Combining the Pharmaceutical and Toxicological Properties of Selected Essential Oils with their Chemical Components by GC‐MS Analysis

Author:

Nilofar 12,Ahmed Shakeel3,Zengin Gokhan2ORCID,Di Simone Simonetta Cristina1,Acquaviva Alessandra1,Libero Maria Loreta1,Chiavaroli Annalisa1,Orlando Giustino1,Tacchini Massimo4,Di Vito Maura5,Menghini Luigi1,Ferrante Claudio1

Affiliation:

1. Department of Pharmacy Botanic Garden “Giardino dei Semplici”, Università degli Studi “Gabriele d'Annunzio” via dei Vestini 31 66100 Chieti Italy

2. Department of Biology Science Faculty, Selcuk University 42130 Konya Turkey

3. Foodomics Laboratory Instituto de Investigación en Ciencias de la Alimentación CSIC-UAM Nicolás Cabrera 9 28049 Madrid Spain

4. Department of Life Sciences and Biotechnology (SVeB) UR7 Terra&Acqua Tech University of Ferrara 44121 Ferrara Italy

5. Dip. di Scienze biotecnologiche di base cliniche intensivologiche e perioperatorie Università Cattolica del Sacro Cuore 24 Largo Agostino Gemelli 1 00167 Rome Italy

Abstract

AbstractIn the current investigation, a comprehensive analysis was carried out on essential oils (EOs) extracted from six aromatic plant species, namely Rosmarinus officinalis, Pelargonium graveolens, Thymus vulgaris, Origanum vulgare, Laurus nobilis, and Aloysia citrodora. An exploration was conducted into the chemical composition using Gas Chromatography‐Mass Spectrometry (GC/MS), antioxidant properties assessed through DPPH, ABTS, CUPRAC, FRAP, MCA, and PBD assays, ecotoxicological impacts evaluated via allelopathy and the Daphnia magna heartbeat test, as well as bio‐pharmacological effects including anticancer activity and gene expression analysis. Results revealed strong antioxidant activity in all essential oils, with T. vulgaris EO (2748.00 mg TE/g) and O. vulgare EO (2609.29 mg TE/g) leading in CUPRAC assay. R. officinalis EO showed the highest α‐amylase inhibition at 1.58 mmol ACAE/g, while O. vulgare EO excelled in α‐glucosidase inhibition at 1.57 mmol ACAE/g. Additionally, cytotoxic effects were evaluated on human colorectal cancer (HCT116) cells. A. citrodora, O. vulgare, and R. officinalis EOs were found the most potent anticancer, as also witnessed by their higher modulatory effects on the gene expression of BAX and Bcl‐2. Collectively, the present data highlight the importance to implement the knowledge and to valorize the supply chain of aromatic plants.

Publisher

Wiley

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