Bioprinting and Preliminary Testing of Highly Reproducible Novel Bioink for Potential Skin Regeneration

Three-dimensional (3D) bioprinting is considered as a novel approach in biofabricating cell-laden constructs that could potentially be used to promote skin regeneration following injury. In this study, a novel crosslinked chitosan (CH)–genipin (GE) bioink laden with keratinocyte and human dermal fib...

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Main Authors: Forough Hafezi, Susan Shorter, Atabak Ghanizadeh Tabriz, Andrew Hurt, Victoria Elmes, Joshua Boateng, Dennis Douroumis
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/12/6/550
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author Forough Hafezi
Susan Shorter
Atabak Ghanizadeh Tabriz
Andrew Hurt
Victoria Elmes
Joshua Boateng
Dennis Douroumis
author_facet Forough Hafezi
Susan Shorter
Atabak Ghanizadeh Tabriz
Andrew Hurt
Victoria Elmes
Joshua Boateng
Dennis Douroumis
author_sort Forough Hafezi
collection DOAJ
description Three-dimensional (3D) bioprinting is considered as a novel approach in biofabricating cell-laden constructs that could potentially be used to promote skin regeneration following injury. In this study, a novel crosslinked chitosan (CH)–genipin (GE) bioink laden with keratinocyte and human dermal fibroblast cells was developed and printed successfully using an extruder-based bioprinter. By altering the composition and degree of CH–GE crosslinking, bioink printability was further assessed and compared with a commercial bioink. Rheological analysis showed that the viscosity of the optimised bioink was in a suitable range that facilitated reproducible and reliable printing by applying low pressures ranging from 20–40 kPa. The application of low printing pressures proved vital for viability of cells loaded within the bioinks. Further characterisation using MTT assay showed that cells were still viable within the printed construct at 93% despite the crosslinking, processing and after subjecting to physiological conditions for seven days. The morphological study of the printed cells showed that they were mobile within the bioink. Furthermore, the multi-layered 3D printed constructs demonstrated excellent self-supportive structures in a consistent manner.
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spelling doaj.art-8a20fa1902014e89b8bac381464dbf292023-11-20T03:43:05ZengMDPI AGPharmaceutics1999-49232020-06-0112655010.3390/pharmaceutics12060550Bioprinting and Preliminary Testing of Highly Reproducible Novel Bioink for Potential Skin RegenerationForough Hafezi0Susan Shorter1Atabak Ghanizadeh Tabriz2Andrew Hurt3Victoria Elmes4Joshua Boateng5Dennis Douroumis6School of Science, Faculty of Engineering and Science, University of Greenwich, Chatham Maritime, Kent ME4 4TB, UKSchool of Science, Faculty of Engineering and Science, University of Greenwich, Chatham Maritime, Kent ME4 4TB, UKSchool of Science, Faculty of Engineering and Science, University of Greenwich, Chatham Maritime, Kent ME4 4TB, UKSchool of Science, Faculty of Engineering and Science, University of Greenwich, Chatham Maritime, Kent ME4 4TB, UKSchool of Science, Faculty of Engineering and Science, University of Greenwich, Chatham Maritime, Kent ME4 4TB, UKSchool of Science, Faculty of Engineering and Science, University of Greenwich, Chatham Maritime, Kent ME4 4TB, UKSchool of Science, Faculty of Engineering and Science, University of Greenwich, Chatham Maritime, Kent ME4 4TB, UKThree-dimensional (3D) bioprinting is considered as a novel approach in biofabricating cell-laden constructs that could potentially be used to promote skin regeneration following injury. In this study, a novel crosslinked chitosan (CH)–genipin (GE) bioink laden with keratinocyte and human dermal fibroblast cells was developed and printed successfully using an extruder-based bioprinter. By altering the composition and degree of CH–GE crosslinking, bioink printability was further assessed and compared with a commercial bioink. Rheological analysis showed that the viscosity of the optimised bioink was in a suitable range that facilitated reproducible and reliable printing by applying low pressures ranging from 20–40 kPa. The application of low printing pressures proved vital for viability of cells loaded within the bioinks. Further characterisation using MTT assay showed that cells were still viable within the printed construct at 93% despite the crosslinking, processing and after subjecting to physiological conditions for seven days. The morphological study of the printed cells showed that they were mobile within the bioink. Furthermore, the multi-layered 3D printed constructs demonstrated excellent self-supportive structures in a consistent manner.https://www.mdpi.com/1999-4923/12/6/5503D bioprintingbioinkchitosangenipinhuman dermal fibroblastsprimary epidermal keratinocytes
spellingShingle Forough Hafezi
Susan Shorter
Atabak Ghanizadeh Tabriz
Andrew Hurt
Victoria Elmes
Joshua Boateng
Dennis Douroumis
Bioprinting and Preliminary Testing of Highly Reproducible Novel Bioink for Potential Skin Regeneration
Pharmaceutics
3D bioprinting
bioink
chitosan
genipin
human dermal fibroblasts
primary epidermal keratinocytes
title Bioprinting and Preliminary Testing of Highly Reproducible Novel Bioink for Potential Skin Regeneration
title_full Bioprinting and Preliminary Testing of Highly Reproducible Novel Bioink for Potential Skin Regeneration
title_fullStr Bioprinting and Preliminary Testing of Highly Reproducible Novel Bioink for Potential Skin Regeneration
title_full_unstemmed Bioprinting and Preliminary Testing of Highly Reproducible Novel Bioink for Potential Skin Regeneration
title_short Bioprinting and Preliminary Testing of Highly Reproducible Novel Bioink for Potential Skin Regeneration
title_sort bioprinting and preliminary testing of highly reproducible novel bioink for potential skin regeneration
topic 3D bioprinting
bioink
chitosan
genipin
human dermal fibroblasts
primary epidermal keratinocytes
url https://www.mdpi.com/1999-4923/12/6/550
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