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Pd@Pt Nanodendrites as Peroxidase Nanomimics for Enhanced Colorimetric ELISA of Cytokines with Femtomolar Sensitivity
Colorimetric enzyme-linked immunosorbent assay (ELISA) has been widely applied as the gold-standard method for cytokine detection over decades. However, it has become a critical challenge to further improve the detection sensitivity of ELISA as limited by the catalytic activity of enzymes. Herein, w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10688776/ https://www.ncbi.nlm.nih.gov/pubmed/38037588 http://dx.doi.org/10.3390/chemosensors10090359 |
Sumario: | Colorimetric enzyme-linked immunosorbent assay (ELISA) has been widely applied as the gold-standard method for cytokine detection over decades. However, it has become a critical challenge to further improve the detection sensitivity of ELISA as limited by the catalytic activity of enzymes. Herein, we report an enhanced colorimetric ELISA for ultrasensitive detection of interleukin-6 (IL-6, as a model cytokine for demonstration) using [Formula: see text] core@shell nanodendrites ([Formula: see text] NDs) as peroxidase nanomimics (named “ [Formula: see text] ND ELISA”), pushing the sensitivity up to femtomolar level. Specifically, the [Formula: see text] NDs are rationally engineered by depositing Pt atoms on Pd nanocubes (NCs) to generate rough dendrite-like Pt skins on the Pd surfaces via Volmer-Weber growth mode. They can be produced on a large scale with highly uniform size, shape, composition, and structure. They exhibit significantly enhanced peroxidase-like catalytic activity with catalytic constants ([Formula: see text]) more than 2000-fold higher than those of horseradish peroxidase (HRP, an enzyme commonly used in ELISA). Using [Formula: see text] NDs as the signal labels, the [Formula: see text] ND ELISA presents strong colorimetric signals for the quantitative determination of IL-6 with a wide dynamic range of 0.05–100 pg mL-1 and an ultralow detection limit of 0.044 pg mL-1 (1.7 fM). This detection limit is 21-fold lower than that of conventional HRP-based ELISA. The reproducibility and specificity of the [Formula: see text] ND ELISA are excellent. More significantly, the [Formula: see text] ND ELISA was validated for analyzing IL-6 in human serum samples with high accuracy and reliability through recovery tests. Our results demonstrate that the colorimetric [Formula: see text] ND ELISA is a promising biosensing tool for ultrasensitive determination of cytokines and thus is expected to be applied in a variety of clinical diagnoses and fundamental biomedical studies. |
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