Functionalizing bullfrog skin collagen for wound healing

Wound healing is a complex problem and a full healing of the wound through the four phases of wound healing is ideal but not common. Wounds need to be managed with wound dressings in order to avoid infections or the development of chronic wounds. Type I collagen is present in intact dermal tissue...

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Main Author: Foo, Laura Li-En
Other Authors: Dalton Tay Chor Yong
Format: Final Year Project
Language:English
Published: Nanyang Technological University 2020
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Online Access:https://hdl.handle.net/10356/139153
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1391532023-03-04T15:48:15Z Functionalizing bullfrog skin collagen for wound healing Foo, Laura Li-En Dalton Tay Chor Yong School of Materials Science and Engineering cytay@ntu.edu.sg Engineering::Materials::Biomaterials Wound healing is a complex problem and a full healing of the wound through the four phases of wound healing is ideal but not common. Wounds need to be managed with wound dressings in order to avoid infections or the development of chronic wounds. Type I collagen is present in intact dermal tissue and is known to support endothelial cell attachment and keratinocytes regeneration in wound healing. Hence, making it the ideal wound dressing material. In this study, bullfrog skin collagen has been proposed as a non-traditional source of Type I collagen for dermal wound healing applications. The novel mechano-chemical collagen extraction method developed in this project enabled collagen to be extracted at a 70% yield, which is 2 folds higher compared to traditional acid soluble extraction method. The extracted collagen was thoroughly characterized using ATR-FTIR, SDS-PAGE, CD Spectroscopy, DSC and In vitro studies. The pristine bullfrog collagen was subsequently methylated and succinylated with the aim to improve the solubility of the bullfrog collagen fibers in water, as well as to render the collagen with photocrosslinkable properties. Biological performance of the chemically modified bullfrog collagen was examined using Cell proliferation assay, Live/Dead cell viability assay and TNBS assay. Results showed that bullfrog collagen is a type I collagen and it is soluble in water. Methylated and succinylated collagen had much higher denaturation temperatures compared to pristine collagen, hence indicating a better thermal stability. In addition, methylated collagen had higher cell proliferation rates compared to pristine collagen. This would mean that methylated collagen when applied to wounds could help improve the wound healing rate. Modified bullfrog collagen was methacrylated to make it photocrosslinkable. However, the collagen could not crosslink and solidify under UV light. Hence, further optimization of the methacrylation process needs to be done to successfully 3D print collagen for wound healing applications. Bachelor of Engineering (Materials Engineering) 2020-05-16T10:59:53Z 2020-05-16T10:59:53Z 2020 Final Year Project (FYP) https://hdl.handle.net/10356/139153 en application/pdf Nanyang Technological University
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Materials::Biomaterials
spellingShingle Engineering::Materials::Biomaterials
Foo, Laura Li-En
Functionalizing bullfrog skin collagen for wound healing
description Wound healing is a complex problem and a full healing of the wound through the four phases of wound healing is ideal but not common. Wounds need to be managed with wound dressings in order to avoid infections or the development of chronic wounds. Type I collagen is present in intact dermal tissue and is known to support endothelial cell attachment and keratinocytes regeneration in wound healing. Hence, making it the ideal wound dressing material. In this study, bullfrog skin collagen has been proposed as a non-traditional source of Type I collagen for dermal wound healing applications. The novel mechano-chemical collagen extraction method developed in this project enabled collagen to be extracted at a 70% yield, which is 2 folds higher compared to traditional acid soluble extraction method. The extracted collagen was thoroughly characterized using ATR-FTIR, SDS-PAGE, CD Spectroscopy, DSC and In vitro studies. The pristine bullfrog collagen was subsequently methylated and succinylated with the aim to improve the solubility of the bullfrog collagen fibers in water, as well as to render the collagen with photocrosslinkable properties. Biological performance of the chemically modified bullfrog collagen was examined using Cell proliferation assay, Live/Dead cell viability assay and TNBS assay. Results showed that bullfrog collagen is a type I collagen and it is soluble in water. Methylated and succinylated collagen had much higher denaturation temperatures compared to pristine collagen, hence indicating a better thermal stability. In addition, methylated collagen had higher cell proliferation rates compared to pristine collagen. This would mean that methylated collagen when applied to wounds could help improve the wound healing rate. Modified bullfrog collagen was methacrylated to make it photocrosslinkable. However, the collagen could not crosslink and solidify under UV light. Hence, further optimization of the methacrylation process needs to be done to successfully 3D print collagen for wound healing applications.
author2 Dalton Tay Chor Yong
author_facet Dalton Tay Chor Yong
Foo, Laura Li-En
format Final Year Project
author Foo, Laura Li-En
author_sort Foo, Laura Li-En
title Functionalizing bullfrog skin collagen for wound healing
title_short Functionalizing bullfrog skin collagen for wound healing
title_full Functionalizing bullfrog skin collagen for wound healing
title_fullStr Functionalizing bullfrog skin collagen for wound healing
title_full_unstemmed Functionalizing bullfrog skin collagen for wound healing
title_sort functionalizing bullfrog skin collagen for wound healing
publisher Nanyang Technological University
publishDate 2020
url https://hdl.handle.net/10356/139153
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