The present invention features formulations, including liquid, semi-solid or solid pharmaceutical formulations, that improve the oral bioavailability of hydrophobic pharmaceutical agents, such as quinazoline-, nitrothiazole-, and indolinone-based compounds. Also featured are formulations for parenteral delivery of such hydrophobic pharmaceutical agents, as well as methods of making and using both types of formulations.
本发明涉及包括液体、半固体或固体制剂的配方,可以提高疏
水性药物,如
喹唑啉、硝基
噻唑和
吲哚酮类化合物的口服
生物利用度。还包括适用于静脉注射递送这些疏
水性药物的配方,以及制备和使用这两种类型配方的方法。