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Microneedle-array patches loaded with dual mineralized protein/peptide particles for type 2 diabetes therapy
The delivery of therapeutic peptides for diabetes therapy is compromised by short half-lives of drugs with the consequent need for multiple daily injections that reduce patient compliance and increase treatment cost. In this study, we demonstrate a smart exendin-4 (Ex4) delivery device based on micr...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701150/ https://www.ncbi.nlm.nih.gov/pubmed/29176623 http://dx.doi.org/10.1038/s41467-017-01764-1 |
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author | Chen, Wei Tian, Rui Xu, Can Yung, Bryant C. Wang, Guohao Liu, Yijing Ni, Qianqian Zhang, Fuwu Zhou, Zijian Wang, Jingjing Niu, Gang Ma, Ying Fu, Liwu Chen, Xiaoyuan |
author_facet | Chen, Wei Tian, Rui Xu, Can Yung, Bryant C. Wang, Guohao Liu, Yijing Ni, Qianqian Zhang, Fuwu Zhou, Zijian Wang, Jingjing Niu, Gang Ma, Ying Fu, Liwu Chen, Xiaoyuan |
author_sort | Chen, Wei |
collection | PubMed |
description | The delivery of therapeutic peptides for diabetes therapy is compromised by short half-lives of drugs with the consequent need for multiple daily injections that reduce patient compliance and increase treatment cost. In this study, we demonstrate a smart exendin-4 (Ex4) delivery device based on microneedle (MN)-array patches integrated with dual mineralized particles separately containing Ex4 and glucose oxidase (GOx). The dual mineralized particle-based system can specifically release Ex4 while immobilizing GOx as a result of the differential response to the microenvironment induced by biological stimuli. In this manner, the system enables glucose-responsive and closed-loop release to significantly improve Ex4 therapeutic performance. Moreover, integration of mineralized particles can enhance the mechanical strength of alginate-based MN by crosslinking to facilitate skin penetration, thus supporting painless and non-invasive transdermal administration. We believe this smart glucose-responsive Ex4 delivery holds great promise for type 2 diabetes therapy by providing safe, long-term, and on-demand Ex4 therapy. |
format | Online Article Text |
id | pubmed-5701150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57011502017-11-27 Microneedle-array patches loaded with dual mineralized protein/peptide particles for type 2 diabetes therapy Chen, Wei Tian, Rui Xu, Can Yung, Bryant C. Wang, Guohao Liu, Yijing Ni, Qianqian Zhang, Fuwu Zhou, Zijian Wang, Jingjing Niu, Gang Ma, Ying Fu, Liwu Chen, Xiaoyuan Nat Commun Article The delivery of therapeutic peptides for diabetes therapy is compromised by short half-lives of drugs with the consequent need for multiple daily injections that reduce patient compliance and increase treatment cost. In this study, we demonstrate a smart exendin-4 (Ex4) delivery device based on microneedle (MN)-array patches integrated with dual mineralized particles separately containing Ex4 and glucose oxidase (GOx). The dual mineralized particle-based system can specifically release Ex4 while immobilizing GOx as a result of the differential response to the microenvironment induced by biological stimuli. In this manner, the system enables glucose-responsive and closed-loop release to significantly improve Ex4 therapeutic performance. Moreover, integration of mineralized particles can enhance the mechanical strength of alginate-based MN by crosslinking to facilitate skin penetration, thus supporting painless and non-invasive transdermal administration. We believe this smart glucose-responsive Ex4 delivery holds great promise for type 2 diabetes therapy by providing safe, long-term, and on-demand Ex4 therapy. Nature Publishing Group UK 2017-11-24 /pmc/articles/PMC5701150/ /pubmed/29176623 http://dx.doi.org/10.1038/s41467-017-01764-1 Text en © The Author(s) 2017 Open AccessThis 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 Commonslicense, unless indicated otherwise in a credit line to the material. If material is not included in the article’sCreative 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, visithttp://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chen, Wei Tian, Rui Xu, Can Yung, Bryant C. Wang, Guohao Liu, Yijing Ni, Qianqian Zhang, Fuwu Zhou, Zijian Wang, Jingjing Niu, Gang Ma, Ying Fu, Liwu Chen, Xiaoyuan Microneedle-array patches loaded with dual mineralized protein/peptide particles for type 2 diabetes therapy |
title | Microneedle-array patches loaded with dual mineralized protein/peptide particles for type 2 diabetes therapy |
title_full | Microneedle-array patches loaded with dual mineralized protein/peptide particles for type 2 diabetes therapy |
title_fullStr | Microneedle-array patches loaded with dual mineralized protein/peptide particles for type 2 diabetes therapy |
title_full_unstemmed | Microneedle-array patches loaded with dual mineralized protein/peptide particles for type 2 diabetes therapy |
title_short | Microneedle-array patches loaded with dual mineralized protein/peptide particles for type 2 diabetes therapy |
title_sort | microneedle-array patches loaded with dual mineralized protein/peptide particles for type 2 diabetes therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701150/ https://www.ncbi.nlm.nih.gov/pubmed/29176623 http://dx.doi.org/10.1038/s41467-017-01764-1 |
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