions were optimised by operation at low temperature (5 °C) to resolve these key isomeric PAs. Such separation of these isomers by UHPLC, enabled the relative proportions of these PAs present in honey to be compared to alkaloid levels in suspect source plants. Overall plant pyrrolizidine alkaloid profiles were compared to those found in honey samples to help identify the most important plants responsible for honey contamination. The native Australian vines of Parsonsia spp. are proposed as a likely contributor to high levels of lycopsamine in many of the honeys surveyed. Botanical origin information such as this, gained via low temperature chromatographic resolution of isomeric PAs, will be very valuable in identifying region of origin for honey samples. MDPI 2019-12-11 /pmc/articles/PMC6950414/ /pubmed/31835836 http://dx.doi.org/10.3390/toxins11120726 Text en © 2019 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 Hungerford, Natasha L. Carter, Steve J. Anuj, Shalona R. Tan, Benjamin L. L. Hnatko, Darina Martin, Christopher L. Sharma, Elipsha Yin, Mukan Nguyen, Thao T. P. Melksham, Kevin J. Fletcher, Mary T. Analysis of Pyrrolizidine Alkaloids in Queensland Honey: Using Low Temperature Chromatography to Resolve Stereoisomers and Identify Botanical Sources by UHPLC-MS/MS |
title | Analysis of Pyrrolizidine Alkaloids in Queensland Honey: Using Low Temperature Chromatography to Resolve Stereoisomers and Identify Botanical Sources by UHPLC-MS/MS |
title_full | Analysis of Pyrrolizidine Alkaloids in Queensland Honey: Using Low Temperature Chromatography to Resolve Stereoisomers and Identify Botanical Sources by UHPLC-MS/MS |
title_fullStr | Analysis of Pyrrolizidine Alkaloids in Queensland Honey: Using Low Temperature Chromatography to Resolve Stereoisomers and Identify Botanical Sources by UHPLC-MS/MS |
title_full_unstemmed | Analysis of Pyrrolizidine Alkaloids in Queensland Honey: Using Low Temperature Chromatography to Resolve Stereoisomers and Identify Botanical Sources by UHPLC-MS/MS |
title_short | Analysis of Pyrrolizidine Alkaloids in Queensland Honey: Using Low Temperature Chromatography to Resolve Stereoisomers and Identify Botanical Sources by UHPLC-MS/MS |
title_sort | analysis of pyrrolizidine alkaloids in queensland honey: using low temperature chromatography to resolve stereoisomers and identify botanical sources by uhplc-ms/ms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6950414/ https://www.ncbi.nlm.nih.gov/pubmed/31835836 http://dx.doi.org/10.3390/toxins11120726 |
work_keys_str_mv | AT hungerfordnatashal analysisofpyrrolizidinealkaloidsinqueenslandhoneyusinglowtemperaturechromatographytoresolvestereoisomersandidentifybotanicalsourcesbyuhplcmsms AT carterstevej analysisofpyrrolizidinealkaloidsinqueenslandhoneyusinglowtemperaturechromatographytoresolvestereoisomersandidentifybotanicalsourcesbyuhplcmsms AT anujshalonar analysisofpyrrolizidinealkaloidsinqueenslandhoneyusinglowtemperaturechromatographytoresolvestereoisomersandidentifybotanicalsourcesbyuhplcmsms AT tanbenjaminll analysisofpyrrolizidinealkaloidsinqueenslandhoneyusinglowtemperaturechromatographytoresolvestereoisomersandidentifybotanicalsourcesbyuhplcmsms AT hnatkodarina analysisofpyrrolizidinealkaloidsinqueenslandhoneyusinglowtemperaturechromatographytoresolvestereoisomersandidentifybotanicalsourcesbyuhplcmsms AT martinchristopherl analysisofpyrrolizidinealkaloidsinqueenslandhoneyusinglowtemperaturechromatographytoresolvestereoisomersandidentifybotanicalsourcesbyuhplcmsms AT sharmaelipsha analysisofpyrrolizidinealkaloidsinqueenslandhoneyusinglowtemperaturechromatographytoresolvestereoisomersandidentifybotanicalsourcesbyuhplcmsms AT yinmukan analysisofpyrrolizidinealkaloidsinqueenslandhoneyusinglowtemperaturechromatographytoresolvestereoisomersandidentifybotanicalsourcesbyuhplcmsms AT nguyenthaotp analysisofpyrrolizidinealkaloidsinqueenslandhoneyusinglowtemperaturechromatographytoresolvestereoisomersandidentifybotanicalsourcesbyuhplcmsms AT melkshamkevinj analysisofpyrrolizidinealkaloidsinqueenslandhoneyusinglowtemperaturechromatographytoresolvestereoisomersandidentifybotanicalsourcesbyuhplcmsms AT fletchermaryt analysisofpyrrolizidinealkaloidsinqueenslandhoneyusinglowtemperaturechromatographytoresolvestereoisomersandidentifybotanicalsourcesbyuhplcmsms |