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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2008
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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. |
format | Online Article Text |
id | pubmed-6245309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sandrosmarinellag prodrugsincardiovasculartherapy AT sarrafchadyb prodrugsincardiovasculartherapy AT tabrizianmaryam prodrugsincardiovasculartherapy |