H-bonded organic frameworks as ultrasound-programmable delivery platform

• 成果类型: Article
• 署名作者: Wang, Wenliang; Shi, Yanshu; Chai, Wenrui; Tang, Kai Wing Kevin; Pyatnitskiy, Ilya; Xie, Yi; Liu, Xiangping; He, Weilong; Jeong, Jinmo; Hsieh, Ju-Chun; Lozano, Anakaren Romero; Artman, Brinkley; Shi, Xi; Hoefer, Nicole; Shrestha, Binita; Stern, Noah B.; Zhou, Wei; Mccomb, David W.; Porter, Tyrone; Henkelman, Graeme; Chen, Banglin; Wang, Huiliang
• 署名单位: University of Texas System; University of Texas Austin; University of Texas System; University of Texas at San Antonio; University of Texas System; University of Texas Austin; University of Texas System; University of Texas Austin; University System of Ohio; Ohio State University; National Institute of Standards & Technology (NIST) - USA
• 刊物名称: Nature
• ISSN/ISSBN: 0028-2284
• DOI: 10.1038/s41586-024-08401-0
• 发表日期: 2025-02-13
• 关键词: activation

摘要

The precise control of mechanochemical activation within deep tissues using non-invasive ultrasound holds profound implications for advancing our understanding of fundamental biomedical sciences and revolutionizing disease treatments1, 2, 3-4. However, a theory-guided mechanoresponsive materials system with well-defined ultrasound activation has yet to be explored5,6. Here we present the concept of using porous hydrogen-bonded organic frameworks (HOFs) as toolkits for focused ultrasound (FUS) programmably triggered drug activation to control specific cellular events in the deep brain, through on-demand scission of the supramolecular interactions. A theoretical model is developed to potentially visualize the mechanochemical scission and ultrasound mechanics, providing valuable guidelines for the rational design of mechanoresponsive materials to achieve programmable control. To demonstrate the practicality of this approach, we encapsulate the designer drug clozapine N-oxide (CNO) into the optimal HOF nanocrystals for FUS-gated release to activate engineered G-protein-coupled receptors in the ventral tegmental area (VTA) of mice and rats and hence achieve targeted neural circuit modulation even at depth 9 mm with a latency of seconds. This work demonstrates the capability of ultrasound to precisely control molecular interactions and develops ultrasound-programmable HOFs to non-invasively and spatiotemporally control cellular events, thereby facilitating the establishment of precise molecular therapeutic possibilities.