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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8227156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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