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Glycogen as an advantageous polymer carrier in cancer theranostics: Straightforward in vivo evidence
As a natural polysaccharide polymer, glycogen possesses suitable properties for use as a nanoparticle carrier in cancer theranostics. Not only it is inherently biocompatible, it can also be easily chemically modified with various moieties. Synthetic glycogen conjugates can passively accumulate in tu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320016/ https://www.ncbi.nlm.nih.gov/pubmed/32591567 http://dx.doi.org/10.1038/s41598-020-67277-y |
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author | Gálisová, Andrea Jirátová, Markéta Rabyk, Mariia Sticová, Eva Hájek, Milan Hrubý, Martin Jirák, Daniel |
author_facet | Gálisová, Andrea Jirátová, Markéta Rabyk, Mariia Sticová, Eva Hájek, Milan Hrubý, Martin Jirák, Daniel |
author_sort | Gálisová, Andrea |
collection | PubMed |
description | As a natural polysaccharide polymer, glycogen possesses suitable properties for use as a nanoparticle carrier in cancer theranostics. Not only it is inherently biocompatible, it can also be easily chemically modified with various moieties. Synthetic glycogen conjugates can passively accumulate in tumours due to enhanced permeability of tumour vessels and limited lymphatic drainage (the EPR effect). For this study, we developed and examined a glycogen-based carrier containing a gadolinium chelate and near-infrared fluorescent dye. Our aim was to monitor biodistribution and accumulation in tumour-bearing rats using magnetic resonance and fluorescence imaging. Our data clearly show that these conjugates possess suitable imaging and tumour-targeting properties, and are safe under both in vitro and in vivo conditions. Additional modification of glycogen polymers with poly(2-alkyl-2-oxazolines) led to a reduction in the elimination rate and lower uptake in internal organs (lower whole-body background: 45% and 27% lower MRI signals of oxazoline-based conjugates in the liver and kidneys, respectively compared to the unmodified version). Our results highlight the potential of multimodal glycogen-based nanopolymers as a carrier for drug delivery systems in tumour diagnosis and treatment. |
format | Online Article Text |
id | pubmed-7320016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73200162020-06-30 Glycogen as an advantageous polymer carrier in cancer theranostics: Straightforward in vivo evidence Gálisová, Andrea Jirátová, Markéta Rabyk, Mariia Sticová, Eva Hájek, Milan Hrubý, Martin Jirák, Daniel Sci Rep Article As a natural polysaccharide polymer, glycogen possesses suitable properties for use as a nanoparticle carrier in cancer theranostics. Not only it is inherently biocompatible, it can also be easily chemically modified with various moieties. Synthetic glycogen conjugates can passively accumulate in tumours due to enhanced permeability of tumour vessels and limited lymphatic drainage (the EPR effect). For this study, we developed and examined a glycogen-based carrier containing a gadolinium chelate and near-infrared fluorescent dye. Our aim was to monitor biodistribution and accumulation in tumour-bearing rats using magnetic resonance and fluorescence imaging. Our data clearly show that these conjugates possess suitable imaging and tumour-targeting properties, and are safe under both in vitro and in vivo conditions. Additional modification of glycogen polymers with poly(2-alkyl-2-oxazolines) led to a reduction in the elimination rate and lower uptake in internal organs (lower whole-body background: 45% and 27% lower MRI signals of oxazoline-based conjugates in the liver and kidneys, respectively compared to the unmodified version). Our results highlight the potential of multimodal glycogen-based nanopolymers as a carrier for drug delivery systems in tumour diagnosis and treatment. Nature Publishing Group UK 2020-06-26 /pmc/articles/PMC7320016/ /pubmed/32591567 http://dx.doi.org/10.1038/s41598-020-67277-y Text en © The Author(s) 2020 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 Gálisová, Andrea Jirátová, Markéta Rabyk, Mariia Sticová, Eva Hájek, Milan Hrubý, Martin Jirák, Daniel Glycogen as an advantageous polymer carrier in cancer theranostics: Straightforward in vivo evidence |
title | Glycogen as an advantageous polymer carrier in cancer theranostics: Straightforward in vivo evidence |
title_full | Glycogen as an advantageous polymer carrier in cancer theranostics: Straightforward in vivo evidence |
title_fullStr | Glycogen as an advantageous polymer carrier in cancer theranostics: Straightforward in vivo evidence |
title_full_unstemmed | Glycogen as an advantageous polymer carrier in cancer theranostics: Straightforward in vivo evidence |
title_short | Glycogen as an advantageous polymer carrier in cancer theranostics: Straightforward in vivo evidence |
title_sort | glycogen as an advantageous polymer carrier in cancer theranostics: straightforward in vivo evidence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320016/ https://www.ncbi.nlm.nih.gov/pubmed/32591567 http://dx.doi.org/10.1038/s41598-020-67277-y |
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