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Micro Injection Molding of Drug-Loaded Round Window Niche Implants for an Animal Model Using 3D-Printed Molds

A novel approach for the long-term medical treatment of the inner ear is the diffusion of drugs through the round window membrane from a patient-individualized, drug-eluting implant, which is inserted in the middle ear. In this study, drug-loaded (10 wt% Dexamethasone) guinea pig round window niche...

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Autores principales: Mau, Robert, Eickner, Thomas, Jüttner, Gábor, Gao, Ziwen, Wei, Chunjiang, Fiedler, Nicklas, Senz, Volkmar, Lenarz, Thomas, Grabow, Niels, Scheper, Verena, Seitz, Hermann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301927/
https://www.ncbi.nlm.nih.gov/pubmed/37376033
http://dx.doi.org/10.3390/pharmaceutics15061584
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author Mau, Robert
Eickner, Thomas
Jüttner, Gábor
Gao, Ziwen
Wei, Chunjiang
Fiedler, Nicklas
Senz, Volkmar
Lenarz, Thomas
Grabow, Niels
Scheper, Verena
Seitz, Hermann
author_facet Mau, Robert
Eickner, Thomas
Jüttner, Gábor
Gao, Ziwen
Wei, Chunjiang
Fiedler, Nicklas
Senz, Volkmar
Lenarz, Thomas
Grabow, Niels
Scheper, Verena
Seitz, Hermann
author_sort Mau, Robert
collection PubMed
description A novel approach for the long-term medical treatment of the inner ear is the diffusion of drugs through the round window membrane from a patient-individualized, drug-eluting implant, which is inserted in the middle ear. In this study, drug-loaded (10 wt% Dexamethasone) guinea pig round window niche implants (GP-RNIs, ~1.30 mm × 0.95 mm × 0.60 mm) were manufactured with high precision via micro injection molding (µIM, T(mold) = 160 °C, crosslinking time of 120 s). Each implant has a handle (~3.00 mm × 1.00 mm × 0.30 mm) that can be used to hold the implant. A medical-grade silicone elastomer was used as implant material. Molds for µIM were 3D printed from a commercially available resin (T(G) = 84 °C) via a high-resolution DLP process (xy resolution of 32 µm, z resolution of 10 µm, 3D printing time of about 6 h). Drug release, biocompatibility, and bioefficacy of the GP-RNIs were investigated in vitro. GP-RNIs could be successfully produced. The wear of the molds due to thermal stress was observed. However, the molds are suitable for single use in the µIM process. About 10% of the drug load (8.2 ± 0.6 µg) was released after 6 weeks (medium: isotonic saline). The implants showed high biocompatibility over 28 days (lowest cell viability ~80%). Moreover, we found anti-inflammatory effects over 28 days in a TNF-α-reduction test. These results are promising for the development of long-term drug-releasing implants for human inner ear therapy.
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spelling pubmed-103019272023-06-29 Micro Injection Molding of Drug-Loaded Round Window Niche Implants for an Animal Model Using 3D-Printed Molds Mau, Robert Eickner, Thomas Jüttner, Gábor Gao, Ziwen Wei, Chunjiang Fiedler, Nicklas Senz, Volkmar Lenarz, Thomas Grabow, Niels Scheper, Verena Seitz, Hermann Pharmaceutics Article A novel approach for the long-term medical treatment of the inner ear is the diffusion of drugs through the round window membrane from a patient-individualized, drug-eluting implant, which is inserted in the middle ear. In this study, drug-loaded (10 wt% Dexamethasone) guinea pig round window niche implants (GP-RNIs, ~1.30 mm × 0.95 mm × 0.60 mm) were manufactured with high precision via micro injection molding (µIM, T(mold) = 160 °C, crosslinking time of 120 s). Each implant has a handle (~3.00 mm × 1.00 mm × 0.30 mm) that can be used to hold the implant. A medical-grade silicone elastomer was used as implant material. Molds for µIM were 3D printed from a commercially available resin (T(G) = 84 °C) via a high-resolution DLP process (xy resolution of 32 µm, z resolution of 10 µm, 3D printing time of about 6 h). Drug release, biocompatibility, and bioefficacy of the GP-RNIs were investigated in vitro. GP-RNIs could be successfully produced. The wear of the molds due to thermal stress was observed. However, the molds are suitable for single use in the µIM process. About 10% of the drug load (8.2 ± 0.6 µg) was released after 6 weeks (medium: isotonic saline). The implants showed high biocompatibility over 28 days (lowest cell viability ~80%). Moreover, we found anti-inflammatory effects over 28 days in a TNF-α-reduction test. These results are promising for the development of long-term drug-releasing implants for human inner ear therapy. MDPI 2023-05-24 /pmc/articles/PMC10301927/ /pubmed/37376033 http://dx.doi.org/10.3390/pharmaceutics15061584 Text en © 2023 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
Mau, Robert
Eickner, Thomas
Jüttner, Gábor
Gao, Ziwen
Wei, Chunjiang
Fiedler, Nicklas
Senz, Volkmar
Lenarz, Thomas
Grabow, Niels
Scheper, Verena
Seitz, Hermann
Micro Injection Molding of Drug-Loaded Round Window Niche Implants for an Animal Model Using 3D-Printed Molds
title Micro Injection Molding of Drug-Loaded Round Window Niche Implants for an Animal Model Using 3D-Printed Molds
title_full Micro Injection Molding of Drug-Loaded Round Window Niche Implants for an Animal Model Using 3D-Printed Molds
title_fullStr Micro Injection Molding of Drug-Loaded Round Window Niche Implants for an Animal Model Using 3D-Printed Molds
title_full_unstemmed Micro Injection Molding of Drug-Loaded Round Window Niche Implants for an Animal Model Using 3D-Printed Molds
title_short Micro Injection Molding of Drug-Loaded Round Window Niche Implants for an Animal Model Using 3D-Printed Molds
title_sort micro injection molding of drug-loaded round window niche implants for an animal model using 3d-printed molds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301927/
https://www.ncbi.nlm.nih.gov/pubmed/37376033
http://dx.doi.org/10.3390/pharmaceutics15061584
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