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Cell labelling for in vivo use and in process quality control

Cell labelling for in vivo use and in process quality control
用于体内使用和过程质量控制的细胞标记
批准号:
101102
负责人:
金额:
$30.41万
依托单位:
依托单位国家:
英国
项目类别:
Collaborative R&D
财政年份:
2012
资助国家:
英国
项目状态:
已结题
起止时间:
2012 至 --

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中文摘要
翻译
Altrika、爱丁堡大学化学学院、Roslin Cellab和Barts以及The伦敦的联盟将研发、制造、临床和商业化经验带到了体外和体内追踪临床相关细胞群的挑战中。缺乏体内跟踪方法导致研发、制造和临床限制、宝贵的研究人员时间和细胞产量损失以及相关成本。该项目采用了一种创新的无毒细胞标签,该标签稳定,具有成本效益且易于检测。它将证明适用于一系列未满足临床需求的再生医学疗法,以及提高研发活动和制造过程的效率,并提高临床交付的功效。鉴于再生医学的发展,该平台可以在2020年将行业成本降低2.75亿美元。
英文摘要
The consortium of Altrika, the University of Edinburgh’s School of Chemistry, Roslin Cellab and Barts and The London bring R&D, manufacturing, clinical and commercialisation experience to the challenge of tracking clinically relevant cell populations in vitro and in vivo. The absence of an in vivo tracking methodology leads to R&D, manufacturing and clinical constraints, valuable researcher time and cell yield losses, and associated costs. This project utilises an innovative, non-toxic cell label that is stable, cost-effective and easy to detect. It will demonstrate applicability to a range of regenerative medicine therapies for unmet clinical needs, as well as increasing the efficiency of R&D activities and manufacturing processes, and improving the efficacy of clinical delivery. Given the growth of regenerative medicine, this platform could reduce industry costs by as much as $275m in 2020.
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