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filingDate 2007-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ca8fbbab3b3b55047a104214194f9e24
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publicationDate 2011-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2434633-C2
titleOfInvention Pharmaceutical preparative forms of latrunculin
abstract FIELD: medicine, pharmaceutics. ^ SUBSTANCE: water pharmaceutical preparative form contains, at least, one latrunculin, non-ionic surface-active substance and preparation for supporting tonicity, at pH from 4 to 8. Latrunkulin, surface-active substance and preparation for supporting tonicity are compatible in preparative form, and preparative form does not contain more than 0.1% vol/vol dimethylsulfoxide. Latrunculin represents latrunculin A, latrunculin B, desmethyl latrunculin B or latrunculin analogue. Non-ionic surface-active substance is polysorbate, poloxamer or their combination. In accordance with the second version, water pharmaceutical form contains latrunculin, ethanol and preparation for supporting tonicity. Preparative form is intended for reduction of intraocular pressure in mammals. Preparative form by invention is stable during, at least, six months when cooled. ^ EFFECT: preparative form is intended for reduction of intraocular pressure in mammals. ^ 15 cl, 5 dwg, 7 ex
priorityDate 2006-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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