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Size-tunable drug-delivery capsules composed of a magnetic nanoshell
Nano-sized FePt capsules with two types of ultrathin shell were fabricated using a template method for use in a nano-scale drug delivery system. One capsule was composed of an inorganic-organic hybrid shell of a water-soluble polymer and FePt nanoparticles, and the other capsule was composed of a ne...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568115/ https://www.ncbi.nlm.nih.gov/pubmed/23507895 http://dx.doi.org/10.4161/biom.22617 |
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author | Fuchigami, Teruaki Kitamoto, Yoshitaka Namiki, Yoshihisa |
author_facet | Fuchigami, Teruaki Kitamoto, Yoshitaka Namiki, Yoshihisa |
author_sort | Fuchigami, Teruaki |
collection | PubMed |
description | Nano-sized FePt capsules with two types of ultrathin shell were fabricated using a template method for use in a nano-scale drug delivery system. One capsule was composed of an inorganic-organic hybrid shell of a water-soluble polymer and FePt nanoparticles, and the other capsule was composed of a network of fused FePt nanoparticles. We demonstrated that FePt nanoparticles selectively accumulated on the polymer molecules adsorbed on the template silica particles, and investigated the morphologies of the particle accumulation by changing the concentration of the polymer solution with which the template particles were treated. Capsular size was reduced from 340 to less than 90 nm by changing the size of the silica template particles, and the shell thickness was controlled by changing the amount of FePt nanoparticles adsorbed on the template particles. The hybrid shell was maintained by the connection of FePt nanoparticles and polymer molecules, and the shell thickness was 10 nm at the maximum. The FePt network shell was fabricated by hydrothermal treatment of the FePt/polymer-modified silica composite particles. The FePt network shell was produced from only the FePt alloy, and the shell thickness was 3 nm. Water-soluble anti-cancer drugs could be loaded into the hollow space of FePt network capsules, and lipid-coated FePt network capsules loaded with anti-cancer drugs showed cellular toxicity. The nano-sized capsular structure and the ultrathin shell suggest applicability as a drug carrier in magnetically guided drug delivery systems. |
format | Online Article Text |
id | pubmed-3568115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-35681152013-05-22 Size-tunable drug-delivery capsules composed of a magnetic nanoshell Fuchigami, Teruaki Kitamoto, Yoshitaka Namiki, Yoshihisa Biomatter Special Focus Report Nano-sized FePt capsules with two types of ultrathin shell were fabricated using a template method for use in a nano-scale drug delivery system. One capsule was composed of an inorganic-organic hybrid shell of a water-soluble polymer and FePt nanoparticles, and the other capsule was composed of a network of fused FePt nanoparticles. We demonstrated that FePt nanoparticles selectively accumulated on the polymer molecules adsorbed on the template silica particles, and investigated the morphologies of the particle accumulation by changing the concentration of the polymer solution with which the template particles were treated. Capsular size was reduced from 340 to less than 90 nm by changing the size of the silica template particles, and the shell thickness was controlled by changing the amount of FePt nanoparticles adsorbed on the template particles. The hybrid shell was maintained by the connection of FePt nanoparticles and polymer molecules, and the shell thickness was 10 nm at the maximum. The FePt network shell was fabricated by hydrothermal treatment of the FePt/polymer-modified silica composite particles. The FePt network shell was produced from only the FePt alloy, and the shell thickness was 3 nm. Water-soluble anti-cancer drugs could be loaded into the hollow space of FePt network capsules, and lipid-coated FePt network capsules loaded with anti-cancer drugs showed cellular toxicity. The nano-sized capsular structure and the ultrathin shell suggest applicability as a drug carrier in magnetically guided drug delivery systems. Landes Bioscience 2012-10-01 2012-10-01 /pmc/articles/PMC3568115/ /pubmed/23507895 http://dx.doi.org/10.4161/biom.22617 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Special Focus Report Fuchigami, Teruaki Kitamoto, Yoshitaka Namiki, Yoshihisa Size-tunable drug-delivery capsules composed of a magnetic nanoshell |
title | Size-tunable drug-delivery capsules composed of a magnetic nanoshell |
title_full | Size-tunable drug-delivery capsules composed of a magnetic nanoshell |
title_fullStr | Size-tunable drug-delivery capsules composed of a magnetic nanoshell |
title_full_unstemmed | Size-tunable drug-delivery capsules composed of a magnetic nanoshell |
title_short | Size-tunable drug-delivery capsules composed of a magnetic nanoshell |
title_sort | size-tunable drug-delivery capsules composed of a magnetic nanoshell |
topic | Special Focus Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568115/ https://www.ncbi.nlm.nih.gov/pubmed/23507895 http://dx.doi.org/10.4161/biom.22617 |
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