生物正交化学
纳米反应器
点击化学
纳米技术
化学
概念证明
组合化学
生命系统
计算机科学
纳米颗粒
材料科学
人工智能
操作系统
作者
Frédéric Taran,Léa Madegard,Mélissa Girard,Estelle Blochouse,Benjamin Riss‐Yaw,Alberto Palazzolo,Davide Audisio,Pauline Poinot,Sébastien Papot,Mélanie Laquembe
标识
DOI:10.1002/anie.202422627
摘要
The development of innovative strategies enabling chemical reactions in living systems is of great interest for exploring and manipulating biological processes. Herein, we present a pioneering approach based on both bioorthogonal and confined chemistry for intracellular drug synthesis. Exploiting a click‐to‐release reaction, we engineered nanoparticles capable of synthesizing drugs within cellular environments through bioorthogonal reactions with cyclooctynes. Proof of concept experiments showed that this new approach could be successfully applied to the synthesis of the FDA‐approved Sorafenib within cancer cells. The integration of bioorthogonal and confined chemistry not only offers exciting prospects for advancing therapeutic strategies but also opens up new avenues for exploring non‐natural reactions within living systems. This innovative approach represents a fundamental extension of the biorthogonal chemistry concept and holds great promise for pioneering developments in therapeutic applications.
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