Synthesis of novel drug-free cancer targeting nanotherapeutics

Cancer remains the leading cause of death worldwide. Mesoporous silica nanoparticles (MSNs) are seen as one of the promising candidates for anti-cancer therapy, due to its favourable cancer-killing properties. In this research paper, MSNs are being further modified, through attachment of PEG (Polyet...

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Main Author: Cheong, How Min
Other Authors: Dalton Tay Chor Yong
Format: Final Year Project (FYP)
Language:English
Published: Nanyang Technological University 2020
Subjects:
Online Access:https://hdl.handle.net/10356/139298
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author Cheong, How Min
author2 Dalton Tay Chor Yong
author_facet Dalton Tay Chor Yong
Cheong, How Min
author_sort Cheong, How Min
collection NTU
description Cancer remains the leading cause of death worldwide. Mesoporous silica nanoparticles (MSNs) are seen as one of the promising candidates for anti-cancer therapy, due to its favourable cancer-killing properties. In this research paper, MSNs are being further modified, through attachment of PEG (Polyethylene Glycol) chains, in efforts to increase its ability to cause cancer cell death in-vivo, by reducing aggregation and therefore increasing the stability of MSNs. Preliminary in vitro results indicate that PEG conjugation can significantly enhance the stability of MSN in water as well as physiologically-emulated phosphate-buffered saline (PBS). These data lay a solid foundation for the follow-up fabrication of cancer-targeting physiologically-stable silica nanomedicine.
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spelling ntu-10356/1392982023-03-04T15:48:23Z Synthesis of novel drug-free cancer targeting nanotherapeutics Cheong, How Min Dalton Tay Chor Yong School of Materials Science and Engineering cytay@ntu.edu.sg Engineering::Materials::Biomaterials Cancer remains the leading cause of death worldwide. Mesoporous silica nanoparticles (MSNs) are seen as one of the promising candidates for anti-cancer therapy, due to its favourable cancer-killing properties. In this research paper, MSNs are being further modified, through attachment of PEG (Polyethylene Glycol) chains, in efforts to increase its ability to cause cancer cell death in-vivo, by reducing aggregation and therefore increasing the stability of MSNs. Preliminary in vitro results indicate that PEG conjugation can significantly enhance the stability of MSN in water as well as physiologically-emulated phosphate-buffered saline (PBS). These data lay a solid foundation for the follow-up fabrication of cancer-targeting physiologically-stable silica nanomedicine. Bachelor of Engineering (Materials Engineering) 2020-05-18T10:45:58Z 2020-05-18T10:45:58Z 2020 Final Year Project (FYP) https://hdl.handle.net/10356/139298 en application/pdf Nanyang Technological University
spellingShingle Engineering::Materials::Biomaterials
Cheong, How Min
Synthesis of novel drug-free cancer targeting nanotherapeutics
title Synthesis of novel drug-free cancer targeting nanotherapeutics
title_full Synthesis of novel drug-free cancer targeting nanotherapeutics
title_fullStr Synthesis of novel drug-free cancer targeting nanotherapeutics
title_full_unstemmed Synthesis of novel drug-free cancer targeting nanotherapeutics
title_short Synthesis of novel drug-free cancer targeting nanotherapeutics
title_sort synthesis of novel drug free cancer targeting nanotherapeutics
topic Engineering::Materials::Biomaterials
url https://hdl.handle.net/10356/139298
work_keys_str_mv AT cheonghowmin synthesisofnoveldrugfreecancertargetingnanotherapeutics