High throughput screening of protein formulation stability: Practical considerations

被引:97
作者
Capelle, Martinus A. H. [1 ]
Gurny, Robert [1 ]
Arvinte, Tudor [1 ]
机构
[1] Univ Geneva, Univ Lausanne, Dept Pharmaceut & Biopharmaceut, Sch Pharmaceut Sci, CH-1211 Geneva 4, Switzerland
关键词
high throughput screening; protein formulation; spectroscopy; physical and chemical characterization; fluorescence; aggregation; stability;
D O I
10.1016/j.ejpb.2006.09.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The formulation of protein drugs is a difficult and time-consuming process, mainly due to the complexity of protein structure and the very specific physical and chemical properties involved. Understanding protein degradation pathways is essential for the success of a biopharmaceutical drug. The present review concerns the application of high throughput screening techniques in protein formulation development. A protein high throughput formulation (HTF) platform is based on the use of microplates. Basically, the HTF platform consists of two parts: (i) sample preparation and (ii) sample analysis. Sample preparation involves automated systems for dispensing the drug and the formulation ingredients in both liquid and powder form. The sample analysis involves specific methods developed for each protein to investigate physical and chemical properties of the formulations in microplates. Examples are presented of the use of protein intrinsic fluorescence for the analysis of protein aqueous properties (e.g., conformation and aggregation). Different techniques suitable for HTF analysis are discussed and some of the issues concerning implementation are presented with reference to the use of microplates. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:131 / 148
页数:18
相关论文
共 171 条
[51]   An evaluation of fluorescence polarization and lifetime discriminated polarization for high throughput screening of serine/threonine kinases [J].
Fowler, A ;
Swift, D ;
Longman, E ;
Acornley, A ;
Hemsley, P ;
Murray, D ;
Unitt, J ;
Dale, I ;
Sullivan, E ;
Coldwell, M .
ANALYTICAL BIOCHEMISTRY, 2002, 308 (02) :223-231
[52]   High-throughput screening: Searching for higher productivity [J].
Fox, S ;
Farr-Jones, S ;
Sopchak, L ;
Boggs, A ;
Comley, J .
JOURNAL OF BIOMOLECULAR SCREENING, 2004, 9 (04) :354-358
[53]   High throughput screening 2002: Moving toward increased success rates [J].
Fox, S ;
Wang, H ;
Sopchak, L ;
Farr-Jones, S .
JOURNAL OF BIOMOLECULAR SCREENING, 2002, 7 (04) :313-316
[54]   High throughput screening: Early successes indicate a promising future [J].
Fox, S ;
Wang, H ;
Sopchak, L ;
Khoury, R .
JOURNAL OF BIOMOLECULAR SCREENING, 2001, 6 (03) :137-140
[55]   Fluorescence-lifetime technologies for high-throughput screening [J].
French, T ;
Owicki, JC ;
Modlin, DN ;
Deshpande, SS ;
Mineyev, I ;
Crawford, K ;
Burton, W .
SYSTEMS AND TECHNOLOGIES FOR CLINICAL DIAGNOSTICS AND DRUG DISCOVERY, PROCEEDINGS OF, 1998, 3259 :209-218
[56]   A microplate assay for the determination of hemoglobin concentration [J].
Frenchik, MD ;
McFaul, SJ ;
Tsonev, LI .
CLINICA CHIMICA ACTA, 2004, 339 (1-2) :199-201
[57]   High-throughput screening of structural proteomics targets using NMR [J].
Galvao-Botton, LMP ;
Katsuyama, AM ;
Guzzo, CR ;
Almeida, FCL ;
Farah, CS ;
Valente, AP .
FEBS LETTERS, 2003, 552 (2-3) :207-213
[58]   Standardized measurements and differential spectroscopy in microplates [J].
Geiger, G ;
Bernhagen, J ;
Wagner, E ;
Bisswanger, H ;
Brunner, H ;
Vitzthum, F .
ANALYTICAL BIOCHEMISTRY, 2001, 296 (01) :29-40
[59]   Enzyme assays for high-throughput screening [J].
Goddard, JP ;
Reymond, JL .
CURRENT OPINION IN BIOTECHNOLOGY, 2004, 15 (04) :314-322
[60]   Undistorted structural analysis of soluble proteins by attenuated total reflectance infrared spectroscopy [J].
Goldberg, ME ;
Chaffotte, AF .
PROTEIN SCIENCE, 2005, 14 (11) :2781-2792