dc.contributorUniversity of Oxford
dc.contributorQingdao University of Science and Technology
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:28:10Z
dc.date.available2014-05-27T11:28:10Z
dc.date.created2014-05-27T11:28:10Z
dc.date.issued2013-01-15
dc.identifierBiosensors and Bioelectronics, v. 39, n. 1, p. 94-98, 2013.
dc.identifier0956-5663
dc.identifier1873-4235
dc.identifierhttp://hdl.handle.net/11449/74376
dc.identifier10.1016/j.bios.2012.06.051
dc.identifierWOS:000309486300015
dc.identifier2-s2.0-84865764290
dc.identifier0477045906733254
dc.identifier0000-0003-2827-0208
dc.description.abstractC-reactive protein (CRP) is an acute phase protein whose levels are increased in many disorders. There exists, in particular, a great deal of interest in the correlation between blood serum levels and the severity of risk for cardiovascular disease. A sensitive, label-free, non-amplified and reusable electrochemical impedimetric biosensor for the detection of CRP in blood serum was developed herein based on controlled and coverage optimised antibody immobilization on standard polycrystalline gold electrodes. Charge transfer resistance changes were highly target specific, linear with log. CRP. concentration across a 0.5-50. nM range and associated with a limit of detection of 176. pM. Significantly, the detection limits are better than those of current CRP clinical methods and the assays are potentially cheap, relatively automated, reusable, multiplexed and highly portable. The generated interfaces were capable not only of comfortably quantifying CRP across a clinically relevant range of concentrations but also of doing this in whole blood serum with interfaces that were, subsequently, reusable. The importance of optimising receptor layer resistance in maximising assay sensitivity is also detailed. © 2012.
dc.languageeng
dc.relationBiosensors and Bioelectronics
dc.relation8.173
dc.relation2,373
dc.rightsAcesso restrito
dc.sourceScopus
dc.subjectBiosensor
dc.subjectBlood
dc.subjectC-reactive protein
dc.subjectElectrochemical impedance spectroscopy
dc.subjectResistance
dc.subjectSelf-assembly
dc.subjectAcute phase proteins
dc.subjectAntibody immobilization
dc.subjectBlood serum
dc.subjectC-reactive proteins
dc.subjectCardio-vascular disease
dc.subjectCharge transfer resistance
dc.subjectClinical methods
dc.subjectDetection limits
dc.subjectElectrochemical biosensor
dc.subjectHighly-portable
dc.subjectLabel free
dc.subjectLabel-free detection
dc.subjectLimit of detection
dc.subjectPolycrystalline gold
dc.subjectReceptor layers
dc.subjectWhole blood
dc.subjectAssays
dc.subjectCharge transfer
dc.subjectChemical detection
dc.subjectElectric resistance
dc.subjectProteins
dc.subjectSelf assembly
dc.subjectBiosensors
dc.subjectC reactive protein
dc.subjectpolyclonal antibody
dc.subjectbiosensor
dc.subjectblood analysis
dc.subjectcontrolled study
dc.subjectelectric resistance
dc.subjectelectrochemical detection
dc.subjectelectrochemical impedance spectroscopy
dc.subjecthuman
dc.subjectlaboratory automation
dc.subjectlimit of detection
dc.subjectprocess development
dc.subjectprocess optimization
dc.subjectprotein blood level
dc.subjectprotein determination
dc.subjectprotein immobilization
dc.subjectquantitative analysis
dc.subjectsensitivity and specificity
dc.subjectvalidation process
dc.subjectBiosensing Techniques
dc.subjectC-Reactive Protein
dc.subjectCardiovascular Diseases
dc.subjectDielectric Spectroscopy
dc.subjectHumans
dc.subjectImmunoassay
dc.subjectLimit of Detection
dc.subjectSerum
dc.titleAn optimised electrochemical biosensor for the label-free detection of C-reactive protein in blood
dc.typeArtículos de revistas


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