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Porous polymer coatings on metal microneedles for enhanced drug delivery
We present a simple method to coat microneedles (MNs) uniformly with a porous polymer (PLGA) that can deliver drugs at high rates. Stainless steel (SS) MNs of high mechanical strength were coated with a thin porous polymer layer to enhance their delivery rates. Additionally, to improve the interfaci...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5936903/ https://www.ncbi.nlm.nih.gov/pubmed/29765638 http://dx.doi.org/10.1098/rsos.171609 |
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author | Ullah, Asad Kim, Chul Min Kim, Gyu Man |
author_facet | Ullah, Asad Kim, Chul Min Kim, Gyu Man |
author_sort | Ullah, Asad |
collection | PubMed |
description | We present a simple method to coat microneedles (MNs) uniformly with a porous polymer (PLGA) that can deliver drugs at high rates. Stainless steel (SS) MNs of high mechanical strength were coated with a thin porous polymer layer to enhance their delivery rates. Additionally, to improve the interfacial adhesion between the polymer and MNs, the MN surface was modified by plasma treatment followed by dip coating with polyethyleneimine, a polymer with repeating amine units. The average failure load (the minimum force sufficient for detaching the polymer layer from the surface of SS) recorded for the modified surface coating was 25 N, whereas it was 2.2 N for the non-modified surface. Calcein dye was successfully delivered into porcine skin to a depth of 750 µm by the porous polymer-coated MNs, demonstrating that the developed MNs can pierce skin easily without deformation of MNs; additional skin penetration tests confirmed this finding. For visual comparison, rhodamine B dye was delivered using porous-coated and non-coated MNs in gelatin gel which showed that delivery with porous-coated MNs penetrate deeper when compared with non-coated MNs. Finally, lidocaine and rhodamine B dye were delivered in phosphate-buffered saline (PBS) medium by porous polymer-coated and non-coated MNs. For rhodamine B, drug delivery with the porous-coated MNs was five times higher than that with the non-coated MNs, whereas 25 times more lidocaine was delivered by the porous-coated MNs compared with the non-coated MNs. |
format | Online Article Text |
id | pubmed-5936903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-59369032018-05-15 Porous polymer coatings on metal microneedles for enhanced drug delivery Ullah, Asad Kim, Chul Min Kim, Gyu Man R Soc Open Sci Engineering We present a simple method to coat microneedles (MNs) uniformly with a porous polymer (PLGA) that can deliver drugs at high rates. Stainless steel (SS) MNs of high mechanical strength were coated with a thin porous polymer layer to enhance their delivery rates. Additionally, to improve the interfacial adhesion between the polymer and MNs, the MN surface was modified by plasma treatment followed by dip coating with polyethyleneimine, a polymer with repeating amine units. The average failure load (the minimum force sufficient for detaching the polymer layer from the surface of SS) recorded for the modified surface coating was 25 N, whereas it was 2.2 N for the non-modified surface. Calcein dye was successfully delivered into porcine skin to a depth of 750 µm by the porous polymer-coated MNs, demonstrating that the developed MNs can pierce skin easily without deformation of MNs; additional skin penetration tests confirmed this finding. For visual comparison, rhodamine B dye was delivered using porous-coated and non-coated MNs in gelatin gel which showed that delivery with porous-coated MNs penetrate deeper when compared with non-coated MNs. Finally, lidocaine and rhodamine B dye were delivered in phosphate-buffered saline (PBS) medium by porous polymer-coated and non-coated MNs. For rhodamine B, drug delivery with the porous-coated MNs was five times higher than that with the non-coated MNs, whereas 25 times more lidocaine was delivered by the porous-coated MNs compared with the non-coated MNs. The Royal Society Publishing 2018-04-18 /pmc/articles/PMC5936903/ /pubmed/29765638 http://dx.doi.org/10.1098/rsos.171609 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Engineering Ullah, Asad Kim, Chul Min Kim, Gyu Man Porous polymer coatings on metal microneedles for enhanced drug delivery |
title | Porous polymer coatings on metal microneedles for enhanced drug delivery |
title_full | Porous polymer coatings on metal microneedles for enhanced drug delivery |
title_fullStr | Porous polymer coatings on metal microneedles for enhanced drug delivery |
title_full_unstemmed | Porous polymer coatings on metal microneedles for enhanced drug delivery |
title_short | Porous polymer coatings on metal microneedles for enhanced drug delivery |
title_sort | porous polymer coatings on metal microneedles for enhanced drug delivery |
topic | Engineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5936903/ https://www.ncbi.nlm.nih.gov/pubmed/29765638 http://dx.doi.org/10.1098/rsos.171609 |
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