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Enhanced oral delivery of insulin via the colon-targeted nanocomposite system of organoclay/glycol chitosan/Eudragit(®)S100
This study aimed to develop a ternary nanocomposite system of organoclay, glycol-chitosan, and Eudragit(®)S100 as an effective colon targeted drug delivery carrier to enhance the oral absorption of insulin. A nanocomplex of insulin and aminoclay was prepared via spontaneous co-assembly, which was th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382030/ https://www.ncbi.nlm.nih.gov/pubmed/32711522 http://dx.doi.org/10.1186/s12951-020-00662-x |
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author | Lee, Sang Hoon Back, Seung-Yun Song, Jae Geun Han, Hyo-Kyung |
author_facet | Lee, Sang Hoon Back, Seung-Yun Song, Jae Geun Han, Hyo-Kyung |
author_sort | Lee, Sang Hoon |
collection | PubMed |
description | This study aimed to develop a ternary nanocomposite system of organoclay, glycol-chitosan, and Eudragit(®)S100 as an effective colon targeted drug delivery carrier to enhance the oral absorption of insulin. A nanocomplex of insulin and aminoclay was prepared via spontaneous co-assembly, which was then coated with glycol-chitosan and Eudragit S(®)100 (EGAC-Ins). The double coated nanocomplex, EGAC-Ins demonstrated a high entrapment efficiency of greater than 90% and a pH-dependent drug release. The conformational stability of insulin entrapped in EGAC-Ins was effectively maintained in the presence of proteolytic enzymes. When compared to a free insulin solution, EGAC-Ins enhanced drug permeability by approximately sevenfold in Caco-2 cells and enhanced colonic drug absorption in rats. Accordingly, oral EGAC-Ins significantly reduced blood glucose levels in diabetic rats while the hypoglycemic effect of an oral insulin solution was negligible. In conclusion, EGAC-Ins should be a promising colonic delivery system for improving the oral absorption of insulin. |
format | Online Article Text |
id | pubmed-7382030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73820302020-07-27 Enhanced oral delivery of insulin via the colon-targeted nanocomposite system of organoclay/glycol chitosan/Eudragit(®)S100 Lee, Sang Hoon Back, Seung-Yun Song, Jae Geun Han, Hyo-Kyung J Nanobiotechnology Research This study aimed to develop a ternary nanocomposite system of organoclay, glycol-chitosan, and Eudragit(®)S100 as an effective colon targeted drug delivery carrier to enhance the oral absorption of insulin. A nanocomplex of insulin and aminoclay was prepared via spontaneous co-assembly, which was then coated with glycol-chitosan and Eudragit S(®)100 (EGAC-Ins). The double coated nanocomplex, EGAC-Ins demonstrated a high entrapment efficiency of greater than 90% and a pH-dependent drug release. The conformational stability of insulin entrapped in EGAC-Ins was effectively maintained in the presence of proteolytic enzymes. When compared to a free insulin solution, EGAC-Ins enhanced drug permeability by approximately sevenfold in Caco-2 cells and enhanced colonic drug absorption in rats. Accordingly, oral EGAC-Ins significantly reduced blood glucose levels in diabetic rats while the hypoglycemic effect of an oral insulin solution was negligible. In conclusion, EGAC-Ins should be a promising colonic delivery system for improving the oral absorption of insulin. BioMed Central 2020-07-25 /pmc/articles/PMC7382030/ /pubmed/32711522 http://dx.doi.org/10.1186/s12951-020-00662-x Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Lee, Sang Hoon Back, Seung-Yun Song, Jae Geun Han, Hyo-Kyung Enhanced oral delivery of insulin via the colon-targeted nanocomposite system of organoclay/glycol chitosan/Eudragit(®)S100 |
title | Enhanced oral delivery of insulin via the colon-targeted nanocomposite system of organoclay/glycol chitosan/Eudragit(®)S100 |
title_full | Enhanced oral delivery of insulin via the colon-targeted nanocomposite system of organoclay/glycol chitosan/Eudragit(®)S100 |
title_fullStr | Enhanced oral delivery of insulin via the colon-targeted nanocomposite system of organoclay/glycol chitosan/Eudragit(®)S100 |
title_full_unstemmed | Enhanced oral delivery of insulin via the colon-targeted nanocomposite system of organoclay/glycol chitosan/Eudragit(®)S100 |
title_short | Enhanced oral delivery of insulin via the colon-targeted nanocomposite system of organoclay/glycol chitosan/Eudragit(®)S100 |
title_sort | enhanced oral delivery of insulin via the colon-targeted nanocomposite system of organoclay/glycol chitosan/eudragit(®)s100 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382030/ https://www.ncbi.nlm.nih.gov/pubmed/32711522 http://dx.doi.org/10.1186/s12951-020-00662-x |
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