Reversible boric ester-carbene adhesive films

The growing interest in the development of tissue adhesives as an alternative to surgical sutures for wound closure can be attributed to the ease of on-site application, while eliminating the side effects such as tissue necrosis and nerve damage from puncturing soft tissues in the process of suturin...

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Main Author: Lai, Wan Jun
Other Authors: Terry W.J. Steele
Format: Final Year Project
Language:English
Published: Nanyang Technological University 2023
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Online Access:https://hdl.handle.net/10356/165907
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1659072023-05-17T06:51:51Z Reversible boric ester-carbene adhesive films Lai, Wan Jun Terry W.J. Steele School of Materials Science and Engineering WJSTEELE@ntu.edu.sg Engineering::Materials The growing interest in the development of tissue adhesives as an alternative to surgical sutures for wound closure can be attributed to the ease of on-site application, while eliminating the side effects such as tissue necrosis and nerve damage from puncturing soft tissues in the process of suturing. Most of the bioadhesives available in the market currently requires a stimuli such as heat or light for crosslinking. The bioadhesives that do not require activation have an inferior bonding strength, which limits its site of application. Biomimetic adhesives with micro-structured designs have a high and reversible adhesion strength, but they are complicated and expensive to fabricate. A recent development of a bioadhesive leverages on the covalent bonds formed between poly(vinyl alcohol) and boric acid to give a crosslinked structure with strong ester bonds that can undergo debonding in the presence of water. The synthesis of the gel is simple, and the resulting bioadhesive has a high adhesion strength with reversible bond that enhances the flexibility. This project aims to introduce the boronic ester bonds to the hydroxyl groups in diazirine-grafted polycaprolactone (CaproGlu), with the addition of boric acid, trimethyl borate, triethyl borate and tributyl borate. The crosslinking characteristics will be characterised with photorheometry, to obtain the viscosity, storage modulus, loss modulus, and stress-strain curve for different ratio of hydroxyl groups to borate ester sites. Successful crosslinking was observed between polycaprolactone polyol and CaproGlu, with all borate compounds, which was indicated by an increase in the viscosity from neat polycaprolactone polyol or CaproGlu. The highest visocity was observed at a low ratio of hydroxyl groups to borate ester sites. The crosslinked polycaprolactone gel softened when exposed to the atmosphere, possibly from the uptake of water from the environment. After photoactivation, CaproGlu with borate ester bonds showed a higher storage modulus across all borates and ratio tested. Amplitude sweep measurements also showed a higher maximum shear stress at the same shear strain. Further optimisation of the ratio between the hydroxyl groups in CaproGlu and borate ester sites may yield a higher shear strain for the sample, due to the reversibility of the boronic ester bonds. Bachelor of Engineering (Materials Engineering) 2023-05-12T06:50:18Z 2023-05-12T06:50:18Z 2023 Final Year Project (FYP) Lai, W. J. (2023). Reversible boric ester-carbene adhesive films. Final Year Project (FYP), Nanyang Technological University, Singapore. https://hdl.handle.net/10356/165907 https://hdl.handle.net/10356/165907 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
spellingShingle Engineering::Materials
Lai, Wan Jun
Reversible boric ester-carbene adhesive films
description The growing interest in the development of tissue adhesives as an alternative to surgical sutures for wound closure can be attributed to the ease of on-site application, while eliminating the side effects such as tissue necrosis and nerve damage from puncturing soft tissues in the process of suturing. Most of the bioadhesives available in the market currently requires a stimuli such as heat or light for crosslinking. The bioadhesives that do not require activation have an inferior bonding strength, which limits its site of application. Biomimetic adhesives with micro-structured designs have a high and reversible adhesion strength, but they are complicated and expensive to fabricate. A recent development of a bioadhesive leverages on the covalent bonds formed between poly(vinyl alcohol) and boric acid to give a crosslinked structure with strong ester bonds that can undergo debonding in the presence of water. The synthesis of the gel is simple, and the resulting bioadhesive has a high adhesion strength with reversible bond that enhances the flexibility. This project aims to introduce the boronic ester bonds to the hydroxyl groups in diazirine-grafted polycaprolactone (CaproGlu), with the addition of boric acid, trimethyl borate, triethyl borate and tributyl borate. The crosslinking characteristics will be characterised with photorheometry, to obtain the viscosity, storage modulus, loss modulus, and stress-strain curve for different ratio of hydroxyl groups to borate ester sites. Successful crosslinking was observed between polycaprolactone polyol and CaproGlu, with all borate compounds, which was indicated by an increase in the viscosity from neat polycaprolactone polyol or CaproGlu. The highest visocity was observed at a low ratio of hydroxyl groups to borate ester sites. The crosslinked polycaprolactone gel softened when exposed to the atmosphere, possibly from the uptake of water from the environment. After photoactivation, CaproGlu with borate ester bonds showed a higher storage modulus across all borates and ratio tested. Amplitude sweep measurements also showed a higher maximum shear stress at the same shear strain. Further optimisation of the ratio between the hydroxyl groups in CaproGlu and borate ester sites may yield a higher shear strain for the sample, due to the reversibility of the boronic ester bonds.
author2 Terry W.J. Steele
author_facet Terry W.J. Steele
Lai, Wan Jun
format Final Year Project
author Lai, Wan Jun
author_sort Lai, Wan Jun
title Reversible boric ester-carbene adhesive films
title_short Reversible boric ester-carbene adhesive films
title_full Reversible boric ester-carbene adhesive films
title_fullStr Reversible boric ester-carbene adhesive films
title_full_unstemmed Reversible boric ester-carbene adhesive films
title_sort reversible boric ester-carbene adhesive films
publisher Nanyang Technological University
publishDate 2023
url https://hdl.handle.net/10356/165907
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