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High-Resolution Bioprinting of Recombinant Human Collagen Type III

The development of commercial collagen inks for extrusion-based bioprinting has increased the amount of research on pure collagen bioprinting, i.e., collagen inks not mixed with gelatin, alginate, or other more common biomaterial inks. New printing techniques have also improved the resolution achiev...

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Detalles Bibliográficos
Autores principales: Gibney, Rory, Patterson, Jennifer, Ferraris, Eleonora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8434404/
https://www.ncbi.nlm.nih.gov/pubmed/34503013
http://dx.doi.org/10.3390/polym13172973
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author Gibney, Rory
Patterson, Jennifer
Ferraris, Eleonora
author_facet Gibney, Rory
Patterson, Jennifer
Ferraris, Eleonora
author_sort Gibney, Rory
collection PubMed
description The development of commercial collagen inks for extrusion-based bioprinting has increased the amount of research on pure collagen bioprinting, i.e., collagen inks not mixed with gelatin, alginate, or other more common biomaterial inks. New printing techniques have also improved the resolution achievable with pure collagen bioprinting. However, the resultant collagen constructs still appear too weak to replicate dense collagenous tissues, such as the cornea. This work aims to demonstrate the first reported case of bioprinted recombinant collagen films with suitable optical and mechanical properties for corneal tissue engineering. The printing technology used, aerosol jet(®) printing (AJP), is a high-resolution printing method normally used to deposit conductive inks for electronic printing. In this work, AJP was employed to deposit recombinant human collagen type III (RHCIII) in overlapping continuous lines of 60 µm to form thin layers. Layers were repeated up to 764 times to result in a construct that was considered a few hundred microns thick when swollen. Samples were subsequently neutralised and crosslinked using EDC:NHS crosslinking. Nanoindentation and absorbance measurements were conducted, and the results show that the AJP-deposited RHCIII samples possess suitable mechanical and optical properties for corneal tissue engineering: an average effective elastic modulus of 506 ± 173 kPa and transparency ≥87% at all visible wavelengths. Circular dichroism showed that there was some loss of helicity of the collagen due to aerosolisation. SDS-PAGE and pepsin digestion were used to show that while some collagen is degraded due to aerosolisation, it remains an inaccessible substrate for pepsin cleavage.
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spelling pubmed-84344042021-09-12 High-Resolution Bioprinting of Recombinant Human Collagen Type III Gibney, Rory Patterson, Jennifer Ferraris, Eleonora Polymers (Basel) Article The development of commercial collagen inks for extrusion-based bioprinting has increased the amount of research on pure collagen bioprinting, i.e., collagen inks not mixed with gelatin, alginate, or other more common biomaterial inks. New printing techniques have also improved the resolution achievable with pure collagen bioprinting. However, the resultant collagen constructs still appear too weak to replicate dense collagenous tissues, such as the cornea. This work aims to demonstrate the first reported case of bioprinted recombinant collagen films with suitable optical and mechanical properties for corneal tissue engineering. The printing technology used, aerosol jet(®) printing (AJP), is a high-resolution printing method normally used to deposit conductive inks for electronic printing. In this work, AJP was employed to deposit recombinant human collagen type III (RHCIII) in overlapping continuous lines of 60 µm to form thin layers. Layers were repeated up to 764 times to result in a construct that was considered a few hundred microns thick when swollen. Samples were subsequently neutralised and crosslinked using EDC:NHS crosslinking. Nanoindentation and absorbance measurements were conducted, and the results show that the AJP-deposited RHCIII samples possess suitable mechanical and optical properties for corneal tissue engineering: an average effective elastic modulus of 506 ± 173 kPa and transparency ≥87% at all visible wavelengths. Circular dichroism showed that there was some loss of helicity of the collagen due to aerosolisation. SDS-PAGE and pepsin digestion were used to show that while some collagen is degraded due to aerosolisation, it remains an inaccessible substrate for pepsin cleavage. MDPI 2021-09-01 /pmc/articles/PMC8434404/ /pubmed/34503013 http://dx.doi.org/10.3390/polym13172973 Text en © 2021 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
Gibney, Rory
Patterson, Jennifer
Ferraris, Eleonora
High-Resolution Bioprinting of Recombinant Human Collagen Type III
title High-Resolution Bioprinting of Recombinant Human Collagen Type III
title_full High-Resolution Bioprinting of Recombinant Human Collagen Type III
title_fullStr High-Resolution Bioprinting of Recombinant Human Collagen Type III
title_full_unstemmed High-Resolution Bioprinting of Recombinant Human Collagen Type III
title_short High-Resolution Bioprinting of Recombinant Human Collagen Type III
title_sort high-resolution bioprinting of recombinant human collagen type iii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8434404/
https://www.ncbi.nlm.nih.gov/pubmed/34503013
http://dx.doi.org/10.3390/polym13172973
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