Hydroxypropyl Methylcellulose Acetate Succinate-Based Spray-Dried Dispersions: An Overview

被引:470
作者
Friesen, Dwayne T. [1 ]
Shanker, Ravi [2 ]
Crew, Marshall [1 ]
Smithey, Daniel T. [1 ]
Curatolo, W. J. [2 ]
Nightingale, J. A. S. [1 ]
机构
[1] Bend Res Inc, Bend, OR 97701 USA
[2] Pfizer Inc, Global R&D, World Wide Pharmaceut Sci, Groton, CT 06340 USA
关键词
Solid amorphous dispersion; HPMCAS; absorption; oral bioavailability; spray drying; solid solution;
D O I
10.1021/mp8000793
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Spray-dried dispersions (SDDs) of low-solubility drugs have been prepared using the polymer hydroxypropyl methylcellulose acetate succinate (HPMCAS). For a variety of drug structures, these SDDs provide supersaturation in in vitro dissolution determinations and large bioavailability increases in vivo. In bile-salt/lecithin in vitro solutions, these SDDs provide amorphous drug/polymer colloids and an increased concentration of free drug and drug in micelles relative to crystalline or amorphous drug. As dry powders, the SDDs are a single amorphous phase in which the drug remains amorphous and dispersed and does not crystallize over storage times relevant for practical drug products. A melting temperature (T-m)/glass-transition temperature (T-g) (K/K) versus log P map for 139 compounds formulated as SDDs provides a perspective on an appropriate formulation strategy for low-solubility drugs with various physical properties.
引用
收藏
页码:1003 / 1019
页数:17
相关论文
共 67 条