Cargando…
PLLA Coating of Active Implants for Dual Drug Release
Cochlear implants, like other active implants, rely on precise and effective electrical stimulation of the target tissue but become encapsulated by different amounts of fibrous tissue. The current study aimed at the development of a dual drug release from a PLLA coating and from the bulk material to...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875406/ https://www.ncbi.nlm.nih.gov/pubmed/35209205 http://dx.doi.org/10.3390/molecules27041417 |
_version_ | 1784657904582787072 |
---|---|
author | Wulf, Katharina Goblet, Madeleine Raggl, Stefan Teske, Michael Eickner, Thomas Lenarz, Thomas Grabow, Niels Paasche, Gerrit |
author_facet | Wulf, Katharina Goblet, Madeleine Raggl, Stefan Teske, Michael Eickner, Thomas Lenarz, Thomas Grabow, Niels Paasche, Gerrit |
author_sort | Wulf, Katharina |
collection | PubMed |
description | Cochlear implants, like other active implants, rely on precise and effective electrical stimulation of the target tissue but become encapsulated by different amounts of fibrous tissue. The current study aimed at the development of a dual drug release from a PLLA coating and from the bulk material to address short-term and long-lasting release of anti-inflammatory drugs. Inner-ear cytocompatibility of drugs was studied in vitro. A PLLA coating (containing diclofenac) of medical-grade silicone (containing 5% dexamethasone) was developed and release profiles were determined. The influence of different coating thicknesses (2.5, 5 and 10 µm) and loadings (10% and 20% diclofenac) on impedances of electrical contacts were measured with and without pulsatile electrical stimulation. Diclofenac can be applied to the inner ear at concentrations of or below 4 × 10(−5) mol/L. Release of dexamethasone from the silicone is diminished by surface coating but not blocked. Addition of 20% diclofenac enhances the dexamethasone release again. All PLLA coatings serve as insulator. This can be overcome by using removable masking on the contacts during the coating process. Dual drug release with different kinetics can be realized by adding drug-loaded coatings to drug-loaded silicone arrays without compromising electrical stimulation. |
format | Online Article Text |
id | pubmed-8875406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88754062022-02-26 PLLA Coating of Active Implants for Dual Drug Release Wulf, Katharina Goblet, Madeleine Raggl, Stefan Teske, Michael Eickner, Thomas Lenarz, Thomas Grabow, Niels Paasche, Gerrit Molecules Article Cochlear implants, like other active implants, rely on precise and effective electrical stimulation of the target tissue but become encapsulated by different amounts of fibrous tissue. The current study aimed at the development of a dual drug release from a PLLA coating and from the bulk material to address short-term and long-lasting release of anti-inflammatory drugs. Inner-ear cytocompatibility of drugs was studied in vitro. A PLLA coating (containing diclofenac) of medical-grade silicone (containing 5% dexamethasone) was developed and release profiles were determined. The influence of different coating thicknesses (2.5, 5 and 10 µm) and loadings (10% and 20% diclofenac) on impedances of electrical contacts were measured with and without pulsatile electrical stimulation. Diclofenac can be applied to the inner ear at concentrations of or below 4 × 10(−5) mol/L. Release of dexamethasone from the silicone is diminished by surface coating but not blocked. Addition of 20% diclofenac enhances the dexamethasone release again. All PLLA coatings serve as insulator. This can be overcome by using removable masking on the contacts during the coating process. Dual drug release with different kinetics can be realized by adding drug-loaded coatings to drug-loaded silicone arrays without compromising electrical stimulation. MDPI 2022-02-19 /pmc/articles/PMC8875406/ /pubmed/35209205 http://dx.doi.org/10.3390/molecules27041417 Text en © 2022 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 Wulf, Katharina Goblet, Madeleine Raggl, Stefan Teske, Michael Eickner, Thomas Lenarz, Thomas Grabow, Niels Paasche, Gerrit PLLA Coating of Active Implants for Dual Drug Release |
title | PLLA Coating of Active Implants for Dual Drug Release |
title_full | PLLA Coating of Active Implants for Dual Drug Release |
title_fullStr | PLLA Coating of Active Implants for Dual Drug Release |
title_full_unstemmed | PLLA Coating of Active Implants for Dual Drug Release |
title_short | PLLA Coating of Active Implants for Dual Drug Release |
title_sort | plla coating of active implants for dual drug release |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875406/ https://www.ncbi.nlm.nih.gov/pubmed/35209205 http://dx.doi.org/10.3390/molecules27041417 |
work_keys_str_mv | AT wulfkatharina pllacoatingofactiveimplantsfordualdrugrelease AT gobletmadeleine pllacoatingofactiveimplantsfordualdrugrelease AT ragglstefan pllacoatingofactiveimplantsfordualdrugrelease AT teskemichael pllacoatingofactiveimplantsfordualdrugrelease AT eicknerthomas pllacoatingofactiveimplantsfordualdrugrelease AT lenarzthomas pllacoatingofactiveimplantsfordualdrugrelease AT grabowniels pllacoatingofactiveimplantsfordualdrugrelease AT paaschegerrit pllacoatingofactiveimplantsfordualdrugrelease |