3D Bioprinting of Pectin-Cellulose Nanofibers Multicomponent Bioinks

Pectin has found extensive interest in biomedical applications, including wound dressing, drug delivery, and cancer targeting. However, the low viscosity of pectin solutions hinders their applications in 3D bioprinting. Here, we developed multicomponent bioinks prepared by combining pectin with TEMP...

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Autores principales: Matteo Pitton, Andrea Fiorati, Silvia Buscemi, Lucio Melone, Silvia Farè, Nicola Contessi Negrini
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:1836242337694e5485bf8378e6bfd8782021-12-03T05:46:20Z3D Bioprinting of Pectin-Cellulose Nanofibers Multicomponent Bioinks2296-418510.3389/fbioe.2021.732689https://doaj.org/article/1836242337694e5485bf8378e6bfd8782021-12-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fbioe.2021.732689/fullhttps://doaj.org/toc/2296-4185Pectin has found extensive interest in biomedical applications, including wound dressing, drug delivery, and cancer targeting. However, the low viscosity of pectin solutions hinders their applications in 3D bioprinting. Here, we developed multicomponent bioinks prepared by combining pectin with TEMPO-oxidized cellulose nanofibers (TOCNFs) to optimize the inks’ printability while ensuring stability of the printed hydrogels and simultaneously print viable cell-laden inks. First, we screened several combinations of pectin (1%, 1.5%, 2%, and 2.5% w/v) and TOCNFs (0%, 0.5%, 1%, and 1.5% w/v) by testing their rheological properties and printability. Addition of TOCNFs allowed increasing the inks’ viscosity while maintaining shear thinning rheological response, and it allowed us to identify the optimal pectin concentration (2.5% w/v). We then selected the optimal TOCNFs concentration (1% w/v) by evaluating the viability of cells embedded in the ink and eventually optimized the writing speed to be used to print accurate 3D grid structures. Bioinks were prepared by embedding L929 fibroblast cells in the ink printed by optimized printing parameters. The printed scaffolds were stable in a physiological-like environment and characterized by an elastic modulus of E = 1.8 ± 0.2 kPa. Cells loaded in the ink and printed were viable (cell viability >80%) and their metabolic activity increased in time during the in vitro culture, showing the potential use of the developed bioinks for biofabrication and tissue engineering applications.Matteo PittonMatteo PittonAndrea FioratiAndrea FioratiSilvia BuscemiLucio MeloneLucio MeloneLucio MeloneSilvia FarèSilvia FarèNicola Contessi NegriniNicola Contessi NegriniFrontiers Media S.A.articlepectincellulose nanofiberhydrogelbioprintingmulticomponent bioink3D printingBiotechnologyTP248.13-248.65ENFrontiers in Bioengineering and Biotechnology, Vol 9 (2021)
institution DOAJ
collection DOAJ
language EN
topic pectin
cellulose nanofiber
hydrogel
bioprinting
multicomponent bioink
3D printing
Biotechnology
TP248.13-248.65
spellingShingle pectin
cellulose nanofiber
hydrogel
bioprinting
multicomponent bioink
3D printing
Biotechnology
TP248.13-248.65
Matteo Pitton
Matteo Pitton
Andrea Fiorati
Andrea Fiorati
Silvia Buscemi
Lucio Melone
Lucio Melone
Lucio Melone
Silvia Farè
Silvia Farè
Nicola Contessi Negrini
Nicola Contessi Negrini
3D Bioprinting of Pectin-Cellulose Nanofibers Multicomponent Bioinks
description Pectin has found extensive interest in biomedical applications, including wound dressing, drug delivery, and cancer targeting. However, the low viscosity of pectin solutions hinders their applications in 3D bioprinting. Here, we developed multicomponent bioinks prepared by combining pectin with TEMPO-oxidized cellulose nanofibers (TOCNFs) to optimize the inks’ printability while ensuring stability of the printed hydrogels and simultaneously print viable cell-laden inks. First, we screened several combinations of pectin (1%, 1.5%, 2%, and 2.5% w/v) and TOCNFs (0%, 0.5%, 1%, and 1.5% w/v) by testing their rheological properties and printability. Addition of TOCNFs allowed increasing the inks’ viscosity while maintaining shear thinning rheological response, and it allowed us to identify the optimal pectin concentration (2.5% w/v). We then selected the optimal TOCNFs concentration (1% w/v) by evaluating the viability of cells embedded in the ink and eventually optimized the writing speed to be used to print accurate 3D grid structures. Bioinks were prepared by embedding L929 fibroblast cells in the ink printed by optimized printing parameters. The printed scaffolds were stable in a physiological-like environment and characterized by an elastic modulus of E = 1.8 ± 0.2 kPa. Cells loaded in the ink and printed were viable (cell viability >80%) and their metabolic activity increased in time during the in vitro culture, showing the potential use of the developed bioinks for biofabrication and tissue engineering applications.
format article
author Matteo Pitton
Matteo Pitton
Andrea Fiorati
Andrea Fiorati
Silvia Buscemi
Lucio Melone
Lucio Melone
Lucio Melone
Silvia Farè
Silvia Farè
Nicola Contessi Negrini
Nicola Contessi Negrini
author_facet Matteo Pitton
Matteo Pitton
Andrea Fiorati
Andrea Fiorati
Silvia Buscemi
Lucio Melone
Lucio Melone
Lucio Melone
Silvia Farè
Silvia Farè
Nicola Contessi Negrini
Nicola Contessi Negrini
author_sort Matteo Pitton
title 3D Bioprinting of Pectin-Cellulose Nanofibers Multicomponent Bioinks
title_short 3D Bioprinting of Pectin-Cellulose Nanofibers Multicomponent Bioinks
title_full 3D Bioprinting of Pectin-Cellulose Nanofibers Multicomponent Bioinks
title_fullStr 3D Bioprinting of Pectin-Cellulose Nanofibers Multicomponent Bioinks
title_full_unstemmed 3D Bioprinting of Pectin-Cellulose Nanofibers Multicomponent Bioinks
title_sort 3d bioprinting of pectin-cellulose nanofibers multicomponent bioinks
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/1836242337694e5485bf8378e6bfd878
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