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A novel device for chronic intracranial drug delivery via microdialysis

dc.contributor.authorBazzett, Terence J.en_US
dc.contributor.authorBecker, Jill B.en_US
dc.contributor.authorAlbin, Roger L.en_US
dc.date.accessioned2006-04-10T14:31:19Z
dc.date.available2006-04-10T14:31:19Z
dc.date.issued1991-11en_US
dc.identifier.citationBazzett, T. J., Becker, J. B., Albin, R. L. (1991/11)."A novel device for chronic intracranial drug delivery via microdialysis." Journal of Neuroscience Methods 40(1): 1-8. <http://hdl.handle.net/2027.42/29039>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T04-484MD8Y-6N/2/74a19c8b537fe19f07fa2b5b79378a93en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/29039
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1839046&dopt=citationen_US
dc.description.abstractA system is described for chronic intracranial drug administration in the rat using a modified in vivo microdialysis probe coupled to an Alzet model 2002 osmotic minipump. The results presented demonstrate that this system can be used for the chronic administration of quinolinic acid with minimal non-specific damage. Each pump delivered approximately 225 [mu]l of solution over a period of 19-20 days when tested in vitro. The dialysis units were uniform in function, delivering &gt; 93% of the [3H]quinolinic acid initially loaded into the minipump. For in vivo analysis of this apparatus the dose of quinolinic acid tested produced extensive destruction of the striatum. The present system allows reliable drug diffusion over a relatively large area without pressure injection variability. In conclusion, we have developed a simple and inexpensive technique for administration of drugs into brain parenchyma with substantial advantages over previously used techniques.en_US
dc.format.extent606046 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleA novel device for chronic intracranial drug delivery via microdialysisen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPsychologyen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelSocial Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Psychology, Neuroscience and Reproductive Sciences Programs, The University of Michigan, Ann Arbor, MI 48104-1687, U.S.A.; Department of Neurology, Neuroscience Program, The University of Michigan, Ann Arbor, MI 48104-1687, U.S.A.en_US
dc.contributor.affiliationumDepartment of Psychology, Neuroscience and Reproductive Sciences Programs, The University of Michigan, Ann Arbor, MI 48104-1687, U.S.A.en_US
dc.contributor.affiliationumDepartment of Neurology, Neuroscience Program, The University of Michigan, Ann Arbor, MI 48104-1687, U.S.A.en_US
dc.identifier.pmid1839046en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/29039/1/0000072.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0165-0270(91)90111-Cen_US
dc.identifier.sourceJournal of Neuroscience Methodsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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