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dc.contributor.advisorRustad, Eirik
dc.contributor.authorZuboon, Tariq
dc.date.accessioned2025-05-15T08:36:15Z
dc.date.available2025-05-15T08:36:15Z
dc.date.issued2023-05-15
dc.description.abstractGlioblastoma is the most lethal brain cancer, characterized by rapid growth and high mortality. Despite advances in diagnosis, surgery, and radiation therapy, glioblastoma remains resistant to treatment. One of the keys to successful anticancer drugs is their ability to reach the target site while minimizing accumulation in other tissues. Most drugs lack the physical and chemical properties and specificity to successfully enter the brain, limiting their ability to reach the tumor. The extracellular environment surrounding the GBM tumor is reported to be acidic. Considering the acidic pH in the tumor environment, we have previously designed and prepared pH-responsive liposomes for glioblastoma targeting and triggered release. We aim to further develop and characterize multifunctional liposomes that specifically target and deliver chemotherapeutic drugs to glioblastoma tumors. This study investigates the effect of PEGylation on cell uptake. We conducted experiments comparing the uptake of PEGylated liposomes with PEG750 and PEG2000 and non-PEGylated liposomes in GL261-cells, and how PC formation can influence the uptake in these three formulations.en_US
dc.identifier.urihttps://hdl.handle.net/10037/37077
dc.language.isonoben_US
dc.publisherUiT Norges arktiske universiteten_US
dc.publisherUiT The Arctic University of Norwayen_US
dc.rights.holderCopyright 2023 The Author(s)
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0en_US
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)en_US
dc.subject.courseIDFAR-3911
dc.subjectPEGen_US
dc.subjectprotein coronaen_US
dc.titleEffect of PEGylation in liposomal protein corona formation. Characterization of in vitro protein corona formation and the effect of protein corona on cellular uptake of pH-sensitive liposomes in glioblastoma cellsen_US
dc.typeMaster thesisen_US
dc.typeMastergradsoppgaveen_US


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Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)