| 摘要 |
<P>PROBLEM TO BE SOLVED: To provide a spontaneously dispersible N-benzoyl-staurosporine composition for oral administration having high bioavailability levels and reduced variability of bioavailability levels of N-benzoyl-staurosporine. <P>SOLUTION: The spontaneously dispersible N-benzoyl-staurosporin composition is such a colloid structure, for example colloid or an analogous structure, for example a droplet, particle, micelle, for example a swelling micelle, microemulsion and/or aggregate. In addition, its preparation and the use in medical treatment are disclosed. <P>COPYRIGHT: (C)2012,JPO&INPIT |
