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Targeted delivery of doxorubicin by nano-loaded mesenchymal stem cells for lung melanoma metastases therapy
Poor antigenic presentation of tumor tissues and a lack of specific targets currently limit the success of nanoparticle delivery system. Cellular carrier technique has been recently explored extensively as a substitutive or supplement for traditional targeting delivery system. Here, we demonstrate t...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355993/ https://www.ncbi.nlm.nih.gov/pubmed/28303966 http://dx.doi.org/10.1038/srep44758 |
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author | Zhao, Yuekui Tang, Shanshan Guo, Jiamin Alahdal, Murad Cao, Shunxiu Yang, Zhaocong Zhang, Fangfang Shen, Yumeng Sun, Minjie Mo, Ran Zong, Li Jin, Liang |
author_facet | Zhao, Yuekui Tang, Shanshan Guo, Jiamin Alahdal, Murad Cao, Shunxiu Yang, Zhaocong Zhang, Fangfang Shen, Yumeng Sun, Minjie Mo, Ran Zong, Li Jin, Liang |
author_sort | Zhao, Yuekui |
collection | PubMed |
description | Poor antigenic presentation of tumor tissues and a lack of specific targets currently limit the success of nanoparticle delivery system. Cellular carrier technique has been recently explored extensively as a substitutive or supplement for traditional targeting delivery system. Here, we demonstrate the usage of mesenchymal stem cells (MSCs) loaded with doxorubicin containing polymer nanoparticles in pulmonary melanoma metastases therapy, as a modified technique of targeted delivery system. The characterizations of prepared nanoparticles and MSCs sensitivity to DOX and PLGA-DOX were measured. In vitro tumor tropism, and in vivo distributions of nanoparticles loaded MSCs were also investigated. The findings have demonstrated that, the modified system not only integrates the controlled-release property of nanoparticles but also exhibits tumor tropism and penetrative characteristics of MSCs. Furthermore, the in vitro and in vivo anti-tumor study has demonstrated that drug loaded MSCs had potent efficacy in lung melanoma metastases treatment. |
format | Online Article Text |
id | pubmed-5355993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53559932017-03-22 Targeted delivery of doxorubicin by nano-loaded mesenchymal stem cells for lung melanoma metastases therapy Zhao, Yuekui Tang, Shanshan Guo, Jiamin Alahdal, Murad Cao, Shunxiu Yang, Zhaocong Zhang, Fangfang Shen, Yumeng Sun, Minjie Mo, Ran Zong, Li Jin, Liang Sci Rep Article Poor antigenic presentation of tumor tissues and a lack of specific targets currently limit the success of nanoparticle delivery system. Cellular carrier technique has been recently explored extensively as a substitutive or supplement for traditional targeting delivery system. Here, we demonstrate the usage of mesenchymal stem cells (MSCs) loaded with doxorubicin containing polymer nanoparticles in pulmonary melanoma metastases therapy, as a modified technique of targeted delivery system. The characterizations of prepared nanoparticles and MSCs sensitivity to DOX and PLGA-DOX were measured. In vitro tumor tropism, and in vivo distributions of nanoparticles loaded MSCs were also investigated. The findings have demonstrated that, the modified system not only integrates the controlled-release property of nanoparticles but also exhibits tumor tropism and penetrative characteristics of MSCs. Furthermore, the in vitro and in vivo anti-tumor study has demonstrated that drug loaded MSCs had potent efficacy in lung melanoma metastases treatment. Nature Publishing Group 2017-03-17 /pmc/articles/PMC5355993/ /pubmed/28303966 http://dx.doi.org/10.1038/srep44758 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zhao, Yuekui Tang, Shanshan Guo, Jiamin Alahdal, Murad Cao, Shunxiu Yang, Zhaocong Zhang, Fangfang Shen, Yumeng Sun, Minjie Mo, Ran Zong, Li Jin, Liang Targeted delivery of doxorubicin by nano-loaded mesenchymal stem cells for lung melanoma metastases therapy |
title | Targeted delivery of doxorubicin by nano-loaded mesenchymal stem cells for lung melanoma metastases therapy |
title_full | Targeted delivery of doxorubicin by nano-loaded mesenchymal stem cells for lung melanoma metastases therapy |
title_fullStr | Targeted delivery of doxorubicin by nano-loaded mesenchymal stem cells for lung melanoma metastases therapy |
title_full_unstemmed | Targeted delivery of doxorubicin by nano-loaded mesenchymal stem cells for lung melanoma metastases therapy |
title_short | Targeted delivery of doxorubicin by nano-loaded mesenchymal stem cells for lung melanoma metastases therapy |
title_sort | targeted delivery of doxorubicin by nano-loaded mesenchymal stem cells for lung melanoma metastases therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355993/ https://www.ncbi.nlm.nih.gov/pubmed/28303966 http://dx.doi.org/10.1038/srep44758 |
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