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Nano-fibre Integrated Microcapsules: A Nano-in-Micro Platform for 3D Cell Culture
Nano-in-micro (NIM) system is a promising approach to enhance the performance of devices for a wide range of applications in disease treatment and tissue regeneration. In this study, polymeric nanofibre-integrated alginate (PNA) hydrogel microcapsules were designed using NIM technology. Various rati...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765003/ https://www.ncbi.nlm.nih.gov/pubmed/31562351 http://dx.doi.org/10.1038/s41598-019-50380-0 |
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author | Khanal, Shalil Bhattarai, Shanta R. Sankar, Jagannathan Bhandari, Ramji K. Macdonald, Jeffrey M. Bhattarai, Narayan |
author_facet | Khanal, Shalil Bhattarai, Shanta R. Sankar, Jagannathan Bhandari, Ramji K. Macdonald, Jeffrey M. Bhattarai, Narayan |
author_sort | Khanal, Shalil |
collection | PubMed |
description | Nano-in-micro (NIM) system is a promising approach to enhance the performance of devices for a wide range of applications in disease treatment and tissue regeneration. In this study, polymeric nanofibre-integrated alginate (PNA) hydrogel microcapsules were designed using NIM technology. Various ratios of cryo-ground poly (lactide-co-glycolide) (PLGA) nanofibres (CPN) were incorporated into PNA hydrogel microcapsule. Electrostatic encapsulation method was used to incorporate living cells into the PNA microcapsules (~500 µm diameter). Human liver carcinoma cells, HepG2, were encapsulated into the microcapsules and their physio-chemical properties were studied. Morphology, stability, and chemical composition of the PNA microcapsules were analysed by light microscopy, fluorescent microscopy, scanning electron microscopy (SEM), Fourier-Transform Infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA). The incorporation of CPN caused no significant changes in the morphology, size, and chemical structure of PNA microcapsules in cell culture media. Among four PNA microcapsule products (PNA-0, PNA-10, PNA-30, and PNA-50 with size 489 ± 31 µm, 480 ± 40 µm, 473 ± 51 µm and 464 ± 35 µm, respectively), PNA-10 showed overall suitability for HepG2 growth with high cellular metabolic activity, indicating that the 3D PNA-10 microcapsule could be suitable to maintain better vitality and liver-specific metabolic functions. Overall, this novel design of PNA microcapsule and the one-step method of cell encapsulation can be a versatile 3D NIM system for spontaneous generation of organoids with in vivo like tissue architectures, and the system can be useful for numerous biomedical applications, especially for liver tissue engineering, cell preservation, and drug toxicity study. |
format | Online Article Text |
id | pubmed-6765003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67650032019-10-02 Nano-fibre Integrated Microcapsules: A Nano-in-Micro Platform for 3D Cell Culture Khanal, Shalil Bhattarai, Shanta R. Sankar, Jagannathan Bhandari, Ramji K. Macdonald, Jeffrey M. Bhattarai, Narayan Sci Rep Article Nano-in-micro (NIM) system is a promising approach to enhance the performance of devices for a wide range of applications in disease treatment and tissue regeneration. In this study, polymeric nanofibre-integrated alginate (PNA) hydrogel microcapsules were designed using NIM technology. Various ratios of cryo-ground poly (lactide-co-glycolide) (PLGA) nanofibres (CPN) were incorporated into PNA hydrogel microcapsule. Electrostatic encapsulation method was used to incorporate living cells into the PNA microcapsules (~500 µm diameter). Human liver carcinoma cells, HepG2, were encapsulated into the microcapsules and their physio-chemical properties were studied. Morphology, stability, and chemical composition of the PNA microcapsules were analysed by light microscopy, fluorescent microscopy, scanning electron microscopy (SEM), Fourier-Transform Infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA). The incorporation of CPN caused no significant changes in the morphology, size, and chemical structure of PNA microcapsules in cell culture media. Among four PNA microcapsule products (PNA-0, PNA-10, PNA-30, and PNA-50 with size 489 ± 31 µm, 480 ± 40 µm, 473 ± 51 µm and 464 ± 35 µm, respectively), PNA-10 showed overall suitability for HepG2 growth with high cellular metabolic activity, indicating that the 3D PNA-10 microcapsule could be suitable to maintain better vitality and liver-specific metabolic functions. Overall, this novel design of PNA microcapsule and the one-step method of cell encapsulation can be a versatile 3D NIM system for spontaneous generation of organoids with in vivo like tissue architectures, and the system can be useful for numerous biomedical applications, especially for liver tissue engineering, cell preservation, and drug toxicity study. Nature Publishing Group UK 2019-09-27 /pmc/articles/PMC6765003/ /pubmed/31562351 http://dx.doi.org/10.1038/s41598-019-50380-0 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Khanal, Shalil Bhattarai, Shanta R. Sankar, Jagannathan Bhandari, Ramji K. Macdonald, Jeffrey M. Bhattarai, Narayan Nano-fibre Integrated Microcapsules: A Nano-in-Micro Platform for 3D Cell Culture |
title | Nano-fibre Integrated Microcapsules: A Nano-in-Micro Platform for 3D Cell Culture |
title_full | Nano-fibre Integrated Microcapsules: A Nano-in-Micro Platform for 3D Cell Culture |
title_fullStr | Nano-fibre Integrated Microcapsules: A Nano-in-Micro Platform for 3D Cell Culture |
title_full_unstemmed | Nano-fibre Integrated Microcapsules: A Nano-in-Micro Platform for 3D Cell Culture |
title_short | Nano-fibre Integrated Microcapsules: A Nano-in-Micro Platform for 3D Cell Culture |
title_sort | nano-fibre integrated microcapsules: a nano-in-micro platform for 3d cell culture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765003/ https://www.ncbi.nlm.nih.gov/pubmed/31562351 http://dx.doi.org/10.1038/s41598-019-50380-0 |
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