Published May 20, 2025 | Version Published
Journal Article Open

Acoustic percolation switches enable targeted drug delivery controlled by diagnostic ultrasound

Abstract

Delivering biomedicines to specific sites of disease using remote-controlled devices is a long-standing vision in biomedical research. However, most existing externally triggered delivery systems are based on complex micromachines that are controlled with electromagnetic waves and require custom external instrumentation. Here, we present a drug delivery platform based on a simple protein-containing hydrogel that can be both imaged and triggered to release drugs at specific locations using widely available diagnostic ultrasound devices. This technology is based on the addition of air-filled protein nanostructures called gas vesicles (GVs) to hydrogel delivery vehicles. While intact, GVs sterically block the release of drug payloads and allow the vehicle to be imaged with ultrasound. An increase in ultrasound pressure causes the collapse of GVs within the delivery vehicles at the desired anatomical location, instantly creating percolation channels in the hydrogel, massively increasing diffusivity, and leading to rapid drug release. Unlike previous ultrasound-actuated delivery approaches, both the imaging and release are performed using a simple diagnostic ultrasound probe ubiquitously available in clinical settings. We implement this concept by quantifying ultrasound-controlled drug diffusion and release in vitro and demonstrating image-guided protein delivery in vivo in the gastrointestinal (GI) tract following oral administration. We further validate this technology by using it to deliver anti-inflammatory antibodies to effectively treat a rat model of colitis. Targeted acoustic percolation switches (TAPS) open a conduit for local, image-guided drug delivery with a simple formulation and commonplace ultrasound equipment.

Copyright and License

© 2025 the Author(s). Published by PNAS. This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY).

Acknowledgement

We thank Yuxing Yao and John Brady for helpful discussions. M.P.A. was funded by the A*STAR graduate fellowship. M.T.B. was funded by the NSF graduate research fellowship. This research was supported by the Jacobs Institute for Molecular Engineering in Medicine, the David and Lucille Packard Foundation, and the Dreyfus Teacher-Scholar Award. M.G.S. is an Investigator of the HHMI. Portions of the paper were developed from the thesis of M.P.A.

Contributions

M.P.A., A.T.T., M.T.B., and M.G.S. designed research; M.P.A., A.T.T., M.T.B., P.B.-L., Z.J., and D.M. performed research; M.P.A., A.T.T., M.T.B., P.B.-L., and Z.J. analyzed data; and M.P.A. and M.G.S. wrote the paper.

Conflict of Interest

M.P.A. and M.G.S. are co-inventors on a patent application describing this technology (US17/092,215) assigned to the California Institute of Technology.

Supplemental Material

Appendix 01 (PDF)

Files

abundo-et-al-2025-acoustic-percolation-switches-enable-targeted-drug-delivery-controlled-by-diagnostic-ultrasound.pdf

Additional details

Identifiers

Related works

Describes
Journal Article: 40366696 (PMID)
Journal Article: PMC12107142 (PMCID)

Funding

Agency for Science, Technology and Research
National Science Foundation
David and Lucile Packard Foundation
Camille and Henry Dreyfus Foundation

Dates

Submitted
2024-11-06
Accepted
2025-04-09
Available
2025-05-14
Published