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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Format: | Final Year Project |
Language: | English |
Published: |
2013
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Online Access: | http://hdl.handle.net/10356/52083 |
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Institution: | Nanyang Technological University |
Language: | English |
Summary: | 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. |
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