: The detection of protein biomarkers at low concentrations through fluorescence resonance energy transfer (FRET) remains challenging, as conventional homogeneous assays are often affected by uncontrolled donor-acceptor diffusion, fluorophore quenching, and limited reproducibility. In this work, we propose a two-dimensional solid-supported FRET nanoplatform enabling a surface-confined sensing strategy for the stable and reliable detection of the model biomarker Tumor Necrosis Factor-alpha (TNF-α). The approach combines a nanostructured film of fluorine-doped ZnO (F/ZnO) quantum dots deposited on a glass slide with a high-precision pyro-electrohydrodynamic jet (p-jet) printing technique. Microspots of a high-affinity peptide (P52) were printed onto the F/ZnO layer to control donor-acceptor spacing and optimize fluorophore orientation and density, ensuring efficient FRET and reduced variability between samples. The platform provides stable, reproducible, and concentration-dependent FRET signals in the ng mL-1 range, with a limit of detection of 31 ng mL-1, suitable for identifying elevated cytokine levels associated with inflammatory responses. Assay selectivity was evaluated in the presence of non-target proteins, including bovine serum albumin (BSA) and phosphorylated Tau (p-Tau181), and in artificial urine as a complex biological matrix. The results indicate limited interference and minimal matrix effects. Overall, this strategy offers a robust architecture with low reagent consumption and scalable fabrication for future point-of-care diagnostic applications.

Surface-confined FRET nanoplatform printed via pyro-EHD jet for stable and reproducible TNF-α detection / Carbone, S.; Russo, S.; Palma, A.; Mosca, G. J.; La Manna, S.; Cugudda, A.; Coppola, S.; Maffettone, P. L.; Grilli, S.; Vitiello, G.; Di Natale, C.. - In: RSC ADVANCES. - ISSN 2046-2069. - 16:22(2026), pp. 20304-20315. [10.1039/d6ra00144k]

Surface-confined FRET nanoplatform printed via pyro-EHD jet for stable and reproducible TNF-α detection

Carbone S.;Russo S.;Palma A.;Mosca G. J.;La Manna S.;Cugudda A.;Maffettone P. L.;Vitiello G.
Supervision
;
Di Natale C.
Supervision
2026

Abstract

: The detection of protein biomarkers at low concentrations through fluorescence resonance energy transfer (FRET) remains challenging, as conventional homogeneous assays are often affected by uncontrolled donor-acceptor diffusion, fluorophore quenching, and limited reproducibility. In this work, we propose a two-dimensional solid-supported FRET nanoplatform enabling a surface-confined sensing strategy for the stable and reliable detection of the model biomarker Tumor Necrosis Factor-alpha (TNF-α). The approach combines a nanostructured film of fluorine-doped ZnO (F/ZnO) quantum dots deposited on a glass slide with a high-precision pyro-electrohydrodynamic jet (p-jet) printing technique. Microspots of a high-affinity peptide (P52) were printed onto the F/ZnO layer to control donor-acceptor spacing and optimize fluorophore orientation and density, ensuring efficient FRET and reduced variability between samples. The platform provides stable, reproducible, and concentration-dependent FRET signals in the ng mL-1 range, with a limit of detection of 31 ng mL-1, suitable for identifying elevated cytokine levels associated with inflammatory responses. Assay selectivity was evaluated in the presence of non-target proteins, including bovine serum albumin (BSA) and phosphorylated Tau (p-Tau181), and in artificial urine as a complex biological matrix. The results indicate limited interference and minimal matrix effects. Overall, this strategy offers a robust architecture with low reagent consumption and scalable fabrication for future point-of-care diagnostic applications.
2026
Surface-confined FRET nanoplatform printed via pyro-EHD jet for stable and reproducible TNF-α detection / Carbone, S.; Russo, S.; Palma, A.; Mosca, G. J.; La Manna, S.; Cugudda, A.; Coppola, S.; Maffettone, P. L.; Grilli, S.; Vitiello, G.; Di Natale, C.. - In: RSC ADVANCES. - ISSN 2046-2069. - 16:22(2026), pp. 20304-20315. [10.1039/d6ra00144k]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/1044118
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