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Collagen/kerateine multi-protein hydrogels as a thermally stable extracellular matrix for 3D in vitro models

OBJECTIVE: To determine whether the addition of kerateine (reduced keratin) in rat tail collagen type I hydrogels increases thermal stability and changes material properties and supports cell growth for use in cellular hyperthermia studies for tumor treatment. METHODS: Collagen type I extracted from...

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Autores principales: Zuniga, Kameel, Gadde, Manasa, Scheftel, Jacob, Senecal, Kris, Cressman, Erik, Van Dyke, Mark, Rylander, Marissa Nichole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523628/
https://www.ncbi.nlm.nih.gov/pubmed/34058945
http://dx.doi.org/10.1080/02656736.2021.1930202
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author Zuniga, Kameel
Gadde, Manasa
Scheftel, Jacob
Senecal, Kris
Cressman, Erik
Van Dyke, Mark
Rylander, Marissa Nichole
author_facet Zuniga, Kameel
Gadde, Manasa
Scheftel, Jacob
Senecal, Kris
Cressman, Erik
Van Dyke, Mark
Rylander, Marissa Nichole
author_sort Zuniga, Kameel
collection PubMed
description OBJECTIVE: To determine whether the addition of kerateine (reduced keratin) in rat tail collagen type I hydrogels increases thermal stability and changes material properties and supports cell growth for use in cellular hyperthermia studies for tumor treatment. METHODS: Collagen type I extracted from rat tail tendon was combined with kerateine extracted from human hair fibers. Thermal, mechanical, and biocompatibility properties and cell behavior was assessed and compared to 100% collagen type I hydrogels to demonstrate their utility as a tissue model for 3D in vitro testing. RESULTS: A combination (i.e., containing both collagen ‘C/KNT’) hydrogel was more thermally stable than pure collagen hydrogels and resisted thermal degradation when incubated at a hyperthermic temperature of 47°C for heating durations up to 60 min with a higher melting temperature measured by DSC. An increase in the storage modulus was only observed with an increased collagen concentration rather than an increased KTN concentration; however, a change in ECM structure was observed with greater fiber alignment and width with an increase in KTN concentration. The C/KTN hydrogels, specifically 50/50 C/KTN hydrogels, also supported the growth and of fibroblasts and MDA-MB-231 breast cancer cells similar to those seeded in 100% collagen hydrogels. CONCLUSION: This multi-protein C/KTN hydrogel shows promise for future studies involving thermal stress studies without compromising the 3D ECM environment or cell growth.
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spelling pubmed-105236282023-09-27 Collagen/kerateine multi-protein hydrogels as a thermally stable extracellular matrix for 3D in vitro models Zuniga, Kameel Gadde, Manasa Scheftel, Jacob Senecal, Kris Cressman, Erik Van Dyke, Mark Rylander, Marissa Nichole Int J Hyperthermia Article OBJECTIVE: To determine whether the addition of kerateine (reduced keratin) in rat tail collagen type I hydrogels increases thermal stability and changes material properties and supports cell growth for use in cellular hyperthermia studies for tumor treatment. METHODS: Collagen type I extracted from rat tail tendon was combined with kerateine extracted from human hair fibers. Thermal, mechanical, and biocompatibility properties and cell behavior was assessed and compared to 100% collagen type I hydrogels to demonstrate their utility as a tissue model for 3D in vitro testing. RESULTS: A combination (i.e., containing both collagen ‘C/KNT’) hydrogel was more thermally stable than pure collagen hydrogels and resisted thermal degradation when incubated at a hyperthermic temperature of 47°C for heating durations up to 60 min with a higher melting temperature measured by DSC. An increase in the storage modulus was only observed with an increased collagen concentration rather than an increased KTN concentration; however, a change in ECM structure was observed with greater fiber alignment and width with an increase in KTN concentration. The C/KTN hydrogels, specifically 50/50 C/KTN hydrogels, also supported the growth and of fibroblasts and MDA-MB-231 breast cancer cells similar to those seeded in 100% collagen hydrogels. CONCLUSION: This multi-protein C/KTN hydrogel shows promise for future studies involving thermal stress studies without compromising the 3D ECM environment or cell growth. 2021 /pmc/articles/PMC10523628/ /pubmed/34058945 http://dx.doi.org/10.1080/02656736.2021.1930202 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Zuniga, Kameel
Gadde, Manasa
Scheftel, Jacob
Senecal, Kris
Cressman, Erik
Van Dyke, Mark
Rylander, Marissa Nichole
Collagen/kerateine multi-protein hydrogels as a thermally stable extracellular matrix for 3D in vitro models
title Collagen/kerateine multi-protein hydrogels as a thermally stable extracellular matrix for 3D in vitro models
title_full Collagen/kerateine multi-protein hydrogels as a thermally stable extracellular matrix for 3D in vitro models
title_fullStr Collagen/kerateine multi-protein hydrogels as a thermally stable extracellular matrix for 3D in vitro models
title_full_unstemmed Collagen/kerateine multi-protein hydrogels as a thermally stable extracellular matrix for 3D in vitro models
title_short Collagen/kerateine multi-protein hydrogels as a thermally stable extracellular matrix for 3D in vitro models
title_sort collagen/kerateine multi-protein hydrogels as a thermally stable extracellular matrix for 3d in vitro models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523628/
https://www.ncbi.nlm.nih.gov/pubmed/34058945
http://dx.doi.org/10.1080/02656736.2021.1930202
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