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Drug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Cancer

[Image: see text] In this study we have developed biodegradable polymeric nanoparticles (NPs) containing the cytostatic drugs mertansine (MRT) or cabazitaxel (CBZ). The NPs are based on chitosan (CS) conjugate polymers synthesized with different amounts of the photosensitizer tetraphenylchlorin (TPC...

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Autores principales: Pandya, Abhilash D., Øverbye, Anders, Sahariah, Priyanka, Gaware, Vivek S., Høgset, Håkon, Masson, Màr, Høgset, Anders, Mælandsmo, Gunhild M., Skotland, Tore, Sandvig, Kirsten, Iversen, Tore-Geir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307886/
https://www.ncbi.nlm.nih.gov/pubmed/32092254
http://dx.doi.org/10.1021/acs.biomac.0c00061
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author Pandya, Abhilash D.
Øverbye, Anders
Sahariah, Priyanka
Gaware, Vivek S.
Høgset, Håkon
Masson, Màr
Høgset, Anders
Mælandsmo, Gunhild M.
Skotland, Tore
Sandvig, Kirsten
Iversen, Tore-Geir
author_facet Pandya, Abhilash D.
Øverbye, Anders
Sahariah, Priyanka
Gaware, Vivek S.
Høgset, Håkon
Masson, Màr
Høgset, Anders
Mælandsmo, Gunhild M.
Skotland, Tore
Sandvig, Kirsten
Iversen, Tore-Geir
author_sort Pandya, Abhilash D.
collection PubMed
description [Image: see text] In this study we have developed biodegradable polymeric nanoparticles (NPs) containing the cytostatic drugs mertansine (MRT) or cabazitaxel (CBZ). The NPs are based on chitosan (CS) conjugate polymers synthesized with different amounts of the photosensitizer tetraphenylchlorin (TPC). These TPC–CS NPs have high loading capacity and strong drug retention due to π–π stacking interactions between the drugs and the aromatic photosensitizer groups of the polymers. CS polymers with 10% of the side chains containing TPC were found to be optimal in terms of drug loading capacity and NP stability. The TPC–CS NPs loaded with MRT or CBZ displayed higher cytotoxicity than the free form of these drugs in the breast cancer cell lines MDA-MB-231 and MDA-MB-468. Furthermore, light-induced photochemical activation of the NPs elicited a strong photodynamic therapy effect on these breast cancer cells. Biodistribution studies in mice showed that most of the TPC–CS NPs accumulated in liver and lungs, but they were also found to be localized in tumors derived from HCT-116 cells. These data suggest that the drug-loaded TPC–CS NPs have a potential in combinatory anticancer therapy and as contrast agents.
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spelling pubmed-73078862020-06-23 Drug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Cancer Pandya, Abhilash D. Øverbye, Anders Sahariah, Priyanka Gaware, Vivek S. Høgset, Håkon Masson, Màr Høgset, Anders Mælandsmo, Gunhild M. Skotland, Tore Sandvig, Kirsten Iversen, Tore-Geir Biomacromolecules [Image: see text] In this study we have developed biodegradable polymeric nanoparticles (NPs) containing the cytostatic drugs mertansine (MRT) or cabazitaxel (CBZ). The NPs are based on chitosan (CS) conjugate polymers synthesized with different amounts of the photosensitizer tetraphenylchlorin (TPC). These TPC–CS NPs have high loading capacity and strong drug retention due to π–π stacking interactions between the drugs and the aromatic photosensitizer groups of the polymers. CS polymers with 10% of the side chains containing TPC were found to be optimal in terms of drug loading capacity and NP stability. The TPC–CS NPs loaded with MRT or CBZ displayed higher cytotoxicity than the free form of these drugs in the breast cancer cell lines MDA-MB-231 and MDA-MB-468. Furthermore, light-induced photochemical activation of the NPs elicited a strong photodynamic therapy effect on these breast cancer cells. Biodistribution studies in mice showed that most of the TPC–CS NPs accumulated in liver and lungs, but they were also found to be localized in tumors derived from HCT-116 cells. These data suggest that the drug-loaded TPC–CS NPs have a potential in combinatory anticancer therapy and as contrast agents. American Chemical Society 2020-02-24 2020-04-13 /pmc/articles/PMC7307886/ /pubmed/32092254 http://dx.doi.org/10.1021/acs.biomac.0c00061 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Pandya, Abhilash D.
Øverbye, Anders
Sahariah, Priyanka
Gaware, Vivek S.
Høgset, Håkon
Masson, Màr
Høgset, Anders
Mælandsmo, Gunhild M.
Skotland, Tore
Sandvig, Kirsten
Iversen, Tore-Geir
Drug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Cancer
title Drug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Cancer
title_full Drug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Cancer
title_fullStr Drug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Cancer
title_full_unstemmed Drug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Cancer
title_short Drug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Cancer
title_sort drug-loaded photosensitizer-chitosan nanoparticles for combinatorial chemo- and photodynamic-therapy of cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307886/
https://www.ncbi.nlm.nih.gov/pubmed/32092254
http://dx.doi.org/10.1021/acs.biomac.0c00061
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