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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...

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Autores principales: Thong, Qiu Xian, Biabanikhankahdani, Roya, Ho, Kok Lian, Alitheen, Noorjahan Banu, Tan, Wen Siang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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