Design and development of polymeric levodopa nanoparticles for intranasal drug delivery / Mohd Zulhelmy Ahmad
Nasal delivery is an alternative route of delivery to deliver levodopa (L-dopa) to the brain. It provides high permeability towards drugs in the nasal epithelium, rapid absorption across the central nervous system (CNS) and avoidance of first-pass metabolism. Importantly, transport of exogenous mate...
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my.uitm.ir.859102024-03-27T01:17:05Z https://ir.uitm.edu.my/id/eprint/85910/ Design and development of polymeric levodopa nanoparticles for intranasal drug delivery / Mohd Zulhelmy Ahmad Ahmad, Mohd Zulhelmy Nasal delivery is an alternative route of delivery to deliver levodopa (L-dopa) to the brain. It provides high permeability towards drugs in the nasal epithelium, rapid absorption across the central nervous system (CNS) and avoidance of first-pass metabolism. Importantly, transport of exogenous materials directly from nose-to-brain is a potential route for bypassing the blood brain barrier (BBB). In this study, we developed a carrier system for L-dopa using polymers such as poly lactic co-glycolic acid (PLGA) and chitosan. Screening of suitable polymers as a drug carrier is important to ensure optimum percentage of L-dopa encapsulated in the carrier system. Total of three formulations (P1, P2 and P3) using PLGA nanoparticles were prepared using modified water in oil in water (W/O/W) solvent evaporation technique while four formulations of chitosan nanoparticles (C1, C2, C3 and C4) were prepared by ionic gelation method with sodium tripolyphosphate as a crosslinking agent. 2018 Thesis NonPeerReviewed text en https://ir.uitm.edu.my/id/eprint/85910/1/85910.pdf Design and development of polymeric levodopa nanoparticles for intranasal drug delivery / Mohd Zulhelmy Ahmad. (2018) Masters thesis, thesis, Universiti Teknologi MARA (UiTM). |
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Nasal delivery is an alternative route of delivery to deliver levodopa (L-dopa) to the brain. It provides high permeability towards drugs in the nasal epithelium, rapid absorption across the central nervous system (CNS) and avoidance of first-pass metabolism. Importantly, transport of exogenous materials directly from nose-to-brain is a potential route for bypassing the blood brain barrier (BBB). In this study, we developed a carrier system for L-dopa using polymers such as poly lactic co-glycolic acid (PLGA) and chitosan. Screening of suitable polymers as a drug carrier is important to ensure optimum percentage of L-dopa encapsulated in the carrier system. Total of three formulations (P1, P2 and P3) using PLGA nanoparticles were prepared using modified water in oil in water (W/O/W) solvent evaporation technique while four formulations of chitosan nanoparticles (C1, C2, C3 and C4) were prepared by ionic gelation method with sodium tripolyphosphate as a crosslinking agent. |
format |
Thesis |
author |
Ahmad, Mohd Zulhelmy |
spellingShingle |
Ahmad, Mohd Zulhelmy Design and development of polymeric levodopa nanoparticles for intranasal drug delivery / Mohd Zulhelmy Ahmad |
author_facet |
Ahmad, Mohd Zulhelmy |
author_sort |
Ahmad, Mohd Zulhelmy |
title |
Design and development of polymeric levodopa nanoparticles for intranasal drug delivery / Mohd Zulhelmy Ahmad |
title_short |
Design and development of polymeric levodopa nanoparticles for intranasal drug delivery / Mohd Zulhelmy Ahmad |
title_full |
Design and development of polymeric levodopa nanoparticles for intranasal drug delivery / Mohd Zulhelmy Ahmad |
title_fullStr |
Design and development of polymeric levodopa nanoparticles for intranasal drug delivery / Mohd Zulhelmy Ahmad |
title_full_unstemmed |
Design and development of polymeric levodopa nanoparticles for intranasal drug delivery / Mohd Zulhelmy Ahmad |
title_sort |
design and development of polymeric levodopa nanoparticles for intranasal drug delivery / mohd zulhelmy ahmad |
publishDate |
2018 |
url |
https://ir.uitm.edu.my/id/eprint/85910/1/85910.pdf https://ir.uitm.edu.my/id/eprint/85910/ |
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1795017050573242368 |