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符合药品生产质量管理规范的细胞生产中固体组织处理的培养基灌装方法验证

Validation of the Media Fill Method for Solid Tissue Processing in Good Manufacturing Practice-Compliant Cell Production.

作者信息

Öztel Olga Nehir, Aydoğdu Nurullah, Karaöz Erdal

机构信息

Liv Hospital, Center of Regenerative Medicine and Stem Cell Research, Istanbul, Turkey.

Istinye University, Faculty of Medicine, Department of Histology and Embryology, Istanbul, Turkey.

出版信息

Methods Mol Biol. 2021;2286:67-71. doi: 10.1007/7651_2020_331.

Abstract

Over the past few years, a large number of clinical studies for advanced therapy medicinal products have been registered and/or conducted for treating various diseases around the world and many have generated very exciting outcomes. Media fill, the validation of the aseptic manufacturing process, is the simulation of medicinal product manufacturing using nutrient media. The purpose of this study is to explain the media fill procedure stepwise in the context of cellular therapy medicinal products. The aseptic preparation of patient individual cellular product is simulated by using tryptic soy broth as the growth medium, and sterile vials as primary packaging materials.

摘要

在过去几年中,全球范围内已注册和/或开展了大量针对先进治疗药品的临床研究,用于治疗各种疾病,其中许多研究都取得了非常令人振奋的成果。培养基灌装,即无菌生产工艺的验证,是使用营养培养基模拟药品生产过程。本研究的目的是在细胞治疗药品的背景下逐步解释培养基灌装程序。使用胰蛋白胨大豆肉汤作为生长培养基,无菌小瓶作为初级包装材料,模拟患者个体细胞产品的无菌制备过程。

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