Supercritical and enzymatic technologies for the production of lysophosphatidylcholine

BACKGROUND This study focuses on obtaining a highly purified lysophosphatidylcholine from phosphatidylcholine powder via hydrolysis, catalyzed by a phospholipase A2 in a solvent‐free medium, and subsequent purification either by organic solvent or by supercritical fluid extraction. RESULTS A solvent...

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Veröffentlicht in:Journal of chemical technology and biotechnology (1986) 2013-01, Vol.88 (1), p.153-162
Hauptverfasser: Casado, Víctor, Señorans, Francisco.J, Reglero, Guillermo, Torres, Carlos F.
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Sprache:eng
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Zusammenfassung:BACKGROUND This study focuses on obtaining a highly purified lysophosphatidylcholine from phosphatidylcholine powder via hydrolysis, catalyzed by a phospholipase A2 in a solvent‐free medium, and subsequent purification either by organic solvent or by supercritical fluid extraction. RESULTS A solvent‐free hydrolysis reaction of phosphatidylcholine powder to produce lysophosphatidylcholine with residual phosphatidylcholine content lower than 10% has been described and scaled‐up. Supercritical fluid mixtures of carbon dioxide, ethanol and formic acid were studied at 250, bar 50 °C to selectively extract the free fatty acids fraction from hydrolyzed phosphatidylcholine. Finally, a solid product with lysophosphatidylcholine content of c. 95% (w/w) and with free fatty acids content of c. 5% (w/w) was attained. Under optimum conditions, the content of the original phosphatidylcholine in the lysophosphatidylcholine product was lower than 5% (w/w). CONCLUSIONS An efficient hydrolysis of phosphatidylcholine by phospholipase A2 in a solvent‐free reaction was developed. In addition, three novel strategies for the purification of lysophosphatidylcholine have been developed: (1) hexane/formic acid extraction process, (2) supercritical CO2 extraction with ethanol as modifier, and (3) supercritical CO2 extraction with ethanol/formic acid as modifier. Copyright © 2012 Society of Chemical Industry
ISSN:0268-2575
1097-4660
DOI:10.1002/jctb.3842