Unveiling the in vitro activity of extracted Euphorbia trigona via Supercritical Fluid Extraction against pathogenic yeasts, obesity, cancer, and its wound healing properties.

Natural products of plant origin are being explored as safe alternatives for illness management. Their extraction processes play a crucial role in determining their phytochemical and pharmacological properties. In this context, Euphorbia trigona was extracted using Supercritical Fluid Extraction with CO (SFE-CO) at two operating temperatures: 20 °C and 40 °C. Phytochemical characterization was performed via HPLC, along with anti-yeast evaluation using the well diffusion method, anticancer assessment using the MTT assay, wound healing analysis via the scratch assay, and anti-obesity evaluation through the lipase assay of the E. trigona extract. The results indicated that SFE-CO at 40 °C extracted a greater quantity (0.198 g) of E. trigona than SFE-CO at 20 °C (0.156 g). Several compounds, such as rosmarinic acid, gallic acid, daidzein, ellagic acid, naringenin, and ferulic acid, were identified at high concentrations of 10,034.29, 1,800.33, 750.22, 748.11, 462.15, and 207.05 µg/mL, respectively, in the E. trigona extract obtained using SFE-CO at 40 °C, compared to the extract obtained using SFE-CO at 20 °C. High inhibition zones of 24 ± 1.5, 24 ± 0.5, and 23 ± 0.33 mm were recorded against C. albicans, C. tropicalis, and G. candidum, respectively, using the extract from SFE-CO at 40 °C, compared to the inhibition zones of 24 ± 1.5, 24 ± 0.5, and 23 ± 0.33 mm obtained from the extract using SFE-CO at 20 °C. Moreover, the extract from SFE-CO at 40 °C exhibited lower MIC and MFC values against the tested yeasts compared to the efficacy of the extract from SFE-CO at 20 °C. The ultrastructure of the examined yeasts was severely affected by the extract from SFE-CO at 40 °C. A lower IC (98.87 ± 1.26 µg/mL) was recorded for the extract from SFE-CO at 40 °C compared to the IC (333.87 ± 1.8 µg/mL) of the extract from SFE-CO at 20 °C against cancer cells (A431). The wound closure level was 84.08% using the extract from SFE-CO at 40 °C, while it was 71.27% using the extract from SFE-CO at 20 °C. Lipase was inhibited by the extract obtained via SFE-CO at 40 °C and 20 °C, with IC values of 15.77 and 28.14 µg/mL, respectively. Molecular docking indicated that rosmarinic acid is a suitable inhibitor for the tested yeasts.