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噬菌体的生产(共两部分,第一部分):细胞系开发、上游和下游考量因素

Manufacturing Bacteriophages (Part 1 of 2): Cell Line Development, Upstream, and Downstream Considerations.

作者信息

Tanir Tayfun, Orellana Marvin, Escalante Aster, Moraes de Souza Carolina, Koeris Michael S

机构信息

Amgen Bioprocessing Center, Department of Biological Engineering and Management, Keck Graduate Institute, Henry E. Riggs School of Applied Life Sciences, Claremont, CA 91711, USA.

出版信息

Pharmaceuticals (Basel). 2021 Sep 17;14(9):934. doi: 10.3390/ph14090934.

Abstract

Within this first part of the two-part series on phage manufacturing, we will give an overview of the process leading to bacteriophages as a drug substance, before covering the formulation into a drug product in the second part. The principal goal is to provide the reader with a comprehensive framework of the challenges and opportunities that present themselves when developing manufacturing processes for bacteriophage-based products. We will examine cell line development for manufacture, upstream and downstream processes, while also covering the additional opportunities that engineered bacteriophages present.

摘要

在这个关于噬菌体制造的两部分系列文章的第一部分中,我们将概述制备作为药物的噬菌体的过程,然后在第二部分介绍将其制成药品的配方。主要目标是为读者提供一个全面的框架,以了解在开发基于噬菌体的产品制造工艺时所面临的挑战和机遇。我们将研究用于制造的细胞系开发、上游和下游工艺,同时也会涉及工程噬菌体带来的额外机遇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d24/8471501/42387971a9d6/pharmaceuticals-14-00934-g001.jpg

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