4.7 Article

New electrochemical method for programmed death-ligand 1 detection based on a paper-based microfluidic aptasensor

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BIOELECTROCHEMISTRY
卷 140, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.bioelechem.2021.107789

关键词

Electrochemical aptasensor; Programmed death-ligand 1; Differential pulse voltammetry

资金

  1. National Key Research and Development Program of Nano Science and Technology of China [2017YFA0205902]
  2. NSFC [61960206012, 61527815, 61771452, 61673024, 61775216]
  3. Key Research Programs of Frontier Sciences, CAS [QYZDJ-SSW-SYS015]
  4. Beijing Municipal Natural Science Foundation [4202081]

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A paper-based microfluidic aptasensor was developed for label-free electrochemical detection of PD-L1 in liquids, showing good performance such as low cost, portability, and high sensitivity.
As programmed death-ligand 1 (PD-L1) is considered a referenced therapeutic biomarker, a rapid and low-cost method to detect PD-L1 in body fluids is necessary. In this work, a paper-based microfluidic aptasensor for label-free electrochemical detection of PD-L1 in liquids was fabricated. The aptasensor integrates a reaction cell and a three-electrode system, and a differential pulse voltammetry electrochemical method was adopted. PD-L1 aptamer with a low equilibrium dissociation constant was used as a biorecognition molecule. To bind the aptamer and assist in the electrochemical measurement, nanocomposites were synthesized and used to modify the working electrode, which was composed of an amine-functionalized single-walled carbon nanotube, new methylene blue and gold nanoparticles. The basic performance of the aptasensor was tested in phosphate-buffered saline: the linear range was between 10 pg mL(-1) and 2.5 ng mL(-1), and the detection limit was 10 pg mL(-1) (signal/noise = 3). Moreover, the aptasensor was used for the detection of serum samples and compared with an enzyme linked immunosorbent assay (ELISA). The results showed that the aptasensor provides a new low-cost, portable and highly sensitive detection method for PD-L1, as an alternative to ELISA. (C) 2021 Elsevier B.V. All rights reserved.

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