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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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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. |
format | Online Article Text |
id | pubmed-10523628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
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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