Issue 21, 2026, Issue in Progress

Chemical interaction-driven sensitivity enhancement in graphene-integrated photonic crystal biosensors for hormone detection

Abstract

We report the development of a chemically enhanced photonic crystal-based biosensing platform enabling highly sensitive and label-free detection of critical female reproductive hormones, specifically estradiol (E2), progesterone (P4), and luteinizing hormone (LH). The proposed platform integrates a Si3N4/TiO2 photonic crystal slab with a graphene-functionalized interface, where π–π interactions and surface adsorption mechanisms significantly enhance molecular binding efficiency. The sensing mechanism is governed by chemically induced refractive index perturbations at the graphene interface, which are optically converted into measurable resonance shifts. Detailed evaluation of the device's structural and optical parameters indicates that the combined effect of strengthened electromagnetic field confinement and chemically driven adsorption mechanisms results in notable improvements in both sensitivity and spectral resolution. The sensor exhibits a concentration-dependent redshift with sub-ng mL−1 detection capability within physiologically relevant ranges. Furthermore, the thermal response remains minimal compared to analyte-induced variations, thereby confirming the chemical selectivity of the sensing process. The proposed platform establishes a synergistic opto-chemical sensing framework with strong potential for real-time, label-free biosensing in biomedical diagnostics.

Graphical abstract: Chemical interaction-driven sensitivity enhancement in graphene-integrated photonic crystal biosensors for hormone detection

Article information

Article type
Paper
Submitted
25 Mar 2026
Accepted
03 Apr 2026
First published
13 Apr 2026
This article is Open Access
Creative Commons BY license

RSC Adv., 2026,16, 19198-19205

Chemical interaction-driven sensitivity enhancement in graphene-integrated photonic crystal biosensors for hormone detection

V. Revathy and A. H. Aly, RSC Adv., 2026, 16, 19198 DOI: 10.1039/D6RA02484J

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