An electrochemical vertical flow immunoassay (eVFIA) as a point-of-care device for the on-site determination of GFAP demonstrates strong potential for deployment in decentralized healthcare environments, providing clinicians with a rapid and reliable tool for early stroke assessment.
Abstract
Rapid identification of stroke types remains a major clinical challenge, as current diagnostic methods often rely on neuroimaging, which is time-consuming and not always accessible in pre-hospital settings or remote zones. Glial fibrillary acidic protein (GFAP) has emerged as a promising biomarker for distinguishing hemorrhagic from ischemic stroke, paving the way for rapid, quantitative, and portable detection platforms. Here, we report an electrochemical vertical flow immunoassay (eVFIA) as a point-of-care device for the on-site determination of GFAP. The device combines a multilayer paper-based architecture with a screen-printed electrochemical cell, enabling rapid vertical flow immunoassay and electrochemical signal generation within 10 min. Through systematic optimization of assay parameters, the eVFIA offered a detection limit of 85 pg/mL and strong agreement with standard ELISA measurements. The vertical flow format accelerates fluid transport, while the electrochemical readout ensures quantitative, light-independent measurements. This platform thus offers a cost-effective and user-friendly approach to determine biomarkers for stroke type differentiation. Although further large-scale validation is needed, the GFAP-eVFIA demonstrates strong potential for deployment in decentralized healthcare environments, providing clinicians with a rapid and reliable tool for early stroke assessment.
The ability of the automated sample preparation platform to quantify cTnI spiked in human blood plasma at sub-picomolar concentrations is demonstrated, which opens perspectives for integrating the whole immuno-LAMP method from human plasma samples in a microfluidic device including the LAMP amplification and detection.
Valentin Tardieux, Mathilde Aubret, Charlotte Parent et al.· Analytical Methods· 0 citations
Current biobanking guidelines require in-person blood collection and immediate processing for Alzheimer's disease (AD) biomarker assessment. We recently reported that the P100 blood collection tubes containing protease inhibitors improve protein biomarker stability over delayed centrifugation periods. However, whether...
Yron K. Lee, X. Zeng, M. Farinas et al.· medRxiv· 0 citations
Traumatic brain injury (TBI) affects an estimated 69 million people each year and remains difficult to diagnose rapidly because conventional assessment relies heavily on neurological examination and computed tomography, which may miss subtle injuries or be unavailable in many clinical settings. Blood-based biomarkers,...
Jacob Wekalao, Tobias Topisia· Frontiers in Neurology· 0 citations
Glial fibrillary acidic protein (GFAP) is an intermediate filament protein predominantly expressed in astrocytes and certain neural stem/progenitor cells within the central nervous system. Growing evidence indicates that serum/plasma GFAP is associated with traumatic brain injury, neurodegenerative diseases (e.g....
E. Jian-fei, Kang Wang, Guo-Ping Wu et al.· Clinical Chemistry· 0 citations
BACKGROUND AND PURPOSE
Current blood-based diagnostic tests for traumatic brain injury (TBI), such as those measuring UCH-L1 and GFAP, require venous whole blood or plasma samples collection and cold-chain handling. No FDA-cleared TBI test currently supports capillary blood or dried sample formats. We propose incorpora...
Firas H. Kobeissy, E. Elbayoumi, Rawad Daniel Arja et al.· Journal of Advanced Research· 0 citations
Modern clinical diagnostics require highly sensitive, rapid, and technologically simple methods for quantitatively determining biomarkers directly at the patient’s bedside. Fluorescence polarization (FP) meets these criteria, as it enables the homogeneous recording of an analytical signal based on changes in the rotati...
L. Mukhametova, S. Eremin, Andreas Tsakalof· Diagnostics· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.