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COMMUNICATION: Multi-site incorporation of bioactive matrices into MEMS-based neural probes

dc.contributor.authorWilliams, Justin C.en_US
dc.contributor.authorHolecko, Matthew M. II.en_US
dc.contributor.authorMassia, Stephen P.en_US
dc.contributor.authorRousche, Patrick J.en_US
dc.contributor.authorKipke, Daryl R.en_US
dc.date.accessioned2006-12-19T19:21:41Z
dc.date.available2006-12-19T19:21:41Z
dc.date.issued2005-12-01en_US
dc.identifier.citationWilliams, Justin C; Holecko, Matthew M II; Massia, Stephen P; Rousche, Patrick; Kipke, Daryl R (2005). "COMMUNICATION: Multi-site incorporation of bioactive matrices into MEMS-based neural probes." Journal of Neural Engineering. 2(4): L23-L28. <http://hdl.handle.net/2027.42/49187>en_US
dc.identifier.issn1741-2552en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/49187
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=16317225&dopt=citation
dc.description.abstractMethods are presented to incorporate polymer-based bioactive matrices into micro-fabricated implantable microelectrode arrays. Using simple techniques, hydrogels infused with bioactive molecules are deposited within wells in the substrate of the device. This method allows local drug delivery without increasing the footprint of the device. In addition, each well can be loaded individually, allowing spatial and temporal control over diffusion gradients in the microenvironment of the implanted neural interface probe. In vivo testing verified the following: diffusion of the bioactive molecules, integration of the bioactive molecules with the intended neural target and concurrent extracellular recording using nearby electrodes. These results support the feasibility of using polymer gels to deliver bioactive molecules to the region close to microelectrode shanks. This technique for microdrug delivery may serve as a means to intervene with the initial phases of the neuroinflammatory tissue response to permanently implanted microelectrode arrays.en_US
dc.format.extent3118 bytes
dc.format.extent1252982 bytes
dc.format.mimetypetext/plain
dc.format.mimetypeapplication/pdf
dc.language.isoen_US
dc.publisherIOP Publishing Ltden_US
dc.titleCOMMUNICATION: Multi-site incorporation of bioactive matrices into MEMS-based neural probesen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumHarrington Department of Bioengineering, Arizona State University, Tempe, AZ 85287, USA; Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA;en_US
dc.contributor.affiliationumHarrington Department of Bioengineering, Arizona State University, Tempe, AZ 85287, USA; Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA;en_US
dc.contributor.affiliationotherHarrington Department of Bioengineering, Arizona State University, Tempe, AZ 85287, USA;en_US
dc.contributor.affiliationotherHarrington Department of Bioengineering, Arizona State University, Tempe, AZ 85287, USAen_US
dc.contributor.affiliationotherHarrington Department of Bioengineering, Arizona State University, Tempe, AZ 85287, USA;en_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid16317225
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/49187/2/jne5_4_l03.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1088/1741-2560/2/4/L03en_US
dc.identifier.sourceJournal of Neural Engineering.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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