# Inkjet-Printed Electrode Enable Portable Electrochemical Immunosensing of Tau-441 for Early Alzheimer’s Screening

**Authors:** Binglun Li, Chenghao Liu, Chenlu Gu, Shanshan Wei, Shiyong Li, Ziang Liu, Dongdong Zhao, Qunfeng Tang, Yun Chen, Zhencheng Chen

PMC · DOI: 10.3390/bios16020113 · Biosensors · 2026-02-10

## TL;DR

A portable device using inkjet-printed electrodes can detect a key Alzheimer’s biomarker at very low levels, enabling early screening.

## Contribution

A scalable and portable electrochemical immunosensing method for Tau-441 detection using inkjet-printed electrodes and gold nanoparticles.

## Key findings

- The method achieves a detection limit of 16 fg/mL for Tau-441 with high specificity and reproducibility.
- The system provides a linear response from 50 fg/mL to 10 ng/mL of Tau-441.
- The integration of inkjet printing and a handheld reader enables rapid and on-site Alzheimer’s screening.

## Abstract

Early diagnosis of Alzheimer’s disease represents a critical clinical challenge, and the high-sensitive biomarkers measurement holds great potential for enabling early identification and intervention. This study proposes an electrochemical immunosensing strategy based on inkjet printing for the quantitative detection of Tau-441. Conductive patterns were formed by inkjet printing, followed by surface functionalization with gold nanoparticles to immobilize highly specific anti-Tau-441. This process created a stable and high affinity immunorecognition interface that enhances electron transfer and signal amplification. Furthermore, we developed and integrated a low-power portable detection platform to achieve a rapid detection process encompassing sample loading, signal acquisition, and on-device readout. The method shows a linear response from 50 fg/mL to 10 ng/mL and a limit of detection of 16 fg/mL (S/N = 3), with high specificity and good reproducibility. By combining scalable inkjet fabrication with a self-contained handheld reader, this method shortens the path from sample to result and offers a practical route for on-site screening and early intervention in Alzheimer’s disease.

## Linked entities

- **Diseases:** Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}
- **Diseases:** beta-amyloid (MESH:C000718787), dementia (MESH:D003704), neuronal degeneration (MESH:D009410), cognitive impairment (MESH:D003072), neurofibrillary tangles (MESH:D055956), injury to (MESH:D014947), neurodegenerative disorder (MESH:D019636), AD (MESH:D000544)
- **Chemicals:** PET (MESH:C475920), spike (MESH:C010346), H2SO4 (MESH:C033158), PBS (MESH:D007854), Au NPs (-), Graphene (MESH:D006108), S (MESH:D013455), thiol (MESH:D013438), Fe (MESH:D007501), water (MESH:D014867), Ag (MESH:D012834), AgCl (MESH:C037548), PB (MESH:C000170), O (MESH:D010100), ferrocyanide (MESH:C020354), ferricyanide (MESH:C007931), Au (MESH:D006046), polymer (MESH:D011108), C (MESH:D002244), N (MESH:D009584), HAuCl4 (MESH:C024568)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938625/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938625/full.md

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Source: https://tomesphere.com/paper/PMC12938625