# SPR biosensor with a graphene overlayer for carcinoma detection

**Authors:** Talia Tene, Katherine Tixi Gallegos, María José Mendoza Salazar, Lala Gahramanli, Rana Khankishiyeva, Cristian Vacacela Gomez

PMC · DOI: 10.3389/fbioe.2026.1789453 · Frontiers in Bioengineering and Biotechnology · 2026-02-23

## TL;DR

This paper presents a new SPR biosensor design with graphene that improves sensitivity for detecting carcinoma biomarkers.

## Contribution

A novel SPR biosensor architecture with graphene overlayer is proposed, showing enhanced sensitivity and detection accuracy.

## Key findings

- The CaF2/Cu/TiO2/Graphene stack achieved 481.29°/RIU sensitivity and DA = 0.80.
- The graphene-integrated design outperformed TiO2-only and Cu-only baselines in detection performance.
- The design enables cost-effective and sensitive carcinoma biomarker detection.

## Abstract

Early carcinoma detection benefits from label-free, high-sensitivity surface plasmon resonance (SPR) biosensors. We computationally evaluated multilayer SPR architectures based on CaF2/Cu/TiO2/Graphene using the transfer-matrix method at 633 nm. Across 1–5 ng/mL, we analyzed reflectance, resonance-angle shifts, and near-field profiles, and derived sensitivity, detection accuracy (DA), figure of merit, and the limit of detection (LOD). The CaF2/Cu/TiO2/Graphene stack yielded the best performance, achieving 481.29°/RIU sensitivity and DA = 0.80, with pronounced evanescent-field confinement at the sensing interface. Under identical modeling conditions, this graphene-integrated configuration outperformed TiO2-only and Cu-only baselines within the studied range. These results indicate a cost-effective platform for sensitive carcinoma biomarker detection. Calculation details for LOD and other metrics are provided in Methods, and practical considerations for experimental realization are discussed.

## Linked entities

- **Diseases:** carcinoma (MONDO:0004993)

## Full-text entities

- **Genes:** CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, CNOT8 (CCR4-NOT transcription complex subunit 8) [NCBI Gene 9337] {aka CAF1, CALIF, Caf1b, POP2, hCAF1}, SYS1 (SYS1 golgi trafficking protein) [NCBI Gene 90196] {aka C20orf169, dJ453C12.4, dJ453C12.4.1}
- **Diseases:** Carcinomas (MESH:D009369), TMM (MESH:D004195)
- **Chemicals:** Au (MESH:D006046), metal (MESH:D008670), GO (MESH:C000628730), carbon (MESH:D002244), E (MESH:D004540), water (MESH:D014867), CaF2 (MESH:D002124), Copper (MESH:D003300), silver (MESH:D012834), CuO (MESH:C030973), BK7 (-), Graphene (MESH:D006108), Ti (MESH:D014025), TiO2 (MESH:C009495)

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12968620/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968620/full.md

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Source: https://tomesphere.com/paper/PMC12968620