3D‐Printed Microinjection Needle Arrays via a Hybrid DLP‐Direct Laser Writing Strategy

Author:

Sarker Sunandita123ORCID,Colton Adira123ORCID,Wen Ziteng1ORCID,Xu Xin1,Erdi Metecan4ORCID,Jones Anthony123ORCID,Kofinas Peter4ORCID,Tubaldi Eleonora123ORCID,Walczak Piotr4ORCID,Janowski Miroslaw5ORCID,Liang Yajie5ORCID,Sochol Ryan D.12367ORCID

Affiliation:

1. Department of Mechanical Engineering University of Maryland College Park MD 20742 USA

2. Maryland Robotics Center University of Maryland College Park MD 20742 USA

3. Institute for Systems Research University of Maryland College Park MD 20742 USA

4. Department of Chemical and Biomolecular Engineering University of Maryland College Park MD 20742 USA

5. Program in Image Guided Neurointerventions Department of Diagnostic Radiology and Nuclear Medicine University of Maryland School of Medicine Baltimore MD 21201 USA

6. Fischell Department of Bioengineering University of Maryland College Park MD 20742 USA

7. Robert E. Fischell Institute for Biomedical Devices University of Maryland College Park MD 20742 USA

Abstract

AbstractMicroinjection 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.

Funder

National Institutes of Health

Maryland Stem Cell Research Fund

National Science Foundation

National Institute on Aging

National Institute of Neurological Disorders and Stroke

National Institute of Diabetes and Digestive and Kidney Diseases

National Institute of Biomedical Imaging and Bioengineering

Division of Civil, Mechanical and Manufacturing Innovation

Publisher

Wiley

Subject

Industrial and Manufacturing Engineering,Mechanics of Materials,General Materials Science

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