Soluble urokinase plasminogen activator receptor (suPAR) is an inflammatory protein present in blood and a marker of disease presence, severity and prognosis. A heterogeneous sandwich assay is proposed for quantifying suPAR by employing a capture antibody from rat and a biotinylated detection antibody from mouse. Optical detection was achieved by a successive exposure of the biotinylated sandwich to streptavidin labelled with ATTO647N. The heterogeneous assay was implemented on a multichannel polymethylmetacrylate (PMMA) optical biochip, potentially capable of the simultaneous detection of more than one analyte. Capture antibody was immobilized on the PMMA surface of the microfluidic channel and the assay was performed with the following protocol: i) surface blocking with BSA, ii) incubation with suPAR or PBS, iii) incubation with biotinylated suPAR detection Ab and iv) incubation with streptavidin-ATTO647N. Promising preliminary results were obtained with this protocol. Moreover, an improved optical setup is proposed which avoids the mechanical scanning of the chip and consequently the in-series fluorescence excitation and read out, allowing the simultaneous measurement of the fluorescence on all the channels of the microfluidic chip.

Optical heterogeneous bioassay for the detection of the inflammatory biomarker suPAR

S Tombelli;C Trono;B Adinolfi;F Chiavaioli;A Giannetti;R Bernini;I A Grimaldi;G Persichetti;G Testa;F Baldini
2015

Abstract

Soluble urokinase plasminogen activator receptor (suPAR) is an inflammatory protein present in blood and a marker of disease presence, severity and prognosis. A heterogeneous sandwich assay is proposed for quantifying suPAR by employing a capture antibody from rat and a biotinylated detection antibody from mouse. Optical detection was achieved by a successive exposure of the biotinylated sandwich to streptavidin labelled with ATTO647N. The heterogeneous assay was implemented on a multichannel polymethylmetacrylate (PMMA) optical biochip, potentially capable of the simultaneous detection of more than one analyte. Capture antibody was immobilized on the PMMA surface of the microfluidic channel and the assay was performed with the following protocol: i) surface blocking with BSA, ii) incubation with suPAR or PBS, iii) incubation with biotinylated suPAR detection Ab and iv) incubation with streptavidin-ATTO647N. Promising preliminary results were obtained with this protocol. Moreover, an improved optical setup is proposed which avoids the mechanical scanning of the chip and consequently the in-series fluorescence excitation and read out, allowing the simultaneous measurement of the fluorescence on all the channels of the microfluidic chip.
2015
Istituto di Fisica Applicata - IFAC
Istituto per il Rilevamento Elettromagnetico dell'Ambiente - IREA
Inglese
Photonic West 2015
9313
93130W-1
93130W-6
6
http://proceedings.spiedigitallibrary.org/proceeding.aspx?articleid=2195082
07-12/02/2015
San Francisco USA
Soluble urokinase plasminogen activator receptor
heterogeneous assay
immunoas
fluorescence
optical biochip
diffractive optics
10
none
S. Tombelli ; C. Trono ; B. Adinolfi ; F. Chiavaioli ; A. Giannetti ; J. EugenOlsen ; R. Bernini ; I. A. Grimaldi ; G. Persichetti ; G. Testa ; F. Bal...espandi
273
info:eu-repo/semantics/conferenceObject
04 Contributo in convegno::04.01 Contributo in Atti di convegno
   Advanced spectroscopic hemogram for personalized care against live threatening infections using an integrated chip-assisted bio-photonic system
   HEMOSPEC
   FP7
   611682
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/290237
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