Krivitsky Adva, Paunović Nevena, Klein Karina, Coulter Fergal Brian, Schleich Sarah, Karol Agnieszka Anna, Bauer Aline, Krivitsky Vadim, Lohmann Victoria, Carril Paula Cendoya, Bao Yinyin, von Rechenberg Brigitte, Halin Cornelia, Studart André R, Franzen Daniel, Leroux Jean-Christophe
Institute of Pharmaceutical Sciences, Department of Chemistry and Applied Biosciences, ETH Zurich, Zurich, Switzerland.
Musculoskeletal Research Unit, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland.
J Control Release. 2025 Jan 10;377:553-562. doi: 10.1016/j.jconrel.2024.11.031. Epub 2024 Nov 29.
Airway stents are life-saving medical devices used to treat malignant or benign central airway stenoses. Unfortunately, these devices, typically manufactured from silicone alone and/or nitinol, can result in serious complications, such as stent migration, bacterial colonization, and tissue granulation, eventually forcing stent removal. Customized airway stents exhibit reduced migration and they can be tailored to address other complications by releasing drugs, such as the antibiotic levofloxacin and the antifibrotic drug nintedanib. Herein, the incorporation of these molecules in customized, bioresorbable 3D printed airway stents was investigated. Nintedanib (1.5 wt%) and levofloxacin (2.0 wt%) were incorporated in the polymer-based resin, which was used to 3D print tracheal stents with adequate mechanical and drug release properties. The drug-loaded stents were then deployed into rabbit tracheas and found to deliver the drugs locally with minimal systemic exposure. Drug activities were demonstrated by inhibition of bacterial colonization and reduced interleukin 8 (IL8) local expression. Although the application of these tracheal stents requires further exploration in larger animal models, this work paves the way for the rapid manufacturing of personalized medical devices with therapeutic functions.