Cargando…
Chitin Nanofibrils Enabled Core–Shell Microcapsules of Alginate Hydrogel
An engineered 3D architectural network of the biopolymeric hydrogel can mimic the native cell environment that promotes cell infiltration and growth. Among several bio-fabricated hydrogel structures, core–shell microcapsules inherit the potential of cell encapsulation to ensure the growth and transp...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10489914/ https://www.ncbi.nlm.nih.gov/pubmed/37686978 http://dx.doi.org/10.3390/nano13172470 |
_version_ | 1785103719058112512 |
---|---|
author | Sapkota, Thakur Shrestha, Bishnu Kumar Shrestha, Sita Bhattarai, Narayan |
author_facet | Sapkota, Thakur Shrestha, Bishnu Kumar Shrestha, Sita Bhattarai, Narayan |
author_sort | Sapkota, Thakur |
collection | PubMed |
description | An engineered 3D architectural network of the biopolymeric hydrogel can mimic the native cell environment that promotes cell infiltration and growth. Among several bio-fabricated hydrogel structures, core–shell microcapsules inherit the potential of cell encapsulation to ensure the growth and transport of cells and cell metabolites. Herein, a co-axial electrostatic encapsulation strategy is used to create and encapsulate the cells into chitin nanofibrils integrated alginate hydrogel microcapsules. Three parameters that are critical in the electrostatic encapsulation process, hydrogel composition, flow rate, and voltage were optimized. The physicochemical characterization including structure, size, and stability of the core–shell microcapsules was analyzed by scanning electron microscope (SEM), FTIR, and mechanical tests. The cellular responses of the core–shell microcapsules were evaluated through in vitro cell studies by encapsulating NIH/3T3 fibroblast cells. Notably, the bioactive microcapsule showed that the cell viability was found excellent for more than 2 weeks. Thus, the results of this core–shell microcapsule showed a promising approach to creating 3D hydrogel networks suitable for different biomedical applications such as in vitro tissue models for toxicity studies, wound healing, and tissue repair. |
format | Online Article Text |
id | pubmed-10489914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104899142023-09-09 Chitin Nanofibrils Enabled Core–Shell Microcapsules of Alginate Hydrogel Sapkota, Thakur Shrestha, Bishnu Kumar Shrestha, Sita Bhattarai, Narayan Nanomaterials (Basel) Article An engineered 3D architectural network of the biopolymeric hydrogel can mimic the native cell environment that promotes cell infiltration and growth. Among several bio-fabricated hydrogel structures, core–shell microcapsules inherit the potential of cell encapsulation to ensure the growth and transport of cells and cell metabolites. Herein, a co-axial electrostatic encapsulation strategy is used to create and encapsulate the cells into chitin nanofibrils integrated alginate hydrogel microcapsules. Three parameters that are critical in the electrostatic encapsulation process, hydrogel composition, flow rate, and voltage were optimized. The physicochemical characterization including structure, size, and stability of the core–shell microcapsules was analyzed by scanning electron microscope (SEM), FTIR, and mechanical tests. The cellular responses of the core–shell microcapsules were evaluated through in vitro cell studies by encapsulating NIH/3T3 fibroblast cells. Notably, the bioactive microcapsule showed that the cell viability was found excellent for more than 2 weeks. Thus, the results of this core–shell microcapsule showed a promising approach to creating 3D hydrogel networks suitable for different biomedical applications such as in vitro tissue models for toxicity studies, wound healing, and tissue repair. MDPI 2023-09-01 /pmc/articles/PMC10489914/ /pubmed/37686978 http://dx.doi.org/10.3390/nano13172470 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sapkota, Thakur Shrestha, Bishnu Kumar Shrestha, Sita Bhattarai, Narayan Chitin Nanofibrils Enabled Core–Shell Microcapsules of Alginate Hydrogel |
title | Chitin Nanofibrils Enabled Core–Shell Microcapsules of Alginate Hydrogel |
title_full | Chitin Nanofibrils Enabled Core–Shell Microcapsules of Alginate Hydrogel |
title_fullStr | Chitin Nanofibrils Enabled Core–Shell Microcapsules of Alginate Hydrogel |
title_full_unstemmed | Chitin Nanofibrils Enabled Core–Shell Microcapsules of Alginate Hydrogel |
title_short | Chitin Nanofibrils Enabled Core–Shell Microcapsules of Alginate Hydrogel |
title_sort | chitin nanofibrils enabled core–shell microcapsules of alginate hydrogel |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10489914/ https://www.ncbi.nlm.nih.gov/pubmed/37686978 http://dx.doi.org/10.3390/nano13172470 |
work_keys_str_mv | AT sapkotathakur chitinnanofibrilsenabledcoreshellmicrocapsulesofalginatehydrogel AT shresthabishnukumar chitinnanofibrilsenabledcoreshellmicrocapsulesofalginatehydrogel AT shresthasita chitinnanofibrilsenabledcoreshellmicrocapsulesofalginatehydrogel AT bhattarainarayan chitinnanofibrilsenabledcoreshellmicrocapsulesofalginatehydrogel |