4.6 Article

Detection of VEGF165 in Whole Blood by Differential Pulse Voltammetry Based on a Centrifugal Microfluidic Chip

期刊

ACS SENSORS
卷 7, 期 4, 页码 1019-1026

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.1c02641

关键词

centrifugal microfluidic chip; plasma separation; PThi; Au NP nanocomposites; vascular endothelial growth factor 165 (VEGF(165)); differential pulse voltammetry (DPV)

资金

  1. National Key Research and Development Plan [2020YFB2009001]
  2. National Natural Science Foundation of China [62071066, 62071072]
  3. Fundamental Research Funds for the Central Universities [2021CDJKYJH006]
  4. 2020 Chongqing Graduate Research and Innovation Project of School of Optoelectronic Engineering [GDYKC202005]
  5. Project of Intelligent Sensing and Micro-nano Biochemical System (2019 Graduate Tutor Team)

向作者/读者索取更多资源

A microfluidic sensing chip that integrates a centrifugal separation pretreatment unit and a composite nanosensing film was proposed for the rapid and sensitive detection of vascular endothelial growth factor 165 (VEGF165) in clinical blood samples. The method achieved a low detection limit and a wide linear range, meeting the needs of clinical VEGF165 detection.
For the rapid and sensitive detection of vascular endothelial growth factor 165 (VEGF165) in clinical blood samples, amicrofluidic sensing chip that integrates a centrifugal separationpretreatment unit and a composite nanosensingfilm was proposed inthis paper. An efficient sensing strategy and method was established. Theblood sample wasfirst separated and extracted by centrifugal force on thecentrifugal microfluidic chip within 5 min after injection. The separatedplasma can be automatically transferred through the designed micro-channels to the detection area integrated electrodes for subsequentdifferential pulse voltammetric detection. The Au NPs/MCH/Apt2sensingfilm was constructed on the surface of the Au working electrode.A sandwich sensing strategy based ondouble aptamersandnanop-robefor VEGF165detection was established, by which the synthetic Apt1/PThi/Au NP nanoprobe was applied to capture VEGF165in plasma and bind to the sensingfilm. By this method, the detection limit of VEGF165in whole blood was 0.67 pg/mL and the linearrange was between 1 pg and 10 ng, which met the needs of clinical VEGF165detection. It was illustrated that the proposedmethodology based on the centrifugal microfluidic chip had potential application prospects in the development of the point-of-care testing fields

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