http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-665558-A5

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filingDate 1985-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b084f5cad92a578583c9ecde6d12b8e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_973a1e0ecc30b962d94d9e829cc3164a
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publicationDate 1988-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-665558-A5
titleOfInvention Phase sepn. prodn. of microcapsules for water soluble pharmaceuticals - using fluoro-substd. aliphatic hydrocarbon as non-solvent in the hardening stage
abstract In the phase-sepn. process for microencapsulation of water-soluble pharmaceuticals, the new feature is that the capsules are hardened at 0-25 deg.C, and that during this stage at least one fluoro- or fluorohalo-aliphatic hydrocarbon (A) is used as non-solvent. An excess of (A), relative to the total vol. of solvent and non-solvent originating from the phase-sepn. step, is used. (A) is used in at least 5:1 excess, and is particularly CFCl3; CFCl2.CF2Cl or CF2Cl.CF2Cl. The microcapsules are made of poly-L-lactide; poly-D,L-lactide or a copolymer of D,L-lactide and glycolide. USE/ADVANTAGE - The microcapsules are prepd. without formation of aggregates and in a more stable form, particularly with respect to hydrolysis. Their non-solvent content is very low (only about 1/10 that when using heptane as non-solvent) and low processing temps. are not necessary.
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