Development of novel intranasal therapeutic nanoclusters for traumatic brain injury (TBI)

Traumatic brain injury (TBI) is one of the major risk factors for disability and death affecting people of all age groups. Secondary TBI injuries can potentially deteriorate and cause progressive neurodegeneration and neurological disability. Although secondary TBI injuries can be potentially preven...

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Main Author: Fong, Lai Guan
Other Authors: Song Juha
Format: Thesis-Master by Research
Language:English
Published: Nanyang Technological University 2024
Subjects:
Online Access:https://hdl.handle.net/10356/178731
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author Fong, Lai Guan
author2 Song Juha
author_facet Song Juha
Fong, Lai Guan
author_sort Fong, Lai Guan
collection NTU
description Traumatic brain injury (TBI) is one of the major risk factors for disability and death affecting people of all age groups. Secondary TBI injuries can potentially deteriorate and cause progressive neurodegeneration and neurological disability. Although secondary TBI injuries can be potentially prevented, currently, there are still no effective neuroprotective therapeutics that can minimize their detrimental effects due to the heterogeneity and complexity of the pathological mechanisms that ensue after brain injury. It was hypothesized that successful delivery of intact functional microRNA-124 (miR124) could potentially help ameliorate TBI-induced secondary injuries by reducing neuroinflammation, preserving cell survival, and stimulating regeneration after injury. To harness the neuroprotective potential of miR124, this study engineered a wheat germ agglutinin (WGA)-conjugated polymer NP that can be loaded with miR124 (WGA-NP-miR124) and evaluated its therapeutic properties in vitro. Characterization studies indicated that WGA-NP-miR124 possesses the ideal physical and chemical characteristics for intranasal delivery. In vitro cellular model experiments showed that WGA-NP-miR124 has no significant cytotoxicity and can be efficiently taken up by cells. Treatment of the SH-SY5Y scratch injury model with WGA-NP-miR124 significantly improved cell proliferation after injury. The protein expression level of the PARP p85 fragment and the results of the apoptosis assay indicated that WGA-NP-miR124 treatment reduced cell death and enhanced cell proliferation. Overall, these findings in vitro suggest that WGA-NP-miR124 holds promising therapeutic effects in enhancing cell proliferation and inhibiting apoptosis, which could benefit future TBI treatment approaches.
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spelling ntu-10356/1787312024-08-01T08:11:46Z Development of novel intranasal therapeutic nanoclusters for traumatic brain injury (TBI) Fong, Lai Guan Song Juha School of Chemistry, Chemical Engineering and Biotechnology Lee Kong Chian School of Medicine (LKCMedicine) Parasuraman Padmanabhan songjuha@ntu.edu.sg, ppadmanabhan@ntu.edu.sg Engineering Medicine, Health and Life Sciences Neuroscience Nanoparticle Traumatic brain injury miRNA Therapeutic Traumatic brain injury (TBI) is one of the major risk factors for disability and death affecting people of all age groups. Secondary TBI injuries can potentially deteriorate and cause progressive neurodegeneration and neurological disability. Although secondary TBI injuries can be potentially prevented, currently, there are still no effective neuroprotective therapeutics that can minimize their detrimental effects due to the heterogeneity and complexity of the pathological mechanisms that ensue after brain injury. It was hypothesized that successful delivery of intact functional microRNA-124 (miR124) could potentially help ameliorate TBI-induced secondary injuries by reducing neuroinflammation, preserving cell survival, and stimulating regeneration after injury. To harness the neuroprotective potential of miR124, this study engineered a wheat germ agglutinin (WGA)-conjugated polymer NP that can be loaded with miR124 (WGA-NP-miR124) and evaluated its therapeutic properties in vitro. Characterization studies indicated that WGA-NP-miR124 possesses the ideal physical and chemical characteristics for intranasal delivery. In vitro cellular model experiments showed that WGA-NP-miR124 has no significant cytotoxicity and can be efficiently taken up by cells. Treatment of the SH-SY5Y scratch injury model with WGA-NP-miR124 significantly improved cell proliferation after injury. The protein expression level of the PARP p85 fragment and the results of the apoptosis assay indicated that WGA-NP-miR124 treatment reduced cell death and enhanced cell proliferation. Overall, these findings in vitro suggest that WGA-NP-miR124 holds promising therapeutic effects in enhancing cell proliferation and inhibiting apoptosis, which could benefit future TBI treatment approaches. Master's degree 2024-07-04T01:16:59Z 2024-07-04T01:16:59Z 2024 Thesis-Master by Research Fong, L. G. (2024). Development of novel intranasal therapeutic nanoclusters for traumatic brain injury (TBI). Master's thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/178731 https://hdl.handle.net/10356/178731 10.32657/10356/178731 en This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0). application/pdf Nanyang Technological University
spellingShingle Engineering
Medicine, Health and Life Sciences
Neuroscience
Nanoparticle
Traumatic brain injury
miRNA
Therapeutic
Fong, Lai Guan
Development of novel intranasal therapeutic nanoclusters for traumatic brain injury (TBI)
title Development of novel intranasal therapeutic nanoclusters for traumatic brain injury (TBI)
title_full Development of novel intranasal therapeutic nanoclusters for traumatic brain injury (TBI)
title_fullStr Development of novel intranasal therapeutic nanoclusters for traumatic brain injury (TBI)
title_full_unstemmed Development of novel intranasal therapeutic nanoclusters for traumatic brain injury (TBI)
title_short Development of novel intranasal therapeutic nanoclusters for traumatic brain injury (TBI)
title_sort development of novel intranasal therapeutic nanoclusters for traumatic brain injury tbi
topic Engineering
Medicine, Health and Life Sciences
Neuroscience
Nanoparticle
Traumatic brain injury
miRNA
Therapeutic
url https://hdl.handle.net/10356/178731
work_keys_str_mv AT fonglaiguan developmentofnovelintranasaltherapeuticnanoclustersfortraumaticbraininjurytbi