FIELD: pharmaceutical industry.
SUBSTANCE: group of inventions relates to an anionic drug delivery composition comprising: an anionic drug; cationic compound, selected from polyethyleneimine and cationic lipid of formula 7 (, where n and m = 0–12 under condition 2≤n+m≤12, a and b=1–6, R1 and R2 are selected from saturated and unsaturated C11-25 hydrocarbons); amphiphilic two-block block-copolymer of type AB, consisting of hydrophilic block A selected from monomethoxy polyethylene glycol and polyalkylene glycol, and hydrophobic block B, which is a polyester; and at least one compound of formula 1 (RO-CHZ-[A]n-[B]m-COOM, where A -COO-CHZ-; B -COO-CHY-; R is a hydrogen atom, acetyl, benzoyl, decanoyl, palmitoyl, methyl or ethyl; Z and Y are methyl; M is Na, K or Li; n=1–30, m=0–20 with the condition n+m=7–50) and formula 6 (YO-[-C(O)-(CHX)a-O-]m-C(O)-R-C(O)-[-O-(CHX')b-C(O)-]n-OZ, where X and X' are methyl; Y and Z—Na, K or Li; m and n are integer from 0 to 95 under condition 5<m+n<100; a and b = 1; R -(CH2)k- with the proviso k=2). Anionic drug and cationic compound by electrostatic interaction form complex, which is enclosed in micellar structure of block-copolymer and compound of formula 1 and/or 6.
EFFECT: group of inventions provides improved stability of an anionic drug in blood or body fluid.
22 cl, 2 dwg, 18 tbl, 32 ex
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Authors
Dates
2020-05-20—Published
2016-09-12—Filed