Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/15190
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dc.contributor.authorLiebetrau J.M.
dc.contributor.authorMiller H.M.
dc.contributor.authorBaur J.E.
dc.contributor.authorTakacs S.A.
dc.contributor.authorAnupunpisit V.
dc.contributor.authorGarris P.A.
dc.contributor.authorWipf D.O.
dc.date.accessioned2021-04-05T04:32:55Z-
dc.date.available2021-04-05T04:32:55Z-
dc.date.issued2003
dc.identifier.issn32700
dc.identifier.other2-s2.0-0037312636
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/15190-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0037312636&doi=10.1021%2fac026166v&partnerID=40&md5=6b9b86bf7069cd6c12771cc5a650dc9f
dc.description.abstractLiving PC12 cells, a model cell type for studying neuronal function, were imaged using the negative feedback mode of a scanning electrochemical microscope (SECM). Six biocompatible redox mediators were successfully identified from a large pool of candidates and were then used for imaging PC12 cells before and after exposure to nerve growth factor (NGF). When exposed to NGF, cells differentiate into a neuron phenotype by growing narrow neurites (1-2 μm wide) that can extend >100 μm from the cell proper. We demonstrate that carbon fiber electrodes with reduced tip diameters can be used for imaging both the cell proper and these neurites. Regions of decreased current, possibly resulting from raised features not identifiable by light microscopy, are clearly evident in the SECM images. Changes in the morphology of undifferentiated PC12 cells could be detected in real time with the SECM. After exposure to hypotonic and hypertonic solutions, reversible changes in cell height of <2 μm were measured.
dc.subjectBiocompatibility
dc.subjectCarbon fibers
dc.subjectCells
dc.subjectImaging techniques
dc.subjectMicroscopic examination
dc.subjectMorphology
dc.subjectNeurology
dc.subjectScanning electrochemical microscopy (SECM)
dc.subjectElectrochemistry
dc.subjectdopamine
dc.subjectanimal cell
dc.subjectarticle
dc.subjectcell strain
dc.subjectcell structure
dc.subjectcell type
dc.subjectcyclic potentiometry
dc.subjectdopamine release
dc.subjectelectrochemical analysis
dc.subjectelectrode
dc.subjecthigh performance liquid chromatography
dc.subjectmicroscopy
dc.subjectmodel
dc.subjectmorphology
dc.subjectnerve cell
dc.subjectnerve cell differentiation
dc.subjectneurotransmitter release
dc.subjectnonhuman
dc.subjectrat
dc.subjectscanning electrochemical microscopy
dc.subjectscanning electron microscopy
dc.subjectAnimals
dc.subjectDiagnostic Imaging
dc.subjectElectrochemistry
dc.subjectMicroelectrodes
dc.subjectMicroscopy, Electron, Scanning
dc.subjectNerve Growth Factor
dc.subjectNeurons
dc.subjectPC12 Cells
dc.subjectRats
dc.titleScanning electrochemical microscopy of model neurons: Imaging and real-time detection of morphological changes
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationAnalytical Chemistry. Vol 75, No.3 (2003), p.563-571
dc.identifier.doi10.1021/ac026166v
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