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dc.contributor.authorNewland, Ben
dc.contributor.authorDunnett, Stephen B.
dc.contributor.authorDowd, Eilís
dc.date.accessioned2018-09-20T16:19:12Z
dc.date.available2018-09-20T16:19:12Z
dc.date.issued2016-08-01
dc.identifier.citationNewland, Ben; Dunnett, Stephen B. Dowd, Eilís (2016). Targeting delivery in parkinson's disease. Drug Discovery Today 21 (8), 1313-1320
dc.identifier.issn1359-6446
dc.identifier.urihttp://hdl.handle.net/10379/13110
dc.description.abstractDisease-modifying therapies for Parkinson's disease (PD), with the potential to halt the neurodegenerative process and to stimulate the protection, repair, and regeneration of dopaminergic neurons, remain a vital but unmet clinical need. Targeting the delivery of current and new therapeutics directly to the diseased brain region (in particular the nigrostriatal pathway) could result in greater improvements in the motor functions that characterise PD. Here, we highlight some of the opportunities and challenges facing the development of the next generation of therapies for patients with PD.
dc.publisherElsevier BV
dc.relation.ispartofDrug Discovery Today
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.subjectlactoferrin-modified nanoparticles
dc.subjectfactor gene-therapy
dc.subjectglial-cell line
dc.subjectstem-cells
dc.subjectneurotrophic factor
dc.subjectdopamine neurons
dc.subjectrat model
dc.subjecthemiparkinsonian rats
dc.subjectsubstantia-nigra
dc.subjectdrug-delivery
dc.titleTargeting delivery in parkinson's disease
dc.typeArticle
dc.identifier.doi10.1016/j.drudis.2016.06.003
dc.local.publishedsourcehttp://orca.cf.ac.uk/106085/1/Targeting%20Delivery%20in%20Parkinson%3Fs%20Disease.pdf
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Attribution-NonCommercial-NoDerivs 3.0 Ireland
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Ireland