• English
    • norsk
  • English 
    • English
    • norsk
  • Login
View Item 
  •   All institutions
  • Norges teknisk-naturvitenskapelige universitet
  • Fakultet for naturvitenskap (NV)
  • Institutt for fysikk
  • View Item
  •   All institutions
  • Norges teknisk-naturvitenskapelige universitet
  • Fakultet for naturvitenskap (NV)
  • Institutt for fysikk
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

Intracellular Localization of Polymeric Nanoparticles and the Effect of Encapsulated Drug in vitro

Levik, Kjetil Viste
Master thesis
Thumbnail
View/Open
13608_FULLTEXT.pdf (5.725Mb)
13608_COVER.pdf (307.3Kb)
Permanent link
http://hdl.handle.net/11250/2353108
Issue date
2015
Share
Metadata
Show full item record
Collections
  • Institutt for fysikk [1074]
Abstract
Chemotherapy could be greatly improved if drug carriers could deliver the chemotherapeutic agents specifically to the cancer cells. SINTEF Materials and Chemistry have developed a novel, multimodal polymeric nanoparticle platform which is promising for drug delivery and other medical applications. In this thesis, nanoparticles made of biodegradable poly(butyl cyanoacrylate) were used to investigate intracellular localization of the nanoparticles. In addition, the effect of drug encapsulated in the nanoparticles was evaluated. PC3 cells and HeLa cells were used.

Confocal laser scanning microscopy was used to study colocalization between the nanoparticles and lysosomes. Lysosomes were stained with CellLight Lysosomes-GFP, while the nanoparticles were loaded with the fluorescent dye NR668. Very few nanoparticles were taken up by PC3 cells, but most of them was found to colocalize with lysosomes. The results from these experiments strengthens the hypothesize of endocytotic uptake of the nanoparticles.

AlamarBlue cell viability assay was used to study the impact of encapsulated drug on cell proliferation, while flow cytometry was used to assess the impact of encapsulated drug on the cell cycle distribution. Drug encapsulated in nanoparticles was found to work very similar to free drug. This indicates that the nanoparticles or the released drug are able to escape the lysosomes. In addition it proves that the encapsulation process does not alter this drug in such a way that it becomes ineffective.
Publisher
NTNU

Contact Us

Search NORA
Powered by DSpace software

Service from BIBSYS
 

 

Browse this CollectionIssue DateAuthorsTitlesSubjectsDocument TypesJournalsBrowse all ArchivesArchives & CollectionsIssue DateAuthorsTitlesSubjectsDocument TypesJournals

My Account

Login

Statistics

Google Analytics StatisticsView Usage Statistics

Contact Us

Search NORA
Powered by DSpace software

Service from BIBSYS