# Valorization of Onion By-Products and Assessment of Their Biological Activities

**Authors:** Maymouneh Rabie, Salma Khazaal, Mayyas M. Othman, Elie Salem Sokhn, Espérance Debs, Suhair Sunoqrot, Bilal Azakir, Nicolas Louka, Nada El Darra

PMC · DOI: 10.3390/foods15040637 · 2026-02-10

## TL;DR

This study explores the potential of red onion waste as a source of antioxidants, antibacterial agents, and anticancer compounds.

## Contribution

The study introduces optimized extraction parameters and identifies key compounds in red onion waste with biological activities.

## Key findings

- ROW extract showed highest antibacterial activity against Staphylococcus aureus.
- Isorhamnetin, hyperoside, and quercetin were the major compounds detected in ROW extract.
- ROW extract exhibited cytotoxic effects against H460 and Caco-2 cancer cell lines.

## Abstract

Onions represent one of the most widely consumed vegetables within the Allium genus, generating a significant amount of waste. Onion waste is mainly composed of non-edible fractions, including roots, outer dry skins, and the outer fleshy scale. This study aimed to valorize red onion waste (ROW) and assess its total phenolic content and antioxidant activity using a water bath extraction method with distilled water as the extraction solvent. response surface methodology was employed to optimize the extraction parameters, namely temperature and time. The phenolic composition of freeze-dried ROW extract was analyzed using liquid chromatography–mass spectrometry analysis. The antibacterial activity was assessed using the disk diffusion and broth dilution methods against Gram-positive and Gram-negative bacteria, and the anticancer activity was tested against H460 lung, Caco-2 colon, and HT-29 colorectal cancer cell lines. The ideal extraction parameters were 1:40 g/mL, 98 °C for 27 min. The major detected compounds were isorhamnetin (55.32%), hyperoside (19.44%), and quercetin (13.65%). ROW extract showed antibacterial activity against Bacillus cereus, Staphylococcus aureus, Listeria monocytogenes, Escherichia coli, Pseudomonas aeruginosa, and Salmonella Typhimurium, with the highest activity observed against S. aureus. A cytotoxic effect against H460 and Caco-2 was shown by the ROW extract, with IC50 values detected within the tested concentrations. The results suggest that ROW extract has potential for effective application as an antioxidant, antibacterial, and anticancer agent, demonstrating its potential for incorporation into functional foods and nutraceutical development.

## Linked entities

- **Chemicals:** isorhamnetin (PubChem CID 5281654), hyperoside (PubChem CID 5281643), quercetin (PubChem CID 5280343)
- **Diseases:** lung cancer (MONDO:0005138), colon cancer (MONDO:0002032), colorectal cancer (MONDO:0005575)
- **Species:** Bacillus cereus (taxon 1396), Staphylococcus aureus (taxon 1280), Listeria monocytogenes (taxon 1639), Escherichia coli (taxon 562), Pseudomonas aeruginosa (taxon 287)

## Full-text entities

- **Diseases:** MBC (MESH:C567712), injury to (MESH:D014947), lung cancer (MESH:D008175), Cancer (MESH:D009369), colon cancer (MESH:D015179), cytotoxic (MESH:D064420)
- **Chemicals:** L (MESH:D007930), L-tyrosine (MESH:D014443), Water (MESH:D014867), kaempferol (MESH:C006552), S-Allyl-L-cysteine (MESH:C065299), phenolic acids (MESH:C017616), ferulic acid (MESH:C004999), S-adenosyl-L-methionine (MESH:D012436), Hyperoside (MESH:C021304), cinnamic acid (MESH:C029010), 2-Methoxy-4-vinylphenol (MESH:C526552), ascorbic acid (MESH:D001205), Gentamicin (MESH:D005839), ethanol (MESH:D000431), flavonol (MESH:C041477), quercetin-3,4'-O-diglucoside (MESH:C000613585), adenosine (MESH:D000241), TE (MESH:D013691), L-proline (MESH:D011392), methanol (MESH:D000432), T (MESH:D014316), trypan blue (MESH:D014343), Trolox (MESH:C010643), acid (MESH:D000143), formic acid (MESH:C030544), formazan (MESH:D005562), trigonelline (MESH:C009560), GA (MESH:D005707), propyl allyl disulfide (MESH:C006469), L-histidine (MESH:D006639), Quercetin (MESH:D011794), acetonitrile (MESH:C032159), DPPH (MESH:C004931), stilbenes (MESH:D013267), Agar (MESH:D000362), streptomycin (MESH:D013307), Imipenem (MESH:D015378), lignin (MESH:D008031), Polyphenols (MESH:D059808), CO2 (MESH:D002245), citric acid (MESH:D019343), Na2CO3 (MESH:C005686), myristic acid (MESH:D019814), coumarins (MESH:D003374), (+-)-tryptophan (MESH:D014364), caffeic acid (MESH:C040048), H (MESH:D006859), 3-O-methylquercetin (MESH:C047368), anthocyanin (MESH:D000872), DMSO (MESH:D004121), flavonoid (MESH:D005419), eriodictyol (MESH:C007619), glycosides (MESH:D006027), CA (MESH:D002118), 6-hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid (-), 1,2,3-benzenetriol (MESH:D011748), S (MESH:D013455), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MESH:C022616), 4-hydroxycoumarin (MESH:C068805), FC (MESH:C095424)
- **Species:** Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Escherichia coli (E. coli, species) [taxon 562], Bacillus cereus (species) [taxon 1396], Pseudomonas aeruginosa (species) [taxon 287], Listeria (genus) [taxon 1637], Allium cepa (onion, species) [taxon 4679], Listeria monocytogenes (species) [taxon 1639], Staphylococcus aureus (species) [taxon 1280], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Allium (genus) [taxon 4678], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** 3  C for T, T) of 60
- **Cell lines:** H460 — Homo sapiens (Human), Lung large cell carcinoma, Cancer cell line (CVCL_0459), ATCC 19115 — Homo sapiens (Human), Transformed cell line (CVCL_0X39), A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), HT-29 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0320), HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030), H69 — Homo sapiens (Human), Transformed cell line (CVCL_8121), Caco-2 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0025)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940003/full.md

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Source: https://tomesphere.com/paper/PMC12940003