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Development and Validation of a Reversed-Phase HPLC Method with UV Detection for the Determination of L-Dopa in Vicia faba L. Broad Beans

L-Dopa (LD), a substance used medically in the treatment of Parkinson’s disease, is found in several natural products, such as Vicia faba L., also known as broad beans. Due to its low chemical stability, LD analysis in plant matrices requires an appropriate optimization of the chosen analytical meth...

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Autores principales: Tesoro, Carmen, Ciriello, Rosanna, Lelario, Filomena, Di Capua, Angela, Pascale, Raffaella, Bianco, Giuliana, Dell’Agli, Mario, Piazza, Stefano, Guerrieri, Antonio, Scrano, Laura, Bufo, Sabino A., Acquavia, Maria Assunta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654252/
https://www.ncbi.nlm.nih.gov/pubmed/36364292
http://dx.doi.org/10.3390/molecules27217468
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author Tesoro, Carmen
Ciriello, Rosanna
Lelario, Filomena
Di Capua, Angela
Pascale, Raffaella
Bianco, Giuliana
Dell’Agli, Mario
Piazza, Stefano
Guerrieri, Antonio
Scrano, Laura
Bufo, Sabino A.
Acquavia, Maria Assunta
author_facet Tesoro, Carmen
Ciriello, Rosanna
Lelario, Filomena
Di Capua, Angela
Pascale, Raffaella
Bianco, Giuliana
Dell’Agli, Mario
Piazza, Stefano
Guerrieri, Antonio
Scrano, Laura
Bufo, Sabino A.
Acquavia, Maria Assunta
author_sort Tesoro, Carmen
collection PubMed
description L-Dopa (LD), a substance used medically in the treatment of Parkinson’s disease, is found in several natural products, such as Vicia faba L., also known as broad beans. Due to its low chemical stability, LD analysis in plant matrices requires an appropriate optimization of the chosen analytical method to obtain reliable results. This work proposes an HPLC-UV method, validated according to EURACHEM guidelines as regards linearity, limits of detection and quantification, precision, accuracy, and matrix effect. The LD extraction was studied by evaluating its aqueous stability over 3 months. The best chromatographic conditions were found by systematically testing several C(18) stationary phases and acidic mobile phases. In addition, the assessment of the best storage treatment of Vicia faba L. broad beans able to preserve a high LD content was performed. The best LD determination conditions include sun-drying storage, extraction in HCl 0.1 M, chromatographic separation with a Discovery C(18) column, 250 × 4.6 mm, 5 µm particle size, and 99% formic acid 0.2% v/v and 1% methanol as the mobile phase. The optimized method proposed here overcomes the problems linked to LD stability and separation, thus contributing to the improvement of its analytical determination.
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spelling pubmed-96542522022-11-15 Development and Validation of a Reversed-Phase HPLC Method with UV Detection for the Determination of L-Dopa in Vicia faba L. Broad Beans Tesoro, Carmen Ciriello, Rosanna Lelario, Filomena Di Capua, Angela Pascale, Raffaella Bianco, Giuliana Dell’Agli, Mario Piazza, Stefano Guerrieri, Antonio Scrano, Laura Bufo, Sabino A. Acquavia, Maria Assunta Molecules Article L-Dopa (LD), a substance used medically in the treatment of Parkinson’s disease, is found in several natural products, such as Vicia faba L., also known as broad beans. Due to its low chemical stability, LD analysis in plant matrices requires an appropriate optimization of the chosen analytical method to obtain reliable results. This work proposes an HPLC-UV method, validated according to EURACHEM guidelines as regards linearity, limits of detection and quantification, precision, accuracy, and matrix effect. The LD extraction was studied by evaluating its aqueous stability over 3 months. The best chromatographic conditions were found by systematically testing several C(18) stationary phases and acidic mobile phases. In addition, the assessment of the best storage treatment of Vicia faba L. broad beans able to preserve a high LD content was performed. The best LD determination conditions include sun-drying storage, extraction in HCl 0.1 M, chromatographic separation with a Discovery C(18) column, 250 × 4.6 mm, 5 µm particle size, and 99% formic acid 0.2% v/v and 1% methanol as the mobile phase. The optimized method proposed here overcomes the problems linked to LD stability and separation, thus contributing to the improvement of its analytical determination. MDPI 2022-11-02 /pmc/articles/PMC9654252/ /pubmed/36364292 http://dx.doi.org/10.3390/molecules27217468 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tesoro, Carmen
Ciriello, Rosanna
Lelario, Filomena
Di Capua, Angela
Pascale, Raffaella
Bianco, Giuliana
Dell’Agli, Mario
Piazza, Stefano
Guerrieri, Antonio
Scrano, Laura
Bufo, Sabino A.
Acquavia, Maria Assunta
Development and Validation of a Reversed-Phase HPLC Method with UV Detection for the Determination of L-Dopa in Vicia faba L. Broad Beans
title Development and Validation of a Reversed-Phase HPLC Method with UV Detection for the Determination of L-Dopa in Vicia faba L. Broad Beans
title_full Development and Validation of a Reversed-Phase HPLC Method with UV Detection for the Determination of L-Dopa in Vicia faba L. Broad Beans
title_fullStr Development and Validation of a Reversed-Phase HPLC Method with UV Detection for the Determination of L-Dopa in Vicia faba L. Broad Beans
title_full_unstemmed Development and Validation of a Reversed-Phase HPLC Method with UV Detection for the Determination of L-Dopa in Vicia faba L. Broad Beans
title_short Development and Validation of a Reversed-Phase HPLC Method with UV Detection for the Determination of L-Dopa in Vicia faba L. Broad Beans
title_sort development and validation of a reversed-phase hplc method with uv detection for the determination of l-dopa in vicia faba l. broad beans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654252/
https://www.ncbi.nlm.nih.gov/pubmed/36364292
http://dx.doi.org/10.3390/molecules27217468
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