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Compatibility of Staining Protocols for Bone Tissue with Raman Imaging

dc.contributor.authorGomez, Luis E.en_US
dc.contributor.authorMorris, Michael D.en_US
dc.contributor.authorCrane, Nicole J.en_US
dc.contributor.authorIgnelzi, Michael A.en_US
dc.date.accessioned2006-09-11T19:39:17Z
dc.date.available2006-09-11T19:39:17Z
dc.date.issued2004-01en_US
dc.identifier.citationMorris, Michael D.; Crane, Nicole J.; Gomez, Luis E.; Ignelzi, Michael A.; (2004). "Compatibility of Staining Protocols for Bone Tissue with Raman Imaging." Calcified Tissue International 74(1): 86-94. <http://hdl.handle.net/2027.42/48009>en_US
dc.identifier.issn0171-967Xen_US
dc.identifier.issn1432-0827en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/48009
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=14564434&dopt=citationen_US
dc.description.abstractWe report the use of Raman microscopy to image mouse calvaria stained with hematoxylin, eosin and toluidine blue. Raman imaging of stained specimens allows for direct correlation of histological and spectral information. A line-focus 785 nm laser imaging system with specialized near-infrared (NIR) microscope objectives and CCD detector were used to collect approximately 100 × 450 µm Raman images. Principal components analysis, a multivariate analysis technique, was used to determine whether the histological stains cause spectral interference (band shifts or intensity changes) or result in thermal damage to the examined tissue. Image analysis revealed factors for tissue components and the embedding medium, glycol methacrylate, only. Thus, Raman imaging proved to be compatible with histological stains such as hematoxylin, eosin and toluidine blue.en_US
dc.format.extent357136 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherToluidine Blueen_US
dc.subject.otherHistological Stainingen_US
dc.subject.otherMineralized Tissueen_US
dc.subject.otherRaman Spectroscopyen_US
dc.subject.otherPhilosophyen_US
dc.subject.otherH&Een_US
dc.subject.otherBoneen_US
dc.titleCompatibility of Staining Protocols for Bone Tissue with Raman Imagingen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelDentistryen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, 930 N. University Avenue, Ann Arbor, MI 48109-1055, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, 930 N. University Avenue, Ann Arbor, MI 48109-1055, USAen_US
dc.contributor.affiliationumDepartment of Orthodontics and Pediatric Dentistry, University of Michigan School of Dentistry, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Orthodontics and Pediatric Dentistry, University of Michigan School of Dentistry, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid14564434en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/48009/1/223_2003_Article_38.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s00223-003-0038-0en_US
dc.identifier.sourceCalcified Tissue Internationalen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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