Developing an Free Bioprocess toProduce Pharmaceutical Quality Grade

C. PerryChou
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Abstract

In 2005, the American Chemical Society (ACS) Green Chemistry Institute (GCI) and global pharmaceutical companies established the ACS GCI Pharmaceutical Roundtable to encourage the integration of green chemistry and engineering into the pharmaceutical industry. The Roundtable developed a list of key research areas in green chemistry in 2007, which has served as a guide for focusing green chemistry research. Following that publication, the Roundtable companies have identified a list of the key green engineering research areas that is intended to be the required companion of the first list. Intense efforts in bioprocessing development have been made to improve the production of Chinese hamster ovary-based biopharmaceuticals. However, lacking an efficient host cell has hampered therapeutic protein production. This article reviews means by which biopharmaceutical production can be improved via cell engineering. Finally, rational cell engineering facilitated with ‘omics technologies is presented.
开发自由生物工艺生产药品质量等级
2005年,美国化学会(ACS)绿色化学研究所(GCI)和全球制药公司建立了ACS GCI制药圆桌会议,以鼓励将绿色化学和工程融入制药行业。2007年,圆桌会议制定了绿色化学重点研究领域清单,为绿色化学研究提供了指导。在该出版物发布后,圆桌会议公司确定了一份关键绿色工程研究领域的清单,旨在作为第一份清单的必要配套。为了提高中国仓鼠卵巢生物制剂的生产水平,人们在生物加工方面做出了巨大的努力。然而,缺乏有效的宿主细胞阻碍了治疗性蛋白的产生。本文综述了利用细胞工程技术改进生物制药生产的方法。最后,提出了利用组学技术实现合理的细胞工程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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