Evidence map›Paper›PMID 37893383›Full record

ArticleMicromachines2023

The Study of Performance of a Nanoribbon Biosensor, Sensitized with Aptamers and Antibodies, upon Detection of Core Antigen of Hepatitis C Virus.

Yuri D Ivanov, Kristina A Malsagova, Kristina V Goldaeva, Tatyana O Pleshakova, Andrey F Kozlov, Rafael A Galiullin, Ivan D Shumov, Vladimir P Popov, Irina K Abramova, Vadim S Ziborov and 3 more

Abstract read
In one paragraph

Article in Micromachines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Yuri D IvanovInstitute of Biomedical Chemistry (IBMC), 119121 Moscow, Russia.ORCID 0000-0001-5041-1914
Kristina A MalsagovaInstitute of Biomedical Chemistry (IBMC), 119121 Moscow, Russia.ORCID 0000-0001-9404-1660
Kristina V GoldaevaInstitute of Biomedical Chemistry (IBMC), 119121 Moscow, Russia.ORCID 0000-0002-4082-1247
Tatyana O PleshakovaInstitute of Biomedical Chemistry (IBMC), 119121 Moscow, Russia.
Andrey F KozlovInstitute of Biomedical Chemistry (IBMC), 119121 Moscow, Russia.
Rafael A GaliullinInstitute of Biomedical Chemistry (IBMC), 119121 Moscow, Russia.
Ivan D ShumovInstitute of Biomedical Chemistry (IBMC), 119121 Moscow, Russia.ORCID 0000-0002-9795-7065
Vladimir P PopovRzhanov Institute of Semiconductor Physics, Siberian Branch of Russian Academy of Sciences, 630090 Novosibirsk, Russia.ORCID 0000-0002-7415-1405
Irina K AbramovaInstitute of Biomedical Chemistry (IBMC), 119121 Moscow, Russia.
Vadim S ZiborovInstitute of Biomedical Chemistry (IBMC), 119121 Moscow, Russia.
Oleg F PetrovJoint Institute for High Temperatures of Russian Academy of Sciences, 125412 Moscow, Russia.
Alexander Yu DolgoborodovJoint Institute for High Temperatures of Russian Academy of Sciences, 125412 Moscow, Russia.ORCID 0000-0001-7054-7341
Alexander I ArchakovInstitute of Biomedical Chemistry (IBMC), 119121 Moscow, Russia.

Funding

Program for Basic Research in the Russian Federation for a long-term period (2021-2030) 122030100168-2The Ministry of Science and Higher Education of the Russian Federation 075-01129-23-00
6 · The paper itself

Abstract

The development of highly sensitive diagnostic systems for the early revelation of diseases in humans is one of the most important tasks of modern biomedical research, and the detection of the core antigen of the hepatitis C virus (HCVcoreAg)-a protein marker of the hepatitis C virus-is just the case. Our study is aimed at testing the performance of the nanoribbon biosensor in the case of the use of two different types of molecular probes: the antibodies and the aptamers against HCVcoreAg. The nanoribbon sensor chips employed are based on "silicon-on-insulator structures" (SOI-NR). Two different HCVcoreAg preparations are tested: recombinant β-galactosidase-conjugated HCVcoreAg ("Virogen", Watertown, MA, USA) and recombinant HCVcoreAg ("Vector-Best", Novosibirsk, Russia). Upon the detection of either type of antigen preparation, the lowest concentration of the antigen detectable in buffer with pH 5.1 was found to be approximately equal, amounting to ~10

Indexed as

antibodyaptamerdiagnosticsHCVcoreAgnanoribbon biosensor

Identifiers

PMID37893383
PMCPMC10609547

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.