High throughput screening of protein formulation stability: Practical considerations
- 作者：Martinus A.H. Capelle ; Robert Gurny ; Tudor Arvinte
- 关键词：High throughput screening ; Protein formulation ; Spectroscopy ; Physical and chemical characterization ; Fluorescence ; Aggregation ; Stability
- 刊名：European Journal of Pharmaceutics and Biopharmaceutics
- 出版年：2007
- 期刊代码：16_09396411
- 类别：pha
- 出版时间：February 2007
- 卷：65
- 期：2
- 页码：131-148
- 文件大小：363 K
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.