Cargando…
Natural material-decorated mesoporous silica nanoparticle container for multifunctional membrane-controlled targeted drug delivery
To avoid the side effects caused by nonspecific targeting, premature release, weak selectivity, and poor therapeutic efficacy of current nanoparticle-based systems used for drug delivery, we fabricated natural material-decorated nanoparticles as a multifunctional, membrane-controlled targeted drug d...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702528/ https://www.ncbi.nlm.nih.gov/pubmed/29200852 http://dx.doi.org/10.2147/IJN.S148438 |
_version_ | 1783281548610502656 |
---|---|
author | Hu, Yan Ke, Lei Chen, Hao Zhuo, Ma Yang, Xinzhou Zhao, Dan Zeng, Suying Xiao, Xincai |
author_facet | Hu, Yan Ke, Lei Chen, Hao Zhuo, Ma Yang, Xinzhou Zhao, Dan Zeng, Suying Xiao, Xincai |
author_sort | Hu, Yan |
collection | PubMed |
description | To avoid the side effects caused by nonspecific targeting, premature release, weak selectivity, and poor therapeutic efficacy of current nanoparticle-based systems used for drug delivery, we fabricated natural material-decorated nanoparticles as a multifunctional, membrane-controlled targeted drug delivery system. The nanocomposite material coated with a membrane was biocompatible and integrated both specific tumor targeting and responsiveness to stimulation, which improved transmission efficacy and controlled drug release. Mesoporous silica nanoparticles (MSNs), which are known for their biocompatibility and high drug-loading capacity, were selected as a model drug container and carrier. The membrane was established by the polyelectrolyte composite method from chitosan (CS) which was sensitive to the acidic tumor microenvironment, folic acid-modified CS which recognizes the folate receptor expressed on the tumor cell surface, and a CD(44) receptor-targeted polysaccharide hyaluronic acid. We characterized the structure of the nanocomposite as well as the drug release behavior under the control of the pH-sensitive membrane switch and evaluated the antitumor efficacy of the system in vitro. Our results provide a basis for the design and fabrication of novel membrane-controlled nanoparticles with improved tumor-targeting therapy. |
format | Online Article Text |
id | pubmed-5702528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57025282017-11-30 Natural material-decorated mesoporous silica nanoparticle container for multifunctional membrane-controlled targeted drug delivery Hu, Yan Ke, Lei Chen, Hao Zhuo, Ma Yang, Xinzhou Zhao, Dan Zeng, Suying Xiao, Xincai Int J Nanomedicine Original Research To avoid the side effects caused by nonspecific targeting, premature release, weak selectivity, and poor therapeutic efficacy of current nanoparticle-based systems used for drug delivery, we fabricated natural material-decorated nanoparticles as a multifunctional, membrane-controlled targeted drug delivery system. The nanocomposite material coated with a membrane was biocompatible and integrated both specific tumor targeting and responsiveness to stimulation, which improved transmission efficacy and controlled drug release. Mesoporous silica nanoparticles (MSNs), which are known for their biocompatibility and high drug-loading capacity, were selected as a model drug container and carrier. The membrane was established by the polyelectrolyte composite method from chitosan (CS) which was sensitive to the acidic tumor microenvironment, folic acid-modified CS which recognizes the folate receptor expressed on the tumor cell surface, and a CD(44) receptor-targeted polysaccharide hyaluronic acid. We characterized the structure of the nanocomposite as well as the drug release behavior under the control of the pH-sensitive membrane switch and evaluated the antitumor efficacy of the system in vitro. Our results provide a basis for the design and fabrication of novel membrane-controlled nanoparticles with improved tumor-targeting therapy. Dove Medical Press 2017-11-22 /pmc/articles/PMC5702528/ /pubmed/29200852 http://dx.doi.org/10.2147/IJN.S148438 Text en © 2017 Hu 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 Hu, Yan Ke, Lei Chen, Hao Zhuo, Ma Yang, Xinzhou Zhao, Dan Zeng, Suying Xiao, Xincai Natural material-decorated mesoporous silica nanoparticle container for multifunctional membrane-controlled targeted drug delivery |
title | Natural material-decorated mesoporous silica nanoparticle container for multifunctional membrane-controlled targeted drug delivery |
title_full | Natural material-decorated mesoporous silica nanoparticle container for multifunctional membrane-controlled targeted drug delivery |
title_fullStr | Natural material-decorated mesoporous silica nanoparticle container for multifunctional membrane-controlled targeted drug delivery |
title_full_unstemmed | Natural material-decorated mesoporous silica nanoparticle container for multifunctional membrane-controlled targeted drug delivery |
title_short | Natural material-decorated mesoporous silica nanoparticle container for multifunctional membrane-controlled targeted drug delivery |
title_sort | natural material-decorated mesoporous silica nanoparticle container for multifunctional membrane-controlled targeted drug delivery |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702528/ https://www.ncbi.nlm.nih.gov/pubmed/29200852 http://dx.doi.org/10.2147/IJN.S148438 |
work_keys_str_mv | AT huyan naturalmaterialdecoratedmesoporoussilicananoparticlecontainerformultifunctionalmembranecontrolledtargeteddrugdelivery AT kelei naturalmaterialdecoratedmesoporoussilicananoparticlecontainerformultifunctionalmembranecontrolledtargeteddrugdelivery AT chenhao naturalmaterialdecoratedmesoporoussilicananoparticlecontainerformultifunctionalmembranecontrolledtargeteddrugdelivery AT zhuoma naturalmaterialdecoratedmesoporoussilicananoparticlecontainerformultifunctionalmembranecontrolledtargeteddrugdelivery AT yangxinzhou naturalmaterialdecoratedmesoporoussilicananoparticlecontainerformultifunctionalmembranecontrolledtargeteddrugdelivery AT zhaodan naturalmaterialdecoratedmesoporoussilicananoparticlecontainerformultifunctionalmembranecontrolledtargeteddrugdelivery AT zengsuying naturalmaterialdecoratedmesoporoussilicananoparticlecontainerformultifunctionalmembranecontrolledtargeteddrugdelivery AT xiaoxincai naturalmaterialdecoratedmesoporoussilicananoparticlecontainerformultifunctionalmembranecontrolledtargeteddrugdelivery |