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

dc.contributorHáskóli Íslandsen_US
dc.contributorUniversity of Icelanden_US
dc.contributor.authorPandya, Abhilash D.
dc.contributor.authorØverbye, Anders
dc.contributor.authorSahariah, Priyanka
dc.contributor.authorGaware, Vivek S.
dc.contributor.authorHøgset, Håkon
dc.contributor.authorMásson, Már
dc.contributor.authorHøgset, Anders
dc.contributor.authorMælandsmo, Gunhild M.
dc.contributor.authorSkotland, Tore
dc.contributor.authorSandvig, Kirsten
dc.contributor.authorIversen, Tore-Geir
dc.contributor.departmentLyfjafræðideild (HÍ)en_US
dc.contributor.departmentFaculty of Pharmaceutical Sciences (UI)en_US
dc.contributor.schoolHeilbrigðisvísindasvið (HÍ)en_US
dc.contributor.schoolSchool of Health Sciences (UI)en_US
dc.date.accessioned2021-01-15T11:14:57Z
dc.date.available2021-01-15T11:14:57Z
dc.date.issued2020-02-24
dc.descriptionPublisher's version (útgefin grein)en_US
dc.description.abstractIn 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-πstacking 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.en_US
dc.description.sponsorshipThis work was supported by The Research Council of Norway [NANO2021; Project Number 228200/O70] and The Norwegian Cancer Society. We thank Anne Engen for excellent assistance with cell culturing and Monika Håkerud for professional assistance regarding illumination of cells. We would also like to thank The Norwegian Radium Hospital Research Foundation (RADFORSK) for financial support and The Simon Fougner Hartmann Family Fund for providing means to analytical instrumentation. We also acknowledge a contribution from the University of Iceland Research Fund for the work in Iceland.en_US
dc.description.versionPeer Revieweden_US
dc.format.extent1489-1498en_US
dc.identifier.citationPandya, A.D., Øverbye, A., Sahariah, P., Gaware, V.S., Høgset, H., Masson, M., Høgset, A., Mælandsmo, G.M., Skotland, T., Sandvig, K., Iversen, T.-G., 2020. Drug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Cancer. Biomacromolecules 21, 1489–1498. doi:10.1021/acs.biomac.0c00061en_US
dc.identifier.doi10.1021/acs.biomac.0c00061
dc.identifier.issn1525-7797
dc.identifier.issn1526-4602 (eISSN)
dc.identifier.journalBiomacromoleculesen_US
dc.identifier.urihttps://hdl.handle.net/20.500.11815/2378
dc.language.isoenen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.ispartofseriesBiomacromolecules;21(4)
dc.relation.urlhttps://pubs.acs.org/doi/10.1021/acs.biomac.0c00061en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBiodegradable polymersen_US
dc.subjectMertansineen_US
dc.subjectCabazitaxelen_US
dc.subjectBreast cancer cellsen_US
dc.subjectLyfjaefnafræðien_US
dc.subjectFjölliðuren_US
dc.subjectBrjóstakrabbameinen_US
dc.titleDrug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Canceren_US
dc.typeinfo:eu-repo/semantics/articleen_US
dcterms.licenseThis is an open access article published under a Creative Commons Attribution (CC-BY)License, which permits unrestricted use, distribution and reproduction in any medium,provided the author and source are citeden_US

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