Strategies for formulating and delivering poorly water-soluble drugs

被引:124
|
作者
Rodriguez-Aller, Marta [1 ]
Guillarme, Davy [1 ]
Veuthey, Jean-Luc [1 ]
Gurny, Robert [1 ]
机构
[1] Univ Lausanne, Univ Geneva, Sch Pharmaceut Sci, CH-1211 Geneva 4, Switzerland
关键词
Insoluble drugs; Formulation; Delivery; pH; Pharmaceutical strategies; Alternative administration route; HYDROXYPROPYL-BETA-CYCLODEXTRIN; IMPROVED ORAL BIOAVAILABILITY; BLOCK-COPOLYMER MICELLES; PHARMACEUTICAL APPLICATIONS; SOLID DISPERSION; IN-VIVO; SPONTANEOUS EMULSIFICATION; FLUOROPYRIMIDINE CARBAMATE; PHYSICOCHEMICAL PROPERTIES; MICROEMULSION FORMULATION;
D O I
10.1016/j.jddst.2015.05.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Water solubility is a key parameter in drug formulation since it highly influences drug pharmacokinetics and pharmacodynamics. In the past decades, the challenge with poorly water soluble drugs has been growing continuously. As a matter of fact, poorly soluble compounds represent 40% of the top 200 oral drugs marketed in the US, 33% of drugs listed in the US Pharmacopeia, 75% of compounds under development and 90% of new chemical entities. The present article presents and discusses the pharmaceutical strategies available to overcome poor water solubility in light of final drug product examples. First, chemical modifications based on the adjustment of the pH and the design of prodrugs are presented and discussed. Physical modifications based on modified solid states of the drug, small drug. particles, cosolvents, surfactants, lipids and cyclodextrins are discussed in a second part. Finally, the option of modifying the route of administration is briefly presented. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:342 / 351
页数:10
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