Anogeissus latifolia leaf, flower and stem extracts: UPLC/ESI-qTOF-HRMS/MS profile with cytotoxicity and antiviral activity evaluation

Document Type : Original Article

Authors

1 Department of Pharmacognosy, Faculty of Pharmacy (for Girls), Al-Azhar University, P.O. Box 11651, Nasr City, Cairo, Egypt.

2 Chemistry of Tanning Materials and Leather Technology Department, Chemical Industries Research Institute, National Research Centre, 33 El‑Bohouth St. (Former El‑Tahrir St.), Dokki, Cairo 12622, Egypt.

Abstract

Further phytochemical and biological investigations for A. latifolia extracts were designed through LC/qTOF-MS/MS characterization alongside cytotoxicity and antiviral activity were examined against four cancer cell lines and two viruses. Phytochemical profiles of leaf and flower were determined by UPLC/HRESI-MS/MS. MTT assay was used for cytotoxicity evaluation against four human cancer cell lines. In vitro anti-HSV1 and HAV activity was evaluated with three different protocols to test protective, anti-replicative, and anti-infective antiviral activities, and three separate replications of each experiment were conducted using MTT colorimetric assay and IC50 with selectivity index (SI) using Vero cell line. By LC/ESIMS, 66 and 27 metabolites were identified. In-vitro, all extracts inhibited HepG-2, Caco-2/ATB-37, MCF-7/HTB-22 and Panc-1 growth in concentration dependent manner. Leaf-extract showed the moderate activity against Caco-2 (IC50=81.78±0.43 μg/ml & SI= 11.83); stem, leaf and flower demonstrated nearly weak cytotoxicity against HepG-2 (IC50=203.3±5.33, 221.71±4.44, 329.35 ± 9.27 μg/ml). Flower-extract recorded weak activity against MCF-7 (IC50=288±20.1) and promising protective activity against HSV1 with no significant difference with acyclovir (65.53±3.24 vs 68.44±7.62). Leaf -extract demonstrated pronounced protective (82.99±1.56) and anti-infectivity (73.19±3.1) activities against HAV. Stem-extract exhibited least activity against HSV1 and no activity against HAV. Significant cytotoxicity and antiviral activity could be attributed mainly to constitutive polyphenols.
 

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Articles in Press, Accepted Manuscript
Available Online from 21 February 2024
  • Receive Date: 30 December 2023
  • Revise Date: 14 February 2024
  • Accept Date: 21 February 2024