Department of Chemistry, University of Tennessee, Knoxville, TN 37996-1600, USA.
J Chromatogr A. 2011 Dec 9;1218(49):8836-58. doi: 10.1016/j.chroma.2011.09.008. Epub 2011 Sep 14.
The impact of economic change, advances in science, therapy and production processes resulted in considerable growth in the area of biopharmaceuticals. Progress in selection of microorganisms and improvements in cell culture and bioreactors is evidenced by increased yields of the desired products in the complex fermentation mixture. At this stage the downstream process of extraction and purification of the desired biopharmaceutical requires considerable attention in the design and operation of the units used for preparative chromatography. Understanding of the process, optimization of column design and experimental conditions have become critical to the biopharmaceutical industry in order to minimize production costs while satisfying new regulatory requirements. Optimization of the purification of biopharmaceuticals by preparative liquid chromatography including an examination of column preparation and bed properties is the focus of this manuscript.
经济变革、科学进步、治疗方法和生产工艺的发展使得生物制药领域有了显著的增长。微生物的选择、细胞培养和生物反应器的改进方面的进展,在复杂发酵混合物中提高了所需产物的产量。在这个阶段,下游的提取和纯化所需生物制药的过程需要在设计和操作用于制备色谱的单元时给予相当的关注。为了在满足新的监管要求的同时最小化生产成本,对工艺的理解、对柱设计和实验条件的优化已经成为生物制药行业的关键。本文的重点是通过制备液相色谱法优化生物制药的纯化,包括对柱制备和床层性质的检查。