# Integrated Microfluidic Giant Magnetoresistance (GMR) Biosensor Platform for Magnetoresistive Immunoassay of Myoglobin

**Authors:** Yikai Wang, Huaiyu Wang, Yunyun Zhang, Shuhui Cui, Fei Hu, Bo’an Li

PMC · DOI: 10.3390/bios16010008 · Biosensors · 2025-12-22

## TL;DR

A new biosensor platform detects myoglobin, an early marker for heart attacks, using microfluidic and magnetic technologies for faster and more accurate diagnosis.

## Contribution

An integrated microfluidic-GMR biosensor platform is developed for rapid and specific myoglobin detection.

## Key findings

- The platform detected myoglobin at 75 ng/mL with a magnetoresistance change of ≥ 0.202%.
- The system showed high specificity for myoglobin, distinguishing it from BSA and troponin I.
- Optimal conditions included 1 μm magnetic beads and a 60 Oe magnetic field for detection.

## Abstract

Acute myocardial infarction (AMI) is a rapidly progressing cardiovascular condition associated with high mortality. Myoglobin is an early biomarker of AMI; however, its detection using conventional methods is limited by complex workflows and low resistance to interference. In this study, we developed an integrated myoglobin detection platform that combined magneto-immunoassay with microfluidic technology. A giant magnetoresistance (GMR) sensor was fabricated using micro-electro-mechanical systems (MEMS). The designed microfluidic chip integrated sample pretreatment, immunoreaction, and magnetic signal capture functionalities. Its built-in GMR sensor, labeled with magnetic nanoparticles, directly converted the “antigen–antibody” biochemical signal into detectable magnetoresistance changes, thereby enabling the indirect detection of myoglobin. A magneto-immunoassay analysis system consisted of a fluidic drive, magnetic field control, and data acquisition functions. Various key parameters were optimized, including EDC/NHS concentration, antibody concentration, and magnetic bead size. Under the optimal conditions and using 1 μm magnetic beads as labels and an external detection magnetic field of 60 Oe, the platform successfully detected myoglobin at 75 ng/mL with ∆MR ≥ 0.202%. Specificity tests demonstrated that the platform had high specificity for myoglobin and could effectively distinguish myoglobin from bovine serum albumin (BSA) and troponin I. This study presents a rapid, accurate myoglobin detection platform that can be applied for the early diagnosis of AMI.

## Linked entities

- **Proteins:** LOC105216124 (uncharacterized LOC105216124), LOC105904758 (troponin I, fast skeletal muscle-like)
- **Chemicals:** NHS (PubChem CID 80170)
- **Diseases:** acute myocardial infarction (MONDO:0004781)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, MB (myoglobin) [NCBI Gene 4151] {aka MYOSB, PVALB}
- **Diseases:** AMI (MESH:D009203), cardiovascular condition (MESH:D002318)
- **Chemicals:** EDC (MESH:C024565)
- **Species:** Bos taurus (bovine, species) [taxon 9913]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12838720/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12838720/full.md

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Source: https://tomesphere.com/paper/PMC12838720