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Smart Microneedles with Porous Polymer Layer for Glucose-Responsive Insulin Delivery

A closed-loop system imitating the function of pancreatic cells, connected to microneedles (MNs) that automatically “release” insulin in response to the blood glucose (BG) levels would be highly satisfactory for improving the quality of life and health for diabetes patients. This paper describes an...

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Autores principales: Ullah, Asad, Choi, Hye Jin, Jang, Mijin, An, Sanghyun, Kim, Gyu Man
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407179/
https://www.ncbi.nlm.nih.gov/pubmed/32629825
http://dx.doi.org/10.3390/pharmaceutics12070606
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author Ullah, Asad
Choi, Hye Jin
Jang, Mijin
An, Sanghyun
Kim, Gyu Man
author_facet Ullah, Asad
Choi, Hye Jin
Jang, Mijin
An, Sanghyun
Kim, Gyu Man
author_sort Ullah, Asad
collection PubMed
description A closed-loop system imitating the function of pancreatic cells, connected to microneedles (MNs) that automatically “release” insulin in response to the blood glucose (BG) levels would be highly satisfactory for improving the quality of life and health for diabetes patients. This paper describes an easy, fast and simple technique of coating a porous polymer layer on stainless steel (SS) MNs that release insulin in a glucose-responsive fashion. It was fabricated by sealing insulin, sodium bicarbonate (a pH-sensitive element [NaHCO(3)]) and glucose oxidase (glucose-specific enzymes [GOx]) into the pores of a porous polymer coating. Glucose can passively diffuse into the pores and become oxidized to gluconic acid by GOx, thereby causing a decrease in local pH. The subsequent reaction of protons with NaHCO(3) forms carbon dioxide (CO(2)) which creates pressure inside the pores, thereby rupturing the thin polymer film and releasing the encapsulated insulin. Field emission scanning electron microscopy (FE-SEM) images displayed that upon the exposure of MNs to glucose-free phosphate buffer saline (PBS) with pH 7.4, the pores of the porous MNs were closed, while in MNs exposed to a hyperglycemic glucose level, the pores were opened and the thin film burst. These MNs demonstrated both in vitro (in porcine skin and PBS) and in vivo (in diabetic rats) glucose-mediated insulin release under hyperglycemic conditions with rapid responsiveness. This study validated that the release of insulin from porous MNs was effectively correlated with glucose concentration.
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spelling pubmed-74071792020-08-11 Smart Microneedles with Porous Polymer Layer for Glucose-Responsive Insulin Delivery Ullah, Asad Choi, Hye Jin Jang, Mijin An, Sanghyun Kim, Gyu Man Pharmaceutics Article A closed-loop system imitating the function of pancreatic cells, connected to microneedles (MNs) that automatically “release” insulin in response to the blood glucose (BG) levels would be highly satisfactory for improving the quality of life and health for diabetes patients. This paper describes an easy, fast and simple technique of coating a porous polymer layer on stainless steel (SS) MNs that release insulin in a glucose-responsive fashion. It was fabricated by sealing insulin, sodium bicarbonate (a pH-sensitive element [NaHCO(3)]) and glucose oxidase (glucose-specific enzymes [GOx]) into the pores of a porous polymer coating. Glucose can passively diffuse into the pores and become oxidized to gluconic acid by GOx, thereby causing a decrease in local pH. The subsequent reaction of protons with NaHCO(3) forms carbon dioxide (CO(2)) which creates pressure inside the pores, thereby rupturing the thin polymer film and releasing the encapsulated insulin. Field emission scanning electron microscopy (FE-SEM) images displayed that upon the exposure of MNs to glucose-free phosphate buffer saline (PBS) with pH 7.4, the pores of the porous MNs were closed, while in MNs exposed to a hyperglycemic glucose level, the pores were opened and the thin film burst. These MNs demonstrated both in vitro (in porcine skin and PBS) and in vivo (in diabetic rats) glucose-mediated insulin release under hyperglycemic conditions with rapid responsiveness. This study validated that the release of insulin from porous MNs was effectively correlated with glucose concentration. MDPI 2020-06-30 /pmc/articles/PMC7407179/ /pubmed/32629825 http://dx.doi.org/10.3390/pharmaceutics12070606 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ullah, Asad
Choi, Hye Jin
Jang, Mijin
An, Sanghyun
Kim, Gyu Man
Smart Microneedles with Porous Polymer Layer for Glucose-Responsive Insulin Delivery
title Smart Microneedles with Porous Polymer Layer for Glucose-Responsive Insulin Delivery
title_full Smart Microneedles with Porous Polymer Layer for Glucose-Responsive Insulin Delivery
title_fullStr Smart Microneedles with Porous Polymer Layer for Glucose-Responsive Insulin Delivery
title_full_unstemmed Smart Microneedles with Porous Polymer Layer for Glucose-Responsive Insulin Delivery
title_short Smart Microneedles with Porous Polymer Layer for Glucose-Responsive Insulin Delivery
title_sort smart microneedles with porous polymer layer for glucose-responsive insulin delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407179/
https://www.ncbi.nlm.nih.gov/pubmed/32629825
http://dx.doi.org/10.3390/pharmaceutics12070606
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