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Gambogic acid-loaded biomimetic nanoparticles in colorectal cancer treatment
Gambogic acid (GA) is expected to be a potential new antitumor drug, but its poor aqueous solubility and inevitable side effects limit its clinical application. Despite these inhe rent defects, various nanocarriers can be used to promote the solubility and tumor targeting of GA, improving antitumor...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339001/ https://www.ncbi.nlm.nih.gov/pubmed/28280328 http://dx.doi.org/10.2147/IJN.S127256 |
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author | Zhang, Zhen Qian, Hanqing Yang, Mi Li, Rutian Hu, Jing Li, Li Yu, Lixia Liu, Baorui Qian, Xiaoping |
author_facet | Zhang, Zhen Qian, Hanqing Yang, Mi Li, Rutian Hu, Jing Li, Li Yu, Lixia Liu, Baorui Qian, Xiaoping |
author_sort | Zhang, Zhen |
collection | PubMed |
description | Gambogic acid (GA) is expected to be a potential new antitumor drug, but its poor aqueous solubility and inevitable side effects limit its clinical application. Despite these inhe rent defects, various nanocarriers can be used to promote the solubility and tumor targeting of GA, improving antitumor efficiency. In addition, a cell membrane-coated nanoparticle platform that was reported recently, unites the customizability and flexibility of a synthetic copolymer, as well as the functionality and complexity of natural membrane, and is a new synthetic biomimetic nanocarrier with improved stability and biocompatibility. Here, we combined poly(lactic-co-glycolic acid) (PLGA) with red blood-cell membrane (RBCm), and evaluated whether GA-loaded RBCm nanoparticles can retain and improve the antitumor efficacy of GA with relatively lower toxicity in colorectal cancer treatment compared with free GA. We also confirmed the stability, biocompatibility, passive targeting, and few side effects of RBCm-GA/PLGA nanoparticles. We expect to provide a new drug carrier in the treatment of colorectal cancer, which has strong clinical application prospects. In addition, the potential antitumor drug GA and other similar drugs could achieve broader clinical applications via this biomimetic nanocarrier. |
format | Online Article Text |
id | pubmed-5339001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53390012017-03-09 Gambogic acid-loaded biomimetic nanoparticles in colorectal cancer treatment Zhang, Zhen Qian, Hanqing Yang, Mi Li, Rutian Hu, Jing Li, Li Yu, Lixia Liu, Baorui Qian, Xiaoping Int J Nanomedicine Original Research Gambogic acid (GA) is expected to be a potential new antitumor drug, but its poor aqueous solubility and inevitable side effects limit its clinical application. Despite these inhe rent defects, various nanocarriers can be used to promote the solubility and tumor targeting of GA, improving antitumor efficiency. In addition, a cell membrane-coated nanoparticle platform that was reported recently, unites the customizability and flexibility of a synthetic copolymer, as well as the functionality and complexity of natural membrane, and is a new synthetic biomimetic nanocarrier with improved stability and biocompatibility. Here, we combined poly(lactic-co-glycolic acid) (PLGA) with red blood-cell membrane (RBCm), and evaluated whether GA-loaded RBCm nanoparticles can retain and improve the antitumor efficacy of GA with relatively lower toxicity in colorectal cancer treatment compared with free GA. We also confirmed the stability, biocompatibility, passive targeting, and few side effects of RBCm-GA/PLGA nanoparticles. We expect to provide a new drug carrier in the treatment of colorectal cancer, which has strong clinical application prospects. In addition, the potential antitumor drug GA and other similar drugs could achieve broader clinical applications via this biomimetic nanocarrier. Dove Medical Press 2017-02-28 /pmc/articles/PMC5339001/ /pubmed/28280328 http://dx.doi.org/10.2147/IJN.S127256 Text en © 2017 Zhang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Zhang, Zhen Qian, Hanqing Yang, Mi Li, Rutian Hu, Jing Li, Li Yu, Lixia Liu, Baorui Qian, Xiaoping Gambogic acid-loaded biomimetic nanoparticles in colorectal cancer treatment |
title | Gambogic acid-loaded biomimetic nanoparticles in colorectal cancer treatment |
title_full | Gambogic acid-loaded biomimetic nanoparticles in colorectal cancer treatment |
title_fullStr | Gambogic acid-loaded biomimetic nanoparticles in colorectal cancer treatment |
title_full_unstemmed | Gambogic acid-loaded biomimetic nanoparticles in colorectal cancer treatment |
title_short | Gambogic acid-loaded biomimetic nanoparticles in colorectal cancer treatment |
title_sort | gambogic acid-loaded biomimetic nanoparticles in colorectal cancer treatment |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339001/ https://www.ncbi.nlm.nih.gov/pubmed/28280328 http://dx.doi.org/10.2147/IJN.S127256 |
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