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Identification of common horsetail (Equisetum arvense L.; Equisetaceae) using Thin Layer Chromatography versus DNA barcoding

The global herbal products market has grown in recent years, making regulation of these products paramount for public healthcare. For instance, the common horsetail (Equisetum arvense L.) is used in numerous herbal products, but it can be adulterated with closely related species, especially E. palus...

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Autores principales: Saslis-Lagoudakis, C. Haris, Bruun-Lund, Sam, Iwanycki, Natalie E., Seberg, Ole, Petersen, Gitte, Jäger, Anna K., Rønsted, Nina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499799/
https://www.ncbi.nlm.nih.gov/pubmed/26165523
http://dx.doi.org/10.1038/srep11942
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author Saslis-Lagoudakis, C. Haris
Bruun-Lund, Sam
Iwanycki, Natalie E.
Seberg, Ole
Petersen, Gitte
Jäger, Anna K.
Rønsted, Nina
author_facet Saslis-Lagoudakis, C. Haris
Bruun-Lund, Sam
Iwanycki, Natalie E.
Seberg, Ole
Petersen, Gitte
Jäger, Anna K.
Rønsted, Nina
author_sort Saslis-Lagoudakis, C. Haris
collection PubMed
description The global herbal products market has grown in recent years, making regulation of these products paramount for public healthcare. For instance, the common horsetail (Equisetum arvense L.) is used in numerous herbal products, but it can be adulterated with closely related species, especially E. palustre L. that can produce toxic alkaloids. As morphology-based identification is often difficult or impossible, the identification of processed material can be aided by molecular techniques. In this study, we explore two molecular identification techniques as methods of testing the purity of these products: a Thin Layer Chromatography approach (TLC-test) included in the European Pharmacopoeia and a DNA barcoding approach, used in recent years to identify material in herbal products. We test the potential of these methods for distinguishing and identifying these species using material from herbarium collections and commercial herbal products. We find that both methods can discriminate between the two species and positively identify E. arvense. The TLC-test is more cost- and time-efficient, but DNA barcoding is more powerful in determining the identity of adulterant species. Our study shows that, although DNA barcoding presents certain advantages, other established laboratory methods can perform as well or even better in confirming species’ identity in herbal products.
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spelling pubmed-44997992015-07-17 Identification of common horsetail (Equisetum arvense L.; Equisetaceae) using Thin Layer Chromatography versus DNA barcoding Saslis-Lagoudakis, C. Haris Bruun-Lund, Sam Iwanycki, Natalie E. Seberg, Ole Petersen, Gitte Jäger, Anna K. Rønsted, Nina Sci Rep Article The global herbal products market has grown in recent years, making regulation of these products paramount for public healthcare. For instance, the common horsetail (Equisetum arvense L.) is used in numerous herbal products, but it can be adulterated with closely related species, especially E. palustre L. that can produce toxic alkaloids. As morphology-based identification is often difficult or impossible, the identification of processed material can be aided by molecular techniques. In this study, we explore two molecular identification techniques as methods of testing the purity of these products: a Thin Layer Chromatography approach (TLC-test) included in the European Pharmacopoeia and a DNA barcoding approach, used in recent years to identify material in herbal products. We test the potential of these methods for distinguishing and identifying these species using material from herbarium collections and commercial herbal products. We find that both methods can discriminate between the two species and positively identify E. arvense. The TLC-test is more cost- and time-efficient, but DNA barcoding is more powerful in determining the identity of adulterant species. Our study shows that, although DNA barcoding presents certain advantages, other established laboratory methods can perform as well or even better in confirming species’ identity in herbal products. Nature Publishing Group 2015-07-13 /pmc/articles/PMC4499799/ /pubmed/26165523 http://dx.doi.org/10.1038/srep11942 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Saslis-Lagoudakis, C. Haris
Bruun-Lund, Sam
Iwanycki, Natalie E.
Seberg, Ole
Petersen, Gitte
Jäger, Anna K.
Rønsted, Nina
Identification of common horsetail (Equisetum arvense L.; Equisetaceae) using Thin Layer Chromatography versus DNA barcoding
title Identification of common horsetail (Equisetum arvense L.; Equisetaceae) using Thin Layer Chromatography versus DNA barcoding
title_full Identification of common horsetail (Equisetum arvense L.; Equisetaceae) using Thin Layer Chromatography versus DNA barcoding
title_fullStr Identification of common horsetail (Equisetum arvense L.; Equisetaceae) using Thin Layer Chromatography versus DNA barcoding
title_full_unstemmed Identification of common horsetail (Equisetum arvense L.; Equisetaceae) using Thin Layer Chromatography versus DNA barcoding
title_short Identification of common horsetail (Equisetum arvense L.; Equisetaceae) using Thin Layer Chromatography versus DNA barcoding
title_sort identification of common horsetail (equisetum arvense l.; equisetaceae) using thin layer chromatography versus dna barcoding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499799/
https://www.ncbi.nlm.nih.gov/pubmed/26165523
http://dx.doi.org/10.1038/srep11942
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