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1.
Biosens Bioelectron ; 192: 113497, 2021 Nov 15.
Article in English | MEDLINE | ID: mdl-34274624

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 2 (SARS-CoV-2) spike protein 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 protein interaction was evaluated as a response to SARS-CoV-2 spike protein 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 protein 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.


Subject(s)
Biosensing Techniques , COVID-19 , Spike Glycoprotein, Coronavirus/analysis , COVID-19/diagnosis , Humans , Sensitivity and Specificity
2.
Food Chem ; 311: 126013, 2020 May 01.
Article in English | MEDLINE | ID: mdl-31855768

ABSTRACT

Cost effective, simple and accurate two voltammetric methods for determination of boron in hazelnut, peanut, almond, raisin, prune and date samples were described. Metal nanoparticles-carbon nanotube modified glassy carbon electrode (MNP/CNT/GCE, M = Au or Cu) and poly xylenol orange modified pencil graphite electrode (p-XO/PGE) were used as working electrodes. The oxidation of alizarin red s (ARS) in the boron-ARS complex at MNP/CNT/GCE and the oxidation of tiron in the B-tiron complex at p-XO/PGE were monitored as response. The limit of determination values (based on visual evaluation) for CuNP/CNT/GCE, AuNP/CNT/GCE and p-XO/PGE were calculated as 100 µg/L, 125 µg/L and 80 µg/L, respectively. The results were compared with the results obtained by inductively coupled plasma mass spectrometric method and no significant difference between the results was observed. The accuracy experiments of the methods and uncertainty calculations were also performed using a certified reference material (UME CRM 1202 Elements in Hazelnut).


Subject(s)
Boron/analysis , Fruit/chemistry , Nuts/chemistry , Potentiometry , Anthraquinones/chemistry , Electrodes , Fruit/metabolism , Graphite/chemistry , Metal Nanoparticles/chemistry , Nanotubes, Carbon/chemistry , Nuts/metabolism
3.
Anal Chim Acta ; 572(2): 253-8, 2006 Jul 21.
Article in English | MEDLINE | ID: mdl-17723486

ABSTRACT

A novel voltammetric method for boron determination in ppb level is described. Boron complexes with Alizarin Red S (ARS) and the complex, as well as the free ligand, both adsorbs on a hanging mercury drop electrode. The method is based on the monitoring the anodic peak of the complex at -0.47 V in ammonium acetate-phosphate buffer (pH 7). The maximum peak current was obtained by scanning the potential from -700 mV versus Ag/AgCl to more positive potentials without accumulation in the presence of 1 x 10(-6) mol L(-1) of ARS. The instrumental parameters were mainly differential pulse mode with a pulse duration of 0.02 s and a scan rate of 5 mV s(-1). The limit of detection based on signal to ratio of 3 was calculated as 15 microgL(-1). The calibration plot for boron was linear in the range of 0-500 microg L(-1). The interference of various ions was examined and serious interference was observed from antimony(III). The relative standard deviation was found to be 5.1% for the 100 microg L(-1) boron level (n=10). The method was applied to the determination of boron in water and seawater samples with high boron content. The results obtained from the developed method were compared with Azomethine-H-method and no statistically significant difference was found.

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