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Enhanced stabilization of collagen-based dermal regeneration scaffolds through the combination of physical and chemical crosslinking

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Enhanced stabilization of collagen-based dermal regeneration scaffolds through the combination of physical and chemical crosslinking. / Wessels, Quenton; Pretorius, E.

In: South African Journal of Science , Vol. 104, No. 11-12, 11.2008, p. 513-516.

Research output: Contribution to Journal/MagazineLetterpeer-review

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Wessels Q, Pretorius E. Enhanced stabilization of collagen-based dermal regeneration scaffolds through the combination of physical and chemical crosslinking. South African Journal of Science . 2008 Nov;104(11-12):513-516.

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Wessels, Quenton ; Pretorius, E. / Enhanced stabilization of collagen-based dermal regeneration scaffolds through the combination of physical and chemical crosslinking. In: South African Journal of Science . 2008 ; Vol. 104, No. 11-12. pp. 513-516.

Bibtex

@article{b16663ec971b4ffdbd01776426700455,
title = "Enhanced stabilization of collagen-based dermal regeneration scaffolds through the combination of physical and chemical crosslinking",
abstract = "The use of collagen in the biomedical device industry has led to major advances in soft tissue repair. This is attributed largely to the favourable biological and physiochemical properties of collagen. Regenerative medicine and tissue engineering favoured the use of this biomaterial and various commercial products have become available in the past few decades. This study aims to develop a collagen and chondroitin-6-sulphate dermal regeneration scaffold with enhanced resistance against enzymatic degradation. Frozen slurries (0.5% collagen) were dried under vacuum, coated with silicone, crosslinked and then thoroughly rinsed. The scaffolds were subjected to a range of quantitative and qualitative tests that included: scanning electron microscopy analysis, collagenase enzymatic degradation, and cytotoxicity assessment. Scaffold resistance to enzymatic degradation was manipulated after dehydrothermal treatment by employing combinations of crosslinking agents, such as glutaraldehyde and / or carbodiimide, with or without the presence of L-lysine. Results indicate that highly porous (mean pore diameter of 87.3 µm), bioactive, non-cytotoxic tissue engineering matrices were obtained. Enhanced stability of these scaffolds was achieved through extensive crosslinking and suggests the potential to prevent in vivo wound contraction sufficiently. ",
keywords = "collagen-based scaffolds , physical crosslinking, dermal regeneration",
author = "Quenton Wessels and E. Pretorius",
year = "2008",
month = nov,
language = "English",
volume = "104",
pages = "513--516",
journal = "South African Journal of Science ",
issn = "0038-2353",
publisher = "Academy of Science of South Africa",
number = "11-12",

}

RIS

TY - JOUR

T1 - Enhanced stabilization of collagen-based dermal regeneration scaffolds through the combination of physical and chemical crosslinking

AU - Wessels, Quenton

AU - Pretorius, E.

PY - 2008/11

Y1 - 2008/11

N2 - The use of collagen in the biomedical device industry has led to major advances in soft tissue repair. This is attributed largely to the favourable biological and physiochemical properties of collagen. Regenerative medicine and tissue engineering favoured the use of this biomaterial and various commercial products have become available in the past few decades. This study aims to develop a collagen and chondroitin-6-sulphate dermal regeneration scaffold with enhanced resistance against enzymatic degradation. Frozen slurries (0.5% collagen) were dried under vacuum, coated with silicone, crosslinked and then thoroughly rinsed. The scaffolds were subjected to a range of quantitative and qualitative tests that included: scanning electron microscopy analysis, collagenase enzymatic degradation, and cytotoxicity assessment. Scaffold resistance to enzymatic degradation was manipulated after dehydrothermal treatment by employing combinations of crosslinking agents, such as glutaraldehyde and / or carbodiimide, with or without the presence of L-lysine. Results indicate that highly porous (mean pore diameter of 87.3 µm), bioactive, non-cytotoxic tissue engineering matrices were obtained. Enhanced stability of these scaffolds was achieved through extensive crosslinking and suggests the potential to prevent in vivo wound contraction sufficiently.

AB - The use of collagen in the biomedical device industry has led to major advances in soft tissue repair. This is attributed largely to the favourable biological and physiochemical properties of collagen. Regenerative medicine and tissue engineering favoured the use of this biomaterial and various commercial products have become available in the past few decades. This study aims to develop a collagen and chondroitin-6-sulphate dermal regeneration scaffold with enhanced resistance against enzymatic degradation. Frozen slurries (0.5% collagen) were dried under vacuum, coated with silicone, crosslinked and then thoroughly rinsed. The scaffolds were subjected to a range of quantitative and qualitative tests that included: scanning electron microscopy analysis, collagenase enzymatic degradation, and cytotoxicity assessment. Scaffold resistance to enzymatic degradation was manipulated after dehydrothermal treatment by employing combinations of crosslinking agents, such as glutaraldehyde and / or carbodiimide, with or without the presence of L-lysine. Results indicate that highly porous (mean pore diameter of 87.3 µm), bioactive, non-cytotoxic tissue engineering matrices were obtained. Enhanced stability of these scaffolds was achieved through extensive crosslinking and suggests the potential to prevent in vivo wound contraction sufficiently.

KW - collagen-based scaffolds

KW - physical crosslinking

KW - dermal regeneration

M3 - Letter

VL - 104

SP - 513

EP - 516

JO - South African Journal of Science

JF - South African Journal of Science

SN - 0038-2353

IS - 11-12

ER -