Plasmon Nanocomposite-Enhanced Optical and Electrochemical Signals for Sensitive Virus Detection

• Published in: ACS sensors Vol. 6; no. 7; pp. 2605 - 2612
• Main Authors: Takemura, Kenshin, Ganganboina, Akhilesh Babu, Khoris, Indra Memdi, Chowdhury, Ankan Dutta, Park, Enoch Y
• Format: Journal Article
• Language: English
• Published: American Chemical Society 23.07.2021
• Subjects: influenza virus; multiability nanocomposites; virus detection; localized surface plasmon resonance; electrochemical signal; CdSe quantum dots
• ISSN: 2379-3694; 2379-3694
• DOI: 10.1021/acssensors.1c00308

The social impact of virus spread is immeasurable. Vaccine prophylaxes take considerable time to develop because clinical trials are required. The best initial response to an emerging virus is establishing a virus detection technology adapted by simply preparing virus-specific antibodies. A virus detection system that detects two signals from one analyte has been developed to detect the target virus more sensitively and reliably. Plasmon regions on the surface of nanoparticles are effective in enhancing optical and electrochemical signals. Thus, CdSeTeS quantum dots (QDs) have been used as optical and electrochemical signal-generating materials. In contrast, gold nanoparticle–magnetic nanoparticle–carbon nanotube (AuNP–MNP–CNT) nanocomposites are used for the magnetic separation of the virus from interferences and for signal enhancement. In the presence of the target virus, the QDs optically show a virus concentration-dependent fluorescence enhancement effect due to the localized surface plasmon resonance (LSPR) of AuNPs. Regarding the electrochemical signal, Cd ions eluted by acid degradation of the QDs in solution show a virus concentration-dependent increase in the current peak on an electrode whose electrochemical properties are improved by the deposition of these nanocomposites. Both nanomaterials are conjugated with antibodies specific to influenza virus A (IFV/A), binding this target in a sandwich structure. We are successfully detecting the virus from these two signals during actual virus detection, even when the virus particles are in a human serum matrix. The limit of detection is 2.16 fg/mL for optical detection and 13.66 fg/mL for electrochemical detection.