The COVID-19 pandemic highlighted the global necessity to develop fast, affordable, and user-friendly diagnostic alternatives. Alongside recognized tests such as ELISA, nanotechnologies have since been explored for direct and indirect diagnosis of SARS-CoV-2, the etiological agent of COVID-19. Accordingly, in this work, we report a method to detect anti-SARS-CoV-2 antibodies based on graphene-based field-effect transistors (GFETs), using a nanostructured platform of graphene with added gold nanorods (GNRs) and a specific viral protein. To detect anti-N-protein IgG antibodies for COVID-19 in human sera, gold nanorods were functionalized with the nucleocapsid (N) protein of SARS-CoV-2, and subsequently deposited onto graphene devices. Our test results demonstrate that the sensor is highly sensitive and can detect antibody concentrations as low as 100 pg/mL. Using the sensor to test human sera that were previously diagnosed with ELISA showed a 90% accuracy rate compared to the ELISA results, with the test completed in under 15 min. Integrating graphene and nanorods eliminates the need for a blocker, simplifying sensor fabrication. This hybrid sensor holds robust potential to serve as a simple and efficient point-of-care platform.

Cell membranes and the cytoskeleton play crucial roles in the regulation of cellular responses by mediating mechanical forces and physical stimuli from the microenvironment through their viscoelastic properties. Investigating these properties provides valuable insights into disease mechanisms and therapeutic strategies. Gold nanorods (GNRs), especially under irradiation, exhibit lethal effects against Leishmania parasites through plasmonic photothermal conversion. In this study, we focus on evaluating the effects of non-irradiated GNRs on macrophage properties to better understand their intrinsic interactions with cells and support the development of future phototherapy applications. Here, defocusing microscopy (DM), a quantitative phase microscopy technique, was used to analyze membrane fluctuations in macrophages ($M\varnothing s$) exposed to GNRs (average length of $43\pm 8 \mathrm{n}\mathrm{m}$ and diameter of $20\pm 4 \mathrm{n}\mathrm{m}$) and infected with Leishmania amazonensis. By quantifying membrane–cytoskeleton fluctuation from defocused images, we extracted viscoelastic parameters, including bending modulus ($k_c$) and viscosity ($\eta$), to characterize membrane behavior in detail. Our results show that infection increases both $k_c$ and $\eta$, while treatment at IC₅₀ reduces infection and selectively increases $k_c$ without affecting $\eta$. In healthy macrophages, exposure to GNRs resulted in a reduction in both parameters, indicative of increased membrane fluidity and cytoskeletal rearrangement. These findings provide new insights into the biomechanical effects of GNRs on macrophages and may enlighten the design of future phototherapeutic approaches.

Cell membranes and cytoskeleton play a crucial role in regulating cellular responses by mediating mechanical forces and physical stimuli from the microenvironment through their viscoelastic properties. Investigating these properties provides valuable insights into disease mechanisms and therapeutic strategies. Gold nanorods (GNRs), especially under irradiation, exhibit lethal effects against Leishmania parasites through plasmonic photothermal conversion. However, their mechanical interaction with cells remains poorly understood. Here, Defocusing Microscopy (DM), a quantitative phase microscopy technique, was employed to analyze membrane fluctuations in macrophages (M∅s) exposed to GNRs and infected with Leishmania amazonensis. Measuring the membrane-cytoskeleton fluctuation of defocused images, we quantified viscoelastic parameters such as bending modulus (kc) and viscosity (η), enabling a detailed char-acterization of membrane behavior. Results indicate that infection increases both kc and η, while IC50 treatment reduces infection and selectively increases kc without affecting viscosity. In healthy macrophages, GNRs reduced both parameters, suggesting a fluidizing effect. These findings contribute to a deeper understanding of GNRs' therapeutic performance and cytotoxicity, contributing to improved phototherapy applications.