Affiliation:
1. Department of Chemical and Biological Engineering University of Colorado Boulder 3415 Colorado Ave Boulder CO 80303 USA
2. Department of Mechanical Engineering University of Colorado Boulder 1111 Engineering Drive UCB 427 Boulder CO 80309 USA
3. Biomedical Engineering Program University of Colorado Boulder 1111 Engineering Drive, UCB 422 Boulder CO 80309 USA
Abstract
AbstractRemotely powered microrobots are proposed as next‐generation vehicles for drug delivery. However, most microrobots swim with linear trajectories and lack the capacity to robustly adhere to soft tissues. This limits their ability to navigate complex biological environments and sustainably release drugs at target sites. In this work, bubble‐based microrobots with complex geometries are shown to efficiently swim with non‐linear trajectories in a mouse bladder, robustly pin to the epithelium, and slowly release therapeutic drugs. The asymmetric fins on the exterior bodies of the microrobots induce a rapid rotational component to their swimming motions of up to ≈150 body lengths per second. Due to their fast speeds and sharp fins, the microrobots can mechanically pin themselves to the bladder epithelium and endure shear stresses commensurate with urination. Dexamethasone, a small molecule drug used for inflammatory diseases, is encapsulated within the polymeric bodies of the microrobots. The sustained release of the drug is shown to temper inflammation in a manner that surpasses the performance of free drug controls. This system provides a potential strategy to use microrobots to efficiently navigate large volumes, pin at soft tissue boundaries, and release drugs over several days for a range of diseases.
Funder
National Science Foundation
National Institutes of Health
Office of Naval Research
Pew Charitable Trusts
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
13 articles.
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