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dc.contributor.authorBhujbal, Swapnil Vilas
dc.contributor.authorNiclou, Simone
dc.contributor.authorde Vos, Paul
dc.date.accessioned2018-03-21T08:25:44Z
dc.date.available2018-03-21T08:25:44Z
dc.date.created2017-12-01T11:14:00Z
dc.date.issued2014
dc.identifier.issn0169-409X
dc.identifier.urihttp://hdl.handle.net/11250/2491374
dc.description.abstractMalignant brain tumors including glioblastoma are incurable cancers. Over the last years a number of promising novel treatment approaches have been investigated including the application of inhibitors of receptor tyrosine kinases and downstream targets, immune-based therapies and anti-angiogenic agents. Unfortunately so far the major clinical trials in glioblastoma patients did not deliver clear clinical benefits. Systemic brain tumor therapy is seriously hampered by poor drug delivery to the brain. Although in glioblastoma, the blood brain barrier is disrupted in the tumor core, the major part of the tumor is largely protected by an intact blood brain barrier. Active cytotoxic compounds encapsulated into liposomes, micelles, and nanoparticles constitute novel treatment options because they can be designed to facilitate entry into the brain parenchyma. In the case of biological therapeutics, encapsulation of therapeutic cells and their implantation into the surgical cavity represents another promising approach. This technology provides long term release of the active compound at the tumor site and reduces side effects associated with systemic delivery. The proof of principle of encapsulated cell factories has been successfully demonstrated in experimental animal models and should pave the way for clinical application. Here we review the challenges associated with the treatment of brain tumors and the different encapsulation options available for drugs and living cells, with an emphasis on alginate based cell encapsulation technology.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.titleDrug and cell encapsulation: alternative delivery options for the treatment of malignant brain tumorsnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber142-153nb_NO
dc.source.volume67–68nb_NO
dc.source.journalAdvanced Drug Delivery Reviewsnb_NO
dc.identifier.doi10.1016/j.addr.2014.01.010
dc.identifier.cristin1521489
dc.description.localcodeThis article will not be available due to copyright restrictions (c) 2014 by Elseviernb_NO
cristin.unitcode194,66,15,0
cristin.unitnameInstitutt for bioteknologi og matvitenskap
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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