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Breakdown of the Blood-Ocular Barrier as a Strategy for the Systemic Use of Nanosystems

Several drug delivery systems have been proposed to overcome physiological barriers, improving ocular bioavailability. Systemic routes are seldom used due to the blood-ocular barrier. Novel drug delivery systems based on nanotechnology techniques have been developed to overcome ocular physiological...

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Detalles Bibliográficos
Autores principales: Occhiutto, Marcelo L., Freitas, Fatima R., Maranhao, Raul C., Costa, Vital P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834913/
https://www.ncbi.nlm.nih.gov/pubmed/24300231
http://dx.doi.org/10.3390/pharmaceutics4020252
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author Occhiutto, Marcelo L.
Freitas, Fatima R.
Maranhao, Raul C.
Costa, Vital P.
author_facet Occhiutto, Marcelo L.
Freitas, Fatima R.
Maranhao, Raul C.
Costa, Vital P.
author_sort Occhiutto, Marcelo L.
collection PubMed
description Several drug delivery systems have been proposed to overcome physiological barriers, improving ocular bioavailability. Systemic routes are seldom used due to the blood-ocular barrier. Novel drug delivery systems based on nanotechnology techniques have been developed to overcome ocular physiological barriers. This non-systematic review suggests the utilization of a transitory blood-ocular breakdown to allow the access of drugs by nanotechnology drug delivery systems via the systemic route. We discuss the possible ways to cause the breakdown of the blood-ocular barrier: acute inflammation caused by intraocular surgery, induced ocular hypotony, and the use of inflammatory mediators. The suitability of use of the systemic route and its toxic effects are also discussed in this article.
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spelling pubmed-38349132013-11-21 Breakdown of the Blood-Ocular Barrier as a Strategy for the Systemic Use of Nanosystems Occhiutto, Marcelo L. Freitas, Fatima R. Maranhao, Raul C. Costa, Vital P. Pharmaceutics Hypothesis Several drug delivery systems have been proposed to overcome physiological barriers, improving ocular bioavailability. Systemic routes are seldom used due to the blood-ocular barrier. Novel drug delivery systems based on nanotechnology techniques have been developed to overcome ocular physiological barriers. This non-systematic review suggests the utilization of a transitory blood-ocular breakdown to allow the access of drugs by nanotechnology drug delivery systems via the systemic route. We discuss the possible ways to cause the breakdown of the blood-ocular barrier: acute inflammation caused by intraocular surgery, induced ocular hypotony, and the use of inflammatory mediators. The suitability of use of the systemic route and its toxic effects are also discussed in this article. MDPI 2012-05-14 /pmc/articles/PMC3834913/ /pubmed/24300231 http://dx.doi.org/10.3390/pharmaceutics4020252 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Hypothesis
Occhiutto, Marcelo L.
Freitas, Fatima R.
Maranhao, Raul C.
Costa, Vital P.
Breakdown of the Blood-Ocular Barrier as a Strategy for the Systemic Use of Nanosystems
title Breakdown of the Blood-Ocular Barrier as a Strategy for the Systemic Use of Nanosystems
title_full Breakdown of the Blood-Ocular Barrier as a Strategy for the Systemic Use of Nanosystems
title_fullStr Breakdown of the Blood-Ocular Barrier as a Strategy for the Systemic Use of Nanosystems
title_full_unstemmed Breakdown of the Blood-Ocular Barrier as a Strategy for the Systemic Use of Nanosystems
title_short Breakdown of the Blood-Ocular Barrier as a Strategy for the Systemic Use of Nanosystems
title_sort breakdown of the blood-ocular barrier as a strategy for the systemic use of nanosystems
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834913/
https://www.ncbi.nlm.nih.gov/pubmed/24300231
http://dx.doi.org/10.3390/pharmaceutics4020252
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