UHPLC‐MS/MS analysis, cytotoxic, enzyme inhibition, and antioxidant properties of Lantana camara L. extracts obtained by conventional and nonconventional methods

Author:

Cvetanović Kljakić Aleksandra1ORCID,Lončar Biljana1ORCID,Sinan Kouadio Ibrahime2,Etienne Ouattara Katinan3,Božunović Jelena4,Gašić Uroš4,Koyuncu Ismail5,Yuksekdag Ozgur5,Zengin Gokhan2ORCID

Affiliation:

1. Faculty of Technology University of Novi Sad Novi Sad Serbia

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

3. Laboratoire de Botanique et Valorisation de la Diversite vegetale, UFR science de la nature Universite Nangui Abrogoua Abidjan Ivory Coast

4. Department of Plant Physiology, Institute for Biological Research “Siniša Stanković”—National Institute of Republic of Serbia University of Belgrade Belgrade Serbia

5. Department of Medical Biochemistry, Faculty of Medicine Harran University Sanliurfa Turkey

Abstract

AbstractLantana camara is widely known as a garden plant, but its use for various medicinal purposes is widespread in traditional medicine. In the frame of this study, L. camara was subjected to several different extraction techniques, including supercritical carbon dioxide extraction, accelerated solvent extraction (ASE), homogenizer‐assisted extraction, microwave‐assisted extraction, ultrasound‐assisted extraction, maceration, and Soxhlet extraction. The investigation encompasses the analysis of the chemical composition alongside assessments of biological activities, such as antioxidant and enzyme‐inhibition potential and cytotoxicity of the obtained extracts. The obtained results showed that the extract obtained by accelerated‐solvent extraction was the richest in the content of total phenols and of individual compounds. Of the 17 components identified in total, hispidulin was detected in the highest concentration (5.43–475.97 mg/kg). In the antioxidant assays, the extracts obtained by accelerated‐solvent and microwave extraction possessed the highest level of antioxidant and antiradical protection. All obtained extracts showed enzyme‐inhibitory action on amylase, glucosidase, tyrosinase, and cholinesterase, showing a high potential for application against diseases induced by excessive activity of these enzymes. Cytotoxic analysis was performed on normal and tumor cells, whereby the obtained IC50 values were in the range of 7.685–79.26 µg/mL, showing the high cytotoxicity of the obtained extracts. Using Z score analysis, ASE resulted in an optimal combination of tested quality characteristics of the L. camara extracts.

Publisher

Wiley

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