Fundamental aspects of solid dispersion technology for poorly soluble drugs

被引:421
作者
Huang, Yanbin [1 ]
Dai, Wei-Guo [2 ]
机构
[1] Tsinghua Univ, Dept Chem Engn, Key Lab Adv Mat MOE, Beijing 100084, Peoples R China
[2] Johnson & Johnson Co, Janssen Res & Dev, Randor, PA 19087 USA
基金
中国国家自然科学基金;
关键词
Solid dispersion; Poorly soluble drug; Phase separation; Drug-polymer interaction; CRYSTAL-GROWTH; MELT EXTRUSION; PRECIPITATION; POLYMERS; BEHAVIOR; MISCIBILITY; SOLUBILITY; SUPERSATURATION; CRYSTALLIZATION; SULFATHIAZOLE;
D O I
10.1016/j.apsb.2013.11.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The solid dispersion has become an established solubilization technology for poorly water soluble drugs. Since a solid dispersion is basically a drug-polymer two-component system, the drug-polymer interaction is the determining factor in its design and performance. In this review, we summarize our current understanding of solid dispersions both in the solid state and in dissolution, emphasizing the fundamental aspects of this important technology. (C) 2014 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:18 / 25
页数:8
相关论文
共 57 条
[31]   Characterization of Amorphous API:Polymer Mixtures Using X-Ray Powder Diffraction [J].
Newman, Ann ;
Engers, David ;
Bates, Simon ;
Ivanisevic, Igor ;
Kelly, Ron C. ;
Zografi, George .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 97 (11) :4840-4856
[32]   Assessing the performance of amorphous solid dispersions [J].
Newman, Ann ;
Knipp, Gregory ;
Zografi, George .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2012, 101 (04) :1355-1377
[33]   Manufacturing of solid dispersions of poorly water soluble drugs by spray drying: Formulation and process considerations [J].
Paudel, Amrit ;
Worku, Zelalem Ayenew ;
Meeus, Joke ;
Guns, Sandra ;
Van den Mooter, Guy .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2013, 453 (01) :253-284
[34]   Characterisation of solid dispersions of paracetamol and EUDRAGIT® E prepared by hot-melt extrusion using thermal, microthermal and spectroscopic analysis [J].
Qi, Sheng ;
Gryczke, Andreas ;
Belton, Peter ;
Craig, Duncan Q. M. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 354 (1-2) :158-167
[35]   Characterisation and Prediction of Phase Separation in Hot-Melt Extruded Solid Dispersions: A Thermal, Microscopic and NMR Relaxometry Study [J].
Qi, Sheng ;
Belton, Peter ;
Nollenberger, Kathrin ;
Clayden, Nigel ;
Reading, Mike ;
Craig, Duncan Q. M. .
PHARMACEUTICAL RESEARCH, 2010, 27 (09) :1869-1883
[36]   Solution Behavior of PVP-VA and HPMC-AS-Based Amorphous Solid Dispersions and Their Bioavailability Implications [J].
Qian, Feng ;
Wang, Jennifer ;
Hartley, Ruiling ;
Tao, Jing ;
Haddadin, Raja ;
Mathias, Neil ;
Hussain, Munir .
PHARMACEUTICAL RESEARCH, 2012, 29 (10) :2766-2776
[37]   Is a distinctive single Tg a reliable indicator for the homogeneity of amorphous solid dispersion? [J].
Qian, Feng ;
Huang, Jun ;
Zhu, Qing ;
Haddadin, Raja ;
Gawel, John ;
Garmise, Robert ;
Hussain, Munir .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 395 (1-2) :232-235
[38]   Drug-Polymer Solubility and Miscibility: Stability Consideration and Practical Challenges in Amorphous Solid Dispersion Development [J].
Qian, Feng ;
Huang, Jun ;
Hussain, Munir A. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2010, 99 (07) :2941-2947
[39]   Crystallization of hydrocortisone acetate: influence of polymers [J].
Raghavan, SL ;
Trividic, A ;
Davis, AF ;
Hadgraft, J .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 212 (02) :213-221
[40]  
Rubinstein M., 2003, Polymer Physics