Microfluidic Interfaces for Chronic Bidirectional Access to the Brain

Author:

Marcigaglia Simone12ORCID,De Plus Robin12ORCID,Vandendriessche Charysse34ORCID,Schiltz Eleonore12ORCID,Cuypers Marie‐Lynn5ORCID,Cools Jordi16ORCID,Hoffman Luis D.17ORCID,Vandenbroucke Roosmarijn E.34ORCID,Dewilde Maarten58ORCID,Haesler Sebastian12ORCID

Affiliation:

1. Neuroelectronics Research Flanders (NERF) Leuven 3000 Belgium

2. Department of Neurosciences KU Leuven Leuven 3000 Belgium

3. VIB Center for Inflammation Research VIB Ghent 9052 Belgium

4. Department of Biomedical Molecular Biology Ghent University Ghent 9052 Belgium

5. Laboratory for Therapeutic and Diagnostic Antibodies Department of Pharmaceutical and Pharmacological Sciences KU Leuven Leuven 3000 Belgium

6. Current affiliation Thermofisher Scientific (AIG/MSD) Dilbeek 1702 Belgium

7. Current affiliation SWave Photonics Leuven 3001 Belgium

8. PharmAbs‐The KU Leuven Antibody Center KU Leuven Leuven 3000 Belgium

Abstract

AbstractTwo‐photon polymerization (TPP) is an additive manufacturing technique with micron‐scale resolution that is rapidly gaining ground for a range of biomedical applications. TPP is particularly attractive for the creation of microscopic three‐dimensional structures in biocompatible and noncytotoxic resins. Here, TPP is used to develop microfluidic interfaces which provide chronic fluidic access to the brain of preclinical research models. These microcatheters can be used for either convection‐enhanced delivery (CED) or for the repeated collection of liquid biopsies. In a brain phantom, infusions with the micronozzle result in more localized distribution clouds and lower backflow compared to a control catheter. In mice, the delivery interface enables faster, more precise, and physiologically less disruptive fluid injections. A second microcatheter design enables repeated, longitudinal sampling of cerebrospinal fluid (CSF) over time periods as long as 250 days. Moreover, further in vivo studies demonstrate that the blood‐CSF barrier is intact after chronic implantation of the sampling interface and that samples are suitable for downstream molecular analysis for the identification of nucleic acid‐ or peptide‐based biomarkers. Ultimately, the versatility of this fabrication technique implies a great translational potential for simultaneous drug delivery and biomarker tracking in a range of human neurological diseases.

Funder

Fonds Wetenschappelijk Onderzoek

Onderzoeksraad, KU Leuven

Publisher

Wiley

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