Collagen-carbon nanotube composite materials as scaffolds in tissue engineering

Carbon nanotubes (CNT) are attractive for use in fiber‐reinforced composite materials due to their very high aspect ratio, combined with outstanding mechanical and electrical properties. Composite materials comprising a collagen matrix with embedded CNT were prepared by mixing solubilized Type I col...

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Veröffentlicht in:Journal of biomedical materials research 2005-09, Vol.74A (3), p.489-496
Hauptverfasser: MacDonald, Rebecca A., Laurenzi, Brendan F., Viswanathan, Gunaranjan, Ajayan, Pulickel M., Stegemann, Jan P.
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container_end_page 496
container_issue 3
container_start_page 489
container_title Journal of biomedical materials research
container_volume 74A
creator MacDonald, Rebecca A.
Laurenzi, Brendan F.
Viswanathan, Gunaranjan
Ajayan, Pulickel M.
Stegemann, Jan P.
description Carbon nanotubes (CNT) are attractive for use in fiber‐reinforced composite materials due to their very high aspect ratio, combined with outstanding mechanical and electrical properties. Composite materials comprising a collagen matrix with embedded CNT were prepared by mixing solubilized Type I collagen with solutions of carboxylated single‐walled carbon nanotubes (SWNT) at concentrations of 0, 0.2, 0.4, 0.8, and 2.0 weight percent. Living smooth muscle cells were incorporated at the time of collagen gelation to produce cell‐seeded collagen–CNT composite matrices. Constructs containing 2.0 wt % CNT exhibited delayed gel compaction, relative to lower concentrations that compacted at the same rate as pure collagen controls. Cell viability in all constructs was consistently above 85% at both Day 3 and Day 7, whereas cell number in CNT‐containing constructs was lower than in control constructs at Day 3, though statistically unchanged by Day 7. Scanning electron microscopy showed physical interactions between CNT and collagen matrix. Raman spectroscopy confirmed the presence of CNT at the expected diameter (0.85–1.30 nm), but did not indicate strong molecular interactions between the collagen and CNT components. Such collagen–CNT composite matrices may have utility as scaffolds in tissue engineering, or as components of biosensors or other medical devices. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2005
doi_str_mv 10.1002/jbm.a.30386
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Composite materials comprising a collagen matrix with embedded CNT were prepared by mixing solubilized Type I collagen with solutions of carboxylated single‐walled carbon nanotubes (SWNT) at concentrations of 0, 0.2, 0.4, 0.8, and 2.0 weight percent. Living smooth muscle cells were incorporated at the time of collagen gelation to produce cell‐seeded collagen–CNT composite matrices. Constructs containing 2.0 wt % CNT exhibited delayed gel compaction, relative to lower concentrations that compacted at the same rate as pure collagen controls. Cell viability in all constructs was consistently above 85% at both Day 3 and Day 7, whereas cell number in CNT‐containing constructs was lower than in control constructs at Day 3, though statistically unchanged by Day 7. Scanning electron microscopy showed physical interactions between CNT and collagen matrix. Raman spectroscopy confirmed the presence of CNT at the expected diameter (0.85–1.30 nm), but did not indicate strong molecular interactions between the collagen and CNT components. Such collagen–CNT composite matrices may have utility as scaffolds in tissue engineering, or as components of biosensors or other medical devices. © 2005 Wiley Periodicals, Inc. 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Biomed. Mater. Res</addtitle><description>Carbon nanotubes (CNT) are attractive for use in fiber‐reinforced composite materials due to their very high aspect ratio, combined with outstanding mechanical and electrical properties. Composite materials comprising a collagen matrix with embedded CNT were prepared by mixing solubilized Type I collagen with solutions of carboxylated single‐walled carbon nanotubes (SWNT) at concentrations of 0, 0.2, 0.4, 0.8, and 2.0 weight percent. Living smooth muscle cells were incorporated at the time of collagen gelation to produce cell‐seeded collagen–CNT composite matrices. Constructs containing 2.0 wt % CNT exhibited delayed gel compaction, relative to lower concentrations that compacted at the same rate as pure collagen controls. Cell viability in all constructs was consistently above 85% at both Day 3 and Day 7, whereas cell number in CNT‐containing constructs was lower than in control constructs at Day 3, though statistically unchanged by Day 7. Scanning electron microscopy showed physical interactions between CNT and collagen matrix. Raman spectroscopy confirmed the presence of CNT at the expected diameter (0.85–1.30 nm), but did not indicate strong molecular interactions between the collagen and CNT components. Such collagen–CNT composite matrices may have utility as scaffolds in tissue engineering, or as components of biosensors or other medical devices. © 2005 Wiley Periodicals, Inc. 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subjects Animals
Biocompatible Materials
biomaterials
carbon nanotubes
Cells, Cultured
Collagen
composites
Microscopy, Electron, Scanning
Models, Biological
Myocytes, Smooth Muscle - ultrastructure
nanobiotechnology
Nanotubes, Carbon - ultrastructure
Rats
Spectrum Analysis, Raman
Tissue Engineering
title Collagen-carbon nanotube composite materials as scaffolds in tissue engineering
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