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Surface plasmon resonance biosensor for detection of pregnancy associated plasma protein A2 in clinical samples

M. Bocková, X. Chadtová Song, E. Gedeonová, K. Levová, M. Kalousová, T. Zima, J. Homola,

. 2016 ; 408 (26) : 7265-9. [pub] 20160614

Jazyk angličtina Země Německo

Typ dokumentu hodnotící studie, časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc18011161
E-zdroje Online Plný text

NLK ProQuest Central od 2011-01-01 do Před 1 rokem
Medline Complete (EBSCOhost) od 2003-01-01 do Před 1 rokem
Health & Medicine (ProQuest) od 2011-01-01 do Před 1 rokem

Pregnancy associated plasma protein A2 (PAPP-A2) is a metalloproteinase that plays multiple roles in fetal development and post-natal growth. Here we present a novel surface plasmon resonance (SPR) biosensor for the rapid and quantitative detection of PAPP-A2 in blood samples. This biosensor uses a single surface referencing approach and a sandwich assay with functionalized gold nanoparticles for signal enhancement. We demonstrate that this SPR biosensor enables the detection of PAPP-A2 in 30 % blood plasma at levels as low as 3.6 ng/mL. We also characterize the performance of the biosensor and evaluate its cross-reactivity to a PAPP-A analogue. Finally, we utilize this SPR biosensor for the detection of PAPP-A2 in blood serum from two groups of subjects: pregnant women and healthy non-pregnant women and men. Graphical Abstract Temporal sensor response corresponding to respective steps of the assay for detection of PAPP-A2 in buffer.

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$a Pregnancy associated plasma protein A2 (PAPP-A2) is a metalloproteinase that plays multiple roles in fetal development and post-natal growth. Here we present a novel surface plasmon resonance (SPR) biosensor for the rapid and quantitative detection of PAPP-A2 in blood samples. This biosensor uses a single surface referencing approach and a sandwich assay with functionalized gold nanoparticles for signal enhancement. We demonstrate that this SPR biosensor enables the detection of PAPP-A2 in 30 % blood plasma at levels as low as 3.6 ng/mL. We also characterize the performance of the biosensor and evaluate its cross-reactivity to a PAPP-A analogue. Finally, we utilize this SPR biosensor for the detection of PAPP-A2 in blood serum from two groups of subjects: pregnant women and healthy non-pregnant women and men. Graphical Abstract Temporal sensor response corresponding to respective steps of the assay for detection of PAPP-A2 in buffer.
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$a Chadtová Song, Xue $u Department of Optical Sensors, Institute of Photonics and Electronics of the CAS, Chaberska 57, 18251, Prague 8, Czech Republic.
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$a Levová, Kateřina $u Institute of Medical Biochemistry and Laboratory Diagnostics of First Faculty of Medicine, Charles University in Prague and the General University Hospital in Prague, U Nemocnice 2, 12808, Praha 2, Czech Republic.
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$a Kalousová, Marta $u Institute of Medical Biochemistry and Laboratory Diagnostics of First Faculty of Medicine, Charles University in Prague and the General University Hospital in Prague, U Nemocnice 2, 12808, Praha 2, Czech Republic.
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$a Zima, Tomáš $u Institute of Medical Biochemistry and Laboratory Diagnostics of First Faculty of Medicine, Charles University in Prague and the General University Hospital in Prague, U Nemocnice 2, 12808, Praha 2, Czech Republic.
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$a Homola, Jiří $u Department of Optical Sensors, Institute of Photonics and Electronics of the CAS, Chaberska 57, 18251, Prague 8, Czech Republic. homola@ufe.cz.
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