Cargando…

Collagen peptide modified carboxymethyl cellulose as both antioxidant drug and carrier for drug delivery against retinal ischaemia/reperfusion injury

Oxidative stress can cause injury in retinal endothelial cells. Carboxymethyl cellulose modified with collagen peptide (CMCC) is of a distinct antioxidant capacity and potentially a good drug carrier. In this study, the protective effects of CMCC against H(2)O(2)‐induced injury of primary retinal en...

Descripción completa

Detalles Bibliográficos
Autores principales: Mu, Hua, Wang, Yeqing, Wei, Haiying, Lu, Hong, Feng, Zhuolei, Yu, Hongmin, Xing, Yue, Wang, Haijing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156360/
https://www.ncbi.nlm.nih.gov/pubmed/30030883
http://dx.doi.org/10.1111/jcmm.13768
_version_ 1783358084369874944
author Mu, Hua
Wang, Yeqing
Wei, Haiying
Lu, Hong
Feng, Zhuolei
Yu, Hongmin
Xing, Yue
Wang, Haijing
author_facet Mu, Hua
Wang, Yeqing
Wei, Haiying
Lu, Hong
Feng, Zhuolei
Yu, Hongmin
Xing, Yue
Wang, Haijing
author_sort Mu, Hua
collection PubMed
description Oxidative stress can cause injury in retinal endothelial cells. Carboxymethyl cellulose modified with collagen peptide (CMCC) is of a distinct antioxidant capacity and potentially a good drug carrier. In this study, the protective effects of CMCC against H(2)O(2)‐induced injury of primary retinal endothelial cells were investigated. In vitro, we demonstrated that CMCC significantly promoted viability of H(2)O(2)‐treated cells, efficiently restrained cellular reactive oxygen species (ROS) production and cell apoptosis. Then, the CMCC was employed as both drug and anti‐inflammatory drug carrier for treatment of retinal ischaemia/reperfusion (I/R) in rats. Animals were treated with CMCC or interleukin‐10‐loaded CMCC (IL‐10@CMCC), respectively. In comparisons, the IL‐10@CMCC treatment exhibited superior therapeutic effects, including better restoration of retinal structural thickness and less retinal apoptosis. Also, chemiluminescence demonstrated that transplantation of IL‐10@CMCC markedly reduced the retinal oxidative stress level compared with CMCC alone and potently recovered the activities of typical antioxidant enzymes, SOD and CAT. Therefore, it could be concluded that CMCC provides a promising platform to enhance the drug‐based therapy for I/R‐related retinal injury.
format Online
Article
Text
id pubmed-6156360
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-61563602018-10-01 Collagen peptide modified carboxymethyl cellulose as both antioxidant drug and carrier for drug delivery against retinal ischaemia/reperfusion injury Mu, Hua Wang, Yeqing Wei, Haiying Lu, Hong Feng, Zhuolei Yu, Hongmin Xing, Yue Wang, Haijing J Cell Mol Med Original Articles Oxidative stress can cause injury in retinal endothelial cells. Carboxymethyl cellulose modified with collagen peptide (CMCC) is of a distinct antioxidant capacity and potentially a good drug carrier. In this study, the protective effects of CMCC against H(2)O(2)‐induced injury of primary retinal endothelial cells were investigated. In vitro, we demonstrated that CMCC significantly promoted viability of H(2)O(2)‐treated cells, efficiently restrained cellular reactive oxygen species (ROS) production and cell apoptosis. Then, the CMCC was employed as both drug and anti‐inflammatory drug carrier for treatment of retinal ischaemia/reperfusion (I/R) in rats. Animals were treated with CMCC or interleukin‐10‐loaded CMCC (IL‐10@CMCC), respectively. In comparisons, the IL‐10@CMCC treatment exhibited superior therapeutic effects, including better restoration of retinal structural thickness and less retinal apoptosis. Also, chemiluminescence demonstrated that transplantation of IL‐10@CMCC markedly reduced the retinal oxidative stress level compared with CMCC alone and potently recovered the activities of typical antioxidant enzymes, SOD and CAT. Therefore, it could be concluded that CMCC provides a promising platform to enhance the drug‐based therapy for I/R‐related retinal injury. John Wiley and Sons Inc. 2018-07-20 2018-10 /pmc/articles/PMC6156360/ /pubmed/30030883 http://dx.doi.org/10.1111/jcmm.13768 Text en © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Mu, Hua
Wang, Yeqing
Wei, Haiying
Lu, Hong
Feng, Zhuolei
Yu, Hongmin
Xing, Yue
Wang, Haijing
Collagen peptide modified carboxymethyl cellulose as both antioxidant drug and carrier for drug delivery against retinal ischaemia/reperfusion injury
title Collagen peptide modified carboxymethyl cellulose as both antioxidant drug and carrier for drug delivery against retinal ischaemia/reperfusion injury
title_full Collagen peptide modified carboxymethyl cellulose as both antioxidant drug and carrier for drug delivery against retinal ischaemia/reperfusion injury
title_fullStr Collagen peptide modified carboxymethyl cellulose as both antioxidant drug and carrier for drug delivery against retinal ischaemia/reperfusion injury
title_full_unstemmed Collagen peptide modified carboxymethyl cellulose as both antioxidant drug and carrier for drug delivery against retinal ischaemia/reperfusion injury
title_short Collagen peptide modified carboxymethyl cellulose as both antioxidant drug and carrier for drug delivery against retinal ischaemia/reperfusion injury
title_sort collagen peptide modified carboxymethyl cellulose as both antioxidant drug and carrier for drug delivery against retinal ischaemia/reperfusion injury
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156360/
https://www.ncbi.nlm.nih.gov/pubmed/30030883
http://dx.doi.org/10.1111/jcmm.13768
work_keys_str_mv AT muhua collagenpeptidemodifiedcarboxymethylcelluloseasbothantioxidantdrugandcarrierfordrugdeliveryagainstretinalischaemiareperfusioninjury
AT wangyeqing collagenpeptidemodifiedcarboxymethylcelluloseasbothantioxidantdrugandcarrierfordrugdeliveryagainstretinalischaemiareperfusioninjury
AT weihaiying collagenpeptidemodifiedcarboxymethylcelluloseasbothantioxidantdrugandcarrierfordrugdeliveryagainstretinalischaemiareperfusioninjury
AT luhong collagenpeptidemodifiedcarboxymethylcelluloseasbothantioxidantdrugandcarrierfordrugdeliveryagainstretinalischaemiareperfusioninjury
AT fengzhuolei collagenpeptidemodifiedcarboxymethylcelluloseasbothantioxidantdrugandcarrierfordrugdeliveryagainstretinalischaemiareperfusioninjury
AT yuhongmin collagenpeptidemodifiedcarboxymethylcelluloseasbothantioxidantdrugandcarrierfordrugdeliveryagainstretinalischaemiareperfusioninjury
AT xingyue collagenpeptidemodifiedcarboxymethylcelluloseasbothantioxidantdrugandcarrierfordrugdeliveryagainstretinalischaemiareperfusioninjury
AT wanghaijing collagenpeptidemodifiedcarboxymethylcelluloseasbothantioxidantdrugandcarrierfordrugdeliveryagainstretinalischaemiareperfusioninjury