Pharmaceutical compositions for gastrointestinal drug delivery

摘要

A novel pharmaceutical composition, which comprises a therapeutically effective amount of active principle(s) or a pharmaceutically acceptable salt or enantiomer or polymorph thereof, optionally one or more release controlling agent(s) and pharmaceutical acceptable excipient(s) thereof, wherein the composition is formulated to increase the residence time of the said pharmaceutical composition and/or active principle(s) in the gastrointestinal tract. A novel pharmaceutical composition comprising at least two entities wherein one entity is an immediate release/fast release and the other is controlled release. A pharmaceutical composition comprising at least two entities wherein one entity is an immediate release/fast release and the other is bioadhesive. A pharmaceutical composition comprising: at least two entities wherein one entity is controlled release and the other is bioadhesive All the three compositions are formulated to increase the residence time of active principle(s) in the gastrointestinal tract. A multilayered composition with active in a layer which provides immediate release or controlled release of active principles and layer providing increased residence time in the GI tract.

主权项

1. An oral multilayer tablet comprising:
a first layer comprising a pharmaceutical composition comprising rifaximin or a pharmaceutically acceptable salt thereof and that is configured for immediate or fast release of the rifaximin or salt thereof; and a second layer comprising the rifaximin or salt thereof and a polymer having affinity for gastrointestinal mucosa, wherein the polymer adheres to the gastrointestinal mucosa and provides increased residence time of the tablet in the gastrointestinal tract by bioadhesion which is independent of food effect, wherein the composition has an adhesive strength, measured as a force of detachment, of at least 1000 mN in 30 minutes, and wherein bioadhesion is provided for a period greater than 0.5 hour.