A novelrecognitionunitofchemicalsensorforselectivedeterminationoftheinosine,renaldisfunction biomarker,wasdevisedandprepared.Forthatpurpose,inosine-templatedmolecularlyimprinted polymer (MIP) film wasdepositedonanextended-gate field-effect transistor(EG-FET)signaltransducing unit. TheMIP film waspreparedbyelectrochemicalpolymerizationofbis(bithiophene)derivatives bearing cytosineandboronicacidsubstituents,inthepresenceoftheinosinetemplateandathiophene cross-linker.AfterMIP film deposition,thetemplatewasremoved,andwasconfirmed byUV–visible spectroscopy.Subsequently,the film compositionwascharacterizedbyspectroscopictechniques,andits morphology andthicknessweredeterminedbyAFM.The finally MIP film-coated extended-gate fieldeffect transistor(EG-FET)wasusedforsignaltransduction.Thiscombinationisnotwidelystudiedinthe literature,despitethefactthatitallowsforfacileintegrationofelectrodepositedMIP film withFET transducer. The lineardynamicconcentrationrangeofthechemosensorwas0.5–50 μM withinosinedetect- ability of0.62 μM. Theobtaineddetectabilitycompareswelltothelevelsoftheinosineinbody fluids which areintherange0–2.9 mM forpatientswithdiagnoseddiabeticnephropathy,goutorhyperur- icemia, andcanreach25 mM incertaincases.Theimprintingfactorforinosine,determinedfrompie- zomicrogravimetricexperimentswithuseoftheMIP film-coated quartzcrystalresonator,wasfoundto be 5.5.Higherselectivityforinosinewithrespecttocommoninterferentswasalsoachievedwiththe present molecularlyengineeredsensingelement.Theobtainedanalyticalparametersofthedevised chemosensor allowforitsuseforpracticalsamplemeasurements.
Extended-gate field-effect transistor (EG-FET) with molecularly imprinted polymer (MIP) film for selective inosine determination
BENINCORI, TIZIANA;
2015-01-01
Abstract
A novelrecognitionunitofchemicalsensorforselectivedeterminationoftheinosine,renaldisfunction biomarker,wasdevisedandprepared.Forthatpurpose,inosine-templatedmolecularlyimprinted polymer (MIP) film wasdepositedonanextended-gate field-effect transistor(EG-FET)signaltransducing unit. TheMIP film waspreparedbyelectrochemicalpolymerizationofbis(bithiophene)derivatives bearing cytosineandboronicacidsubstituents,inthepresenceoftheinosinetemplateandathiophene cross-linker.AfterMIP film deposition,thetemplatewasremoved,andwasconfirmed byUV–visible spectroscopy.Subsequently,the film compositionwascharacterizedbyspectroscopictechniques,andits morphology andthicknessweredeterminedbyAFM.The finally MIP film-coated extended-gate fieldeffect transistor(EG-FET)wasusedforsignaltransduction.Thiscombinationisnotwidelystudiedinthe literature,despitethefactthatitallowsforfacileintegrationofelectrodepositedMIP film withFET transducer. The lineardynamicconcentrationrangeofthechemosensorwas0.5–50 μM withinosinedetect- ability of0.62 μM. Theobtaineddetectabilitycompareswelltothelevelsoftheinosineinbody fluids which areintherange0–2.9 mM forpatientswithdiagnoseddiabeticnephropathy,goutorhyperur- icemia, andcanreach25 mM incertaincases.Theimprintingfactorforinosine,determinedfrompie- zomicrogravimetricexperimentswithuseoftheMIP film-coated quartzcrystalresonator,wasfoundto be 5.5.Higherselectivityforinosinewithrespecttocommoninterferentswasalsoachievedwiththe present molecularlyengineeredsensingelement.Theobtainedanalyticalparametersofthedevised chemosensor allowforitsuseforpracticalsamplemeasurements.
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