Analytical Profiling of Phenolic and Flavonoid Constituents in Ononis angustissima Using LC–ESI–MS/MS Coupled with Multivariate Optimization

Abstract Ononis angustissima , a member of the Fabaceae family long employed in folk remedies, has remained largely unexplored in terms of its phytochemical composition and bioactivity. In this work, we applied a face-centered central composite design to refine the ethanolic extraction process for phenolic and flavonoid constituents, achieving peak yields of 76.44 ± 0.76 mg GAE/g dry weight (dw) and 66.42 ± 0.83 mg QE/g dw, respectively. Comprehensive LC–ESI–MS/MS analysis unveiled nineteen principal metabolites, among which luteolin (143.55 ± 1.76 µg/g), salicylic acid (45.82 ± 0.24 µg/g dw), and trans-ferulic acid (40.53 ± 0.43 µg/g dw) were most abundant. The chloroform partition demonstrated remarkable butyrylcholinesterase inhibitory activity (IC 50 of 20.52 ± 0.58 µg/mL), showing stronger activity than galantamine under the tested conditions. Additionally, the ethanolic extract exhibited pronounced, selective, and dose-dependent antiproliferative effects against the DLD-1 and CAPAN-1 tumor cell lines, with IC 50 of 0.82 ± 0.07 and 0.87 ± 0.06 mg/mL, respectively, while showing considerably lower cytotoxicity toward the L929 fibroblasts. Molecular docking studies further predicted strong interactions of flavonoids, particularly luteolin and quercetin, with both acetylcholinesterase and butyrylcholinesterase active sites, underscoring their neuroprotective potential. Moreover, ADME profiling of the identified metabolites indicated generally favorable pharmacokinetic properties, with luteolin, caffeic acid, and trans-ferulic acid emerging as promising lead compounds due to their absorption potential, lipophilicity, and bioavailability. Collectively, these results highlight O. angustissima as a valuable source of bioactive compounds worthy of further investigation for potential anticancer and neuroprotective applications. However, given the in vitro and in silico nature of this study, additional research, including bioassay-guided isolation, mechanistic studies, and in vivo validation, is necessary to confirm its therapeutic relevance.

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Journal
Food Analytical Methods
Published
2026-04-14
DOI
https://doi.org/10.1007/s12161-026-03089-6
Primary Topic
Synthesis and Biological Activity
Type
article
Field-Weighted Citation Impact
0.00

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article

Analytical Profiling of Phenolic and Flavonoid Constituents in Ononis angustissima Using LC–ESI–MS/MS Coupled with Multivariate Optimization

Walid Elfalleh, Stefanıa Garzoli, K Rebbas, Radia Ayad et al.
Food Analytical Methods
Synthesis and Biological Activity
article

Analytical Profiling of Phenolic and Flavonoid Constituents in Ononis angustissima Using LC–ESI–MS/MS Coupled with Multivariate Optimization

Walid Elfalleh, Stefanıa Garzoli, K Rebbas, Radia Ayad, Mohamed Lamine Rabhi, Abdesselem Si Mohammed, Larbi Derbak, Hamdi Bendif, Ibrahim Demirtas, Anis Ahmad Chaudhary
article en

Abstract

Abstract Ononis angustissima , a member of the Fabaceae family long employed in folk remedies, has remained largely unexplored in terms of its phytochemical composition and bioactivity. In this work, we applied a face-centered central composite design to refine the ethanolic extraction process for phenolic and flavonoid constituents, achieving peak yields of 76.44 ± 0.76 mg GAE/g dry weight (dw) and 66.42 ± 0.83 mg QE/g dw, respectively. Comprehensive LC–ESI–MS/MS analysis unveiled nineteen principal metabolites, among which luteolin (143.55 ± 1.76 µg/g), salicylic acid (45.82 ± 0.24 µg/g dw), and trans-ferulic acid (40.53 ± 0.43 µg/g dw) were most abundant. The chloroform partition demonstrated remarkable butyrylcholinesterase inhibitory activity (IC 50 of 20.52 ± 0.58 µg/mL), showing stronger activity than galantamine under the tested conditions. Additionally, the ethanolic extract exhibited pronounced, selective, and dose-dependent antiproliferative effects against the DLD-1 and CAPAN-1 tumor cell lines, with IC 50 of 0.82 ± 0.07 and 0.87 ± 0.06 mg/mL, respectively, while showing considerably lower cytotoxicity toward the L929 fibroblasts. Molecular docking studies further predicted strong interactions of flavonoids, particularly luteolin and quercetin, with both acetylcholinesterase and butyrylcholinesterase active sites, underscoring their neuroprotective potential. Moreover, ADME profiling of the identified metabolites indicated generally favorable pharmacokinetic properties, with luteolin, caffeic acid, and trans-ferulic acid emerging as promising lead compounds due to their absorption potential, lipophilicity, and bioavailability. Collectively, these results highlight O. angustissima as a valuable source of bioactive compounds worthy of further investigation for potential anticancer and neuroprotective applications. However, given the in vitro and in silico nature of this study, additional research, including bioassay-guided isolation, mechanistic studies, and in vivo validation, is necessary to confirm its therapeutic relevance.

Food Analytical MethodsVol. 19(6)
University of Jijel (DZ), Ondokuz Mayıs University (TR), Imam Mohammad ibn Saud Islamic University (SA), University Mohamed Boudiaf of M'sila (DZ), Ahmed Zabana University - Relizane (DZ), Centre Hospitalo-Universitaire Bab El Oued (DZ), Sapienza University of Rome (IT)
Imam Mohammed Ibn Saud Islamic University
Openalex Percentile: Top 8%
Synthesis and Biological Activity
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