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Alginate-Poly(ethylene glycol) Hybrid Microspheres for Primary Cell Microencapsulation
The progress of medical therapies, which rely on the transplantation of microencapsulated living cells, depends on the quality of the encapsulating material. Such material has to be biocompatible, and the microencapsulation process must be simple and not harm the cells. Alginate-poly(ethylene glycol...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5453158/ https://www.ncbi.nlm.nih.gov/pubmed/28788456 http://dx.doi.org/10.3390/ma7010275 |
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author | Mahou, Redouan Meier, Raphael P. H. Bühler, Léo H. Wandrey, Christine |
author_facet | Mahou, Redouan Meier, Raphael P. H. Bühler, Léo H. Wandrey, Christine |
author_sort | Mahou, Redouan |
collection | PubMed |
description | The progress of medical therapies, which rely on the transplantation of microencapsulated living cells, depends on the quality of the encapsulating material. Such material has to be biocompatible, and the microencapsulation process must be simple and not harm the cells. Alginate-poly(ethylene glycol) hybrid microspheres (alg-PEG-M) were produced by combining ionotropic gelation of sodium alginate (Na-alg) using calcium ions with covalent crosslinking of vinyl sulfone-terminated multi-arm poly(ethylene glycol) (PEG-VS). In a one-step microsphere formation process, fast ionotropic gelation yields spherical calcium alginate gel beads, which serve as a matrix for simultaneously but slowly occurring covalent cross-linking of the PEG-VS molecules. The feasibility of cell microencapsulation was studied using primary human foreskin fibroblasts (EDX cells) as a model. The use of cell culture media as polymer solvent, gelation bath, and storage medium did not negatively affect the alg-PEG-M properties. Microencapsulated EDX cells maintained their viability and proliferated. This study demonstrates the feasibility of primary cell microencapsulation within the novel microsphere type alg-PEG-M, serves as reference for future therapy development, and confirms the suitability of EDX cells as control model. |
format | Online Article Text |
id | pubmed-5453158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-54531582017-07-28 Alginate-Poly(ethylene glycol) Hybrid Microspheres for Primary Cell Microencapsulation Mahou, Redouan Meier, Raphael P. H. Bühler, Léo H. Wandrey, Christine Materials (Basel) Article The progress of medical therapies, which rely on the transplantation of microencapsulated living cells, depends on the quality of the encapsulating material. Such material has to be biocompatible, and the microencapsulation process must be simple and not harm the cells. Alginate-poly(ethylene glycol) hybrid microspheres (alg-PEG-M) were produced by combining ionotropic gelation of sodium alginate (Na-alg) using calcium ions with covalent crosslinking of vinyl sulfone-terminated multi-arm poly(ethylene glycol) (PEG-VS). In a one-step microsphere formation process, fast ionotropic gelation yields spherical calcium alginate gel beads, which serve as a matrix for simultaneously but slowly occurring covalent cross-linking of the PEG-VS molecules. The feasibility of cell microencapsulation was studied using primary human foreskin fibroblasts (EDX cells) as a model. The use of cell culture media as polymer solvent, gelation bath, and storage medium did not negatively affect the alg-PEG-M properties. Microencapsulated EDX cells maintained their viability and proliferated. This study demonstrates the feasibility of primary cell microencapsulation within the novel microsphere type alg-PEG-M, serves as reference for future therapy development, and confirms the suitability of EDX cells as control model. MDPI 2014-01-09 /pmc/articles/PMC5453158/ /pubmed/28788456 http://dx.doi.org/10.3390/ma7010275 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Mahou, Redouan Meier, Raphael P. H. Bühler, Léo H. Wandrey, Christine Alginate-Poly(ethylene glycol) Hybrid Microspheres for Primary Cell Microencapsulation |
title | Alginate-Poly(ethylene glycol) Hybrid Microspheres for Primary Cell Microencapsulation |
title_full | Alginate-Poly(ethylene glycol) Hybrid Microspheres for Primary Cell Microencapsulation |
title_fullStr | Alginate-Poly(ethylene glycol) Hybrid Microspheres for Primary Cell Microencapsulation |
title_full_unstemmed | Alginate-Poly(ethylene glycol) Hybrid Microspheres for Primary Cell Microencapsulation |
title_short | Alginate-Poly(ethylene glycol) Hybrid Microspheres for Primary Cell Microencapsulation |
title_sort | alginate-poly(ethylene glycol) hybrid microspheres for primary cell microencapsulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5453158/ https://www.ncbi.nlm.nih.gov/pubmed/28788456 http://dx.doi.org/10.3390/ma7010275 |
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