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dc.contributor.authorDingari, Narahara Chari
dc.contributor.authorHorowitz, Gary L.
dc.contributor.authorKang, Jeon Woong
dc.contributor.authorDasari, Ramachandra Rao
dc.contributor.authorBarman, Ishan
dc.date.accessioned2012-06-01T18:55:06Z
dc.date.available2012-06-01T18:55:06Z
dc.date.issued2012-02
dc.date.submitted2011-11
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/70995
dc.description.abstractWe present the first demonstration of glycated albumin detection and quantification using Raman spectroscopy without the addition of reagents. Glycated albumin is an important marker for monitoring the long-term glycemic history of diabetics, especially as its concentrations, in contrast to glycated hemoglobin levels, are unaffected by changes in erythrocyte life times. Clinically, glycated albumin concentrations show a strong correlation with the development of serious diabetes complications including nephropathy and retinopathy. In this article, we propose and evaluate the efficacy of Raman spectroscopy for determination of this important analyte. By utilizing the pre-concentration obtained through drop-coating deposition, we show that glycation of albumin leads to subtle, but consistent, changes in vibrational features, which with the help of multivariate classification techniques can be used to discriminate glycated albumin from the unglycated variant with 100% accuracy. Moreover, we demonstrate that the calibration model developed on the glycated albumin spectral dataset shows high predictive power, even at substantially lower concentrations than those typically encountered in clinical practice. In fact, the limit of detection for glycated albumin measurements is calculated to be approximately four times lower than its minimum physiological concentration. Importantly, in relation to the existing detection methods for glycated albumin, the proposed method is also completely reagent-free, requires barely any sample preparation and has the potential for simultaneous determination of glycated hemoglobin levels as well. Given these key advantages, we believe that the proposed approach can provide a uniquely powerful tool for quantification of glycation status of proteins in biopharmaceutical development as well as for glycemic marker determination in routine clinical diagnostics in the future.en_US
dc.description.sponsorshipNational Center for Research Resources (U.S.) (Grant No. P41-RR02594)en_US
dc.description.sponsorshipMassachusetts Institute of Technology. Laser Biomedical Research Centeren_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0032406en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/en_US
dc.sourcePLoSen_US
dc.titleRaman Spectroscopy Provides a Powerful Diagnostic Tool for Accurate Determination of Albumin Glycationen_US
dc.typeArticleen_US
dc.identifier.citationDingari, Narahara Chari et al. “Raman Spectroscopy Provides a Powerful Diagnostic Tool for Accurate Determination of Albumin Glycation.” Ed. Irene Georgakoudi. PLoS ONE 7.2 (2012): e32406. Web.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Laser Biomedical Research Centeren_US
dc.contributor.departmentMassachusetts Institute of Technology. Spectroscopy Laboratoryen_US
dc.contributor.approverDingari, Narahara Chari
dc.contributor.mitauthorDingari, Narahara Chari
dc.contributor.mitauthorKang, Jeon Woong
dc.contributor.mitauthorDasari, Ramachandra Rao
dc.contributor.mitauthorBarman, Ishan
dc.relation.journalPLoS ONEen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsDingari, Narahara Chari; Horowitz, Gary L.; Kang, Jeon Woong; Dasari, Ramachandra R.; Barman, Ishanen
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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