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Chemical Composition and In Vitro Antioxidant Activity of Salvia aratocensis (Lamiaceae) Essential Oils and Extracts

Salvia aratocensis (Lamiaceae) is an endemic shrub from the Chicamocha River Canyon in Santander (Colombia). Its essential oil (EO) was distilled from the aerial parts of the plant via steam distillation and microwave-assisted hydrodistillation and analyzed using GC/MS and GC/FID. Hydroethanolic ext...

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Autores principales: Henríquez, Juan C., Duarte, Laura V., Sierra, Lady J., Fernández-Alonso, José L., Martínez, Jairo R., Stashenko, Elena E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223537/
https://www.ncbi.nlm.nih.gov/pubmed/37241803
http://dx.doi.org/10.3390/molecules28104062
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author Henríquez, Juan C.
Duarte, Laura V.
Sierra, Lady J.
Fernández-Alonso, José L.
Martínez, Jairo R.
Stashenko, Elena E.
author_facet Henríquez, Juan C.
Duarte, Laura V.
Sierra, Lady J.
Fernández-Alonso, José L.
Martínez, Jairo R.
Stashenko, Elena E.
author_sort Henríquez, Juan C.
collection PubMed
description Salvia aratocensis (Lamiaceae) is an endemic shrub from the Chicamocha River Canyon in Santander (Colombia). Its essential oil (EO) was distilled from the aerial parts of the plant via steam distillation and microwave-assisted hydrodistillation and analyzed using GC/MS and GC/FID. Hydroethanolic extracts were isolated from dry plants before distillation and from the residual plant material after distillation. The extracts were characterized via UHPLC-ESI((+/−))-Orbitrap-HRMS. The S. aratocensis essential oil was rich in oxygenated sesquiterpenes (60–69%) and presented τ-cadinol (44–48%) and 1,10-di-epi-cubenol (21–24%) as its major components. The in vitro antioxidant activity of the EOs, measured via an ABTS(+•) assay, was 32–49 μmol Trolox(®) g(−1) and that measured using the ORAC assay was 1520–1610 μmol Trolox(®) g(−1). Ursolic acid (28.9–39.8 mg g(−1)) and luteolin-7-O-glucuronide (1.16–25.3 mg g(−1)) were the major S. aratocensis extract constituents. The antioxidant activity of the S. aratocensis extract, obtained from undistilled plant material, was higher (82 ± 4 μmol Trolox(®) g(−1), ABTS(+•); 1300 ± 14 μmol Trolox(®) g(−1), ORAC) than that of the extracts obtained from the residual plant material (51–73 μmol Trolox(®) g(−1), ABTS(+•); 752–1205 μmol Trolox(®) g(−1), ORAC). S. aratocensis EO and extract had higher ORAC antioxidant capacity than the reference substances butyl hydroxy toluene (98 μmol Trolox(®) g(−1)) and α-tocopherol (450 μmol Trolox(®) g(−1)). S. aratocensis EOs and extracts have the potential to be used as natural antioxidants for cosmetics and pharmaceutical products.
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spelling pubmed-102235372023-05-28 Chemical Composition and In Vitro Antioxidant Activity of Salvia aratocensis (Lamiaceae) Essential Oils and Extracts Henríquez, Juan C. Duarte, Laura V. Sierra, Lady J. Fernández-Alonso, José L. Martínez, Jairo R. Stashenko, Elena E. Molecules Article Salvia aratocensis (Lamiaceae) is an endemic shrub from the Chicamocha River Canyon in Santander (Colombia). Its essential oil (EO) was distilled from the aerial parts of the plant via steam distillation and microwave-assisted hydrodistillation and analyzed using GC/MS and GC/FID. Hydroethanolic extracts were isolated from dry plants before distillation and from the residual plant material after distillation. The extracts were characterized via UHPLC-ESI((+/−))-Orbitrap-HRMS. The S. aratocensis essential oil was rich in oxygenated sesquiterpenes (60–69%) and presented τ-cadinol (44–48%) and 1,10-di-epi-cubenol (21–24%) as its major components. The in vitro antioxidant activity of the EOs, measured via an ABTS(+•) assay, was 32–49 μmol Trolox(®) g(−1) and that measured using the ORAC assay was 1520–1610 μmol Trolox(®) g(−1). Ursolic acid (28.9–39.8 mg g(−1)) and luteolin-7-O-glucuronide (1.16–25.3 mg g(−1)) were the major S. aratocensis extract constituents. The antioxidant activity of the S. aratocensis extract, obtained from undistilled plant material, was higher (82 ± 4 μmol Trolox(®) g(−1), ABTS(+•); 1300 ± 14 μmol Trolox(®) g(−1), ORAC) than that of the extracts obtained from the residual plant material (51–73 μmol Trolox(®) g(−1), ABTS(+•); 752–1205 μmol Trolox(®) g(−1), ORAC). S. aratocensis EO and extract had higher ORAC antioxidant capacity than the reference substances butyl hydroxy toluene (98 μmol Trolox(®) g(−1)) and α-tocopherol (450 μmol Trolox(®) g(−1)). S. aratocensis EOs and extracts have the potential to be used as natural antioxidants for cosmetics and pharmaceutical products. MDPI 2023-05-12 /pmc/articles/PMC10223537/ /pubmed/37241803 http://dx.doi.org/10.3390/molecules28104062 Text en © 2023 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
Henríquez, Juan C.
Duarte, Laura V.
Sierra, Lady J.
Fernández-Alonso, José L.
Martínez, Jairo R.
Stashenko, Elena E.
Chemical Composition and In Vitro Antioxidant Activity of Salvia aratocensis (Lamiaceae) Essential Oils and Extracts
title Chemical Composition and In Vitro Antioxidant Activity of Salvia aratocensis (Lamiaceae) Essential Oils and Extracts
title_full Chemical Composition and In Vitro Antioxidant Activity of Salvia aratocensis (Lamiaceae) Essential Oils and Extracts
title_fullStr Chemical Composition and In Vitro Antioxidant Activity of Salvia aratocensis (Lamiaceae) Essential Oils and Extracts
title_full_unstemmed Chemical Composition and In Vitro Antioxidant Activity of Salvia aratocensis (Lamiaceae) Essential Oils and Extracts
title_short Chemical Composition and In Vitro Antioxidant Activity of Salvia aratocensis (Lamiaceae) Essential Oils and Extracts
title_sort chemical composition and in vitro antioxidant activity of salvia aratocensis (lamiaceae) essential oils and extracts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223537/
https://www.ncbi.nlm.nih.gov/pubmed/37241803
http://dx.doi.org/10.3390/molecules28104062
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