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Nano-particle engineered atorvastatin delivery to support mesenchymal stem cell survival in infarcted myocardium
Atorvastatin (ATV) may support mesenchymal stem cells (MSC) survival in post-infarct myocardium (MI) as inflammatory reactions, oxidative stress and hypoxia condition get started in such tissues after damage. However, limited aqueous insolubility and rapid first-pass metabolism reduce the systemic a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117435/ https://www.ncbi.nlm.nih.gov/pubmed/30174496 http://dx.doi.org/10.1016/j.sjbs.2017.03.015 |
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author | Yao, Guang-tao Song, Li-ping Xue, Wan-hua Su, Guo-hai Ning, Ai-hua Wang, Jin |
author_facet | Yao, Guang-tao Song, Li-ping Xue, Wan-hua Su, Guo-hai Ning, Ai-hua Wang, Jin |
author_sort | Yao, Guang-tao |
collection | PubMed |
description | Atorvastatin (ATV) may support mesenchymal stem cells (MSC) survival in post-infarct myocardium (MI) as inflammatory reactions, oxidative stress and hypoxia condition get started in such tissues after damage. However, limited aqueous insolubility and rapid first-pass metabolism reduce the systemic availability of ATV. The aim of the present investigation was to develop ATV loaded nanoparticles (ATVNPs) which might ensure the maximum availability of ATV in systemic circulation for longer duration and to strengthen the support to MSC survival. ATVNPs were synthesized using double emulsion solvent evaporation method and characterized as spherical shape, positive charged, nanoparticles of uniform size distribution and higher entrapment efficiency. ATVNPs were non-cytotoxic and showed sustained release (up to 28 days). Assessment of cardiac function (in terms of echocardiographic and left heart catheterization parameters) and cytokines estimation revealed efficient improvement in post-infarct myocardium condition of rat. In conclusion, ATVNP was developed successfully that may ensure safe, cost effective, and efficacious treatment of post-infarct myo-cardium when compared with that of MSC alone and MSC supplemented with ATV solution. |
format | Online Article Text |
id | pubmed-6117435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61174352018-08-31 Nano-particle engineered atorvastatin delivery to support mesenchymal stem cell survival in infarcted myocardium Yao, Guang-tao Song, Li-ping Xue, Wan-hua Su, Guo-hai Ning, Ai-hua Wang, Jin Saudi J Biol Sci Article Atorvastatin (ATV) may support mesenchymal stem cells (MSC) survival in post-infarct myocardium (MI) as inflammatory reactions, oxidative stress and hypoxia condition get started in such tissues after damage. However, limited aqueous insolubility and rapid first-pass metabolism reduce the systemic availability of ATV. The aim of the present investigation was to develop ATV loaded nanoparticles (ATVNPs) which might ensure the maximum availability of ATV in systemic circulation for longer duration and to strengthen the support to MSC survival. ATVNPs were synthesized using double emulsion solvent evaporation method and characterized as spherical shape, positive charged, nanoparticles of uniform size distribution and higher entrapment efficiency. ATVNPs were non-cytotoxic and showed sustained release (up to 28 days). Assessment of cardiac function (in terms of echocardiographic and left heart catheterization parameters) and cytokines estimation revealed efficient improvement in post-infarct myocardium condition of rat. In conclusion, ATVNP was developed successfully that may ensure safe, cost effective, and efficacious treatment of post-infarct myo-cardium when compared with that of MSC alone and MSC supplemented with ATV solution. Elsevier 2018-09 2017-04-04 /pmc/articles/PMC6117435/ /pubmed/30174496 http://dx.doi.org/10.1016/j.sjbs.2017.03.015 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Yao, Guang-tao Song, Li-ping Xue, Wan-hua Su, Guo-hai Ning, Ai-hua Wang, Jin Nano-particle engineered atorvastatin delivery to support mesenchymal stem cell survival in infarcted myocardium |
title | Nano-particle engineered atorvastatin delivery to support mesenchymal stem cell survival in infarcted myocardium |
title_full | Nano-particle engineered atorvastatin delivery to support mesenchymal stem cell survival in infarcted myocardium |
title_fullStr | Nano-particle engineered atorvastatin delivery to support mesenchymal stem cell survival in infarcted myocardium |
title_full_unstemmed | Nano-particle engineered atorvastatin delivery to support mesenchymal stem cell survival in infarcted myocardium |
title_short | Nano-particle engineered atorvastatin delivery to support mesenchymal stem cell survival in infarcted myocardium |
title_sort | nano-particle engineered atorvastatin delivery to support mesenchymal stem cell survival in infarcted myocardium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117435/ https://www.ncbi.nlm.nih.gov/pubmed/30174496 http://dx.doi.org/10.1016/j.sjbs.2017.03.015 |
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