4.8 Article

Electrochemistry-Assisted Surface Plasmon Resonance Biosensor for Detection of CA 15-3

期刊

ANALYTICAL CHEMISTRY
卷 93, 期 22, 页码 7815-7824

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.0c05367

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资金

  1. FCT (Fundacao para a Ciencia e Tecnologia)
  2. European Union (FEDER funds) [Pest-C/QUI/UIDB/00081/2020, NORTE-01-0247-FEDER-017834]
  3. FCT under the QREN - POPH - Advanced Training [SFRH/BSAB/150320/2019, SFRH/BPD/105395/2014]
  4. European Union
  5. national MEC funds
  6. Fundação para a Ciência e a Tecnologia [SFRH/BSAB/150320/2019] Funding Source: FCT

向作者/读者索取更多资源

This study presents an innovative methodology combining SPR and electrochemical responses for detecting CA 15-3 cancer biomarker with high sensitivity and selectivity. By utilizing a two-step approach, the detection limit was significantly improved without the need for complex amplification steps. Additionally, the developed eSPR biosensing methodology showed selectivity for CA 15-3 protein and demonstrated clinical applicability in detecting the biomarker in human serum samples.
In this work, we describe an innovative methodology based on combined surface plasmon resonance (SPR) and electrochemical responses (eSPR) in the same immunoassay for screening CA 15-3 cancer biomarker with high sensitivity (and selectivity), in a very simple, label-free, accurate, and fully automated manner. Detection was achieved by performing two simple steps. In the first step, direct SPR was used to monitor CA 15-3 interaction with surface immobilized antibody. Two linear response ranges were obtained and the detection limit achieved is poor (LOD of 21 U mL(-1)). However, in the second detection step, electrochemical measurements at the SPR gold surface were performed to measure the decrease of redox probe peak current upon antigen-antibody interaction, providing a suitable amplification strategy to lower detection levels of CA 15-3 (LOD of 0.0998 U mL(-1)), without the need of additional complex and/or expensive amplification steps to enhance the sensitivity. Moreover, selectivity studies were performed against other common cancer biomarkers and the results showed that the eSPR immunosensor is selective for the CA 15-3 protein. Finally, the clinical applicability of the developed eSPR biosensing methodology was successfully applied to detect CA 15-3 in human serum samples at clinically relevant levels due to the high sensitivity of electrochemical readout. The same concept may be further extended to other proteins of interest.

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