Hide metadata

dc.date.accessioned2020-08-11T19:15:41Z
dc.date.available2020-08-11T19:15:41Z
dc.date.created2020-04-25T17:41:43Z
dc.date.issued2020
dc.identifier.citationPandya, Abhilash D. Øverbye, Anders Saharia, Priyanka Gaware, Vivek S. Høgset, Håkon Masson, Már Høgset, Anders Mælandsmo, Gunhild Mari Skotland, Tore Sandvig, Kirsten Iversen, Tore Geir . Drug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Cancer. Biomacromolecules. 2020, 21, 1489-1498
dc.identifier.urihttp://hdl.handle.net/10852/78281
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–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.
dc.languageEN
dc.publisherACS Publications
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleDrug-Loaded Photosensitizer-Chitosan Nanoparticles for Combinatorial Chemo- and Photodynamic-Therapy of Cancer
dc.typeJournal article
dc.creator.authorPandya, Abhilash D.
dc.creator.authorØverbye, Anders
dc.creator.authorSaharia, Priyanka
dc.creator.authorGaware, Vivek S.
dc.creator.authorHøgset, Håkon
dc.creator.authorMasson, Már
dc.creator.authorHøgset, Anders
dc.creator.authorMælandsmo, Gunhild Mari
dc.creator.authorSkotland, Tore
dc.creator.authorSandvig, Kirsten
dc.creator.authorIversen, Tore Geir
cristin.unitcode185,15,29,30
cristin.unitnameSeksjon for fysiologi og cellebiologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1808042
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Biomacromolecules&rft.volume=21&rft.spage=1489&rft.date=2020
dc.identifier.jtitleBiomacromolecules
dc.identifier.volume21
dc.identifier.issue4
dc.identifier.startpage1489
dc.identifier.endpage1498
dc.identifier.doihttps://doi.org/10.1021/acs.biomac.0c00061
dc.identifier.urnURN:NBN:no-81368
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1525-7797
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/78281/2/Biomacromolecules%2B2020%2BIversen.pdf
dc.type.versionPublishedVersion
dc.relation.projectNFR/228200


Files in this item

Appears in the following Collection

Hide metadata

Attribution 4.0 International
This item's license is: Attribution 4.0 International