# Phytochemistry and In Vitro Bioactivities of Elaeagnus angustifolia L. Leaves: Influence of Solvent Polarity, Antioxidant Properties, and α-Amylase Inhibition

**Authors:** Rayene Bouaita, Randa Djemil, Samira Bouhalit, Sabrina Lekmine, Ouided Benslama, Saber Boutellaa, Nabil Touzout, Gema Nieto, Ivan Mustać, Gabrijel Ondrašek, Muhammad Imtiaz Rashid

PMC · DOI: 10.3390/molecules31050861 · 2026-03-05

## TL;DR

This study explores how different solvents affect the extraction of bioactive compounds from Elaeagnus angustifolia leaves and their potential as natural antidiabetic agents.

## Contribution

The study identifies solvent-specific phytochemical profiles and evaluates antioxidant and α-amylase inhibition activities in Elaeagnus angustifolia leaf extracts.

## Key findings

- Hydroethanolic extract had the highest yield (18.00%) and strong antioxidant activity.
- n-Hexane extract showed the highest α-amylase inhibition (IC50 = 36.70 µg/mL), better than acarbose.
- Rutin, chlorogenic acid, and chicoric acid were identified as potential α-amylase inhibitors via molecular docking.

## Abstract

This study investigated the effect of solvent polarity on extraction yield, phytochemical composition, antioxidant activity, and α-amylase inhibition of Elaeagnus angustifolia L. leaf extracts to evaluate their antidiabetic potential. Extraction yields varied with solvent polarity, with the hydroethanolic extract showing the highest (18.00%) and n-hexane the lowest (0.05%) yield. The n-butanol and ethyl acetate fractions contained the most phenolics (309.05 and 290.97 mg GAE/g), ethyl acetate was the richest in flavonoids (102.11 mg QE/g), and tannins were concentrated in dichloromethane (66.24 mg CE/g). HPLC revealed solvent-specific profiles: rutin and gallic acid dominated in n-butanol, quercetin in ethyl acetate, and 4-hydroxybenzoic and ferulic acids in dichloromethane, while chicoric acid appeared in hydroethanolic and n-hexane extracts. Antioxidant assays (DPPH, ABTS, and FRAP) showed strong activity in polar extracts, particularly hydroethanolic and ethyl acetate fractions. The n-hexane extract exhibited the highest α-amylase inhibition (IC50 = 36.70 µg/mL), surpassing acarbose (IC50 = 126.14 µg/mL), while other fractions were inactive (IC50 > 400 µg/mL). Molecular docking highlighted rutin, chlorogenic acid, and chicoric acid as potential enzyme binders. These findings demonstrate the chemical diversity and significant bioactivities of E. angustifolia leaves, supporting their potential as natural antidiabetic agents.

## Linked entities

- **Chemicals:** rutin (PubChem CID 5280805), gallic acid (PubChem CID 370), quercetin (PubChem CID 5280343), 4-hydroxybenzoic acid (PubChem CID 135), ferulic acid (PubChem CID 445858), chicoric acid (PubChem CID 5281764), chlorogenic acid (PubChem CID 1794427), acarbose (PubChem CID 9811704)
- **Diseases:** diabetes (MONDO:0005015)

## Full-text entities

- **Chemicals:** rutin (MESH:D012431), dichloromethane (MESH:D008752), ethyl acetate (MESH:C007650), flavonoids (MESH:D005419), DPPH (MESH:C004931), chicoric acid (MESH:C100435), chlorogenic acid (MESH:D002726), quercetin (MESH:D011794), n-butanol (MESH:D020001), CE (MESH:D002563), acarbose (MESH:D020909), 4-hydroxybenzoic (-), gallic acid (MESH:D005707), n-hexane (MESH:C026385), ferulic acids (MESH:C004999), tannins (MESH:D013634), ABTS (MESH:C002502)
- **Species:** Elaeagnus angustifolia (oleaster, species) [taxon 36777]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12986330/full.md

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Source: https://tomesphere.com/paper/PMC12986330