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用于生物制药生产的连续加工

Continuous processing for production of biopharmaceuticals.

作者信息

Rathore Anurag S, Agarwal Harshit, Sharma Abhishek Kumar, Pathak Mili, Muthukumar S

机构信息

a Department of Chemical Engineering , Indian Institute of Technology , New Delhi , India.

出版信息

Prep Biochem Biotechnol. 2015;45(8):836-49. doi: 10.1080/10826068.2014.985834.

Abstract

The merits of continuous processing over batch processing are well known in the manufacturing industry. Continuous operation results in shorter process times due to omission of hold steps, higher productivity due to reduced shutdown costs, and lowers labor requirement. Over the past decade, there has been an increasing interest in continuous processing within the bioprocessing community, specifically those involved in production of biotherapeutics. Continuous operations in upstream processing (perfusion) have been performed for decades. However, recent development of continuous downstream operations has led the industry to envisage an integrated bioprocessing platform for efficient production. The regulators, key players in the biotherapeutic industry, have also expressed their interest and willingness in this migration from the traditional batch processing. This paper aims to review major developments in continuous bioprocessing in the past decade. A discussion of pros and cons of the different proposed approaches has also been presented.

摘要

在制造业中,连续加工相对于分批加工的优点是众所周知的。连续操作由于省略了保持步骤而使加工时间更短,由于降低了停机成本而提高了生产率,并且降低了劳动力需求。在过去十年中,生物加工领域对连续加工的兴趣与日俱增,特别是那些涉及生物治疗药物生产的领域。上游加工(灌注)中的连续操作已经进行了数十年。然而,连续下游操作的最新发展促使该行业设想一个用于高效生产的集成生物加工平台。监管机构作为生物治疗行业的关键参与者,也表达了他们对从传统分批加工向连续加工转变的兴趣和意愿。本文旨在回顾过去十年中连续生物加工的主要发展。还对不同提议方法的优缺点进行了讨论。

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