Promising synergistic interactions and mixture optimization of safranal, crocin, and crocetin from Moroccan Crocus sativus L. with enhanced antimicrobial activity
This study explores the antimicrobial activity of three principal bioactive constituents of <i>Crocus sativus</i> L.-safranal, crocin, and crocetin-using a simplex-centroid mixture design to evaluate their individual and synergistic effects. Twelve formulations were tested against <i>Staphylococcus aureus</i>, <i>Escherichia coli</i>, <i>Candida albicans</i>, and <i>Geotrichum candidum</i>. Minimum inhibitory concentrations (MICs) were determined via microdilution assays, and the results were fitted using special cubic regression models. The models exhibited strong predictive accuracy (R<sup>2</sup> = 0.97-0.99). Safranal showed the highest individual activity against <i>S. aureus</i> (σ<sub>1</sub> = 169.77, <i>p</i> = 0.0053), while crocin exerted the strongest effect on <i>E. coli</i> (σ<sub>2</sub> = 166.63, <i>p</i> < 0.0001). Significant synergistic interactions were observed between crocin and crocetin for both bacterial strains (σ<sub>23</sub> = -290.34 for <i>S. aureus</i>; -170.28 for <i>E. coli</i>). Ternary mixtures displayed superior efficacy compared to single compounds, producing the lowest MIC values across all pathogens. The optimal antibacterial formulation-33.31% safranal, 33.29% crocin, and 33.39% crocetin-yielded MICs of 41.14% <i>(v/v)</i> (predicted) and 39.5% ± 0.75% <i>(v/v)</i> (experimental) against <i>E. coli</i>. Against <i>S. aureus</i>, a blend of 27% safranal, 33% crocin, and 38% crocetin resulted in a predicted MIC of 42.15% <i>(v/v)</i>, confirmed experimentally at 38.13% ± 1.33% <i>(v/v)</i>. For <i>G. candidum</i>, the optimized mixture reached MIC values of 9.13% <i>(v/v)</i> (predicted) and 10.24% ± 2.05% <i>(v/v)</i> (observed). These findings demonstrate that synergistic combinations of saffron-derived metabolites markedly enhance antimicrobial potency. Moreover, mixture design modeling emerges as an effective predictive and optimization strategy for developing reproducible, plant-based antimicrobial formulations targeting antibiotic resistance.
Authors
- Abdellah Baraich (ORCID: https://orcid.org/0000-0002-7483-6738)
- Omer M. Almarfadi (ORCID: https://orcid.org/0000-0002-5663-3064)
- Bassem Jaouadi (ORCID: https://orcid.org/0000-0002-5182-7353)
- François Mesnard (ORCID: https://orcid.org/0000-0002-7626-3902)
- Mothana RA
- Mohammed F. Hawwal (ORCID: https://orcid.org/0000-0002-9192-7260)
- Abdessamad Beraich (ORCID: https://orcid.org/0009-0005-5814-9929)
- Ibrahim Sadougui
- Amine Elbouzidi
- Mounir Haddou
- Mohamed Taibi
- Mohamed Addi
- Abdeslam Asehraou
- Ennouamane Saalaoui
- Fatima Zahrae El Moussaoui
Institutions
- King Saud University (SA)
- Laboratoire de Chimie Physique (FR)
- Biologie des Plantes et Innovation (FR)
- Centre of Biotechnology of Sfax (TN)
- Université Hassan II Mohammedia (MA)
- Université de Picardie Jules Verne (FR)
- Premier University (BD)
Publication Details
- Journal
- Frontiers in Pharmacology
- Published
- 2026-02-13
- DOI
- https://doi.org/10.3389/fphar.2026.1734075
- Primary Topic
- Saffron Plant Research Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- European Commission
- King Saud University