Pharmaceutical preparations comprising a salt of an...

A - Human Necessities – 61 – K

Patent

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A61K 31/7036 (2006.01) A61K 9/00 (2006.01) A61K 9/22 (2006.01) A61K 31/192 (2006.01) A61K 31/405 (2006.01) A61K 31/661 (2006.01) A61K 45/06 (2006.01) A61L 31/08 (2006.01) A61L 31/16 (2006.01) A61P 31/04 (2006.01)

Patent

CA 2432009

The invention relates to hardly soluble antiphlogistic salts and antiphlogistic-antibiotic pharmaceutical preparations and their use. The hardly water soluble antiphlogistic antibiotics salts are characterized in that their cationic component is a representative from the antibiotics gentamicin, clindamycin, neomycin, streptomycin, tetracycline, doxicyline, oxytetracycline and rolitetracycline and that their anionic component is a representative from the antiphlogistics ibuprofen, naproxen, indomethacin, dexamethasone-21-phosphate, dexamethasone- 21-sulfate, triamcinolone-21-phosphate and triamcinolone-21-sulfate. The antiphlogistic antibiotics salts are used in pharmaceutical preparations as controlled-release antibiotic/antibiotics drugs. The invention describes antiphlogistic-antibiotic pharmaceutical preparations for which mixtures in the solid state of aggregation are used, which are composed of an easily water soluble salt of gentamicin, clindamycin, neomycin, streptomycin, tetracycline, doxicycline, oxytetracycline and/or rolitetracycline and at least one easily water soluble salt of ibuprofen, naproxen, indomethacin, dexamethasone-21-phosphate, dexamethasone-21-sulfate, triamcinolone-21- phosphate and/or triamcinolone-21-sulfate and at least one inorganic and/or organic pharmaceutical adjuvant and which are used as permanent or temporary implants in the form of tablets and/or molded bodies.

L'invention porte sur des sels antiphlogistiques très peu solubles et des préparations pharmaceutiques antiphlogistiques antibiotiques, ainsi que leur utilisation. Les sels antiphlogistiques antibiotiques très peu hydrosolubles se caractérisent par leur composante cationique choisie parmi les antibiotiques suivants : gentamicine, clindamycine, néomycine, streptomycine, tétracycline, doxicyline, oxytétracycline et rolitétracycline. Ils se caractérisent également par leur composante anionique sélectionnée parmi les antiphlogistiques suivants : ibuprofène, naproxène, indométhacine, dexaméthasone-21-phosphate, dexaméthasone-21- sulfate, triamcinolone-21-phosphate et triamcinolone-21-sulfate. Les sels antiphlogistiques antibiotiques sont utilisés dans des préparations pharmaceutiques en tant qu'antibiotiques à libération contrôlée. L'invention décrit des préparations pharmaceutiques antiphlogistiques antibiotiques issues de mélanges à l'état d'agrégation solide, qui sont composés d'un sel très hydrosoluble de gentamicine, de clindamycine, de néomycine, de streptomycine, de tétracycline, de doxycycline, d'oxytétracycline et/ou de rolitétracycline et d'au moins un sel très hydrosoluble d'ibuprofène, de naproxène, d'indométhacine, de dexaméthasone-21-phosphate, de dexaméthasone-21-sulfate, de triamcinolone-21-phosphate et/ou de triamcinolone-21-sulfate et d'au moins un adjuvant pharmaceutique inorganique et/ou organique, et qui sont utilisés comme implants permanents ou temporaires sous forme de comprimés et/ou d'entités moulées.

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