4.8 Article

An ultrasensitive human cardiac troponin T graphene screen-printed electrode based on electropolymerized-molecularly imprinted conducting polymer

Journal

BIOSENSORS & BIOELECTRONICS
Volume 77, Issue -, Pages 978-985

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2015.10.068

Keywords

Cardiac troponin T; Molecularly imprinted polymer; Pyrrole; Acid carboxylic-3-pyrrole; Graphene; Point-of-care testing

Funding

  1. National Council of Technological and Scientific Development (CNPq/Brazil) foundation
  2. FACEPE/Brazil foundation
  3. Pernambuco state research foundation
  4. Improvement of Higher Education Personnel (CAPES), Brazil foundation

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A nano-molecularly imprinted polymer (N-MIP) assembled on a screen-printed electrode for the cardiac troponin T (cTnT) was developed. The biomimetic surface was obtained by a co-polymer matrix assembled on the reduced graphene oxide (RGO) electrode surface. The cTnT active sites were engineered using pyrrole and carboxylated pyrrole that was one-step electropolymerized jointly with cTnT by cyclic voltammetry. The stepwise preparation of the biomimetic surface was characterized by cyclic and differential pulse voltammetries using the ferrocyanide/ferricyanide as redox probe. Structural and morphological characterization was also performed. The optimal relation of pyrrole and pyrrole-3-acid carboxylic to perform the cTnT biomimetic nanosurface was obtained at 1:5 ratio. The analytical performance of cTnT N-MIP performed by differential pulse voltammetry showed a linear range from 0.01 to 0.1 ng mL(-1) (r= 0.995, p << 0.01), with a very low limit of detection (0.006 ng mL(-1)). The synergic effect of conductive polymer and graphene forming 3D structures of reactive sites resulted in a N-MIP with excellent affinity to cTnT binding (K-D=7.3 10(-13) mol L-1). The N-MIP proposed is based on a simple method of antibody obtaining with a large potential for point-of-care testing applications. (C) 2015 Elsevier B.V. All rights reserved.

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