Cargando…

A pH-dependent Antibacterial Peptide Release Nano-system Blocks Tumor Growth in vivo without Toxicity

In this study, we designed a nano-system where a novel antibacterial peptide RGD-hylin a1 with reduced hemolysis than the commonly studied melittin was loaded onto mesoporous silica (HMS). We found out that the designed nano-system, RGD-hylin a1-HMS, released RGD-hylin a1 in a pH-dependent manner. I...

Descripción completa

Detalles Bibliográficos
Autores principales: Cao, Jing, Zhang, Yan, Shan, Yanke, Wang, Jingui, Liu, Fei, Liu, Hongrui, Xing, Gang, Lei, Jing, Zhou, Jiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593885/
https://www.ncbi.nlm.nih.gov/pubmed/28894233
http://dx.doi.org/10.1038/s41598-017-11687-y
_version_ 1783263115090067456
author Cao, Jing
Zhang, Yan
Shan, Yanke
Wang, Jingui
Liu, Fei
Liu, Hongrui
Xing, Gang
Lei, Jing
Zhou, Jiyong
author_facet Cao, Jing
Zhang, Yan
Shan, Yanke
Wang, Jingui
Liu, Fei
Liu, Hongrui
Xing, Gang
Lei, Jing
Zhou, Jiyong
author_sort Cao, Jing
collection PubMed
description In this study, we designed a nano-system where a novel antibacterial peptide RGD-hylin a1 with reduced hemolysis than the commonly studied melittin was loaded onto mesoporous silica (HMS). We found out that the designed nano-system, RGD-hylin a1-HMS, released RGD-hylin a1 in a pH-dependent manner. It caused apoptosis of cancer cells at low dosage of the antibacterial peptide at pH = 5.5, but was safe to the cells at pH = 7. The hemolytic activity of RGD-hylin a1 itself was reduced by 50~100% by the nano-system depending on the dosage. When this nano-system was administered to tumor-bearing mice at low dosage via intravenous injection, the growth of the solid tumor was blocked by the RGD-hylin a1-HMS nano-system with a 50–60% inhibition rate relative to the PBS-treated control group in terms of tumor volume and weight. Further, the hemolytic activity of RGD-hylin a1 was completely eliminated within the delivery system with no other side effects observed. This study demonstrates that this smart pH-dependent antibacterial peptide release nano-system has superior potential for solid tumor treatments through intravenous administration. This smart-releasing system has great potential in further clinical applications.
format Online
Article
Text
id pubmed-5593885
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-55938852017-09-13 A pH-dependent Antibacterial Peptide Release Nano-system Blocks Tumor Growth in vivo without Toxicity Cao, Jing Zhang, Yan Shan, Yanke Wang, Jingui Liu, Fei Liu, Hongrui Xing, Gang Lei, Jing Zhou, Jiyong Sci Rep Article In this study, we designed a nano-system where a novel antibacterial peptide RGD-hylin a1 with reduced hemolysis than the commonly studied melittin was loaded onto mesoporous silica (HMS). We found out that the designed nano-system, RGD-hylin a1-HMS, released RGD-hylin a1 in a pH-dependent manner. It caused apoptosis of cancer cells at low dosage of the antibacterial peptide at pH = 5.5, but was safe to the cells at pH = 7. The hemolytic activity of RGD-hylin a1 itself was reduced by 50~100% by the nano-system depending on the dosage. When this nano-system was administered to tumor-bearing mice at low dosage via intravenous injection, the growth of the solid tumor was blocked by the RGD-hylin a1-HMS nano-system with a 50–60% inhibition rate relative to the PBS-treated control group in terms of tumor volume and weight. Further, the hemolytic activity of RGD-hylin a1 was completely eliminated within the delivery system with no other side effects observed. This study demonstrates that this smart pH-dependent antibacterial peptide release nano-system has superior potential for solid tumor treatments through intravenous administration. This smart-releasing system has great potential in further clinical applications. Nature Publishing Group UK 2017-09-11 /pmc/articles/PMC5593885/ /pubmed/28894233 http://dx.doi.org/10.1038/s41598-017-11687-y Text en © The Author(s) 2017 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
Cao, Jing
Zhang, Yan
Shan, Yanke
Wang, Jingui
Liu, Fei
Liu, Hongrui
Xing, Gang
Lei, Jing
Zhou, Jiyong
A pH-dependent Antibacterial Peptide Release Nano-system Blocks Tumor Growth in vivo without Toxicity
title A pH-dependent Antibacterial Peptide Release Nano-system Blocks Tumor Growth in vivo without Toxicity
title_full A pH-dependent Antibacterial Peptide Release Nano-system Blocks Tumor Growth in vivo without Toxicity
title_fullStr A pH-dependent Antibacterial Peptide Release Nano-system Blocks Tumor Growth in vivo without Toxicity
title_full_unstemmed A pH-dependent Antibacterial Peptide Release Nano-system Blocks Tumor Growth in vivo without Toxicity
title_short A pH-dependent Antibacterial Peptide Release Nano-system Blocks Tumor Growth in vivo without Toxicity
title_sort ph-dependent antibacterial peptide release nano-system blocks tumor growth in vivo without toxicity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593885/
https://www.ncbi.nlm.nih.gov/pubmed/28894233
http://dx.doi.org/10.1038/s41598-017-11687-y
work_keys_str_mv AT caojing aphdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT zhangyan aphdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT shanyanke aphdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT wangjingui aphdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT liufei aphdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT liuhongrui aphdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT xinggang aphdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT leijing aphdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT zhoujiyong aphdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT caojing phdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT zhangyan phdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT shanyanke phdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT wangjingui phdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT liufei phdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT liuhongrui phdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT xinggang phdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT leijing phdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity
AT zhoujiyong phdependentantibacterialpeptidereleasenanosystemblockstumorgrowthinvivowithouttoxicity