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Polydeoxyribonucleotide-delivering therapeutic hydrogel for diabetic wound healing
Patients with diabetes experience delayed wound healing because of the uncontrolled glucose level in their bloodstream, which leads to impaired function of white blood cells, poor circulation, decreased production and repair of new blood vessels. Treatment using polydeoxyribonucleotide (PDRN), which...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546631/ https://www.ncbi.nlm.nih.gov/pubmed/33033366 http://dx.doi.org/10.1038/s41598-020-74004-0 |
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author | Shin, Da Yong Park, Ji-Ung Choi, Min-Ha Kim, Sukwha Kim, Hyoun-Ee Jeong, Seol-Ha |
author_facet | Shin, Da Yong Park, Ji-Ung Choi, Min-Ha Kim, Sukwha Kim, Hyoun-Ee Jeong, Seol-Ha |
author_sort | Shin, Da Yong |
collection | PubMed |
description | Patients with diabetes experience delayed wound healing because of the uncontrolled glucose level in their bloodstream, which leads to impaired function of white blood cells, poor circulation, decreased production and repair of new blood vessels. Treatment using polydeoxyribonucleotide (PDRN), which is a DNA extracted from the sperm cells of salmon, has been introduced to accelerate the healing process of diabetic wounds. To accelerate the wound-healing process, sustained delivery of PDRN is critical. In this study, taking advantage of the non-invasive gelation property of alginate, PDRN was loaded inside the hydrogel (Alg-PDRN). The release behavior of PDRN was altered by controlling the crosslinking density of the Alg hydrogel. The amount of PDRN was the greatest inside the hydrogel with the highest crosslinking density because of the decreased diffusion. However, there was an optimal degree of crosslinking for the effective release of PDRN. In vitro studies using human dermal fibroblasts and diabetes mellitus fibroblasts and an in ovo chorioallantoic membrane assay confirmed that the Alg-PDRN hydrogel effectively induced cell proliferation and expression of angiogenic growth factors and promoted new blood vessel formation. Its effectiveness for accelerated diabetic wound healing was also confirmed in an in-vivo animal experiment using a diabetic mouse model. |
format | Online Article Text |
id | pubmed-7546631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75466312020-10-14 Polydeoxyribonucleotide-delivering therapeutic hydrogel for diabetic wound healing Shin, Da Yong Park, Ji-Ung Choi, Min-Ha Kim, Sukwha Kim, Hyoun-Ee Jeong, Seol-Ha Sci Rep Article Patients with diabetes experience delayed wound healing because of the uncontrolled glucose level in their bloodstream, which leads to impaired function of white blood cells, poor circulation, decreased production and repair of new blood vessels. Treatment using polydeoxyribonucleotide (PDRN), which is a DNA extracted from the sperm cells of salmon, has been introduced to accelerate the healing process of diabetic wounds. To accelerate the wound-healing process, sustained delivery of PDRN is critical. In this study, taking advantage of the non-invasive gelation property of alginate, PDRN was loaded inside the hydrogel (Alg-PDRN). The release behavior of PDRN was altered by controlling the crosslinking density of the Alg hydrogel. The amount of PDRN was the greatest inside the hydrogel with the highest crosslinking density because of the decreased diffusion. However, there was an optimal degree of crosslinking for the effective release of PDRN. In vitro studies using human dermal fibroblasts and diabetes mellitus fibroblasts and an in ovo chorioallantoic membrane assay confirmed that the Alg-PDRN hydrogel effectively induced cell proliferation and expression of angiogenic growth factors and promoted new blood vessel formation. Its effectiveness for accelerated diabetic wound healing was also confirmed in an in-vivo animal experiment using a diabetic mouse model. Nature Publishing Group UK 2020-10-08 /pmc/articles/PMC7546631/ /pubmed/33033366 http://dx.doi.org/10.1038/s41598-020-74004-0 Text en © The Author(s) 2020 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 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/. |
spellingShingle | Article Shin, Da Yong Park, Ji-Ung Choi, Min-Ha Kim, Sukwha Kim, Hyoun-Ee Jeong, Seol-Ha Polydeoxyribonucleotide-delivering therapeutic hydrogel for diabetic wound healing |
title | Polydeoxyribonucleotide-delivering therapeutic hydrogel for diabetic wound healing |
title_full | Polydeoxyribonucleotide-delivering therapeutic hydrogel for diabetic wound healing |
title_fullStr | Polydeoxyribonucleotide-delivering therapeutic hydrogel for diabetic wound healing |
title_full_unstemmed | Polydeoxyribonucleotide-delivering therapeutic hydrogel for diabetic wound healing |
title_short | Polydeoxyribonucleotide-delivering therapeutic hydrogel for diabetic wound healing |
title_sort | polydeoxyribonucleotide-delivering therapeutic hydrogel for diabetic wound healing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546631/ https://www.ncbi.nlm.nih.gov/pubmed/33033366 http://dx.doi.org/10.1038/s41598-020-74004-0 |
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