HPLC-DAD/TOF-MS Chemical Compounds Analysis and Evaluation of Antibacterial Activity of Aristolochia longa Root Extracts

Author:

El Omari Nasreddine1ORCID,Akkaoui Sanae2,El Blidi Omar1,Ghchime Rokia3,Bouyahya Abdelhakim4ORCID,Kharbach Mourad56,Yagoubi Maâmar7,Balahbib Abdelaali8,Chokairi Omar1,Barkiyou Malika1

Affiliation:

1. Laboratory of Histology, Embryology and Cytogenetic, Faculty of Medicine and Pharmacy, Mohammed V University in Rabat, Morocco

2. Research Laboratory on Oral Biology and Biotechnology, Faculty of Medicine Dentistry, Mohammed V University in Rabat, Morocco

3. Department of Clinical Neurophysiology, Hospital of Specialities, Ibn Sina University Hospital, Rabat Institute, Morocco

4. Laboratory of Human Pathology Biology, Faculty of Sciences, Genomic Center of Human Pathology, Faculty of Medicine and Pharmacy, Mohammed V University in Rabat, Morocco

5. Department of Analytical Chemistry, Applied Chemometrics and Molecular Modelling, CePhaR, Vrije Universiteit Brussel (VUB), Belgium

6. Bio-Pharmaceutical and Toxicological Analysis Research Team, Laboratory of Pharmacology and Toxicology, Faculty of Medicine and Pharmacy, University Mohammed V in Rabat, Morocco

7. Laboratory of Microbiology, Department of Clinical Medical Biology, Faculty of Medicine and Pharmacy, Mohammed V University in Rabat, Morocco

8. Laboratory of Zoology and General Biology, Faculty of Sciences, Mohammed V University in Rabat, Morocco

Abstract

The present study aimed to determine the phenolic compounds of Aristolochia longa root extracts and to evaluate their antibacterial activities on multiresistant strains. Phytochemical analysis revealed the presence of flavonoids, tannins, terpenoids, and alkaloids. The HPLC-DAD analysis of A. longa extracts showed the presence of several major bioactive compounds such as ferulic acid, 4-hydroxycinnamic acid, citric acid, and quinic acid. The agar diffusion method was used for the sensitivity test, while minimal inhibitory concentration (MIC) and minimal bactericidal concentration values were determined by microdilution assay. Different tests were carried out on 3 clinical multiresistant strains and 3 reference strains. The diameter of inhibition of Staphylococcus aureus ATCC 25923 induced by the ethyl acetate fraction at 200 mg/mL was 25 ± 1 mm. Moreover, Escherichia coli ATCC 29522 showed a great sensitivity toward all the concentrations tested. The MICs of the active extracts vary between 12.5 and 100 mg/mL with a bacteriostatic effect on Pseudomonas aeruginosa ATCC 27853, Enterococcus faecalis, and S. aureus ATCC 25923.

Publisher

SAGE Publications

Subject

Complementary and alternative medicine,Plant Science,Drug Discovery,Pharmacology,General Medicine

Reference29 articles.

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