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-List Of Titles -An experimental platform for systemic drug delivery to the retina

Please use this identifier to cite or link to this item: http://hdl.handle.net/1959.14/137893

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Title
An experimental platform for systemic drug delivery to the retina
Related
Proceedings of the National Academy of Sciences of the United States of America, Vol. 106, Issue 42, (2009), p.17817-17822
DOI
10.1073/pnas.0908561106
Publisher
National Academy of Sciences
Date
2009
Author/Creator
Campbell, Matthew
Author/Creator
Nguyen, Anh T.H
Author/Creator
Humphries, Peter
Author/Creator
Kiang, Anna-Sophia
Author/Creator
Tam, Lawrence C. S
Author/Creator
Gobbo, Oliviero L
Author/Creator
Kerskens, Christian
Author/Creator
Dhubhghaill, Sorcha Ni
Author/Creator
Humphries, Marian M
Author/Creator
Farrar, G. Jane
Author/Creator
Kenna, Paul F
Description
Degenerative retinopathies, including age-related macular degeneration, diabetic retinopathy, and hereditary retinal disorders - major causes of world blindness - are potentially treatable by using low-molecular weight neuroprotective, antiapoptotic, or antineovascular drugs. These agents are, however, not in current systemic use owing to, among other factors, their inability to passively diffuse across the microvasculature of the retina because of the presence of the inner blood-retina barrier (iBRB). Moreover, preclinical assessment of the efficacies o f new formulations in the treatment of such conditions is similarly compromised. We describe here an experimental process for RNAi-mediated, size-selective, transient, and reversible modulation of the iBRB in mice to molecules up to 800 Da by suppression of transcripts encoding claudin-5, a protein component of the tight junctions of the inner retinal vasculature. MRI produced no evidence indicative of brain or retinal edema, and the process resulted in minimal disturbance of global transcriptional patterns analyzed in neuronal tissue. We show that visual function can be improved in IMPDH1-/- mice, a model of autosomal recessive retinitis pigmentosa, and that the rate of photoreceptor cell death can be reduced in a model of light-induced retinal degeneration by systemic drug delivery after reversible barrier opening. These findings provide a platform for high-throughput drug screening in models of retinal degeneration, and they ultimately could result in the development of a novel "humanized" approach to therapy for conditions with little or no current forms of treatment.
Description
6 page(s)
Subject Keyword
Blood-retina barrier
Subject Keyword
Claudin-5
Subject Keyword
Retinitis pigmentosa
Subject Keyword
RNAi
Subject Keyword
Tight junctions
Resource Type
journal article
Organisation
Macquarie University. Dept. of Chemistry and Biomolecular Sciences

Identifier
http://hdl.handle.net/1959.14/137893
Identifier
ISSN:0027-8424
Identifier
mq_res-ext-2-s2.0-70449577160
Language
eng
Reviewed
Reviewed
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Citation Format
E-mail Address
Subject
"Proceedings of the National Academy of Sciences of the United States of America"
 
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