Cargando…
Electrofluidic control of bioactive molecule delivery into soft tissue models based on gelatin methacryloyl hydrogels using threads and surgical sutures
The delivery of bioactive molecules (drugs) with control over spatial distribution remains a challenge. Herein, we demonstrate for the first time an electrofluidic approach to controlled delivery into soft tissue models based on gelatin methacryloyl (GelMA) hydrogels. This was achieved using a surgi...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188853/ https://www.ncbi.nlm.nih.gov/pubmed/32345999 http://dx.doi.org/10.1038/s41598-020-63785-z |
_version_ | 1783527382400892928 |
---|---|
author | Cabot, Joan M. Daikuara, Luciana Y. Yue, Zhilian Hayes, Patricia Liu, Xiao Wallace, Gordon G. Paull, Brett |
author_facet | Cabot, Joan M. Daikuara, Luciana Y. Yue, Zhilian Hayes, Patricia Liu, Xiao Wallace, Gordon G. Paull, Brett |
author_sort | Cabot, Joan M. |
collection | PubMed |
description | The delivery of bioactive molecules (drugs) with control over spatial distribution remains a challenge. Herein, we demonstrate for the first time an electrofluidic approach to controlled delivery into soft tissue models based on gelatin methacryloyl (GelMA) hydrogels. This was achieved using a surgical suture, whereby transport of bioactive molecules, including drugs and proteins, was controlled by imposition of an electric field. Commonly employed surgical sutures or acrylic threads were integrated through the hydrogels to facilitate the directed introduction of bioactive species. The platform consisted of two reservoirs into which the ends of the thread were immersed. The anode and cathode were placed separately into each reservoir. The thread was taken from one reservoir to the other through the gel. When current was applied, biomolecules loaded onto the thread were directed into the gel. Under the same conditions, the rate of movement of the biomolecules along GelMA was dependent on the magnitude of the current. Using 5% GelMA and a current of 100 µA, 2 uL of fluorescein travelled through the hydrogel at a constant velocity of 7.17 ± 0.50 um/s and took less than 8 minutes to exit on the thread. Small molecules such as riboflavin migrated faster (5.99 ± 0.40 μm/s) than larger molecules such as dextran (2.26 ± 0.55 μm/s with 4 kDa) or BSA (0.33 ± 0.07 μm/s with 66.5 kDa). A number of commercial surgical sutures were tested and found to accommodate the controlled movement of biomolecules. Polyester, polyglactin 910, glycolide/lactide copolymer and polyglycolic acid braided sutures created adequate fluid connection between the electrodes and the hydrogel. With a view to application in skin inflammatory diseases and wound treatment, wound healing, slow and controlled delivery of dexamethasone 21-phosphate disodium salt (DSP), an anti-inflammatory prodrug, was achieved using medical surgicryl PGA absorbable suture. After 2 hours of electrical stimulation, still 81.1% of the drug loaded was encapsulated within the hydrogel. |
format | Online Article Text |
id | pubmed-7188853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71888532020-05-04 Electrofluidic control of bioactive molecule delivery into soft tissue models based on gelatin methacryloyl hydrogels using threads and surgical sutures Cabot, Joan M. Daikuara, Luciana Y. Yue, Zhilian Hayes, Patricia Liu, Xiao Wallace, Gordon G. Paull, Brett Sci Rep Article The delivery of bioactive molecules (drugs) with control over spatial distribution remains a challenge. Herein, we demonstrate for the first time an electrofluidic approach to controlled delivery into soft tissue models based on gelatin methacryloyl (GelMA) hydrogels. This was achieved using a surgical suture, whereby transport of bioactive molecules, including drugs and proteins, was controlled by imposition of an electric field. Commonly employed surgical sutures or acrylic threads were integrated through the hydrogels to facilitate the directed introduction of bioactive species. The platform consisted of two reservoirs into which the ends of the thread were immersed. The anode and cathode were placed separately into each reservoir. The thread was taken from one reservoir to the other through the gel. When current was applied, biomolecules loaded onto the thread were directed into the gel. Under the same conditions, the rate of movement of the biomolecules along GelMA was dependent on the magnitude of the current. Using 5% GelMA and a current of 100 µA, 2 uL of fluorescein travelled through the hydrogel at a constant velocity of 7.17 ± 0.50 um/s and took less than 8 minutes to exit on the thread. Small molecules such as riboflavin migrated faster (5.99 ± 0.40 μm/s) than larger molecules such as dextran (2.26 ± 0.55 μm/s with 4 kDa) or BSA (0.33 ± 0.07 μm/s with 66.5 kDa). A number of commercial surgical sutures were tested and found to accommodate the controlled movement of biomolecules. Polyester, polyglactin 910, glycolide/lactide copolymer and polyglycolic acid braided sutures created adequate fluid connection between the electrodes and the hydrogel. With a view to application in skin inflammatory diseases and wound treatment, wound healing, slow and controlled delivery of dexamethasone 21-phosphate disodium salt (DSP), an anti-inflammatory prodrug, was achieved using medical surgicryl PGA absorbable suture. After 2 hours of electrical stimulation, still 81.1% of the drug loaded was encapsulated within the hydrogel. Nature Publishing Group UK 2020-04-28 /pmc/articles/PMC7188853/ /pubmed/32345999 http://dx.doi.org/10.1038/s41598-020-63785-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cabot, Joan M. Daikuara, Luciana Y. Yue, Zhilian Hayes, Patricia Liu, Xiao Wallace, Gordon G. Paull, Brett Electrofluidic control of bioactive molecule delivery into soft tissue models based on gelatin methacryloyl hydrogels using threads and surgical sutures |
title | Electrofluidic control of bioactive molecule delivery into soft tissue models based on gelatin methacryloyl hydrogels using threads and surgical sutures |
title_full | Electrofluidic control of bioactive molecule delivery into soft tissue models based on gelatin methacryloyl hydrogels using threads and surgical sutures |
title_fullStr | Electrofluidic control of bioactive molecule delivery into soft tissue models based on gelatin methacryloyl hydrogels using threads and surgical sutures |
title_full_unstemmed | Electrofluidic control of bioactive molecule delivery into soft tissue models based on gelatin methacryloyl hydrogels using threads and surgical sutures |
title_short | Electrofluidic control of bioactive molecule delivery into soft tissue models based on gelatin methacryloyl hydrogels using threads and surgical sutures |
title_sort | electrofluidic control of bioactive molecule delivery into soft tissue models based on gelatin methacryloyl hydrogels using threads and surgical sutures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188853/ https://www.ncbi.nlm.nih.gov/pubmed/32345999 http://dx.doi.org/10.1038/s41598-020-63785-z |
work_keys_str_mv | AT cabotjoanm electrofluidiccontrolofbioactivemoleculedeliveryintosofttissuemodelsbasedongelatinmethacryloylhydrogelsusingthreadsandsurgicalsutures AT daikuaralucianay electrofluidiccontrolofbioactivemoleculedeliveryintosofttissuemodelsbasedongelatinmethacryloylhydrogelsusingthreadsandsurgicalsutures AT yuezhilian electrofluidiccontrolofbioactivemoleculedeliveryintosofttissuemodelsbasedongelatinmethacryloylhydrogelsusingthreadsandsurgicalsutures AT hayespatricia electrofluidiccontrolofbioactivemoleculedeliveryintosofttissuemodelsbasedongelatinmethacryloylhydrogelsusingthreadsandsurgicalsutures AT liuxiao electrofluidiccontrolofbioactivemoleculedeliveryintosofttissuemodelsbasedongelatinmethacryloylhydrogelsusingthreadsandsurgicalsutures AT wallacegordong electrofluidiccontrolofbioactivemoleculedeliveryintosofttissuemodelsbasedongelatinmethacryloylhydrogelsusingthreadsandsurgicalsutures AT paullbrett electrofluidiccontrolofbioactivemoleculedeliveryintosofttissuemodelsbasedongelatinmethacryloylhydrogelsusingthreadsandsurgicalsutures |