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High-yield dimethyl ether-based recovery of astaxanthin and fatty acids directly from wet Haematococcus pluvialis
[Display omitted] •Green processes involving l-DME and DMSO were developed for microalgal biorefinery.•Drying and cell-wall-disruption steps of wet H. pluvialis were not employed.•Complete recovery of astaxanthin and fatty acids from the wet cysts was achieved.•The dry extract exhibited strong antio...
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Published in: | Separation and purification technology 2023-09, Vol.320, p.124226, Article 124226 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Green processes involving l-DME and DMSO were developed for microalgal biorefinery.•Drying and cell-wall-disruption steps of wet H. pluvialis were not employed.•Complete recovery of astaxanthin and fatty acids from the wet cysts was achieved.•The dry extract exhibited strong antioxidative activities.
Efficient and eco-friendly methods for extracting bioactive molecules are crucial for achieving economically viable microalgae biorefinery. In this study, high-value-added intracellular bioactive compounds were efficiently recovered directly from the red cysts of wet Haematococcus pluvialis. An integrated processes involving liquid dimethyl ether (l-DME) extraction at 45 °C and 2 MPa for 90 min and subsequent dimethyl sulfoxide (DMSO) extraction at 65 °C for 5 min enabled almost complete recovery of astaxanthin (99.6%) and total fatty acids (99.8%) from wet H. pluvialis cyst cells. Notably, this green and sustainable strategy did not involve high-cost and energy-intensive drying, or cell wall-disruption steps. l-DME extraction produced a solvent-free, dry extract with high astaxanthin (43.9 mg g−1 dry extract) and essential fatty acids (ω3, ω6, and ω9; 290.1 mg g−1 dry extract) contents; whereas the astaxanthin and fatty acid contents of the DMSO extract produced from raw H. pluvialis cyst cells (freeze-dried and ball-milled at 200 rpm for 30 min) were 1.5- and 1.7-fold lower, respectively. The dry extract also exhibited 1.6-fold greater antioxidant activity than the DMSO extract, thereby indicating its potential for direct application in nutraceutical, pharmaceutical, and cosmeceutical formulations with high bioactivity and safety. |
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ISSN: | 1383-5866 1873-3794 |
DOI: | 10.1016/j.seppur.2023.124226 |