Remote control of mechanochemical reactions under physiological conditions using biocompatible focused ultrasound

Author:

Yao Yuxing1ORCID,McFadden Molly E.1,Luo Stella M.1,Barber Ross W.1,Kang Elin1,Bar-Zion Avinoam1,Smith Cameron A. B.1,Jin Zhiyang2,Legendre Mark1ORCID,Ling Bill1,Malounda Dina1,Torres Andrea1,Hamza Tiba1ORCID,Edwards Chelsea E. R.1ORCID,Shapiro Mikhail G.123ORCID,Robb Maxwell J.1ORCID

Affiliation:

1. Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125

2. Division of Engineering and Applied Science, California Institute of Technology, Pasadena, CA 91125

3. HHMI, Pasadena, CA 91125

Abstract

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.

Funder

California Institute of Technology

Arnold and Mabel Beckman Foundation

David and Lucile Packard Foundation

Resnick Sustainability Institute for Science, Energy and Sustainability, California Institute of Technology

UC | UCSB | Institute for Collaborative Biotechnologies

National Science Foundation

Alfred P. Sloan Foundation

Camille and Henry Dreyfus Foundation

HHS | NIH | National Institute of General Medical Sciences

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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