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A Wirelessly Controlled Scalable 3D-Printed Microsystem for Drug Delivery

Here we present a 3D-printed, wirelessly controlled microsystem for drug delivery, comprising a refillable microreservoir and a phase-change peristaltic micropump. The micropump structure was inkjet-printed on the back of a printed circuit board around a catheter microtubing. The enclosure of the mi...

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Autores principales: Forouzandeh, Farzad, Ahamed, Nuzhet N., Zhu, Xiaoxia, Bazard, Parveen, Goyal, Krittika, Walton, Joseph P., Frisina, Robert D., Borkholder, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227156/
https://www.ncbi.nlm.nih.gov/pubmed/34199855
http://dx.doi.org/10.3390/ph14060538
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author Forouzandeh, Farzad
Ahamed, Nuzhet N.
Zhu, Xiaoxia
Bazard, Parveen
Goyal, Krittika
Walton, Joseph P.
Frisina, Robert D.
Borkholder, David A.
author_facet Forouzandeh, Farzad
Ahamed, Nuzhet N.
Zhu, Xiaoxia
Bazard, Parveen
Goyal, Krittika
Walton, Joseph P.
Frisina, Robert D.
Borkholder, David A.
author_sort Forouzandeh, Farzad
collection PubMed
description Here we present a 3D-printed, wirelessly controlled microsystem for drug delivery, comprising a refillable microreservoir and a phase-change peristaltic micropump. The micropump structure was inkjet-printed on the back of a printed circuit board around a catheter microtubing. The enclosure of the microsystem was fabricated using stereolithography 3D printing, with an embedded microreservoir structure and integrated micropump. In one configuration, the microsystem was optimized for murine inner ear drug delivery with an overall size of 19 × 13 × 3 mm(3). Benchtop results confirmed the performance of the device for reliable drug delivery. The suitability of the device for long-term subcutaneous implantation was confirmed with favorable results of implantation of a microsystem in a mouse for six months. The drug delivery was evaluated in vivo by implanting four different microsystems in four mice, while the outlet microtubing was implanted into the round window membrane niche for infusion of a known ototoxic compound (sodium salicylate) at 50 nL/min for 20 min. Real-time shifts in distortion product otoacoustic emission thresholds and amplitudes were measured during the infusion, demonstrating similar results with syringe pump infusion. Although demonstrated for one application, this low-cost design and fabrication methodology is scalable for use in larger animals and humans for different clinical applications/delivery sites.
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spelling pubmed-82271562021-06-26 A Wirelessly Controlled Scalable 3D-Printed Microsystem for Drug Delivery Forouzandeh, Farzad Ahamed, Nuzhet N. Zhu, Xiaoxia Bazard, Parveen Goyal, Krittika Walton, Joseph P. Frisina, Robert D. Borkholder, David A. Pharmaceuticals (Basel) Article Here we present a 3D-printed, wirelessly controlled microsystem for drug delivery, comprising a refillable microreservoir and a phase-change peristaltic micropump. The micropump structure was inkjet-printed on the back of a printed circuit board around a catheter microtubing. The enclosure of the microsystem was fabricated using stereolithography 3D printing, with an embedded microreservoir structure and integrated micropump. In one configuration, the microsystem was optimized for murine inner ear drug delivery with an overall size of 19 × 13 × 3 mm(3). Benchtop results confirmed the performance of the device for reliable drug delivery. The suitability of the device for long-term subcutaneous implantation was confirmed with favorable results of implantation of a microsystem in a mouse for six months. The drug delivery was evaluated in vivo by implanting four different microsystems in four mice, while the outlet microtubing was implanted into the round window membrane niche for infusion of a known ototoxic compound (sodium salicylate) at 50 nL/min for 20 min. Real-time shifts in distortion product otoacoustic emission thresholds and amplitudes were measured during the infusion, demonstrating similar results with syringe pump infusion. Although demonstrated for one application, this low-cost design and fabrication methodology is scalable for use in larger animals and humans for different clinical applications/delivery sites. MDPI 2021-06-04 /pmc/articles/PMC8227156/ /pubmed/34199855 http://dx.doi.org/10.3390/ph14060538 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Forouzandeh, Farzad
Ahamed, Nuzhet N.
Zhu, Xiaoxia
Bazard, Parveen
Goyal, Krittika
Walton, Joseph P.
Frisina, Robert D.
Borkholder, David A.
A Wirelessly Controlled Scalable 3D-Printed Microsystem for Drug Delivery
title A Wirelessly Controlled Scalable 3D-Printed Microsystem for Drug Delivery
title_full A Wirelessly Controlled Scalable 3D-Printed Microsystem for Drug Delivery
title_fullStr A Wirelessly Controlled Scalable 3D-Printed Microsystem for Drug Delivery
title_full_unstemmed A Wirelessly Controlled Scalable 3D-Printed Microsystem for Drug Delivery
title_short A Wirelessly Controlled Scalable 3D-Printed Microsystem for Drug Delivery
title_sort wirelessly controlled scalable 3d-printed microsystem for drug delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227156/
https://www.ncbi.nlm.nih.gov/pubmed/34199855
http://dx.doi.org/10.3390/ph14060538
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