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A New NO-Releasing Nanoformulation for the Treatment of Pulmonary Arterial Hypertension
Pulmonary arterial hypertension (PAH) is a chronic and progressive disease which continues to carry an unacceptably high mortality and morbidity. The nitric oxide (NO) pathway has been implicated in the pathophysiology and progression of the disease. Its extremely short half-life and systemic effect...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830862/ https://www.ncbi.nlm.nih.gov/pubmed/26960567 http://dx.doi.org/10.1007/s12265-016-9684-2 |
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author | Mohamed, Nura A. Ahmetaj-Shala, Blerina Duluc, Lucie Mackenzie, Louise S. Kirkby, Nicholas S. Reed, Daniel M. Lickiss, Paul D. Davies, Robert P. Freeman, Gemma R. Wojciak-Stothard, Beata Chester, Adrian H. El-Sherbiny, Ibrahim M. Mitchell, Jane A. Yacoub, Magdi H. |
author_facet | Mohamed, Nura A. Ahmetaj-Shala, Blerina Duluc, Lucie Mackenzie, Louise S. Kirkby, Nicholas S. Reed, Daniel M. Lickiss, Paul D. Davies, Robert P. Freeman, Gemma R. Wojciak-Stothard, Beata Chester, Adrian H. El-Sherbiny, Ibrahim M. Mitchell, Jane A. Yacoub, Magdi H. |
author_sort | Mohamed, Nura A. |
collection | PubMed |
description | Pulmonary arterial hypertension (PAH) is a chronic and progressive disease which continues to carry an unacceptably high mortality and morbidity. The nitric oxide (NO) pathway has been implicated in the pathophysiology and progression of the disease. Its extremely short half-life and systemic effects have hampered the clinical use of NO in PAH. In an attempt to circumvent these major limitations, we have developed a new NO-nanomedicine formulation. The formulation was based on hydrogel-like polymeric composite NO-releasing nanoparticles (NO-RP). The kinetics of NO release from the NO-RP showed a peak at about 120 min followed by a sustained release for over 8 h. The NO-RP did not affect the viability or inflammation responses of endothelial cells. The NO-RP produced concentration-dependent relaxations of pulmonary arteries in mice with PAH induced by hypoxia. In conclusion, NO-RP drugs could considerably enhance the therapeutic potential of NO therapy for PAH. |
format | Online Article Text |
id | pubmed-4830862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-48308622016-04-22 A New NO-Releasing Nanoformulation for the Treatment of Pulmonary Arterial Hypertension Mohamed, Nura A. Ahmetaj-Shala, Blerina Duluc, Lucie Mackenzie, Louise S. Kirkby, Nicholas S. Reed, Daniel M. Lickiss, Paul D. Davies, Robert P. Freeman, Gemma R. Wojciak-Stothard, Beata Chester, Adrian H. El-Sherbiny, Ibrahim M. Mitchell, Jane A. Yacoub, Magdi H. J Cardiovasc Transl Res Correspondence Pulmonary arterial hypertension (PAH) is a chronic and progressive disease which continues to carry an unacceptably high mortality and morbidity. The nitric oxide (NO) pathway has been implicated in the pathophysiology and progression of the disease. Its extremely short half-life and systemic effects have hampered the clinical use of NO in PAH. In an attempt to circumvent these major limitations, we have developed a new NO-nanomedicine formulation. The formulation was based on hydrogel-like polymeric composite NO-releasing nanoparticles (NO-RP). The kinetics of NO release from the NO-RP showed a peak at about 120 min followed by a sustained release for over 8 h. The NO-RP did not affect the viability or inflammation responses of endothelial cells. The NO-RP produced concentration-dependent relaxations of pulmonary arteries in mice with PAH induced by hypoxia. In conclusion, NO-RP drugs could considerably enhance the therapeutic potential of NO therapy for PAH. Springer US 2016-03-09 2016 /pmc/articles/PMC4830862/ /pubmed/26960567 http://dx.doi.org/10.1007/s12265-016-9684-2 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Correspondence Mohamed, Nura A. Ahmetaj-Shala, Blerina Duluc, Lucie Mackenzie, Louise S. Kirkby, Nicholas S. Reed, Daniel M. Lickiss, Paul D. Davies, Robert P. Freeman, Gemma R. Wojciak-Stothard, Beata Chester, Adrian H. El-Sherbiny, Ibrahim M. Mitchell, Jane A. Yacoub, Magdi H. A New NO-Releasing Nanoformulation for the Treatment of Pulmonary Arterial Hypertension |
title | A New NO-Releasing Nanoformulation for the Treatment of Pulmonary Arterial Hypertension |
title_full | A New NO-Releasing Nanoformulation for the Treatment of Pulmonary Arterial Hypertension |
title_fullStr | A New NO-Releasing Nanoformulation for the Treatment of Pulmonary Arterial Hypertension |
title_full_unstemmed | A New NO-Releasing Nanoformulation for the Treatment of Pulmonary Arterial Hypertension |
title_short | A New NO-Releasing Nanoformulation for the Treatment of Pulmonary Arterial Hypertension |
title_sort | new no-releasing nanoformulation for the treatment of pulmonary arterial hypertension |
topic | Correspondence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830862/ https://www.ncbi.nlm.nih.gov/pubmed/26960567 http://dx.doi.org/10.1007/s12265-016-9684-2 |
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