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Drug Delivery Systems for Imaging and Therapy of Parkinson's Disease
Background: Although a variety of therapeutic approaches are available for the treatment of Parkinson’s disease, challenges limit effective therapy. Among these challenges are delivery of drugs through the blood brain barier to the target brain tissue and the side effects observed during long term a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876593/ https://www.ncbi.nlm.nih.gov/pubmed/26714584 http://dx.doi.org/10.2174/1570159X14666151230124904 |
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author | Gunay, Mine Silindir Ozer, A. Yekta Chalon, Sylvie |
author_facet | Gunay, Mine Silindir Ozer, A. Yekta Chalon, Sylvie |
author_sort | Gunay, Mine Silindir |
collection | PubMed |
description | Background: Although a variety of therapeutic approaches are available for the treatment of Parkinson’s disease, challenges limit effective therapy. Among these challenges are delivery of drugs through the blood brain barier to the target brain tissue and the side effects observed during long term administration of antiparkinsonian drugs. The use of drug delivery systems such as liposomes, niosomes, micelles, nanoparticles, nanocapsules, gold nanoparticles, microspheres, microcapsules, nanobubbles, microbubbles and dendrimers is being investigated for diagnosis and therapy. Methods: This review focuses on formulation, development and advantages of nanosized drug delivery systems which can penetrate the central nervous system for the therapy and/or diagnosis of PD, and highlights future nanotechnological approaches. Results: It is esential to deliver a sufficient amount of either therapeutic or radiocontrast agents to the brain in order to provide the best possible efficacy or imaging without undesired degradation of the agent. Current treatments focus on motor symptoms, but these treatments generally do not deal with modifying the course of Parkinson’s disease. Beyond pharmacological therapy, the identification of abnormal proteins such as α-synuclein, parkin or leucine-rich repeat serine/threonine protein kinase 2 could represent promising alternative targets for molecular imaging and therapy of Parkinson's disease. Conclusion: Nanotechnology and nanosized drug delivery systems are being investigated intensely and could have potential effect for Parkinson’s disease. The improvement of drug delivery systems could dramatically enhance the effectiveness of Parkinson’s Disease therapy and reduce its side effects. |
format | Online Article Text |
id | pubmed-4876593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-48765932016-11-01 Drug Delivery Systems for Imaging and Therapy of Parkinson's Disease Gunay, Mine Silindir Ozer, A. Yekta Chalon, Sylvie Curr Neuropharmacol Article Background: Although a variety of therapeutic approaches are available for the treatment of Parkinson’s disease, challenges limit effective therapy. Among these challenges are delivery of drugs through the blood brain barier to the target brain tissue and the side effects observed during long term administration of antiparkinsonian drugs. The use of drug delivery systems such as liposomes, niosomes, micelles, nanoparticles, nanocapsules, gold nanoparticles, microspheres, microcapsules, nanobubbles, microbubbles and dendrimers is being investigated for diagnosis and therapy. Methods: This review focuses on formulation, development and advantages of nanosized drug delivery systems which can penetrate the central nervous system for the therapy and/or diagnosis of PD, and highlights future nanotechnological approaches. Results: It is esential to deliver a sufficient amount of either therapeutic or radiocontrast agents to the brain in order to provide the best possible efficacy or imaging without undesired degradation of the agent. Current treatments focus on motor symptoms, but these treatments generally do not deal with modifying the course of Parkinson’s disease. Beyond pharmacological therapy, the identification of abnormal proteins such as α-synuclein, parkin or leucine-rich repeat serine/threonine protein kinase 2 could represent promising alternative targets for molecular imaging and therapy of Parkinson's disease. Conclusion: Nanotechnology and nanosized drug delivery systems are being investigated intensely and could have potential effect for Parkinson’s disease. The improvement of drug delivery systems could dramatically enhance the effectiveness of Parkinson’s Disease therapy and reduce its side effects. Bentham Science Publishers 2016-05 2016-05 /pmc/articles/PMC4876593/ /pubmed/26714584 http://dx.doi.org/10.2174/1570159X14666151230124904 Text en © 2016 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Gunay, Mine Silindir Ozer, A. Yekta Chalon, Sylvie Drug Delivery Systems for Imaging and Therapy of Parkinson's Disease |
title | Drug Delivery Systems for Imaging and Therapy of Parkinson's Disease |
title_full | Drug Delivery Systems for Imaging and Therapy of Parkinson's Disease |
title_fullStr | Drug Delivery Systems for Imaging and Therapy of Parkinson's Disease |
title_full_unstemmed | Drug Delivery Systems for Imaging and Therapy of Parkinson's Disease |
title_short | Drug Delivery Systems for Imaging and Therapy of Parkinson's Disease |
title_sort | drug delivery systems for imaging and therapy of parkinson's disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876593/ https://www.ncbi.nlm.nih.gov/pubmed/26714584 http://dx.doi.org/10.2174/1570159X14666151230124904 |
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