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人脐带间充质干细胞片的临床应用制造与质量控制。

Manufacture and Quality Control of Human Umbilical Cord-Derived Mesenchymal Stem Cell Sheets for Clinical Use.

机构信息

BOE Regenerative Medicine Technology Co., Ltd., Beijing 100015, China.

Children Heart Center, Fuwai Central China Cardiovascular Hospital, Zhengzhou 450018, China.

出版信息

Cells. 2022 Sep 1;11(17):2732. doi: 10.3390/cells11172732.

Abstract

Human umbilical cord-derived mesenchymal stem cell (UC-MSC) sheets have attracted much attention in cell therapy. However, the culture media and coating matrix used for the preparation of UC-MSC sheets have not been safe enough to comply with current clinical drug standards. Moreover, the UC-MSC sheet preservation systems developed before did not comply with Good Manufacturing Practice (GMP) regulations. In this study, the culture medium and coating matrix were developed for UC-MSC sheet production to comply with clinical drug standards. Additionally, the GMP-compliant preservation solution and method for the UC-MSC sheet were developed. Then, quality standards of the UC-MSC sheet were formulated according to national and international regulations for drugs. Finally, the production process of UC-MSC sheets on a large scale was standardized, and three batches of trial production were conducted and tested to meet the established quality standards. This research provides the possibility for clinical trials of UC-MSC sheet products in the development stage of new drugs and lays the foundation for industrial large-scale production after the new drug is launched.

摘要

人脐带间充质干细胞(UC-MSC)片在细胞治疗中受到广泛关注。然而,用于制备 UC-MSC 片的培养基和涂层基质还不够安全,无法符合当前的临床药物标准。此外,以前开发的 UC-MSC 片保存系统不符合良好生产规范(GMP)规定。在这项研究中,开发了符合临床药物标准的 UC-MSC 片生产用培养基和涂层基质。此外,还开发了符合 GMP 的 UC-MSC 片保存液和保存方法。然后,根据国家和国际药物法规制定了 UC-MSC 片的质量标准。最后,对 UC-MSC 片的大规模生产工艺进行了标准化,并进行了三批试生产,以满足既定的质量标准。这项研究为新药开发阶段的 UC-MSC 片产品临床试验提供了可能性,并为新药上市后的工业大规模生产奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fa4/9454431/4c27f3e98681/cells-11-02732-g001.jpg

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