Since emerging in China in December 2019, COVID-19 has spread globally, wreaked havoc for public health and economies worldwide and, given the high infectivity and unexpectedly rapid spread of the virus responsible—that is, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)—urged the World Health Organization to declare it a pandemic. In response, reducing the virus’s adverse effects requires developing methods of early diagnosis that are reliable, are inexpensive and offer rapid response. As demonstrated in this article, the colorimetric and electrochemical detection of SARS-CoV-2 spike antigens with gold nanoparticle-based biosensors may be one such method. In the presence of the SARS-CoV-2 antigen, gold nanoparticles aggregated rapidly and irreversibly due to antibody–antigen interaction and consequently changed in colour from red to purple, as easily observable with the naked eye or UV-Vis spectrometry by way of spectral redshifting with a detection limit of 48 ng/mL. Moreover, electrochemical detection was achieved by dropping developed probe solution onto the commercially available and disposable screen-printed gold electrode without requiring any electrode preparation and modification. The method identified 1 pg/mL of the SARS-CoV-2 spike antigen and showed a linear response to the SARS-CoV-2 spike antigen ranging from 1 pg/mL to 10 ng/mL. Both methods were highly specific to detecting the SARS-CoV-2 antigen but not other antigens, including influenza A (i.e. H1N1), MERS-CoV and Streptococcus pneumoniae , even at high concentrations.

Graphical abstract

The ongoing coronavirus disease 2019 (COVID-19) pandemic continues to threaten public health systems all around the world. In controlling the viral outbreak, early diagnosis of COVID-19 is pivotal. This article describes a novel method of voltammetrically determining severe acute respiratory syndrome coronavirus 2019 (SARS-CoV-2) with a newly designed sensor involving bovine serum albumin, SARS-CoV-2 spike antibody and a functionalised graphene oxide modified glassy carbon electrode (BSA/AB/ f -GO/GCE) or screen-printed electrode (BSA/AB/ f -GO/SPE). The oxidation reaction based on the antibody–antigen interaction was evaluated as a response to SARS-CoV-2 spike antigen at -200 mV and 1430 mV with the BSA/AB/ f -GO/SPE and BSA/AB/ f -GO/GCE, respectively. The developed sensors, BSA/AB/ f -GO/SPE and BSA/AB/ f -GO/GCE, could detect 1 ag/mL of virus spike protein in synthetic, saliva and oropharyngeal swab samples in 5 min and 35 min, and both sensors demonstrated a dynamic response to the SARS-CoV-2 spike antigen between 1 ag/mL and 10 fg/mL. Real-time polymerase chain reaction (RT-PCR), rapid antigen test and the proposed method were applied to saliva samples. When compared to RT-PCR, it was observed that the developed method had a 92.5% specificity and 93.3% sensitivity. Moreover, BSA/AB/ f -GO/SPE sensor achieved 91.7% accuracy compared to 66.7% accuracy of rapid antigen test kit in positive samples. In view of these findings, the developed sensor provides great potential for the diagnosing of COVID-19 in real samples.

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A unified pH scale of absolute values (pHabs scale) enables the comparison of acidities in different solvents. To date, very few different experimental setups have been used for the measurement of values on this scale. The article describes the design and performance of the different symmetric cells used for unified pH measurement by several institutions. Well-established and reliable standard aqueous buffer solutions are the first step of method validation necessary to achieve a robust metrological level for more complex media. The pH of aqueous standard buffers was measured by differential potentiometry, where the potential between two glass electrodes is measured directly. All the tested electrochemical cells prove to be suitable for unified pH measurements. This validation highlights that the method is, to a large extent, independent of the used equipment, including the cell geometry. The inherent symmetry of the cell design helps to reduce the experimental workload and improve the accuracy of obtained results.