http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H02196713-A

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filingDate 1989-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 1990-08-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02196713-A
titleOfInvention Liposome for effectively packing and controllably releasing amphipathic molecule
abstract PURPOSE: To efficiently pack an amphipathic medicine in a large packing amount simply and rapidly by forming the gradient of ammonium ion between an internal aqueous phase and an external aqueous phase of liposome. CONSTITUTION: A suspension of liposome is prepared in the presence of ammonium sulfate. The external aqueous phase of the prepared suspension is diluted with a proper salt or buffer solution or ammonia is removed from an external aqueous phase, a natural ammonia molecule is diffused from an inner aqueous phase to the external aqueous phase to form a gradient of ammonium from the inside to the outside and a gradient of pH from the outside to the inside between the internal aqueous phase and the external aqueous phase. Then a deprotonized amphipathic medicine is packed from the outside into the inside, bonded to a liberated protein left in the aqueous phase and accumulated in the liposome. When a reverse pH gradient state occurs, the bonded medicine is dissociated into a proton and the deprotonized medicine to release the deprotonized medicine or the liposome.
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Total number of triples: 48.