Development of hybrid exosome-mimetic nanoparticles for eye disease

Topical instillation is the most common route of ocular drug delivery due to its ease of administration and high patient compliance. However, with the complex structure and numerous barriers of the eye, the bioavailability of drugs administered topically is <5%. Thus, there is a need to introd...

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Main Author: Tan, Aaron Ming Hao
Other Authors: Czarny Bertrand Marcel Stanislas
Format: Final Year Project
Language:English
Published: Nanyang Technological University 2021
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Online Access:https://hdl.handle.net/10356/148728
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1487282021-05-15T13:39:12Z Development of hybrid exosome-mimetic nanoparticles for eye disease Tan, Aaron Ming Hao Czarny Bertrand Marcel Stanislas School of Materials Science and Engineering bczarny@ntu.edu.sg Engineering::Materials::Biomaterials Topical instillation is the most common route of ocular drug delivery due to its ease of administration and high patient compliance. However, with the complex structure and numerous barriers of the eye, the bioavailability of drugs administered topically is <5%. Thus, there is a need to introduce a new drug delivery system for ocular medications to overcome the low bioavailability. Cell-derived nanovesicles (CDNs) are exosome-mimetic vesicles with a superior production capability and possess membrane proteins that aid in cellular uptake. However, the CDNs exhibit a negative surface charge and would experience electrostatic repulsion to the corneal tissues. Consequently, the electrostatic repulsion would reduce the adsorption of the CDNs onto the corneal surface, affecting their cellular uptake and permeation. Thus, in this study, the aim was to hybridize CDNs with cationic materials to introduce a positive surface charge. This was done by centrifugal serial extrusion. Hybrid CDNs were synthesized using chitosan, polyallylamine hydrochloride (PAH), and dioleoyl-3-trimethylammonium propane (DOTAP). The hybrid CDNs were then characterized by nanoparticle tracking analysis and zeta potential (ZP), for hydrodynamic size and surface charge, respectively. The hybridization was shown to reduce the negative surface charge of the CDNs through the integration of cationic materials with the CDN membrane. DOTAP and PAH had shown good integration with CDNs, creating cationic hybrid CDNs with a zeta potential of 2.73 mV and 2.19 mV, respectively. Hence, DOTAP and PAH hybrid CDNs have the potential to be used as an ocular drug delivery system. Although chitosan had integrated with CDNs, the chitosan-hybrid CDNs failed to exhibit a positive ZP and were deemed unsuitable for this application. Bachelor of Engineering (Materials Engineering) 2021-05-15T13:39:12Z 2021-05-15T13:39:12Z 2021 Final Year Project (FYP) Tan, A. M. H. (2021). Development of hybrid exosome-mimetic nanoparticles for eye disease. Final Year Project (FYP), Nanyang Technological University, Singapore. https://hdl.handle.net/10356/148728 https://hdl.handle.net/10356/148728 en application/pdf Nanyang Technological University
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Materials::Biomaterials
spellingShingle Engineering::Materials::Biomaterials
Tan, Aaron Ming Hao
Development of hybrid exosome-mimetic nanoparticles for eye disease
description Topical instillation is the most common route of ocular drug delivery due to its ease of administration and high patient compliance. However, with the complex structure and numerous barriers of the eye, the bioavailability of drugs administered topically is <5%. Thus, there is a need to introduce a new drug delivery system for ocular medications to overcome the low bioavailability. Cell-derived nanovesicles (CDNs) are exosome-mimetic vesicles with a superior production capability and possess membrane proteins that aid in cellular uptake. However, the CDNs exhibit a negative surface charge and would experience electrostatic repulsion to the corneal tissues. Consequently, the electrostatic repulsion would reduce the adsorption of the CDNs onto the corneal surface, affecting their cellular uptake and permeation. Thus, in this study, the aim was to hybridize CDNs with cationic materials to introduce a positive surface charge. This was done by centrifugal serial extrusion. Hybrid CDNs were synthesized using chitosan, polyallylamine hydrochloride (PAH), and dioleoyl-3-trimethylammonium propane (DOTAP). The hybrid CDNs were then characterized by nanoparticle tracking analysis and zeta potential (ZP), for hydrodynamic size and surface charge, respectively. The hybridization was shown to reduce the negative surface charge of the CDNs through the integration of cationic materials with the CDN membrane. DOTAP and PAH had shown good integration with CDNs, creating cationic hybrid CDNs with a zeta potential of 2.73 mV and 2.19 mV, respectively. Hence, DOTAP and PAH hybrid CDNs have the potential to be used as an ocular drug delivery system. Although chitosan had integrated with CDNs, the chitosan-hybrid CDNs failed to exhibit a positive ZP and were deemed unsuitable for this application.
author2 Czarny Bertrand Marcel Stanislas
author_facet Czarny Bertrand Marcel Stanislas
Tan, Aaron Ming Hao
format Final Year Project
author Tan, Aaron Ming Hao
author_sort Tan, Aaron Ming Hao
title Development of hybrid exosome-mimetic nanoparticles for eye disease
title_short Development of hybrid exosome-mimetic nanoparticles for eye disease
title_full Development of hybrid exosome-mimetic nanoparticles for eye disease
title_fullStr Development of hybrid exosome-mimetic nanoparticles for eye disease
title_full_unstemmed Development of hybrid exosome-mimetic nanoparticles for eye disease
title_sort development of hybrid exosome-mimetic nanoparticles for eye disease
publisher Nanyang Technological University
publishDate 2021
url https://hdl.handle.net/10356/148728
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