FIELD: medicine.
SUBSTANCE: present invention relates to medicine, namely to pharmaceutical composition and a process for its preparation. Claimed pharmaceutical composition is prepared by mixing Twin-80 and water to obtain an aqueous solution of Twin-80, simultaneous dissolution of hydroxypropyl-beta-cyclodextrin and methyl ester 133-N-(N-methylnicotinil) bacteriopurpurinimide with uniform stirring and heating to temperature of 60 °C to give an aqueous solution of Twin-80, hydroxypropyl-beta-cyclodextrin and methyl ester 133-N-(N-methylnicotinil) bacteriopurpurinimide, filtering the aqueous solution of Twin-80, hydroxypropyl-beta-cyclodextrin and methyl ester 133-N-(N-methylnicotinyl) bacteriopurpurinimide to obtain an aqueous solution of the claimed pharmaceutical composition, drying the aqueous solution of the claimed pharmaceutical composition to obtain the claimed pharmaceutical composition. Resulting composition has the following composition, wt.%: methyl ester 133-N-(N-methylnicotinyl) bacteriopurpurinimide 1.0÷2.0; hydroxypropyl-beta-cyclodextrin 94÷96; Twin-80 3.0÷4.0.
EFFECT: claimed pharmaceutical composition exhibits a high level of photostability, as well as a high level of efficacy of therapy for foci of bacterial damage and is used to prepare dosage forms for parenteral administration.
3 cl, 4 ex, 9 tbl
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Authors
Dates
2018-07-23—Published
2017-10-03—Filed