Cargando…
Validation of the optimal scaffold pore size of nasal implants using the 3-dimensional culture technique
BACKGROUND: To produce patient-specific nasal implants, it is necessary to harvest and grow autologous cartilage. It is crucial to the proliferation and growth of these cells for scaffolds similar to the extracellular matrix to be prepared. The pore size of the scaffold is critical to cell growth an...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Plastic and Reconstructive Surgeons
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398817/ https://www.ncbi.nlm.nih.gov/pubmed/32718109 http://dx.doi.org/10.5999/aps.2020.00213 |
_version_ | 1783566026510696448 |
---|---|
author | Nam, Jeoung Hyun Lee, So Yun Khan, Galina Park, Eun Soo |
author_facet | Nam, Jeoung Hyun Lee, So Yun Khan, Galina Park, Eun Soo |
author_sort | Nam, Jeoung Hyun |
collection | PubMed |
description | BACKGROUND: To produce patient-specific nasal implants, it is necessary to harvest and grow autologous cartilage. It is crucial to the proliferation and growth of these cells for scaffolds similar to the extracellular matrix to be prepared. The pore size of the scaffold is critical to cell growth and interaction. Thus, the goal of this study was to determine the optimal pore size for the growth of chondrocytes and fibroblasts. METHODS: Porous disc-shaped scaffolds with 100-, 200-, 300-, and 400-µm pores were produced using polycaprolactone (PCL). Chondrocytes and fibroblasts were cultured after seeding the scaffolds with these cells, and morphologic evaluation was performed on days 2, 14, 28, and 56 after cell seeding. On each of those days, the number of viable cells was evaluated quantitatively using an MTT assay. RESULTS: The number of cells had moderately increased by day 28. This increase was noteworthy for the 300- and 400-µm pore sizes for fibroblasts; otherwise, no remarkable difference was observed at any size except the 100-µm pore size for chondrocytes. By day 56, the number of cells was observed to increase with pore size, and the number of chondrocytes had markedly increased at the 400-µm pore size. The findings of the morphologic evaluation were consistent with those of the quantitative evaluation. CONCLUSIONS: Experiments using disc-type PCL scaffolds showed (via both morphologic and quantitative analysis) that chondrocytes and fibroblasts proliferated most extensively at the 400-µm pore size in 56 days of culture. |
format | Online Article Text |
id | pubmed-7398817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Korean Society of Plastic and Reconstructive Surgeons |
record_format | MEDLINE/PubMed |
spelling | pubmed-73988172020-08-10 Validation of the optimal scaffold pore size of nasal implants using the 3-dimensional culture technique Nam, Jeoung Hyun Lee, So Yun Khan, Galina Park, Eun Soo Arch Plast Surg Original Article BACKGROUND: To produce patient-specific nasal implants, it is necessary to harvest and grow autologous cartilage. It is crucial to the proliferation and growth of these cells for scaffolds similar to the extracellular matrix to be prepared. The pore size of the scaffold is critical to cell growth and interaction. Thus, the goal of this study was to determine the optimal pore size for the growth of chondrocytes and fibroblasts. METHODS: Porous disc-shaped scaffolds with 100-, 200-, 300-, and 400-µm pores were produced using polycaprolactone (PCL). Chondrocytes and fibroblasts were cultured after seeding the scaffolds with these cells, and morphologic evaluation was performed on days 2, 14, 28, and 56 after cell seeding. On each of those days, the number of viable cells was evaluated quantitatively using an MTT assay. RESULTS: The number of cells had moderately increased by day 28. This increase was noteworthy for the 300- and 400-µm pore sizes for fibroblasts; otherwise, no remarkable difference was observed at any size except the 100-µm pore size for chondrocytes. By day 56, the number of cells was observed to increase with pore size, and the number of chondrocytes had markedly increased at the 400-µm pore size. The findings of the morphologic evaluation were consistent with those of the quantitative evaluation. CONCLUSIONS: Experiments using disc-type PCL scaffolds showed (via both morphologic and quantitative analysis) that chondrocytes and fibroblasts proliferated most extensively at the 400-µm pore size in 56 days of culture. Korean Society of Plastic and Reconstructive Surgeons 2020-07 2020-07-15 /pmc/articles/PMC7398817/ /pubmed/32718109 http://dx.doi.org/10.5999/aps.2020.00213 Text en Copyright © 2020 The Korean Society of Plastic and Reconstructive Surgeons This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Nam, Jeoung Hyun Lee, So Yun Khan, Galina Park, Eun Soo Validation of the optimal scaffold pore size of nasal implants using the 3-dimensional culture technique |
title | Validation of the optimal scaffold pore size of nasal implants using the 3-dimensional culture technique |
title_full | Validation of the optimal scaffold pore size of nasal implants using the 3-dimensional culture technique |
title_fullStr | Validation of the optimal scaffold pore size of nasal implants using the 3-dimensional culture technique |
title_full_unstemmed | Validation of the optimal scaffold pore size of nasal implants using the 3-dimensional culture technique |
title_short | Validation of the optimal scaffold pore size of nasal implants using the 3-dimensional culture technique |
title_sort | validation of the optimal scaffold pore size of nasal implants using the 3-dimensional culture technique |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398817/ https://www.ncbi.nlm.nih.gov/pubmed/32718109 http://dx.doi.org/10.5999/aps.2020.00213 |
work_keys_str_mv | AT namjeounghyun validationoftheoptimalscaffoldporesizeofnasalimplantsusingthe3dimensionalculturetechnique AT leesoyun validationoftheoptimalscaffoldporesizeofnasalimplantsusingthe3dimensionalculturetechnique AT khangalina validationoftheoptimalscaffoldporesizeofnasalimplantsusingthe3dimensionalculturetechnique AT parkeunsoo validationoftheoptimalscaffoldporesizeofnasalimplantsusingthe3dimensionalculturetechnique |