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3D-Printed Microinjection Needle Arrays via a Hybrid DLP-Direct Laser Writing Strategy
Microinjection protocols are ubiquitous throughout biomedical fields, with hollow microneedle arrays (MNAs) offering distinctive benefits in both research and clinical settings. Unfortunately, manufacturing-associated barriers remain a critical impediment to emerging applications that demand high-de...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104452/ https://www.ncbi.nlm.nih.gov/pubmed/37064271 http://dx.doi.org/10.1002/admt.202201641 |
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author | Sarker, Sunandita Colton, Adira Wen, Ziteng Xu, Xin Erdi, Metecan Jones, Anthony Kofinas, Peter Tubaldi, Eleonora Walczak, Piotr Janowski, Miroslaw Liang, Yajie Sochol, Ryan D. |
author_facet | Sarker, Sunandita Colton, Adira Wen, Ziteng Xu, Xin Erdi, Metecan Jones, Anthony Kofinas, Peter Tubaldi, Eleonora Walczak, Piotr Janowski, Miroslaw Liang, Yajie Sochol, Ryan D. |
author_sort | Sarker, Sunandita |
collection | PubMed |
description | Microinjection protocols are ubiquitous throughout biomedical fields, with hollow microneedle arrays (MNAs) offering distinctive benefits in both research and clinical settings. Unfortunately, manufacturing-associated barriers remain a critical impediment to emerging applications that demand high-density arrays of hollow, high-aspect-ratio microneedles. To address such challenges, here, a hybrid additive manufacturing approach that combines digital light processing (DLP) 3D printing with “ex situ direct laser writing (esDLW)” is presented to enable new classes of MNAs for fluidic microinjections. Experimental results for esDLW-based 3D printing of arrays of high-aspect-ratio microneedles—with 30 μm inner diameters, 50 μm outer diameters, and 550 μm heights, and arrayed with 100 μm needle-to-needle spacing—directly onto DLP-printed capillaries reveal uncompromised fluidic integrity at the MNA-capillary interface during microfluidic cyclic burst-pressure testing for input pressures in excess of 250 kPa (n = 100 cycles). Ex vivo experiments perform using excised mouse brains reveal that the MNAs not only physically withstand penetration into and retraction from brain tissue but also yield effective and distributed microinjection of surrogate fluids and nanoparticle suspensions directly into the brains. In combination, the results suggest that the presented strategy for fabricating high-aspect-ratio, high-density, hollow MNAs could hold unique promise for biomedical microinjection applications. |
format | Online Article Text |
id | pubmed-10104452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-101044522023-04-14 3D-Printed Microinjection Needle Arrays via a Hybrid DLP-Direct Laser Writing Strategy Sarker, Sunandita Colton, Adira Wen, Ziteng Xu, Xin Erdi, Metecan Jones, Anthony Kofinas, Peter Tubaldi, Eleonora Walczak, Piotr Janowski, Miroslaw Liang, Yajie Sochol, Ryan D. Adv Mater Technol Article Microinjection protocols are ubiquitous throughout biomedical fields, with hollow microneedle arrays (MNAs) offering distinctive benefits in both research and clinical settings. Unfortunately, manufacturing-associated barriers remain a critical impediment to emerging applications that demand high-density arrays of hollow, high-aspect-ratio microneedles. To address such challenges, here, a hybrid additive manufacturing approach that combines digital light processing (DLP) 3D printing with “ex situ direct laser writing (esDLW)” is presented to enable new classes of MNAs for fluidic microinjections. Experimental results for esDLW-based 3D printing of arrays of high-aspect-ratio microneedles—with 30 μm inner diameters, 50 μm outer diameters, and 550 μm heights, and arrayed with 100 μm needle-to-needle spacing—directly onto DLP-printed capillaries reveal uncompromised fluidic integrity at the MNA-capillary interface during microfluidic cyclic burst-pressure testing for input pressures in excess of 250 kPa (n = 100 cycles). Ex vivo experiments perform using excised mouse brains reveal that the MNAs not only physically withstand penetration into and retraction from brain tissue but also yield effective and distributed microinjection of surrogate fluids and nanoparticle suspensions directly into the brains. In combination, the results suggest that the presented strategy for fabricating high-aspect-ratio, high-density, hollow MNAs could hold unique promise for biomedical microinjection applications. 2023-03-10 2023-02-05 /pmc/articles/PMC10104452/ /pubmed/37064271 http://dx.doi.org/10.1002/admt.202201641 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Article Sarker, Sunandita Colton, Adira Wen, Ziteng Xu, Xin Erdi, Metecan Jones, Anthony Kofinas, Peter Tubaldi, Eleonora Walczak, Piotr Janowski, Miroslaw Liang, Yajie Sochol, Ryan D. 3D-Printed Microinjection Needle Arrays via a Hybrid DLP-Direct Laser Writing Strategy |
title | 3D-Printed Microinjection Needle Arrays via a Hybrid DLP-Direct Laser
Writing Strategy |
title_full | 3D-Printed Microinjection Needle Arrays via a Hybrid DLP-Direct Laser
Writing Strategy |
title_fullStr | 3D-Printed Microinjection Needle Arrays via a Hybrid DLP-Direct Laser
Writing Strategy |
title_full_unstemmed | 3D-Printed Microinjection Needle Arrays via a Hybrid DLP-Direct Laser
Writing Strategy |
title_short | 3D-Printed Microinjection Needle Arrays via a Hybrid DLP-Direct Laser
Writing Strategy |
title_sort | 3d-printed microinjection needle arrays via a hybrid dlp-direct laser
writing strategy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104452/ https://www.ncbi.nlm.nih.gov/pubmed/37064271 http://dx.doi.org/10.1002/admt.202201641 |
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