Rapid and accurate diagnosis of cardiovascular diseases (CVDs) at the earliest stage is of paramount importance to improve the treatment outcomes and avoid irreversible damage to a patient's cardiovascular system. Microfluidic paper-based devices (μPADs) represent a promising platform for rapid CVD diagnosis at the point of care (POC). This paper presents an electrochemical μPAD (E-μPAD) with an all-in-one origami design for rapid and POC testing of cardiac protein markers in whole blood. Based on the label-free, electrochemical impedance spectroscopy (EIS) immunoassay, the E-μPAD integrates all essential components on a single chip, including three electrochemical cells, a plasma separation membrane, and a buffer absorption pad, enabling easy and streamlined operations for multiplexed detection of three cardiac protein markers [cardiac troponin I (cTnI), brain natriuretic peptide (BNP)-32, and D-Dimer] on a finger-prick whole blood sample within 46 min. Superior analytical performance is achieved through sensitive EIS measurement on carbon electrodes decorated with semiconductor zinc oxide nanowires (ZnO NWs). Using spiked human plasma samples, ultralow limits of detection (LODs) of E-μPAD are achieved at 4.6 pg/mL (190 fM) for cTnI, 1.2 pg/mL (40 fM) for BNP-32, and 146 pg/mL (730 fM) for D-Dimer. Real human blood samples spiked with purified proteins are also tested, and the device's analytical performance was proven to be comparable to commercial ELISA kits. The all-in-one E-μPAD will allow rapid and sensitive testing of cardiac protein markers through easy operations, which holds great potential for on-site screening of acute CVDs in nonlaboratory settings such as emergency rooms, doctor's offices, or patient homes.
Keyphrases
- label free
- loop mediated isothermal amplification
- left ventricular
- protein protein
- gold nanoparticles
- cardiovascular disease
- reduced graphene oxide
- high throughput
- case report
- amino acid
- room temperature
- emergency department
- public health
- endothelial cells
- type diabetes
- binding protein
- single cell
- circulating tumor cells
- small molecule
- induced apoptosis
- resting state
- functional connectivity
- ionic liquid
- heart failure
- single molecule
- cell death
- intensive care unit
- molecularly imprinted
- liver failure
- climate change
- multiple sclerosis
- cell cycle arrest
- magnetic resonance
- pluripotent stem cells
- atrial fibrillation
- visible light
- mechanical ventilation
- acute respiratory distress syndrome
- cardiovascular events
- hepatitis b virus