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On-demand electrochemically controlled compound release from an ultrasonically powered implant.
Wang, Max L; Chamberlayne, Christian F; Xu, Haixia; Mofidfar, Mohammad; Baltsavias, Spyridon; Annes, Justin P; Zare, Richard N; Arbabian, Amin.
Afiliación
  • Wang ML; Department of Electrical Engineering, Stanford University Stanford CA USA arbabian@stanford.edu.
  • Chamberlayne CF; Department of Chemistry, Stanford University Stanford CA USA.
  • Xu H; Department of Medicine, Division of Endocrinology, Stanford University Stanford CA USA.
  • Mofidfar M; Department of Chemistry, Stanford University Stanford CA USA.
  • Baltsavias S; Department of Electrical Engineering, Stanford University Stanford CA USA arbabian@stanford.edu.
  • Annes JP; Department of Medicine, Division of Endocrinology, Stanford University Stanford CA USA.
  • Zare RN; Department of Chemistry, Stanford University Stanford CA USA.
  • Arbabian A; Department of Electrical Engineering, Stanford University Stanford CA USA arbabian@stanford.edu.
RSC Adv ; 12(36): 23337-23345, 2022 Aug 16.
Article en En | MEDLINE | ID: mdl-36090393
On-demand drug delivery systems are promising for a wide range of therapeutic applications. When combined with wireless implants for controlled drug delivery, they can reduce overall dosage and side effects. Here, we demonstrate release of fluorescein from a novel on-demand release system for negatively charged compounds. The release system is based on a modified electroresponsive polypyrrole nanoparticulate film designed to minimize ion exchange with the stored compound - a major passive leakage mechanism. We further designed an ultrasonically powered mm-sized implant to electronically control the on-demand drug delivery system in vivo. Release kinetics are characterized both in vitro and in vivo in mice using fluorescein as a model drug, demonstrating the feasibility of wireless, controllable drug release using an ultrasonically powered implant.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2022 Tipo del documento: Article
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