Multi-Approach Assessment of Albizia saponaria Bioactivity Against Dandruff-Related Bacteria and Fungi
Abstract
Dandruff and fungal-associated alopecia result from microbial dysbiosis, including Malassezia furfur, M. globosa, Trichophyton rubrum, and Staphylococcus epidermidis, highlighting the need for alternative therapeutics with improved safety. This study evaluates the antimicrobial activity of Albizia saponaria stem bark against dandruff-associated microorganisms and identifies the key bioactive metabolites responsible. The work combines in vitro bioassays and GC-MS profiling. Pharmacokinetic screening and molecular docking provide mechanistic insights. Ethanolic extracts were fractionated using hexane, ethyl acetate, butanol, and water, followed by antimicrobial evaluation. The hexane fraction showed the most potent antifungal activity, with inhibition zones of 18.25±1.53 mm (M. furfur), 21.64±1.80 mm (M. globosa), and 22.00±2.35 mm (T. rubrum), significantly higher than other fractions (p<0.05). Its activity against T. rubrum was comparable to ketoconazole (p>0.05). GC-MS identified 21 predominantly lipophilic metabolites, including fatty acid esters, terpenoids, phenolics, and sterol derivatives. Docking analysis revealed notable binding affinities, ranging from -4.3 to -9.5 kcal/mol, with 4-campestene-3-one and norambreinolide exhibiting interactions comparable to ketoconazole at CYP51 and TcaR. Collectively, the results demonstrate that the hexane fraction contains multiple bioactive metabolites with strong antimicrobial potency, mechanistic relevance to ergosterol disruption, biofilm inhibition, and metabolic interference. These findings highlight the hexane fraction as a credible natural antidandruff candidate, warranting further isolation studies and in vivo evaluation.
Keywords: Albizia saponaria; Antimicrobial; GC-MS; Molecular docking.
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