为未来的精准医疗做准备:合成细胞药物调控。

IF 2.6 Q2 BIOCHEMICAL RESEARCH METHODS Synthetic biology (Oxford, England) Pub Date : 2024-01-27 eCollection Date: 2024-01-01 DOI:10.1093/synbio/ysae004
Kira Sampson, Carlise Sorenson, Katarzyna P Adamala
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引用次数: 0

摘要

合成细胞是一类新型的类细胞生物反应器,为合成生物学和生物医学的独特发展提供了潜力。要实现这些技术的潜力,基于合成细胞的药物需要通过药物审批流程。在这里,我们讨论了几个监管难题,既有合成细胞所特有的,也有任何新生物医学技术所面临的典型难题。克服这些困难可以为市场带来变革性疗法,并为尖端合成生物学疗法的开发和审批开辟道路。图表摘要。
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Preparing for the future of precision medicine: synthetic cell drug regulation.

Synthetic cells are a novel class of cell-like bioreactors, offering the potential for unique advancements in synthetic biology and biomedicine. To realize the potential of those technologies, synthetic cell-based drugs need to go through the drug approval pipeline. Here, we discussed several regulatory challenges, both unique to synthetic cells, as well as challenges typical for any new biomedical technology. Overcoming those difficulties could bring transformative therapies to the market and will create a path to the development and approval of cutting-edge synthetic biology therapies. Graphical Abstract.

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