Study on fabrication of composite hydrogel/hydrophobic polymer microparticle for drug release

Recently, much emphasis has been placed on the creation of drug delivery systems that are able to encapsulate and deliver water-soluble drugs in vivo to treat a wide variety of diseases. Hydrogel-hydrophobic polymer composite microparticles have been developed to encapsulate water-soluble d...

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Main Author: Tan, Sherwyn Keith Yew Jin.
Other Authors: Loo Say Chye Joachim
Format: Final Year Project
Language:English
Published: 2013
Subjects:
Online Access:http://hdl.handle.net/10356/52083
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-520832023-03-04T15:35:00Z Study on fabrication of composite hydrogel/hydrophobic polymer microparticle for drug release Tan, Sherwyn Keith Yew Jin. Loo Say Chye Joachim School of Materials Science and Engineering DRNTU::Engineering::Materials::Biomaterials Recently, much emphasis has been placed on the creation of drug delivery systems that are able to encapsulate and deliver water-soluble drugs in vivo to treat a wide variety of diseases. Hydrogel-hydrophobic polymer composite microparticles have been developed to encapsulate water-soluble drugs due to the improved encapsulation efficiency and controlled release obtained from these drug delivery systems. In this project, alginate-poly(lactic-co-glycolic acid) microparticles (Alg- PLGA MP) and alginate-poly(L-lactic acid) microparticles (Alg-PLLA MP) were fabricated based on the water-in-oil-in-water double emulsion solvent evaporation technique. The alginate materials were encapsulated within the hollow of the hardened PLGA and PLLA shells, thereby indicating that the ionotropic gelation of alginate and the solvent evaporation process took place concurrently. Subsequently, three process parameters were varied, which involved the addition of an osmolyte and a water-soluble drug in the internal water phase, and varying the volume of the external water phase. These fabricated microparticles were analysed via scanning electron microscopy and Fourier transform infra-red spectroscopy in order to observe the changes in the formation and morphology of the alginate components. It was observed that layered alginate structures formed when there was a zero osmotic pressure difference between the internal and external water phases of the double emulsion system. However, alginate ball-like core structures were prevalent after the addition of the water-soluble drug and a decrease in the volume of the external water phase. It is hoped that this study would lead to a better understanding on how certain process parameters affect the formation and morphology of the alginate material, thus allowing future improvements to be made to this drug delivery system. Bachelor of Engineering (Materials Engineering) 2013-04-22T05:16:24Z 2013-04-22T05:16:24Z 2013 2013 Final Year Project (FYP) http://hdl.handle.net/10356/52083 en Nanyang Technological University 59 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Engineering::Materials::Biomaterials
spellingShingle DRNTU::Engineering::Materials::Biomaterials
Tan, Sherwyn Keith Yew Jin.
Study on fabrication of composite hydrogel/hydrophobic polymer microparticle for drug release
description Recently, much emphasis has been placed on the creation of drug delivery systems that are able to encapsulate and deliver water-soluble drugs in vivo to treat a wide variety of diseases. Hydrogel-hydrophobic polymer composite microparticles have been developed to encapsulate water-soluble drugs due to the improved encapsulation efficiency and controlled release obtained from these drug delivery systems. In this project, alginate-poly(lactic-co-glycolic acid) microparticles (Alg- PLGA MP) and alginate-poly(L-lactic acid) microparticles (Alg-PLLA MP) were fabricated based on the water-in-oil-in-water double emulsion solvent evaporation technique. The alginate materials were encapsulated within the hollow of the hardened PLGA and PLLA shells, thereby indicating that the ionotropic gelation of alginate and the solvent evaporation process took place concurrently. Subsequently, three process parameters were varied, which involved the addition of an osmolyte and a water-soluble drug in the internal water phase, and varying the volume of the external water phase. These fabricated microparticles were analysed via scanning electron microscopy and Fourier transform infra-red spectroscopy in order to observe the changes in the formation and morphology of the alginate components. It was observed that layered alginate structures formed when there was a zero osmotic pressure difference between the internal and external water phases of the double emulsion system. However, alginate ball-like core structures were prevalent after the addition of the water-soluble drug and a decrease in the volume of the external water phase. It is hoped that this study would lead to a better understanding on how certain process parameters affect the formation and morphology of the alginate material, thus allowing future improvements to be made to this drug delivery system.
author2 Loo Say Chye Joachim
author_facet Loo Say Chye Joachim
Tan, Sherwyn Keith Yew Jin.
format Final Year Project
author Tan, Sherwyn Keith Yew Jin.
author_sort Tan, Sherwyn Keith Yew Jin.
title Study on fabrication of composite hydrogel/hydrophobic polymer microparticle for drug release
title_short Study on fabrication of composite hydrogel/hydrophobic polymer microparticle for drug release
title_full Study on fabrication of composite hydrogel/hydrophobic polymer microparticle for drug release
title_fullStr Study on fabrication of composite hydrogel/hydrophobic polymer microparticle for drug release
title_full_unstemmed Study on fabrication of composite hydrogel/hydrophobic polymer microparticle for drug release
title_sort study on fabrication of composite hydrogel/hydrophobic polymer microparticle for drug release
publishDate 2013
url http://hdl.handle.net/10356/52083
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