Advances in LC platforms for drug discovery

被引:14
|
作者
Nicoli, Raul [1 ]
Martel, Sophie [1 ]
Rudaz, Serge [1 ]
Wolfender, Jean-Luc [1 ]
Veuthey, Jean-Luc [1 ]
Carrupt, Pierre-Alain [1 ]
Guillarme, Davy [1 ]
机构
[1] Univ Lausanne, Univ Geneva, Sch Pharmaceut Sci, CH-1211 Geneva 4, Switzerland
关键词
drug discovery; drug metabolism; drug permeability; LC; LC-MS; lipophilicity; pK(a); UHPLC; UHPLC-MS; PERFORMANCE LIQUID-CHROMATOGRAPHY; BIOPARTITIONING MICELLAR CHROMATOGRAPHY; ULTRA-HIGH-PRESSURE; HYDROPHILIC INTERACTION CHROMATOGRAPHY; MASS-SPECTROMETRIC QUANTIFICATION; NATURAL-PRODUCT LIBRARY; BLOOD-BRAIN-BARRIER; IN-VITRO TECHNIQUE; HIGH-THROUGHPUT; LIPOPHILICITY MEASUREMENT;
D O I
10.1517/17460441003733874
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Areas covered in this review: Significant advances in terms of LC platforms achieved in the last 5 years are highlighted in this review. Special attention is paid to novel LC strategies used in the discovery of new bioactive molecules and the determination of lipophilicity, pK(a) values, passive drug permeability and in vitro metabolism of new chemical entities. What the reader will gain: Many improvements were achieved in terms of LC instrumentation, columns technology and analytes detection to attain ultra-fast and/or high-resolution chromatographic separations. These advances are particularly beneficial to face the complexity and high number of samples studied in the early phases of the discovery process. Advantages and drawbacks of each strategy are discussed. Take home message: LC and ultra high pressure liquid chromatography coupled with mass spectrometry detection constitute the most promising strategies to achieve high-throughput and/or high-resolution analyses in a drug discovery environment.
引用
收藏
页码:475 / 489
页数:15
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