Abstract
Sensitive impedimetric detection of miR-222, a miRNA sequence found in many lung tumors, was investigated by using gold-nanostructured disposable carbon electrodes and enzyme-decorated liposomes. The proposed method was based on the immobilization of thiolated DNA capture probes onto gold-nanostructured carbon surfaces. Afterwards, the capture probes were allowed to hybridize to the target miRNAs. Finally, enzyme-decorated liposomes were used as labels to amplify the miRNA sensing, by their association with the probe-miRNA hybrids generated on the nanostructured transducer. By using this amplification route a limit of detection of 0.400 pM, a limit of quantification of 1.70 pM, and an assay range spanning three orders of magnitude (1.70-900 pM) were obtained (RSD % = 13). This limit of quantification was 20 times lower than that obtained using a simple enzyme conjugate for the detection. A comparison was also made with gold screen-printed transducers. In this case, a limit of quantification approximately 70 times lower was found by using the nanostructured transducers. Application of the optimized assay in serum samples was also demonstrated.
Lingua originale | English |
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pagine (da-a) | 7271-81-7281 |
Rivista | Analytical and Bioanalytical Chemistry |
Volume | 408 |
DOI | |
Stato di pubblicazione | Pubblicato - 2016 |
Keywords
- Alkaline Phosphatase
- Alkaline phosphatase
- Biosensing Techniques
- DNA Probes
- Dielectric Spectroscopy
- Electrochemical impedance spectroscopy
- Electrodes
- Enzymes, Immobilized
- Gold
- Gold nanoparticles
- Humans
- Immobilized Nucleic Acids
- Limit of Detection
- Liposome
- Liposomes
- Metal Nanoparticles
- MicroRNAs
- Nanostructures
- Nucleic Acid Hybridization
- Screen-printed electrodes