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...

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Main Authors: Jeoung Hyun Nam, So Yun Lee, Galina Khan, Eun Soo Park
Format: Article
Language:English
Published: Thieme Medical Publishers, Inc. 2020-07-01
Series:Archives of Plastic Surgery
Subjects:
Online Access:http://www.thieme-connect.de/DOI/DOI?10.5999/aps.2020.00213
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author Jeoung Hyun Nam
So Yun Lee
Galina Khan
Eun Soo Park
author_facet Jeoung Hyun Nam
So Yun Lee
Galina Khan
Eun Soo Park
author_sort Jeoung Hyun Nam
collection DOAJ
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.
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spelling doaj.art-c0de3171b74049b99edb970bc05f28f32022-12-22T02:19:08ZengThieme Medical Publishers, Inc.Archives of Plastic Surgery2234-61632234-61712020-07-01470431031610.5999/aps.2020.002133751Validation of the optimal scaffold pore size of nasal implants using the 3-dimensional culture techniqueJeoung Hyun Nam0So Yun Lee1Galina Khan2Eun Soo Park3Department of Plastic and Reconstructive Surgery, Soonchunhyang University Bucheon Hospital, Bucheon, KoreaDepartment of Plastic and Reconstructive Surgery, Soonchunhyang University Bucheon Hospital, Bucheon, KoreaDepartment of Plastic and Reconstructive Surgery, Soonchunhyang University Bucheon Hospital, Bucheon, KoreaDepartment of Plastic and Reconstructive Surgery, Soonchunhyang University Bucheon Hospital, Bucheon, KoreaBackground 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.http://www.thieme-connect.de/DOI/DOI?10.5999/aps.2020.00213porosityrhinoplastyartificial implantchondrocytefibroblast
spellingShingle Jeoung Hyun Nam
So Yun Lee
Galina Khan
Eun Soo Park
Validation of the optimal scaffold pore size of nasal implants using the 3-dimensional culture technique
Archives of Plastic Surgery
porosity
rhinoplasty
artificial implant
chondrocyte
fibroblast
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 porosity
rhinoplasty
artificial implant
chondrocyte
fibroblast
url http://www.thieme-connect.de/DOI/DOI?10.5999/aps.2020.00213
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