Detection of Cardiovascular CRP Protein Biomarker Using a Novel Nanofibrous Substrate
Document Type
Article
Publication Date
6-24-2020
Abstract
It is known that different diseases have characteristic biomarkers that are secreted very early on, even before the symptoms have developed. Before any kind of therapeutic approach can be used, it is necessary that such biomarkers be detected at a minimum concentration in the bodily fluids. Here, we report the fabrication of an interdigitated sensing device integrated with polyvinyl alcohol (PVA) nanofibers and carbon nanotubes (CNT) for the detection of an inflammatory biomarker, C-reactive protein (CRP). The limit of detection (LOD) was achieved in a range of 100 ng mL−1 and 1 fg mL−1 in both phosphate buffered saline (PBS) and human serum (hs). Furthermore, a significant change in the electrochemical impedance from 45% to 70% (hs) and 38% to 60% (PBS) over the loading range of CRP was achieved. The finite element analysis indicates that a non-redox charge transduction at the solid/liquid interface on the electrode surface is responsible for the enhanced sensitivity. Furthermore, the fabricated biosensor consists of a large electro-active surface area, along with better charge transfer characteristics that enabled improved specific binding with CRP. This was determined both experimentally and from the simulated electrochemical impedance of the PVA nanofiber patterned gold electrode.
Publication Title
Biosensors
Repository Citation
Macwan, Isaac; Aphale, Ashish; Bhagvath, Prathamesh; Prasad, Shalini; and Patra, Prabir K., "Detection of Cardiovascular CRP Protein Biomarker Using a Novel Nanofibrous Substrate" (2020). Engineering Faculty Publications. 308.
https://digitalcommons.fairfield.edu/engineering-facultypubs/308
Published Citation
Macwan, Isaac, Ashish Aphale, Prathamesh Bhagvath, Shalini Prasad, and Prabir Patra. “Detection of Cardiovascular CRP Protein Biomarker Using a Novel Nanofibrous Substrate.” Biosensors 10, no. 6 (June 24, 2020): 72. doi:10.3390/bios10060072.
DOI
10.3390/bios10060072
Peer Reviewed
Comments
© 2020 by the authors.
A link to freely available text has been provided.