A rapid and sensitive sandwich electrochemical immunosensor was developed based on the fabrication of the graphene/polyaniline (GP/PANI) nanocomposite onto screen-printed gold electrode (SPGE) for detection of tuberculosis biomarker 10-kDa culture filtrate protein (CFP10). The prepared GP/PANI nanocomposite was characterized using Fourier transform infrared spectroscopy (FTIR) and field emission scanning electron microscopy (FESEM). The chemical bonding and morphology of GP/PANI-modified SPGE were studied by Raman spectroscopy and FESEM coupled with energy dispersive X-ray spectroscopy, respectively. From both studies, it clearly showed that GP/PANI was successfully coated onto SPGE through drop cast technique. Cyclic voltammetry was used to study the electrochemical properties of the modified electrode. The effective surface area for GP/PANI-modified SPGE was enhanced about five times compared with bare SPGE. Differential pulse voltammetry was used to detect the CFP10 antigen. The GP/PANI-modified SPGE that was fortified with sandwich type immunosensor exhibited a wide linear range (20–100 ng/mL) with a low detection limit of 15 ng/mL. This proposed electrochemical immunosensor is sensitive, low sample volume, rapid and disposable, which is suitable for tuberculosis detection in real samples.
Electrochemical application has been widely used in the study of biosensors. Small biomolecules need a sensitive sensor, as the transducer that can relay the signal produced by biomolecule interactions. Therefore, we are improvising a sensor electrode to enhance electrochemical conductivity for the detection of small DNA molecule interaction. This work describes the enhanced electrochemical conductivity studies of copper nanowires/gold nanoparticles (CuNWs/AuNPs), using the screen-printed gold electrode (SPGE). The AuNPs were synthesized using the Turkevich method as well as characterized by the high-resolution transmission electron microscopy (HRTEM) and ultraviolet-visible (UV-Vis) analysis for the particle size and absorption nature, respectively. Further, the surface morphology and elemental analysis of a series of combinations of different ratios of CuNWs-AuNPs-modified SPGE were analyzed by field emission scanning electron microscopy (FESEM) combined with an energy dispersive X-ray (EDX). The results indicate that the nanocomposites of CuNWs-AuNPs have been randomly distributed and compacted on the surface of SPGE, with AuNPs filling the pores of CuNWs, thereby enhancing its electrochemical conductivity. The cyclic voltammetry (CV) method was used for the evaluation of SPGE performance, while the characterization of the electrochemical conductivity of the electrode modified with various concentrations of AuNPs, CuNWs, and different volumes of dithiopropionic acid (DTPA) has been conducted. Of the various parameters tested, the SPGE modified with a mixture of 5 mg/mL CuNWs and 0.25 mM AuNPs exhibited an efficient electrochemical conductivity of 20.3 µA. The effective surface area for the CuNWs-AuNPs-modified SPGE was enhanced by 2.3-fold compared with the unmodified SPGE, thereby conforming the presence of a large active biomolecule interaction area and enhanced electrochemical activity on the electrode surface, thus make it promising for biosensor application.
In this study, an electrochemical DNA biosensor was developed based on the fabrication of silicon nanowires/platinum nanoparticles (SiNWs/PtNPs) on a screen-printed carbon electrode (SPCE) for the detection of Sus scrofa mitochondrial DNA (mtDNA) in food utilizing a new hybrid indicator, ferrocenylnaphthalene diimide (FND). The morphology and elemental composition of the SiNWs/PtNPs-modified SPCE was analyzed by field emission scanning electron microscopy (FESEM) combined with energy dispersive X-ray spectroscopy (EDX). Cyclic voltammetry (CV) was used to study the electrical contact between the PtNPs and the screen-printed working electrode through SiNWs, while electrochemical impedance spectroscopy (EIS) was used to measure the charge transfer resistance of the modified electrode. The results clearly showed that the SiNWs/PtNPs were successfully coated onto the electrode and the effective surface area for the SiNWs/PtNPs-modified SPCE was increased 16.8 times as compared with that of the bare SPCE. Differential pulse voltammetry used for the detection of porcine DNA with FND as an intercalator confirmed its specific binding to the double-stranded DNA (dsDNA) sequences. The developed biosensor showed a selective response towards complementary target DNA and was able to distinguish non-complementary and mismatched DNA oligonucleotides. The SiNWs/PtNPs-modified SPCE that was fortified with DNA hybridization demonstrated good linearity in the range of 3 × 10−9 M to 3 × 10−5 M (R2 = 0.96) with a detection limit of 2.4 × 10−9 M. A cross-reactivity study against various types of meat and processed food showed good reliability for porcine samples.