Developing ultrasound-responsive and drug delivery nanoparticles for acoustic implantation
Atherosclerotic lesions that leads to stroke and acute myocardial infarction remains an issue without a perfect cure. This project focuses on targeted therapy for atherosclerosis, which is achieved using ultrasound-induced cavitation to transport and embed therapeutic drug-loaded agents directly at...
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sg-ntu-dr.10356-755922023-03-03T15:40:08Z Developing ultrasound-responsive and drug delivery nanoparticles for acoustic implantation Chen, Jia Yi James Jing Kwan School of Chemical and Biomedical Engineering DRNTU::Engineering::Bioengineering Atherosclerotic lesions that leads to stroke and acute myocardial infarction remains an issue without a perfect cure. This project focuses on targeted therapy for atherosclerosis, which is achieved using ultrasound-induced cavitation to transport and embed therapeutic drug-loaded agents directly at the site of the lesion Gold nanocone were fabricated and physically and acoustically analyzed. These Gold nanocones had an average diameter of 105.6nm. It was evident that forming nanocones was sensitive to the protocol. In order to nucleate cavitation, Gold nanocones must trap a nanobubble. Thus, Gold nanocones were first pegylated before freeze drying. The PEG prevents agglomeration when suspended for a gas nanobubble to be trapped in the crevice. From the resuspended nanocones, ultrasound was applied to determine if there are any cavitation activities. Bachelor of Engineering (Chemical and Biomolecular Engineering) 2018-06-05T01:55:23Z 2018-06-05T01:55:23Z 2018 Final Year Project (FYP) http://hdl.handle.net/10356/75592 en Nanyang Technological University 41 p. application/pdf |
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DRNTU::Engineering::Bioengineering Chen, Jia Yi Developing ultrasound-responsive and drug delivery nanoparticles for acoustic implantation |
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Atherosclerotic lesions that leads to stroke and acute myocardial infarction remains an issue without a perfect cure. This project focuses on targeted therapy for atherosclerosis, which is achieved using ultrasound-induced cavitation to transport and embed therapeutic drug-loaded agents directly at the site of the lesion Gold nanocone were fabricated and physically and acoustically analyzed. These Gold nanocones had an average diameter of 105.6nm. It was evident that forming nanocones was sensitive to the protocol. In order to nucleate cavitation, Gold nanocones must trap a nanobubble. Thus, Gold nanocones were first pegylated before freeze drying. The PEG prevents agglomeration when suspended for a gas nanobubble to be trapped in the crevice. From the resuspended nanocones, ultrasound was applied to determine if there are any cavitation activities. |
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James Jing Kwan |
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James Jing Kwan Chen, Jia Yi |
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Final Year Project |
author |
Chen, Jia Yi |
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Chen, Jia Yi |
title |
Developing ultrasound-responsive and drug delivery nanoparticles for acoustic implantation |
title_short |
Developing ultrasound-responsive and drug delivery nanoparticles for acoustic implantation |
title_full |
Developing ultrasound-responsive and drug delivery nanoparticles for acoustic implantation |
title_fullStr |
Developing ultrasound-responsive and drug delivery nanoparticles for acoustic implantation |
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Developing ultrasound-responsive and drug delivery nanoparticles for acoustic implantation |
title_sort |
developing ultrasound-responsive and drug delivery nanoparticles for acoustic implantation |
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2018 |
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http://hdl.handle.net/10356/75592 |
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1759857656098455552 |