Controlled drug release from multi-phase polymeric particles

The study of the fabrication of multi-phase particles (i.e. double-layered ternary-phase microparticles, triple-layered and quadruple-layered microparticles) and their drug release profiles is reported in this thesis. The overall objective is to investigate the use of multi-phase/multi-layered micro...

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Main Author: Lee, Wei Li
Other Authors: Loo Say Chye Joachim
Format: Theses and Dissertations
Language:English
Published: 2012
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Online Access:https://hdl.handle.net/10356/48050
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-480502023-03-04T16:48:07Z Controlled drug release from multi-phase polymeric particles Lee, Wei Li Loo Say Chye Joachim School of Materials Science & Engineering DRNTU::Engineering::Materials::Biomaterials The study of the fabrication of multi-phase particles (i.e. double-layered ternary-phase microparticles, triple-layered and quadruple-layered microparticles) and their drug release profiles is reported in this thesis. The overall objective is to investigate the use of multi-phase/multi-layered microparticles with different morphologies and layer configurations as a means to control and fine-tune the drug release profiles. The results obtained show conclusive evidence that different microparticle configurations (i.e. polymer distribution and dimensions) can be achieved through the manipulation of process parameters in a one-step solvent evaporation technique. A starting polymer solution prepared below the cloud point, low stirring speed and an increased oil-to-water ratio facilitated the polymers to configure themselves towards thermodynamic equilibrium configurations. A considerably high polymer precipitation rate was needed to kinetically trap the triple-layered structure when the polymer solution was prepared above cloud point. Layer thickness and configuration were altered by changing the polymer mass ratios. Drugs can be localized within specific layers of the microparticles. A correlation of these process parameters to the final particle morphology was thus established. The ternary-phase and triple-layered microparticles were observed to provide unique and better controlled drug release as compared to single-layered and double-layered microparticles. This was due to their distinctive structural attributes and degradation behaviors of the multiple-polymer system. Drug release profiles can be further altered by changing the physicochemical properties of each polymer phase. A modeled relationship between the physicochemical processes and drug release was established for triple-layered microparticles of different layer thicknesses and particle sizes. It is concluded that the multi-phase/multi-layered microparticles can be used to better control the drug release profiles and kinetics. DOCTOR OF PHILOSOPHY (MSE) 2012-02-27T03:30:37Z 2012-02-27T03:30:37Z 2012 2012 Thesis Lee, W. L. (2012). Controlled drug release from multi-phase polymeric particles. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/48050 10.32657/10356/48050 en 225 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
Lee, Wei Li
Controlled drug release from multi-phase polymeric particles
description The study of the fabrication of multi-phase particles (i.e. double-layered ternary-phase microparticles, triple-layered and quadruple-layered microparticles) and their drug release profiles is reported in this thesis. The overall objective is to investigate the use of multi-phase/multi-layered microparticles with different morphologies and layer configurations as a means to control and fine-tune the drug release profiles. The results obtained show conclusive evidence that different microparticle configurations (i.e. polymer distribution and dimensions) can be achieved through the manipulation of process parameters in a one-step solvent evaporation technique. A starting polymer solution prepared below the cloud point, low stirring speed and an increased oil-to-water ratio facilitated the polymers to configure themselves towards thermodynamic equilibrium configurations. A considerably high polymer precipitation rate was needed to kinetically trap the triple-layered structure when the polymer solution was prepared above cloud point. Layer thickness and configuration were altered by changing the polymer mass ratios. Drugs can be localized within specific layers of the microparticles. A correlation of these process parameters to the final particle morphology was thus established. The ternary-phase and triple-layered microparticles were observed to provide unique and better controlled drug release as compared to single-layered and double-layered microparticles. This was due to their distinctive structural attributes and degradation behaviors of the multiple-polymer system. Drug release profiles can be further altered by changing the physicochemical properties of each polymer phase. A modeled relationship between the physicochemical processes and drug release was established for triple-layered microparticles of different layer thicknesses and particle sizes. It is concluded that the multi-phase/multi-layered microparticles can be used to better control the drug release profiles and kinetics.
author2 Loo Say Chye Joachim
author_facet Loo Say Chye Joachim
Lee, Wei Li
format Theses and Dissertations
author Lee, Wei Li
author_sort Lee, Wei Li
title Controlled drug release from multi-phase polymeric particles
title_short Controlled drug release from multi-phase polymeric particles
title_full Controlled drug release from multi-phase polymeric particles
title_fullStr Controlled drug release from multi-phase polymeric particles
title_full_unstemmed Controlled drug release from multi-phase polymeric particles
title_sort controlled drug release from multi-phase polymeric particles
publishDate 2012
url https://hdl.handle.net/10356/48050
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