Novel cationic carotenoid lipids as delivery vectors of antisense oligonucleotides for exon skipping in duchenne muscular dystrophy
dc.contributor.author | Popplewell, Linda | |
dc.contributor.author | Abu-Dayya, Aseel | |
dc.contributor.author | Khanna, Tushar | |
dc.contributor.author | Flinterman, Marcella | |
dc.contributor.author | Abdul Khalique, nada | |
dc.contributor.author | Raju, Liji | |
dc.contributor.author | Øpstad, Christer Lorentz | |
dc.contributor.author | Sliwka, Hans-Richard | |
dc.contributor.author | Partali, Vassilia | |
dc.contributor.author | Dickson, George | |
dc.contributor.author | Pungente, Michael | |
dc.date.accessioned | 2015-09-30T12:30:27Z | |
dc.date.accessioned | 2015-11-05T14:53:27Z | |
dc.date.available | 2015-09-30T12:30:27Z | |
dc.date.available | 2015-11-05T14:53:27Z | |
dc.date.issued | 2012 | |
dc.identifier.citation | Molecules 2012, 17(2):1138-1148 | nb_NO |
dc.identifier.issn | 1420-3049 | |
dc.identifier.uri | http://hdl.handle.net/11250/2359499 | |
dc.description.abstract | Duchenne Muscular Dystrophy (DMD) is a common, inherited, incurable, fatal muscle wasting disease caused by deletions that disrupt the reading frame of the DMD gene such that no functional dystrophin protein is produced. Antisense oligonucleotide (AO)-directed exon skipping restores the reading frame of the DMD gene, and truncated, yet functional dystrophin protein is expressed. The aim of this study was to assess the efficiency of two novel rigid, cationic carotenoid lipids, C30-20 and C20-20, in the delivery of a phosphorodiamidate morpholino (PMO) AO, specifically designed for the targeted skipping of exon 45 of DMD mRNA in normal human skeletal muscle primary cells (hSkMCs). The cationic carotenoid lipid/PMO-AO lipoplexes yielded significant exon 45 skipping relative to a known commercial lipid, 1,2-dimyristoyl-sn-glycero-3- ethylphosphocholine (EPC). | nb_NO |
dc.language.iso | eng | nb_NO |
dc.publisher | MDPI | nb_NO |
dc.title | Novel cationic carotenoid lipids as delivery vectors of antisense oligonucleotides for exon skipping in duchenne muscular dystrophy | nb_NO |
dc.type | Journal article | nb_NO |
dc.type | Peer reviewed | en_GB |
dc.date.updated | 2015-09-30T12:30:27Z | |
dc.source.volume | 17 | nb_NO |
dc.source.journal | Molecules | nb_NO |
dc.source.issue | 2 | nb_NO |
dc.identifier.doi | 10.3390/molecules17021138 | |
dc.identifier.cristin | 905400 | |
dc.description.localcode | Open access article. Creative Commons Attribution License. | nb_NO |
Files in this item
This item appears in the following Collection(s)
-
Institutt for kjemi [1397]
-
Publikasjoner fra CRIStin - NTNU [38294]