4.7 Article

Fabrication of novel electrochemical immunosensor by mussel-inspired chemistry and surface-initiated PET-ATRP for the simultaneous detection of CEA and AFP

期刊

REACTIVE & FUNCTIONAL POLYMERS
卷 154, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.reactfunctpolym.2020.104632

关键词

Electrochemical immunosensor; Atom transfer radical polymerization; Mussel-inspired chemistry; Tumor markers; Simultaneous detection

资金

  1. National Natural Science Foundation of China [51573075, 51773086, 51973086]
  2. Major Program of Shandong Province Natural Science Foundation [ZR2018ZC0946]
  3. Natural Science Foundation of Shandong Province [ZR2018BB027]
  4. Key Technology Research and Development Program of Shandong Province [2019GGX102012]
  5. Youth Innovation Technology Program of Shandong Province Higher Educational Science [2019KJA011]
  6. Project of Shandong Province Higher Educational Science [J18KA080]

向作者/读者索取更多资源

A functional electrochemical immunosensor was successfully designed for simultaneous and high sensitivity detection of carcinoembryonic antigen (CEA) and alpha-fetoprotein (AFP). This electrochemical immunosensor was mainly designed by surface-initiated poly(glycidyl methacrylate) (PGMA) from multi-walled carbon nanotubes (MWCNTs) with the methodology of mussel-inspired chemistry (polydopamine, PDA) and metal-free photoinduced electron transfer-atom transfer radical polymerization (PET-ATRP). Controlled PGMA was initiated from MWCNTs, in which Br-functional PDA-modified MWCNTs and eosin Y (EY) were used as initiator and photocatalyst, respectively. The epoxy group of PGMA is reacted with ethylenediamine (EDA) by a ring-opening reaction, the amino and hydroxyl groups in the polymer chain provide numerous effective binding sites for carboxyl groups of signal molecules and capture antibodies, realizing highly sensitive electrochemical detection. Under optimized conditions, the obtained hybrid nanoprobes (Aq/PGMA-g-MWCNTs and Fc/PGMA-g-MWCNTs) were used as efficient electrochemical immunosensor to simultaneously detect CEA and AFP. It is worth noting that the electrochemical immunosensor performed a wide detection range and a low detection limit of CEA (163 fg/mL similar to 163 ng/mL, 56.1 fg/mL) and AFP (100 fg/mL similar to 100 ng/mL, 32.8 fg/mL), respectively. This high sensitivity and selectivity detection platform has a potential application in the simultaneous detection of more tumor markers.

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