FIELD: medicine.
SUBSTANCE: invention relates to pharmacology and medicine and represents pharmaceutical composition for parenteral introduction, including diaspartate or disuccinate or diglutamate salt of somatostatin analogue of formula III, where C-2 atom is in (R) or (S) configuration, or their mixture, and where R stands for NR10R11(C2-C6)alkylene or guanidine(C2-C6)alkylene and each of R10 and R11 independently represents H or C1-C4alkyl and water, in which pH value constitutes from 3.0 to 7.0, forming after injection gel-like system-depot in case of contact with liquid medium in organism, in which salts of somatostatin analogues are characterised by ratio salt/base within the interval from 0.1 to 2 and from said gel-like system-depot in patient's organism continuously released is salt of somatostatin analogue: diaspartate, disuccinate or diglutamate during long period of time from 1 to 90 days.
EFFECT: invention ensures obtaining compositions which include diaspartate or disuccinate or diglutamate salt of somatostatin analogue with retarded release.
17 cl, 5 ex, 4 tbl
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Authors
Dates
2010-07-27—Published
2005-12-20—Filed