http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2017048082-A1

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filingDate 2016-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e9a6e3e683d259598d1231e5f97047d0
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publicationDate 2017-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2017048082-A1
titleOfInvention Method for preparing liposomal freeze-dried powder using novel freeze-drying assisting agent and novel phospholipid-dissolving mixed solvent
abstract The present invention relates to a liposome preparation method characterized in that a mixed solvent of ethyl acetate and n-hexane is used as a phospholipid-dissolving solvent used for liposome preparation, and to a liposomal freeze-dried powder preparation method characterized in that a container containing a liposome is placed into a container filled with at least one selected from among isopropyl alcohol, ethanol, and methanol, and then freeze-dried. The present invention uses a phospholipid by dissolving the phospholipid in a mixed solvent of ethyl acetate and n-hexane, and thus has the advantage of being usable in the food industry, unlike typical methods which use toxic chloroform. Moreover, in the present invention, since a container containing a prepared liposome is placed into a container filled with at least one selected from among isopropyl alcohol, ethanol, and methanol, and then freeze-dried, the time passing through the zone of maximum ice crystal formation is short. Thus, the present invention has the advantage in which a reduction in the stability of liposome, such as destruction of the liposome structure during the freeze-drying process and leakage of active material, may be prevented, and the advantage in which when restorating the powder, the powder almost completely returns to its original state.
priorityDate 2015-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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