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Exendin-4–encapsulated dissolving microneedle arrays for efficient treatment of type 2 diabetes
Dissolving microneedles (DMNs) are microscopic needles capable of delivering encapsulated compounds and releasing them into the skin in a minimally invasive manner. Most studies indicate that encapsulating therapeutics in DMNs is an efficacious approach; however, the importance of evaluating the act...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773556/ https://www.ncbi.nlm.nih.gov/pubmed/29348573 http://dx.doi.org/10.1038/s41598-018-19789-x |
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author | Fakhraei Lahiji, Shayan Jang, Yoojung Huh, Inyoung Yang, Huisuk Jang, Mingyu Jung, Hyungil |
author_facet | Fakhraei Lahiji, Shayan Jang, Yoojung Huh, Inyoung Yang, Huisuk Jang, Mingyu Jung, Hyungil |
author_sort | Fakhraei Lahiji, Shayan |
collection | PubMed |
description | Dissolving microneedles (DMNs) are microscopic needles capable of delivering encapsulated compounds and releasing them into the skin in a minimally invasive manner. Most studies indicate that encapsulating therapeutics in DMNs is an efficacious approach; however, the importance of evaluating the activity of encapsulated compounds, during the fabrication process, has not been examined in detail. Conducting an analysis of thermal, chemical, and physical stress factors, including temperature, pH, and the interaction of the polymer and therapeutics mixture during preparation, is essential for retaining the activity of encapsulated therapeutics during and after fabrication. Here, we optimised the thermal, chemical, and physical parameters for the fabrication of exendin-4 (Ex-4)–encapsulated DMNs (Ex-4 DMNs). Ex-4, a peptide agonist of glucagon-like peptide (GLP) receptor, is used for glycaemic control in patients with type 2 diabetes. Our findings indicate that optimising the parameters involved in DMN fabrication retained the activity of Ex-4 by up to 98.3 ± 1.5%. Ex-4 DMNs reduced the blood-glucose level in diabetic mice with efficiency similar to that of a subcutaneous injection. We believe that this study paves way for the commercialisation of an efficient and minimally invasive treatment for patients with type 2 diabetes. |
format | Online Article Text |
id | pubmed-5773556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57735562018-01-26 Exendin-4–encapsulated dissolving microneedle arrays for efficient treatment of type 2 diabetes Fakhraei Lahiji, Shayan Jang, Yoojung Huh, Inyoung Yang, Huisuk Jang, Mingyu Jung, Hyungil Sci Rep Article Dissolving microneedles (DMNs) are microscopic needles capable of delivering encapsulated compounds and releasing them into the skin in a minimally invasive manner. Most studies indicate that encapsulating therapeutics in DMNs is an efficacious approach; however, the importance of evaluating the activity of encapsulated compounds, during the fabrication process, has not been examined in detail. Conducting an analysis of thermal, chemical, and physical stress factors, including temperature, pH, and the interaction of the polymer and therapeutics mixture during preparation, is essential for retaining the activity of encapsulated therapeutics during and after fabrication. Here, we optimised the thermal, chemical, and physical parameters for the fabrication of exendin-4 (Ex-4)–encapsulated DMNs (Ex-4 DMNs). Ex-4, a peptide agonist of glucagon-like peptide (GLP) receptor, is used for glycaemic control in patients with type 2 diabetes. Our findings indicate that optimising the parameters involved in DMN fabrication retained the activity of Ex-4 by up to 98.3 ± 1.5%. Ex-4 DMNs reduced the blood-glucose level in diabetic mice with efficiency similar to that of a subcutaneous injection. We believe that this study paves way for the commercialisation of an efficient and minimally invasive treatment for patients with type 2 diabetes. Nature Publishing Group UK 2018-01-18 /pmc/articles/PMC5773556/ /pubmed/29348573 http://dx.doi.org/10.1038/s41598-018-19789-x Text en © The Author(s) 2018 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 Fakhraei Lahiji, Shayan Jang, Yoojung Huh, Inyoung Yang, Huisuk Jang, Mingyu Jung, Hyungil Exendin-4–encapsulated dissolving microneedle arrays for efficient treatment of type 2 diabetes |
title | Exendin-4–encapsulated dissolving microneedle arrays for efficient treatment of type 2 diabetes |
title_full | Exendin-4–encapsulated dissolving microneedle arrays for efficient treatment of type 2 diabetes |
title_fullStr | Exendin-4–encapsulated dissolving microneedle arrays for efficient treatment of type 2 diabetes |
title_full_unstemmed | Exendin-4–encapsulated dissolving microneedle arrays for efficient treatment of type 2 diabetes |
title_short | Exendin-4–encapsulated dissolving microneedle arrays for efficient treatment of type 2 diabetes |
title_sort | exendin-4–encapsulated dissolving microneedle arrays for efficient treatment of type 2 diabetes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773556/ https://www.ncbi.nlm.nih.gov/pubmed/29348573 http://dx.doi.org/10.1038/s41598-018-19789-x |
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