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Thermally-responsive Virus-like Particle for Targeted Delivery of Cancer Drug
Multifunctional nanocarriers displaying specific ligands and simultaneously response to stimuli offer great potentials for targeted and controlled drug delivery. Several synthetic thermally-responsive nanocarriers have been studied extensively for hyperthermia incorporated chemotherapy. However, no...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6408444/ https://www.ncbi.nlm.nih.gov/pubmed/30850643 http://dx.doi.org/10.1038/s41598-019-40388-x |
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author | Thong, Qiu Xian Biabanikhankahdani, Roya Ho, Kok Lian Alitheen, Noorjahan Banu Tan, Wen Siang |
author_facet | Thong, Qiu Xian Biabanikhankahdani, Roya Ho, Kok Lian Alitheen, Noorjahan Banu Tan, Wen Siang |
author_sort | Thong, Qiu Xian |
collection | PubMed |
description | Multifunctional nanocarriers displaying specific ligands and simultaneously response to stimuli offer great potentials for targeted and controlled drug delivery. Several synthetic thermally-responsive nanocarriers have been studied extensively for hyperthermia incorporated chemotherapy. However, no information is available on the application of virus-like particle (VLP) in thermally-controlled drug delivery systems. Here, we describe the development of a novel multifunctional nanovehicle based on the VLP of Macrobrachium rosenbergii nodavirus (MrNVLP). Folic acid (FA) was covalently conjugated to lysine residues located on the surface of MrNVLP, while doxorubicin (Dox) was loaded inside the VLP using an infusion method. This thermally-responsive nanovehicle, namely FA-MrNVLP-Dox, released Dox in a sustained manner and the rate of drug release increased in response to a hyperthermia temperature at 43 °C. The FA-MrNVLP-Dox enhanced the delivery of Dox to HT29 cancer cells expressing high level of folate receptor (FR) as compared to CCD841CoN normal cells and HepG2 cancer cells, which express low levels of FR. As a result, FA-MrNVLP-Dox increased the cytotoxicity of Dox on HT29 cells, and decreased the drug’s cytotoxicity on CCD841CoN and HepG2 cells. This study demonstrated the potential of FA-MrNVLP-Dox as a thermally-responsive nanovehicle for targeted delivery of Dox to cancer cells rich in FR. |
format | Online Article Text |
id | pubmed-6408444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64084442019-03-12 Thermally-responsive Virus-like Particle for Targeted Delivery of Cancer Drug Thong, Qiu Xian Biabanikhankahdani, Roya Ho, Kok Lian Alitheen, Noorjahan Banu Tan, Wen Siang Sci Rep Article Multifunctional nanocarriers displaying specific ligands and simultaneously response to stimuli offer great potentials for targeted and controlled drug delivery. Several synthetic thermally-responsive nanocarriers have been studied extensively for hyperthermia incorporated chemotherapy. However, no information is available on the application of virus-like particle (VLP) in thermally-controlled drug delivery systems. Here, we describe the development of a novel multifunctional nanovehicle based on the VLP of Macrobrachium rosenbergii nodavirus (MrNVLP). Folic acid (FA) was covalently conjugated to lysine residues located on the surface of MrNVLP, while doxorubicin (Dox) was loaded inside the VLP using an infusion method. This thermally-responsive nanovehicle, namely FA-MrNVLP-Dox, released Dox in a sustained manner and the rate of drug release increased in response to a hyperthermia temperature at 43 °C. The FA-MrNVLP-Dox enhanced the delivery of Dox to HT29 cancer cells expressing high level of folate receptor (FR) as compared to CCD841CoN normal cells and HepG2 cancer cells, which express low levels of FR. As a result, FA-MrNVLP-Dox increased the cytotoxicity of Dox on HT29 cells, and decreased the drug’s cytotoxicity on CCD841CoN and HepG2 cells. This study demonstrated the potential of FA-MrNVLP-Dox as a thermally-responsive nanovehicle for targeted delivery of Dox to cancer cells rich in FR. Nature Publishing Group UK 2019-03-08 /pmc/articles/PMC6408444/ /pubmed/30850643 http://dx.doi.org/10.1038/s41598-019-40388-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Thong, Qiu Xian Biabanikhankahdani, Roya Ho, Kok Lian Alitheen, Noorjahan Banu Tan, Wen Siang Thermally-responsive Virus-like Particle for Targeted Delivery of Cancer Drug |
title | Thermally-responsive Virus-like Particle for Targeted Delivery of Cancer Drug |
title_full | Thermally-responsive Virus-like Particle for Targeted Delivery of Cancer Drug |
title_fullStr | Thermally-responsive Virus-like Particle for Targeted Delivery of Cancer Drug |
title_full_unstemmed | Thermally-responsive Virus-like Particle for Targeted Delivery of Cancer Drug |
title_short | Thermally-responsive Virus-like Particle for Targeted Delivery of Cancer Drug |
title_sort | thermally-responsive virus-like particle for targeted delivery of cancer drug |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6408444/ https://www.ncbi.nlm.nih.gov/pubmed/30850643 http://dx.doi.org/10.1038/s41598-019-40388-x |
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