生物相容性材料
机械化学
聚合物
纳米技术
材料科学
共价键
渗透剂(生化)
化学
生物物理学
生物医学工程
有机化学
医学
生物
作者
Yuxing Yao,Molly E. McFadden,Stella M. Luo,Ross W. Barber,En‐Tang Kang,Avinoam Bar‐Zion,Cameron Smith,Zhiyang Jin,Mark Legendre,Bill Ling,Dina Malounda,Andrea Torres,Tiba Hamza,Chelsea E. R. Edwards,Mikhail G. Shapiro,Maxwell J. Robb
标识
DOI:10.1073/pnas.2309822120
摘要
External control of chemical reactions in biological settings with spatial and temporal precision is a grand challenge for noninvasive diagnostic and therapeutic applications. While light is a conventional stimulus for remote chemical activation, its penetration is severely attenuated in tissues, which limits biological applicability. On the other hand, ultrasound is a biocompatible remote energy source that is highly penetrant and offers a wide range of functional tunability. Coupling ultrasound to the activation of specific chemical reactions under physiological conditions, however, remains a challenge. Here, we describe a synergistic platform that couples the selective mechanochemical activation of mechanophore-functionalized polymers with biocompatible focused ultrasound (FUS) by leveraging pressure-sensitive gas vesicles (GVs) as acousto-mechanical transducers. The power of this approach is illustrated through the mechanically triggered release of covalently bound fluorogenic and therapeutic cargo molecules from polymers containing a masked 2-furylcarbinol mechanophore. Molecular release occurs selectively in the presence of GVs upon exposure to FUS under physiological conditions. These results showcase the viability of this system for enabling remote control of specific mechanochemical reactions with spatiotemporal precision in biologically relevant settings and demonstrate the translational potential of polymer mechanochemistry.
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