Capelle Martinus A H, Gurny Robert, Arvinte Tudor
Department of Pharmaceutics and Biopharmaceutics, University of Geneva, University of Lausanne, CH-1211 Geneva 4, Switzerland.
Eur J Pharm Biopharm. 2007 Feb;65(2):131-48. doi: 10.1016/j.ejpb.2006.09.009. Epub 2006 Sep 29.
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.
蛋白质药物的制剂研发是一个困难且耗时的过程,主要是由于蛋白质结构的复杂性以及所涉及的非常特殊的物理和化学性质。了解蛋白质降解途径对于生物制药的成功至关重要。本综述关注高通量筛选技术在蛋白质制剂研发中的应用。蛋白质高通量制剂(HTF)平台基于微孔板的使用。基本上,HTF平台由两部分组成:(i)样品制备和(ii)样品分析。样品制备涉及用于分配液体和粉末形式的药物及制剂成分的自动化系统。样品分析涉及为每种蛋白质开发的特定方法,以研究微孔板中制剂的物理和化学性质。给出了使用蛋白质固有荧光分析蛋白质水性性质(例如构象和聚集)的示例。讨论了适用于HTF分析的不同技术,并参考微孔板的使用提出了一些关于实施的问题。