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Interaction between porous silica gel microcarriers and peptides for oral administration of functional peptides
Functional peptides, peptides that have biological activities, have attracted attention as active ingredients of functional foods and health foods. In particular, for food applications, because orally ingested peptides are degraded by digestive enzymes in the stomach, novel oral administration metho...
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/PMC6054636/ https://www.ncbi.nlm.nih.gov/pubmed/30030485 http://dx.doi.org/10.1038/s41598-018-29345-2 |
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author | Imai, Kento Shimizu, Kazunori Kamimura, Mitsuhiro Honda, Hiroyuki |
author_facet | Imai, Kento Shimizu, Kazunori Kamimura, Mitsuhiro Honda, Hiroyuki |
author_sort | Imai, Kento |
collection | PubMed |
description | Functional peptides, peptides that have biological activities, have attracted attention as active ingredients of functional foods and health foods. In particular, for food applications, because orally ingested peptides are degraded by digestive enzymes in the stomach, novel oral administration methods that can prevent peptide degradation and successfully deliver them intestinally are desired. In the present study, we focused on porous silica gel, which has many useful characteristics, such as large surface area, pH responsive functional groups, size controllable pores, and approval as food additives. We investigated the possibility of using porous silica gel as a peptide degradation protective microcarrier. As a result, we found that heat treatment of the silica gel at 600 °C for 2 h remarkably enhanced the adsorbed amount of many peptides under acidic conditions, and negatively charged and highly hydrophobic peptides had suitable characteristics for oral intestinal delivery with silica gel. Finally, we demonstrated the degree of protection from pepsin degradation and found that the protection of DFELEDD peptide was 57.1 ± 3.9% when DFELEDD was mixed with the heat-treated silica gel. These results indicated that the heat-treated silica gel is promising for efficient oral intestinal delivery of hydrophobic negatively charged peptides. |
format | Online Article Text |
id | pubmed-6054636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60546362018-07-23 Interaction between porous silica gel microcarriers and peptides for oral administration of functional peptides Imai, Kento Shimizu, Kazunori Kamimura, Mitsuhiro Honda, Hiroyuki Sci Rep Article Functional peptides, peptides that have biological activities, have attracted attention as active ingredients of functional foods and health foods. In particular, for food applications, because orally ingested peptides are degraded by digestive enzymes in the stomach, novel oral administration methods that can prevent peptide degradation and successfully deliver them intestinally are desired. In the present study, we focused on porous silica gel, which has many useful characteristics, such as large surface area, pH responsive functional groups, size controllable pores, and approval as food additives. We investigated the possibility of using porous silica gel as a peptide degradation protective microcarrier. As a result, we found that heat treatment of the silica gel at 600 °C for 2 h remarkably enhanced the adsorbed amount of many peptides under acidic conditions, and negatively charged and highly hydrophobic peptides had suitable characteristics for oral intestinal delivery with silica gel. Finally, we demonstrated the degree of protection from pepsin degradation and found that the protection of DFELEDD peptide was 57.1 ± 3.9% when DFELEDD was mixed with the heat-treated silica gel. These results indicated that the heat-treated silica gel is promising for efficient oral intestinal delivery of hydrophobic negatively charged peptides. Nature Publishing Group UK 2018-07-20 /pmc/articles/PMC6054636/ /pubmed/30030485 http://dx.doi.org/10.1038/s41598-018-29345-2 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 Imai, Kento Shimizu, Kazunori Kamimura, Mitsuhiro Honda, Hiroyuki Interaction between porous silica gel microcarriers and peptides for oral administration of functional peptides |
title | Interaction between porous silica gel microcarriers and peptides for oral administration of functional peptides |
title_full | Interaction between porous silica gel microcarriers and peptides for oral administration of functional peptides |
title_fullStr | Interaction between porous silica gel microcarriers and peptides for oral administration of functional peptides |
title_full_unstemmed | Interaction between porous silica gel microcarriers and peptides for oral administration of functional peptides |
title_short | Interaction between porous silica gel microcarriers and peptides for oral administration of functional peptides |
title_sort | interaction between porous silica gel microcarriers and peptides for oral administration of functional peptides |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054636/ https://www.ncbi.nlm.nih.gov/pubmed/30030485 http://dx.doi.org/10.1038/s41598-018-29345-2 |
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