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Prodrugs in Cardiovascular Therapy

Prodrugs are biologically inactive derivatives of an active drug intended to solve certain problems of the parent drug such as toxicity, instability, minimal solubility and non-targeting capabilities. The majority of drugs for cardiovascular diseases undergo first-pass metabolism, resulting in drug...

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Detalles Bibliográficos
Autores principales: Sandros, Marinella G., Sarraf, Chady B., Tabrizian, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245309/
https://www.ncbi.nlm.nih.gov/pubmed/18560335
http://dx.doi.org/10.3390/molecules13051156
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author Sandros, Marinella G.
Sarraf, Chady B.
Tabrizian, Maryam
author_facet Sandros, Marinella G.
Sarraf, Chady B.
Tabrizian, Maryam
author_sort Sandros, Marinella G.
collection PubMed
description Prodrugs are biologically inactive derivatives of an active drug intended to solve certain problems of the parent drug such as toxicity, instability, minimal solubility and non-targeting capabilities. The majority of drugs for cardiovascular diseases undergo first-pass metabolism, resulting in drug inactivation and generation of toxic metabolites, which makes them appealing targets for prodrug design. Since prodrugs undergo a chemical reaction to form the parent drug once inside the body, this makes them very effective in controlling the release of a variety of compounds to the targeted site. This review will provide the reader with an insight on the latest developments of prodrugs that are available for treating a variety of cardiovascular diseases. In addition, we will focus on several drug delivery methodologies that have merged with the prodrug approach to provide enhanced target specificity and controlled drug release with minimal side effects.
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spelling pubmed-62453092018-11-26 Prodrugs in Cardiovascular Therapy Sandros, Marinella G. Sarraf, Chady B. Tabrizian, Maryam Molecules Review Prodrugs are biologically inactive derivatives of an active drug intended to solve certain problems of the parent drug such as toxicity, instability, minimal solubility and non-targeting capabilities. The majority of drugs for cardiovascular diseases undergo first-pass metabolism, resulting in drug inactivation and generation of toxic metabolites, which makes them appealing targets for prodrug design. Since prodrugs undergo a chemical reaction to form the parent drug once inside the body, this makes them very effective in controlling the release of a variety of compounds to the targeted site. This review will provide the reader with an insight on the latest developments of prodrugs that are available for treating a variety of cardiovascular diseases. In addition, we will focus on several drug delivery methodologies that have merged with the prodrug approach to provide enhanced target specificity and controlled drug release with minimal side effects. MDPI 2008-05-14 /pmc/articles/PMC6245309/ /pubmed/18560335 http://dx.doi.org/10.3390/molecules13051156 Text en © 2008 by the authors. Licensee Molecular Diversity Preservation International, Basel, Switzerland. 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 Review
Sandros, Marinella G.
Sarraf, Chady B.
Tabrizian, Maryam
Prodrugs in Cardiovascular Therapy
title Prodrugs in Cardiovascular Therapy
title_full Prodrugs in Cardiovascular Therapy
title_fullStr Prodrugs in Cardiovascular Therapy
title_full_unstemmed Prodrugs in Cardiovascular Therapy
title_short Prodrugs in Cardiovascular Therapy
title_sort prodrugs in cardiovascular therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245309/
https://www.ncbi.nlm.nih.gov/pubmed/18560335
http://dx.doi.org/10.3390/molecules13051156
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