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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2020
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sg-ntu-dr.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 |
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Engineering::Materials::Biomaterials Cheong, How Min Synthesis of novel drug-free cancer targeting nanotherapeutics |
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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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Dalton Tay Chor Yong |
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Dalton Tay Chor Yong Cheong, How Min |
format |
Final Year Project |
author |
Cheong, How Min |
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Cheong, How Min |
title |
Synthesis of novel drug-free cancer targeting nanotherapeutics |
title_short |
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 |
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Synthesis of novel drug-free cancer targeting nanotherapeutics |
title_sort |
synthesis of novel drug-free cancer targeting nanotherapeutics |
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Nanyang Technological University |
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2020 |
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https://hdl.handle.net/10356/139298 |
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