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Novel stable cytokine delivery system in physiological pH solution: chitosan oligosaccharide/heparin nanoparticles
BACKGROUND: Cell therapy is a promising strategy for tissue regeneration. Key to this strategy is mobilization and recruitment of exogenous or autologous stem/progenitor cells by cytokines. However, there is no effective cytokine delivery system available for clinic application, in particular for my...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431508/ https://www.ncbi.nlm.nih.gov/pubmed/26056441 http://dx.doi.org/10.2147/IJN.S82091 |
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author | Wang, Bin Tan, Ling Deng, Dengpu Lu, Ting Zhou, Changwei Li, Zhongkui Tang, Zhenjie Wu, Zhongshi Tang, Hao |
author_facet | Wang, Bin Tan, Ling Deng, Dengpu Lu, Ting Zhou, Changwei Li, Zhongkui Tang, Zhenjie Wu, Zhongshi Tang, Hao |
author_sort | Wang, Bin |
collection | PubMed |
description | BACKGROUND: Cell therapy is a promising strategy for tissue regeneration. Key to this strategy is mobilization and recruitment of exogenous or autologous stem/progenitor cells by cytokines. However, there is no effective cytokine delivery system available for clinic application, in particular for myocardial regeneration. The aim of this study was to develop a novel cytokine delivery system that is stable in solution at physiological pH. METHODS: Four groups of self-assembled chitosan oligosaccharide/heparin (CSO/H) nanoparticles were prepared with various volume ratios of chitosan oligosaccharide to heparin (5:2, 5:4, 4:15, 1:5) and characterized by laser diffraction, particle size analysis, and transmission electron microscopy. The encapsulation efficiency and loading content of two cytokines, ie, stromal cell-derived factor (SDF)-1α and vascular endothelial growth factor (VEGF) were quantified using an enzyme-linked immunosorbent assay. The biological activity of the loaded SDF-1α and VEGF was evaluated using the transwell migration assay and MTT assay. The dispersion profiles for the cytokine-loaded nanoparticles were quantified using fluorescence molecular tomography. RESULTS: CSO/H nanoparticles were prepared successfully in solution with physiological pH. The particle sizes in the four treatment groups were in the range of 96.2–210.5 nm and the zeta potential ranged from −29.4 mV to 24.2 mV. The loading efficiency in the CSO/H nanoparticle groups with the first three ratios was more than 90%. SDF-1α loaded into CSO/H nanoparticles retained its migration activity and VEGF loaded into CSO/H nanoparticles continued to show proliferation activity. The in vivo dispersion test showed that the CSO/H nanoparticles enabled to VEGF to accumulate locally for a longer period of time. CONCLUSION: CSO/H nanoparticles have a high cytokine loading capacity and allow cytokines to maintain their bioactivity for longer, are stable in an environment with physiological pH, and may be a promising cytokine delivery system for tissue regeneration. |
format | Online Article Text |
id | pubmed-4431508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44315082015-06-08 Novel stable cytokine delivery system in physiological pH solution: chitosan oligosaccharide/heparin nanoparticles Wang, Bin Tan, Ling Deng, Dengpu Lu, Ting Zhou, Changwei Li, Zhongkui Tang, Zhenjie Wu, Zhongshi Tang, Hao Int J Nanomedicine Methodology BACKGROUND: Cell therapy is a promising strategy for tissue regeneration. Key to this strategy is mobilization and recruitment of exogenous or autologous stem/progenitor cells by cytokines. However, there is no effective cytokine delivery system available for clinic application, in particular for myocardial regeneration. The aim of this study was to develop a novel cytokine delivery system that is stable in solution at physiological pH. METHODS: Four groups of self-assembled chitosan oligosaccharide/heparin (CSO/H) nanoparticles were prepared with various volume ratios of chitosan oligosaccharide to heparin (5:2, 5:4, 4:15, 1:5) and characterized by laser diffraction, particle size analysis, and transmission electron microscopy. The encapsulation efficiency and loading content of two cytokines, ie, stromal cell-derived factor (SDF)-1α and vascular endothelial growth factor (VEGF) were quantified using an enzyme-linked immunosorbent assay. The biological activity of the loaded SDF-1α and VEGF was evaluated using the transwell migration assay and MTT assay. The dispersion profiles for the cytokine-loaded nanoparticles were quantified using fluorescence molecular tomography. RESULTS: CSO/H nanoparticles were prepared successfully in solution with physiological pH. The particle sizes in the four treatment groups were in the range of 96.2–210.5 nm and the zeta potential ranged from −29.4 mV to 24.2 mV. The loading efficiency in the CSO/H nanoparticle groups with the first three ratios was more than 90%. SDF-1α loaded into CSO/H nanoparticles retained its migration activity and VEGF loaded into CSO/H nanoparticles continued to show proliferation activity. The in vivo dispersion test showed that the CSO/H nanoparticles enabled to VEGF to accumulate locally for a longer period of time. CONCLUSION: CSO/H nanoparticles have a high cytokine loading capacity and allow cytokines to maintain their bioactivity for longer, are stable in an environment with physiological pH, and may be a promising cytokine delivery system for tissue regeneration. Dove Medical Press 2015-05-08 /pmc/articles/PMC4431508/ /pubmed/26056441 http://dx.doi.org/10.2147/IJN.S82091 Text en © 2015 Wang et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Methodology Wang, Bin Tan, Ling Deng, Dengpu Lu, Ting Zhou, Changwei Li, Zhongkui Tang, Zhenjie Wu, Zhongshi Tang, Hao Novel stable cytokine delivery system in physiological pH solution: chitosan oligosaccharide/heparin nanoparticles |
title | Novel stable cytokine delivery system in physiological pH solution: chitosan oligosaccharide/heparin nanoparticles |
title_full | Novel stable cytokine delivery system in physiological pH solution: chitosan oligosaccharide/heparin nanoparticles |
title_fullStr | Novel stable cytokine delivery system in physiological pH solution: chitosan oligosaccharide/heparin nanoparticles |
title_full_unstemmed | Novel stable cytokine delivery system in physiological pH solution: chitosan oligosaccharide/heparin nanoparticles |
title_short | Novel stable cytokine delivery system in physiological pH solution: chitosan oligosaccharide/heparin nanoparticles |
title_sort | novel stable cytokine delivery system in physiological ph solution: chitosan oligosaccharide/heparin nanoparticles |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431508/ https://www.ncbi.nlm.nih.gov/pubmed/26056441 http://dx.doi.org/10.2147/IJN.S82091 |
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