Enhancing anti-diabetic activity and reducing cytotoxicity of T. crispa extracts through sustainable approach of pressurized hot water extraction and micelle-mediated separation
In this study, pressurized hot water extraction (PHWE) was evaluated for the recovery of anti-diabetic borapetoside C (BPC) from T. crispa stems. The maximum BPC extraction efficiency obtained at 100 ˚C, 2.5 MPa and 5.0 mL/min was considerably higher than that obtained by the conventional methods. U...
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Veröffentlicht in: | The Journal of supercritical fluids 2024-12, Vol.214, p.106377, Article 106377 |
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Sprache: | eng |
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Zusammenfassung: | In this study, pressurized hot water extraction (PHWE) was evaluated for the recovery of anti-diabetic borapetoside C (BPC) from T. crispa stems. The maximum BPC extraction efficiency obtained at 100 ˚C, 2.5 MPa and 5.0 mL/min was considerably higher than that obtained by the conventional methods. Under optimized conditions, one-site kinetic desorption model could most accurately describe the PHWE behavior, suggesting an intra-particle diffusion-controlled mechanism. The undesirable compounds in the extract were further removed by micelle-mediated separation (MMS), in which Tween 80 was added, followed by NaCl addition and slight temperature increase to induce phase separation. At the most suitable MMS condition, with 0.028 mM Tween 80, 0.4 M NaCl, at 85 ˚C, the majority (87 %) of BPC could be recovered in the aqueous phase after 40 min. After MMS, the resulting extract exhibited low cytotoxicity against L6 and HepG2 cells while maintaining significant α-glucosidase and α-amylase inhibition activities.
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•Pressurized hot water extraction (PHWE) of BPC from T. crispa was optimized.•Optimal PHWE conditions were found to be 100 °C, 5 mL/min and 2.5 MPa.•The optimized PHWE conditions accurately fit the one-site kinetic desorption model.•Micelle-mediated separation with Tween 80 selectively removes undesirable compounds from PHWE extracts.•PHWE/MMS extracts exhibit comparable activity to acarbose with low toxicity to L6 cells. |
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ISSN: | 0896-8446 |
DOI: | 10.1016/j.supflu.2024.106377 |