Thermo-responsive injectable hydrogels for sustained drug delivery

Hydrogels are widely used in the biomedical field due to their biocompatibility and similarity to the extracellular matrix. Most of the hydrogels used are crosslinked prior to application and are therefore implanted using surgical procedures. Injectable hydrogels are attractive as they are less inva...

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Main Author: Ng, Elson Weilong
Other Authors: Tan Lay Poh
Format: Final Year Project
Language:English
Published: Nanyang Technological University 2023
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Online Access:https://hdl.handle.net/10356/166206
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1662062023-05-13T16:46:30Z Thermo-responsive injectable hydrogels for sustained drug delivery Ng, Elson Weilong Tan Lay Poh School of Materials Science and Engineering A*STAR Institute of Material Research and Engineering LPTan@ntu.edu.sg Engineering::Materials::Biomaterials Hydrogels are widely used in the biomedical field due to their biocompatibility and similarity to the extracellular matrix. Most of the hydrogels used are crosslinked prior to application and are therefore implanted using surgical procedures. Injectable hydrogels are attractive as they are less invasive and do not require open wound surgical procedures. In order to make conventional hydrogels injectable, polymerization has to be done in the body instead. This has risks associated with the unreacted chemicals during in situ polymerization. On the other hand, thermogels, a type of smart hydrogel that is responsive to temperature stimuli, can be safely injected into the body with minimal risk of monomer toxicity. The unique heat-induced sol-to-gel transition allows them to be in solution below body temperature and gel at body temperature, making them an ideal candidate as an injectable hydrogel. However, the use of physical micellar crosslinks in thermogels makes them mechanically weak. Inspired by a strong protein such as collagen that uses hydrogen bonding to get its strength, we attempt to improve the mechanical properties through the incorporation of dihydroxy groups into a particular thermogel of interest. We have studied the effects of how the increase in dihydroxy concentration in the thermogel affects the storage modulus and provided insights into how this affects the functional properties. We found that as the number of hydroxy groups increases, the strength of the thermogel decreases due to the hydrophilicity. However, there is a notable improvement in the processibility at 25 °C and retention of injectability at high concentrations of 25wt% polymer concentration. The high concentrations allow sustained drug delivery due to a decrease in the thermogel mesh size and an increase in its interaction with therapeutics via hydrogen bonding. Bachelor of Engineering (Materials Engineering) 2023-05-10T07:53:52Z 2023-05-10T07:53:52Z 2023 Final Year Project (FYP) Ng, E. W. (2023). Thermo-responsive injectable hydrogels for sustained drug delivery. Final Year Project (FYP), Nanyang Technological University, Singapore. https://hdl.handle.net/10356/166206 https://hdl.handle.net/10356/166206 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
Ng, Elson Weilong
Thermo-responsive injectable hydrogels for sustained drug delivery
description Hydrogels are widely used in the biomedical field due to their biocompatibility and similarity to the extracellular matrix. Most of the hydrogels used are crosslinked prior to application and are therefore implanted using surgical procedures. Injectable hydrogels are attractive as they are less invasive and do not require open wound surgical procedures. In order to make conventional hydrogels injectable, polymerization has to be done in the body instead. This has risks associated with the unreacted chemicals during in situ polymerization. On the other hand, thermogels, a type of smart hydrogel that is responsive to temperature stimuli, can be safely injected into the body with minimal risk of monomer toxicity. The unique heat-induced sol-to-gel transition allows them to be in solution below body temperature and gel at body temperature, making them an ideal candidate as an injectable hydrogel. However, the use of physical micellar crosslinks in thermogels makes them mechanically weak. Inspired by a strong protein such as collagen that uses hydrogen bonding to get its strength, we attempt to improve the mechanical properties through the incorporation of dihydroxy groups into a particular thermogel of interest. We have studied the effects of how the increase in dihydroxy concentration in the thermogel affects the storage modulus and provided insights into how this affects the functional properties. We found that as the number of hydroxy groups increases, the strength of the thermogel decreases due to the hydrophilicity. However, there is a notable improvement in the processibility at 25 °C and retention of injectability at high concentrations of 25wt% polymer concentration. The high concentrations allow sustained drug delivery due to a decrease in the thermogel mesh size and an increase in its interaction with therapeutics via hydrogen bonding.
author2 Tan Lay Poh
author_facet Tan Lay Poh
Ng, Elson Weilong
format Final Year Project
author Ng, Elson Weilong
author_sort Ng, Elson Weilong
title Thermo-responsive injectable hydrogels for sustained drug delivery
title_short Thermo-responsive injectable hydrogels for sustained drug delivery
title_full Thermo-responsive injectable hydrogels for sustained drug delivery
title_fullStr Thermo-responsive injectable hydrogels for sustained drug delivery
title_full_unstemmed Thermo-responsive injectable hydrogels for sustained drug delivery
title_sort thermo-responsive injectable hydrogels for sustained drug delivery
publisher Nanyang Technological University
publishDate 2023
url https://hdl.handle.net/10356/166206
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