Renda Chahna, Hamdi Bendif, Amina Bouzana, Larbi Derbak, Imane Haouame, Dilaycan Çam, Mehmet Öztürk, Khellaf Rebbas, Mohamed A. M. Ali, Chawki Bensouıci, Fehmi Boufahja, Stefania Garzoli
{"title":"Salvia lanigera Poiret Extracts: Study of the Phytochemical Profiling via GC–MS and HPLC–DAD and Bioactivity with ADME Analysis","authors":"Renda Chahna, Hamdi Bendif, Amina Bouzana, Larbi Derbak, Imane Haouame, Dilaycan Çam, Mehmet Öztürk, Khellaf Rebbas, Mohamed A. M. Ali, Chawki Bensouıci, Fehmi Boufahja, Stefania Garzoli","doi":"10.1007/s12161-025-02863-2","DOIUrl":null,"url":null,"abstract":"<div><p>This investigation evaluated the chemical composition and the biological activities of the ethanol and petroleum ether extracts of <i>Salvia lanigera</i> Poiret from the M’sila region, Algeria. Phytochemical analysis identified 17 compounds in the ethanol extract (HPLC–DAD), with cynarin, ellagic acid, and rutin as major components. Petroleum ether extract (GC–MS) revealed 16 compounds, predominantly palmitic acid and stearic acid. Antioxidant activity was assessed using four assays: the ethanol extract showed significant activity in the phenanthroline assay (1.94 ± 0.18 μg/mL), and SNP assay (124.78 ± 0.59 μg/mL), compared to the BHA standard. Both extracts demonstrated antibacterial and antifungal effects, with inhibition zones of 10–13 mm and MIC values ranging from 0.78 to 3.125 mg/mL against tested strains. Enzymatic assays revealed α-glucosidase inhibition by the ethanol extract (IC<sub>50</sub> = 27.07 ± 0.78 μg/mL), while α-amylase inhibition was lower (ethanol: 429.85 ± 1.43 μg/mL; petroleum ether: 520.31 ± 1.63 μg/mL). Acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibition were minimal (IC<sub>50</sub> > 200 μg/mL for AChE; ethanol: 365.84 ± 5.48 μg/mL, petroleum ether: 636.13 ± 4.49 μg/mL for BChE). Urease inhibition was notable for the ethanol extract (54.88%) and comparable for the petroleum ether extract (52.00%). These findings highlight the potential of <i>S. lanigera</i> extracts as sources of bioactive compounds with antioxidant, antimicrobial, and enzymatic inhibitory properties, warranting further exploration for therapeutic applications.</p></div>","PeriodicalId":561,"journal":{"name":"Food Analytical Methods","volume":"18 10","pages":"2258 - 2276"},"PeriodicalIF":3.0000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Food Analytical Methods","FirstCategoryId":"97","ListUrlMain":"https://link.springer.com/article/10.1007/s12161-025-02863-2","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
This investigation evaluated the chemical composition and the biological activities of the ethanol and petroleum ether extracts of Salvia lanigera Poiret from the M’sila region, Algeria. Phytochemical analysis identified 17 compounds in the ethanol extract (HPLC–DAD), with cynarin, ellagic acid, and rutin as major components. Petroleum ether extract (GC–MS) revealed 16 compounds, predominantly palmitic acid and stearic acid. Antioxidant activity was assessed using four assays: the ethanol extract showed significant activity in the phenanthroline assay (1.94 ± 0.18 μg/mL), and SNP assay (124.78 ± 0.59 μg/mL), compared to the BHA standard. Both extracts demonstrated antibacterial and antifungal effects, with inhibition zones of 10–13 mm and MIC values ranging from 0.78 to 3.125 mg/mL against tested strains. Enzymatic assays revealed α-glucosidase inhibition by the ethanol extract (IC50 = 27.07 ± 0.78 μg/mL), while α-amylase inhibition was lower (ethanol: 429.85 ± 1.43 μg/mL; petroleum ether: 520.31 ± 1.63 μg/mL). Acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibition were minimal (IC50 > 200 μg/mL for AChE; ethanol: 365.84 ± 5.48 μg/mL, petroleum ether: 636.13 ± 4.49 μg/mL for BChE). Urease inhibition was notable for the ethanol extract (54.88%) and comparable for the petroleum ether extract (52.00%). These findings highlight the potential of S. lanigera extracts as sources of bioactive compounds with antioxidant, antimicrobial, and enzymatic inhibitory properties, warranting further exploration for therapeutic applications.
期刊介绍:
Food Analytical Methods publishes original articles, review articles, and notes on novel and/or state-of-the-art analytical methods or issues to be solved, as well as significant improvements or interesting applications to existing methods. These include analytical technology and methodology for food microbial contaminants, food chemistry and toxicology, food quality, food authenticity and food traceability. The journal covers fundamental and specific aspects of the development, optimization, and practical implementation in routine laboratories, and validation of food analytical methods for the monitoring of food safety and quality.