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Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children, with a 5-year survival rate of between 30 and 65%. Standard treatment involves surgery, radiation treatment, and chemotherapy. However, there is a high recurrence rate, particularly from locoregional spread. We investigated t...
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/PMC5724714/ https://www.ncbi.nlm.nih.gov/pubmed/29263655 http://dx.doi.org/10.2147/NSA.S148068 |
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author | White, Benjamin Evison, Anna Dombi, Eszter Townley, Helen E |
author_facet | White, Benjamin Evison, Anna Dombi, Eszter Townley, Helen E |
author_sort | White, Benjamin |
collection | PubMed |
description | Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children, with a 5-year survival rate of between 30 and 65%. Standard treatment involves surgery, radiation treatment, and chemotherapy. However, there is a high recurrence rate, particularly from locoregional spread. We investigated the use of the natural compound citral (3,7-dimethyl-2,6-octadienal), which can be found in a number of plants, but is particularly abundant in lemon grass (Cymbopogon citratus) oil, for activity against immortalized RMS cells. Significant cancer cell death was seen at concentrations above 150 μM citral, and mitochondrial morphological changes were seen after incubation with 10 μM citral. However, since citral is a highly volatile molecule, we prepared albumin particles by a desolvation method to encapsulate citral, as a means of stabilization. We then further incorporated the loaded nanoparticles into a biodegradable polyanhydride wafer to generate a slow release system. The wafers were shown to degrade by 50% over the course of 25 days and to release the active compound. We therefore propose the use of the citral-nanoparticle-polymer wafers for implantation into the tumor bed after surgical removal of a sarcoma as a means to control locoregional spread due to any remaining cancerous cells. |
format | Online Article Text |
id | pubmed-5724714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57247142017-12-20 Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers White, Benjamin Evison, Anna Dombi, Eszter Townley, Helen E Nanotechnol Sci Appl Original Research Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children, with a 5-year survival rate of between 30 and 65%. Standard treatment involves surgery, radiation treatment, and chemotherapy. However, there is a high recurrence rate, particularly from locoregional spread. We investigated the use of the natural compound citral (3,7-dimethyl-2,6-octadienal), which can be found in a number of plants, but is particularly abundant in lemon grass (Cymbopogon citratus) oil, for activity against immortalized RMS cells. Significant cancer cell death was seen at concentrations above 150 μM citral, and mitochondrial morphological changes were seen after incubation with 10 μM citral. However, since citral is a highly volatile molecule, we prepared albumin particles by a desolvation method to encapsulate citral, as a means of stabilization. We then further incorporated the loaded nanoparticles into a biodegradable polyanhydride wafer to generate a slow release system. The wafers were shown to degrade by 50% over the course of 25 days and to release the active compound. We therefore propose the use of the citral-nanoparticle-polymer wafers for implantation into the tumor bed after surgical removal of a sarcoma as a means to control locoregional spread due to any remaining cancerous cells. Dove Medical Press 2017-12-06 /pmc/articles/PMC5724714/ /pubmed/29263655 http://dx.doi.org/10.2147/NSA.S148068 Text en © 2017 White 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 White, Benjamin Evison, Anna Dombi, Eszter Townley, Helen E Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers |
title | Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers |
title_full | Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers |
title_fullStr | Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers |
title_full_unstemmed | Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers |
title_short | Improved delivery of the anticancer agent citral using BSA nanoparticles and polymeric wafers |
title_sort | improved delivery of the anticancer agent citral using bsa nanoparticles and polymeric wafers |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724714/ https://www.ncbi.nlm.nih.gov/pubmed/29263655 http://dx.doi.org/10.2147/NSA.S148068 |
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