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Table · dataset · 2026

<p>Dermal irritation scoring in rats.</p>

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<div> <p>Objective</p><p>To evaluate the in vitro inhibitory activity of different <i>Angelica dahurica–Ligusticum sinense</i> extracts (ethanolic, aqueous, and cold-pressed) against planktonic cells and biofilms of <i>Malassezia furfur</i>.</p> <p>Methods</p><p>Ultra-performance liquid chromatography (UPLC) was used to quantify the major constituents. Micro-broth dilution determined the minimum inhibitory concentration (MIC), and time–kill assays assessed fungicidal kinetics.

Crystal violet staining assay (CVA) and XTT reduction assays quantified inhibition of biofilm biomass formation/metabolic activity and reduction of mature biofilms. Dermal irritation of the ethanolic extract was evaluated in rats.</p> <p>Results</p><p>UPLC showed that the ethanolic extract contained the highest levels of ferulic acid, bergapten, oxypeucedanin, imperatorin, and isoimperatorin. The MIC of the ethanolic extract was 5 mg/mL, superior to those of the aqueous and cold-pressed extracts (10 mg/mL each).

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A time–kill study revealed rapid fungicidal activity at 8 × MIC. Biofilm assays demonstrated that 0.5× and 1 × MIC of the ethanolic extract significantly inhibited biofilm formation (P < 0.05), whereas 8 × MIC effectively eradicated pre-formed biofilms, markedly reducing biomass and metabolic activity (P < 0.01). No cutaneous irritation was observed in rats at 8 × MIC.</p> <p>Conclusion</p><p>The <i>A. dahurica-L. sinense ethanolic</i> extract potently inhibited and eradicated <i>M. furfur</i> planktonic cells and biofilms with favorable safety.

This activity may be attributable to its high content of coumarins and phenolic acids, suggesting its potential as a natural agent for the treatment of <i>M. furfur</i>-associated skin disorders.</p></div>

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