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Analysis of amide compounds in different parts of Piper ovatum Vahl by high-performance liquid chromatographic

BACKGROUND: Piper ovatum (Piperaceae) has been used in traditional medicine for the treatment of inflammations and as an analgesic. Previous studies have showed important biological activities of the extracts and amides from P. ovatum leaves. OBJECTIVE: In this study, a high-performance liquid chrom...

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Autores principales: Silva, Daniel R., Brenzan, Mislaine A., Kambara, Lauro M., Cortez, Lucia E. R., Cortez, Diógenes A. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807989/
https://www.ncbi.nlm.nih.gov/pubmed/24174818
http://dx.doi.org/10.4103/0974-8490.118812
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author Silva, Daniel R.
Brenzan, Mislaine A.
Kambara, Lauro M.
Cortez, Lucia E. R.
Cortez, Diógenes A. G.
author_facet Silva, Daniel R.
Brenzan, Mislaine A.
Kambara, Lauro M.
Cortez, Lucia E. R.
Cortez, Diógenes A. G.
author_sort Silva, Daniel R.
collection PubMed
description BACKGROUND: Piper ovatum (Piperaceae) has been used in traditional medicine for the treatment of inflammations and as an analgesic. Previous studies have showed important biological activities of the extracts and amides from P. ovatum leaves. OBJECTIVE: In this study, a high-performance liquid chromatographic (HPLC) method was developed and validated for quantitative determination of the amides in different parts of Piper ovatum. MATERIALS AND METHODS: The analysis was carried out on a Metasil ODS column (150 × 4.6 mm, 5μm) at room temperature. HPLC conditions were as follows: acetonitrile (A), and water (B), 1.0% acetic acid. The gradient elution used was 0–30 min, 0-60% A; 30–40 min, 60% A. Flow rate used was 1.0mL/min, and detection at 280nm. RESULTS: The validation using piperlonguminine, as the standard, demonstrated that the method shows linearity (linear correlation coefficient = 0.998), precision (relative standard deviation <5%) and accuracy (mean recovery = 103.78%) in the concentration range 31.25 – 500μg/mL. The limit of detection and quantification were 1.21 and 4.03μg/mL, respectively. This method allowed the identification and quantification of piperlonguminine and piperovatine in the hydroethanolic extracts of P. ovatum obtained from the leaves, stems and roots. All the extracts showed the same chromatographic profile. The leaves and roots contained the highest concentrations of piperlonguminine and the stems and leaves showed the most concentrations of piperovatine. CONCLUSION: This HPLC method is suitable for routine quantitative analysis of amides in extracts of Piper ovatum and phytopharmaceuticals containing this herb.
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spelling pubmed-38079892013-10-30 Analysis of amide compounds in different parts of Piper ovatum Vahl by high-performance liquid chromatographic Silva, Daniel R. Brenzan, Mislaine A. Kambara, Lauro M. Cortez, Lucia E. R. Cortez, Diógenes A. G. Pharmacognosy Res Original Article BACKGROUND: Piper ovatum (Piperaceae) has been used in traditional medicine for the treatment of inflammations and as an analgesic. Previous studies have showed important biological activities of the extracts and amides from P. ovatum leaves. OBJECTIVE: In this study, a high-performance liquid chromatographic (HPLC) method was developed and validated for quantitative determination of the amides in different parts of Piper ovatum. MATERIALS AND METHODS: The analysis was carried out on a Metasil ODS column (150 × 4.6 mm, 5μm) at room temperature. HPLC conditions were as follows: acetonitrile (A), and water (B), 1.0% acetic acid. The gradient elution used was 0–30 min, 0-60% A; 30–40 min, 60% A. Flow rate used was 1.0mL/min, and detection at 280nm. RESULTS: The validation using piperlonguminine, as the standard, demonstrated that the method shows linearity (linear correlation coefficient = 0.998), precision (relative standard deviation <5%) and accuracy (mean recovery = 103.78%) in the concentration range 31.25 – 500μg/mL. The limit of detection and quantification were 1.21 and 4.03μg/mL, respectively. This method allowed the identification and quantification of piperlonguminine and piperovatine in the hydroethanolic extracts of P. ovatum obtained from the leaves, stems and roots. All the extracts showed the same chromatographic profile. The leaves and roots contained the highest concentrations of piperlonguminine and the stems and leaves showed the most concentrations of piperovatine. CONCLUSION: This HPLC method is suitable for routine quantitative analysis of amides in extracts of Piper ovatum and phytopharmaceuticals containing this herb. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3807989/ /pubmed/24174818 http://dx.doi.org/10.4103/0974-8490.118812 Text en Copyright: © Pharmacognosy Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Silva, Daniel R.
Brenzan, Mislaine A.
Kambara, Lauro M.
Cortez, Lucia E. R.
Cortez, Diógenes A. G.
Analysis of amide compounds in different parts of Piper ovatum Vahl by high-performance liquid chromatographic
title Analysis of amide compounds in different parts of Piper ovatum Vahl by high-performance liquid chromatographic
title_full Analysis of amide compounds in different parts of Piper ovatum Vahl by high-performance liquid chromatographic
title_fullStr Analysis of amide compounds in different parts of Piper ovatum Vahl by high-performance liquid chromatographic
title_full_unstemmed Analysis of amide compounds in different parts of Piper ovatum Vahl by high-performance liquid chromatographic
title_short Analysis of amide compounds in different parts of Piper ovatum Vahl by high-performance liquid chromatographic
title_sort analysis of amide compounds in different parts of piper ovatum vahl by high-performance liquid chromatographic
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807989/
https://www.ncbi.nlm.nih.gov/pubmed/24174818
http://dx.doi.org/10.4103/0974-8490.118812
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