A self-driven, microfluidic, integrated-circuit biosensing chip for detecting four cardiovascular disease biomarkers

Pei Rong Li, Sasi Kiran Boilla, Chih Hung Wang, Pei Chien Lin, Chien Nan Kuo, Tsung Heng Tsai*, Gwo Bin Lee*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Cardiovascular diseases (CVDs) claimed the lives of nearly 21 million people worldwide in 2021, accounting for 30% of global deaths. However, one in five CVD patients is unaware that they have the disease, emphasizing the need for accurate biomarker monitoring. Herein we developed an integrated microfluidic system (IMS) for rapid quantification of four CVD biomarkers, including N-terminal pro B-type natriuretic peptide (NT-proBNP), fibrinogen, cardiac troponin I (cTnI), and C-reactive protein (CRP)- via aptamer-coated interdigitated electrodes (IDE) with integrated circuits (IC) and a self-driven IMS for sample treatment. The device was composed of plasma filtration, metering, and fluidic delay modules, and the former could extract 45% of plasma from a 20-μL blood sample; the metering module could quantify 5 μL of plasma within 90 s. Subsequently, the plasma was transported to a detection chamber, where IC-based IDE sensors made measurements within 5 min. The entire 15-min process allowed us to evaluate biomarkers across a wide dynamic range: NT-proBNP (0.1–10,000 pg/mL), fibrinogen (50-1,000 mg/dL), cTnI (0.1–10,000 pg/mL), and CRP (0.5-9 mg/L). Given that spiked blood samples were measured with reasonable accuracy (>80%), the IMS could see utility in CVD risk assessment and personalized medicine.

Original languageEnglish
Article number115931
JournalBiosensors and Bioelectronics
Volume249
DOIs
StatePublished - 1 Apr 2024

Keywords

  • Biomarker
  • Capillary microfluidics
  • Cardiovascular disease
  • Integrated circuits
  • Interdigitated electrodes
  • Metering
  • Plasma isolation

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