Sustained release tablet containing hydrocolloid and...

A - Human Necessities – 61 – K

Patent

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Details

A61K 9/26 (2006.01) A61K 9/20 (2006.01)

Patent

CA 2354057

The present invention is directed to a solid sustained release pharmaceutical tablet for administering to a host, comprising a therapeutically effective amount of a pharmaceutically active ingredient and a sustained release carrier therefor, said sustained release carrier comprising (a) a hydrocolloid selected from the group consisting of xanthan gum, guar gum, and alginic acid or a pharmaceutically acceptable salt thereof, and (b) a cellulose ether, said hydrocolloid and cellulose ether being present in synergistic effective amount to retard release of said pharmaceutically active ingredient, said hydrocolloid being present in amount ranging from about 0.3 % to about 7.0 % by weight of the tablet and said cellulose ether being present in an amount ranging from 3 % to about 20 % of said tablet, and cellulose ether being present in said carrier in amounts equal to or greater than 33 % by weight and said carrier being present in amounts less than 35 % by weight of said tablet.

La présente invention concerne un comprimé pharmaceutique solide à libération prolongée destiné à être administré à un patient, et comprenant une dose thérapeutiquement efficace d'un principe actif pharmaceutique et un excipient à libération prolongée de ce dernier, ledit excipient comprenant (a) un hydrocolloïde du groupe de la gomme xanthane, de la gomme de guar, et d'un acide alginique ou d'un de ses sels pharmacologiquement acceptable, et (b) un éther de cellulose. L'hydrocolloïdes et l'éther de cellulose sont présents en doses synergétiques efficaces pour une libération retard dudit principe pharmacologiquement actif. L'hydrocolloïde est présent en dose allant d'environ 0,3 % à environ 7 % du poids du comprimé et l'éther de cellulose est présent en dose allant d'environ 3 % à environ 20 % du poids du comprimé dans l'excipient, et l'éther de cellulose est présent en doses au moins égale à 33 % du poids de l'excipient, lequel excipient est présent en doses inférieures à 35 % du poids dudit comprimé.

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