Fabrication of a biodegradable microcarrier system for drug delivery to cancer cells.

The main aim of drug delivery in cancer cell is to deliver anti-cancer drug agent that specifically and efficiently targeted to cancer cell. In this study, a biodegradable microcarrier system that utilized the Layer-by-Layer self assembled polyelectrolyte technique as drug delivery system and target...

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Main Author: Cheah, Petrie Jiing Ei.
Other Authors: Bjoern Holger Neu
Format: Final Year Project
Language:English
Published: 2011
Subjects:
Online Access:http://hdl.handle.net/10356/45648
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-456482023-03-03T15:32:18Z Fabrication of a biodegradable microcarrier system for drug delivery to cancer cells. Cheah, Petrie Jiing Ei. Bjoern Holger Neu School of Chemical and Biomedical Engineering DRNTU::Engineering::Chemical engineering::Biotechnology The main aim of drug delivery in cancer cell is to deliver anti-cancer drug agent that specifically and efficiently targeted to cancer cell. In this study, a biodegradable microcarrier system that utilized the Layer-by-Layer self assembled polyelectrolyte technique as drug delivery system and targeted to human breast cancer cell (MCF-7 & MCF-10a) will be investigated. This PEM systems include the CaCO3 microparticles as template core because of its advantage of biodegradability, biocompatibility and high adsorption ability. It is prepared by alternate coating with positively and negatively charged biodegradable polyelectrolyte (PRM/DSX) and fluorescence labeled with PAH-FITC and PRM-RITC. The result in terms of qualitative and quantitative measurement was promising. The observations and investigations were carried by means of Zeta Potential measurement, Confocal Laser Scanning Microscopy (CLSM), and Flow Cytometry (FCM). The cellular uptake was visualized using membrane stain and lysosomal activity was examined using lysotracker staining. This system was successfully internalized in cells and observed to increase in lysosomal activity. The saturated particle feed ratio was observed in between 1:5 and 1:10. Other than that, the activity of intracellular cysteine protease capthesins B in cell was observed via Immunocytochemistry assay and visualized under CLSM which will extend the project into the incorporation of cystatin, the cysteine protease inhibitors in CaCO3 PEMP in future. Bachelor of Engineering (Chemical and Biomolecular Engineering) 2011-06-15T09:25:08Z 2011-06-15T09:25:08Z 2011 2011 Final Year Project (FYP) http://hdl.handle.net/10356/45648 en Nanyang Technological University 64 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::Chemical engineering::Biotechnology
spellingShingle DRNTU::Engineering::Chemical engineering::Biotechnology
Cheah, Petrie Jiing Ei.
Fabrication of a biodegradable microcarrier system for drug delivery to cancer cells.
description The main aim of drug delivery in cancer cell is to deliver anti-cancer drug agent that specifically and efficiently targeted to cancer cell. In this study, a biodegradable microcarrier system that utilized the Layer-by-Layer self assembled polyelectrolyte technique as drug delivery system and targeted to human breast cancer cell (MCF-7 & MCF-10a) will be investigated. This PEM systems include the CaCO3 microparticles as template core because of its advantage of biodegradability, biocompatibility and high adsorption ability. It is prepared by alternate coating with positively and negatively charged biodegradable polyelectrolyte (PRM/DSX) and fluorescence labeled with PAH-FITC and PRM-RITC. The result in terms of qualitative and quantitative measurement was promising. The observations and investigations were carried by means of Zeta Potential measurement, Confocal Laser Scanning Microscopy (CLSM), and Flow Cytometry (FCM). The cellular uptake was visualized using membrane stain and lysosomal activity was examined using lysotracker staining. This system was successfully internalized in cells and observed to increase in lysosomal activity. The saturated particle feed ratio was observed in between 1:5 and 1:10. Other than that, the activity of intracellular cysteine protease capthesins B in cell was observed via Immunocytochemistry assay and visualized under CLSM which will extend the project into the incorporation of cystatin, the cysteine protease inhibitors in CaCO3 PEMP in future.
author2 Bjoern Holger Neu
author_facet Bjoern Holger Neu
Cheah, Petrie Jiing Ei.
format Final Year Project
author Cheah, Petrie Jiing Ei.
author_sort Cheah, Petrie Jiing Ei.
title Fabrication of a biodegradable microcarrier system for drug delivery to cancer cells.
title_short Fabrication of a biodegradable microcarrier system for drug delivery to cancer cells.
title_full Fabrication of a biodegradable microcarrier system for drug delivery to cancer cells.
title_fullStr Fabrication of a biodegradable microcarrier system for drug delivery to cancer cells.
title_full_unstemmed Fabrication of a biodegradable microcarrier system for drug delivery to cancer cells.
title_sort fabrication of a biodegradable microcarrier system for drug delivery to cancer cells.
publishDate 2011
url http://hdl.handle.net/10356/45648
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