Pharmaceutical preparations

A - Human Necessities – 61 – K

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A61K 9/10 (2006.01) A61K 9/107 (2006.01) A61K 47/00 (2006.01) A61K 47/18 (2006.01) C07D 213/20 (2006.01) C07D 213/30 (2006.01) C07D 213/63 (2006.01) C07D 213/65 (2006.01) C07D 213/68 (2006.01) C07D 213/69 (2006.01) C07D 213/73 (2006.01) C07D 213/80 (2006.01) C07D 213/81 (2006.01) C07D 213/82 (2006.01) C07D 233/54 (2006.01) C07D 235/06 (2006.01) C07D 239/26 (2006.01) C07D 239/30 (2006.01) C07D 239/36 (2006.01) C07D 239/46 (2006.01) C07D 239/47 (2006.01) C07D 239/54 (2006.01) C07D 239/553 (2006.01) C07D 241/2

Patent

CA 1319321

Abstract A pharmaceutical preparation is disclosed which is made up of a micelle or a vesicle each consisting of a cationic tenside with a monovalent ion and a hydrophobic cyclic or linear peptide, dispersed in a solvent whose pH value lies between pH 7 - pH 8, the critical micellization concentration (cmc) lying in the range of 1.0 . 10-7 to 7.0 . 10-5 mol/litre. The preparations disclosed have in particular the advantage that by the increasing of the hydrophobicity of the alkyl or aryl chain or the radical at the N+ tenside both the mem- brane permeability is increased and furthermore the pharma- ceutical active substance, in particular linear and cyclic tyrocidines (A - E), can be transferred actively into the cytosol. They thus act on the transcription level. In addition, linear and cyclic tyrocidines in particular have antiviral effects.

543931

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