Improved oral dosing formulations of dideoxy purine nucleosides

A - Human Necessities – 61 – K

Patent

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Details

A61K 31/70 (2006.01) A61K 9/00 (2006.01) A61K 33/08 (2006.01) A61K 33/10 (2006.01) A61K 33/12 (2006.01) A61K 33/42 (2006.01)

Patent

CA 2074215

Improved oral dosage formulations for acid-labile dideoxy purine nucleoside derivatives such as ddA, ddI, and ddG, have been developed by incorporating selected water-insoluble buffering systems in the formulation. These novel formulations provide reduced mass dosage units in the form of convenient, palatable chewable/ dispersible tablets or a dry powder sachet. The reduced mass requirement, necessary to allow tablets of reasonable size, was achieved in part by an unexpected 20 to 25% increase in drug bioavailability resulting from use of the selected buffering systems comprised of an insoluble magnesium antacid agent and either dihydroxyaluminum sodium carbonate or calcium carbonate.

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