Antioxidant potential of crude and purified fractions from Bostrychia scorpioides (Hudson) Montagne (Rhodomelaceae)
摘要
Natural antioxidants obtained from marine resources such as macroalgae should be studied in order to develop safer and more sustainable alternatives to synthetic compounds used in the food and pharmaceutical industry. Furthermore, multi-assay assessments contribute to a more thorough knowledge of antioxidant mechanisms, allowing researchers to identify bioactive fractions with focused potential for nutraceutical and medicinal applications. Bostrychia scorpioides (Hundson) Montagne 1842 is a red macroalga collected from the Oualidia lagoon (Moroccan atlantic coast). Its crude ethanolic extract, semi-purified and purified fractions of phycobiliproteins and sulfated galactans were evaluated for antioxidant activity using four complementary in vitro assays: nitric oxide (NO−) scavenging, hydrogen peroxide (H2O2) scavenging, lipid peroxidation inhibition, and β-carotene bleaching inhibition. The phycobiliproteins crude extract exhibited broad-spectrum antioxidant activity (93.92% ± 0.06), comparable to Trolox in the lipid peroxidation assay (83.47% ± 0.05). Notably, the second purified phycobiliprotein fraction showed exceptionnel NO scavenging activity (86.01% ± 0.12), surpassing the positive control Trolox (69.31% ± 0.01). In contrast, H2O2 scavenging was generally weaker in all the different samples. Overall, crude and semi-purified extracts had a stable, more broad-spectrum antioxidant effect likely due to synergistic interactions, unlike purified fractions with decreased or selective activity. These results highlight the importance of multi-assay profiling and the potential of B. scorpioides fractions for targeted nutraceutical and biomedical applications.
Graphical abstractGraphical abstract illustrates the comprehensive experimental workflow applied to Bostrychia scorpioides, including the extraction, purification, and characterization of its bioactive compounds, as well as an evaluation of their antioxidant mechanisms