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Author

Zeinab Rahmati

Bio: Zeinab Rahmati is an academic researcher. The author has contributed to research in topics: Aptamer & Electrode. The author has an hindex of 7, co-authored 14 publications receiving 116 citations.

Papers
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Journal ArticleDOI
TL;DR: In this paper, a label-free electrochemical biosensor was presented as a powerful nanobiodevice for SARS-CoV-2 spike protein detection, which was applied on a screen-printed carbon electrode modified with Cu2O nanocubes (Cu2O NCs), which provided a large surface area in a very small space.
Abstract: Severe acute respiratory syndrome SARS-CoV-2 has caused a global pandemic starting in 2020. Accordingly, testing is crucial for mitigating the economic and public health effects. In order to facilitate point-of-care diagnosis, this study aims at presenting a label-free electrochemical biosensor as a powerful nanobiodevice for SARS-CoV-2 spike protein detection. Utilizing the IgG anti-SARS-CoV-2 spike antibody onto the electrode surface as a specific platform in an ordered orientation through staphylococcal protein A (ProtA) is highly significant in fabricating the designed nanobiodevice. In this sense, the screen-printed carbon electrode modified with Cu2O nanocubes (Cu2O NCs), which provide a large surface area in a very small space, was applied in order to increase the ProtA loading on the electrode surface. Accordingly, the sensitivity and stability of the sensing platform significantly increased. The electrochemical evaluations proved that there is a very good linear relationship between the charge transfer resistance (Rct) and spike protein contents via a specific binding reaction in the range 0.25 fg mL−1 to 1 μg mL−1. Moreover, the assay when tested with influenza viruses 1 and 2 was performed in 20 min with a low detection limit of 0.04 fg mL−1 for spike protein without any cross-reactivity. The designed nanobiodevice exhibited an average satisfactory recovery rate of ~ 97–103% in different artificial sample matrices, i.e., saliva, artificial nasal, and universal transport medium (UTM), illustrating its high detection performance and practicability. The nanobiodevice was also tested using real patients and healthy samples, where the results had been already obtained using the standard polymerase chain reaction (PCR) procedure, and showed satisfactory results.

83 citations

Journal ArticleDOI
TL;DR: A biosensor with a dual recognition system was fabricated and founded on a combination of aptasensing and the molecular imprinting union of the chloramphenicol (CAP) selective detection, which exhibited outstanding results when applied to detect CAP in milk samples.

56 citations

Journal ArticleDOI
TL;DR: The DPV was used as a sensitive electrochemical technique for the measurement of CAP with an appropriate linear concentration range which was found to be between 10 pM and 0.2 μM and, with a low limit of detection, it equaled 3.3 pM.

46 citations

Journal ArticleDOI
TL;DR: In this paper, a robust electrochemical biosensor for selective and quantitative analysis of SARS-CoV-2-specific viral antibodies was designed, which showed an average satisfactory recovery rate of ~99-103% for the determination of antibodies in real blood serum samples with the possibility of being widely used in individual serological qualitative monitoring.

35 citations

Journal ArticleDOI
TL;DR: In this paper, a hierarchical porous 3D-NiCo2O4 nanowires, shelled with a thin layer of N-doped carbon with sea-urchin-like morphology, were successfully prepared by a facile protocol.

24 citations


Cited by
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Journal ArticleDOI
TL;DR: In this paper, a label-free electrochemical biosensor was presented as a powerful nanobiodevice for SARS-CoV-2 spike protein detection, which was applied on a screen-printed carbon electrode modified with Cu2O nanocubes (Cu2O NCs), which provided a large surface area in a very small space.
Abstract: Severe acute respiratory syndrome SARS-CoV-2 has caused a global pandemic starting in 2020. Accordingly, testing is crucial for mitigating the economic and public health effects. In order to facilitate point-of-care diagnosis, this study aims at presenting a label-free electrochemical biosensor as a powerful nanobiodevice for SARS-CoV-2 spike protein detection. Utilizing the IgG anti-SARS-CoV-2 spike antibody onto the electrode surface as a specific platform in an ordered orientation through staphylococcal protein A (ProtA) is highly significant in fabricating the designed nanobiodevice. In this sense, the screen-printed carbon electrode modified with Cu2O nanocubes (Cu2O NCs), which provide a large surface area in a very small space, was applied in order to increase the ProtA loading on the electrode surface. Accordingly, the sensitivity and stability of the sensing platform significantly increased. The electrochemical evaluations proved that there is a very good linear relationship between the charge transfer resistance (Rct) and spike protein contents via a specific binding reaction in the range 0.25 fg mL−1 to 1 μg mL−1. Moreover, the assay when tested with influenza viruses 1 and 2 was performed in 20 min with a low detection limit of 0.04 fg mL−1 for spike protein without any cross-reactivity. The designed nanobiodevice exhibited an average satisfactory recovery rate of ~ 97–103% in different artificial sample matrices, i.e., saliva, artificial nasal, and universal transport medium (UTM), illustrating its high detection performance and practicability. The nanobiodevice was also tested using real patients and healthy samples, where the results had been already obtained using the standard polymerase chain reaction (PCR) procedure, and showed satisfactory results.

83 citations

Journal ArticleDOI
TL;DR: In this article, a mesoporous TAPB-DMTP−COF composite was constructed via a covalent linking approach, and the composite significantly improved the electrochemical detection performance.
Abstract: Exploration and construction of novel porous core-shell composites is of crucial significance due to their prospectively enhanced performances and far-ranging applications. Herein, microporous UiO-66-NH2 as a MOF core is coated by a mesoporous TAPB-DMTP−COF shell to construct the UiO-66-NH2@COF composite via a covalent linking approach. Importantly, the composite with retentive crystallinity and hierarchical porosity significantly improves the electrochemical detection performance, for instance ATP and antibiotic, because this composite has the high affinity between the phosphate groups of aptamers and dense Zr(IV) sites, and strong π-π stacking interaction between aptamers and this MOF@COF. The synthetic strategy in this systematic research expands a rational design for other MOF@COF core-shell hybrid materials to expand their promising applications.

74 citations

Journal ArticleDOI
TL;DR: This mini review has summarized the latest developments and new trends in electrochemical sensors for antibiotics, and the existing problems and the future challenges ahead have been proposed.

64 citations

Journal ArticleDOI
15 Aug 2020-Talanta
TL;DR: Recent leading trends about gold (Au) nanostructures based electrochemical aptasensors have been collected, reviewed, and compared and an in-depth analysis has been provided based on the crucial features of all included aptasensor.

56 citations

Journal ArticleDOI
TL;DR: A biosensor with a dual recognition system was fabricated and founded on a combination of aptasensing and the molecular imprinting union of the chloramphenicol (CAP) selective detection, which exhibited outstanding results when applied to detect CAP in milk samples.

56 citations