Evidence map›Paper›PMID 33230700›Full record

ArticleAnalytical and bioanalytical chemistry2021

Upconverting nanoparticle reporter-based highly sensitive rapid lateral flow immunoassay for hepatitis B virus surface antigen.

Iida Martiskainen, Sheikh M Talha, Karoliina Vuorenpää, Teppo Salminen, Etvi Juntunen, Souvick Chattopadhyay, Dinesh Kumar, Tytti Vuorinen, Kim Pettersson, Navin Khanna and 1 more

Open access · hybridAbstract readEvaluation Study
In one paragraph

Article in Analytical and bioanalytical chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.5field-weighted citation impact, top 6% of its field
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

24 citing papers in PubMed, 51 citations in OpenAlex.

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  13. Recent Trends in Lateral Flow Immunoassays with Optical Nanoparticles.International journal of molecular sciences · 2023
    Review
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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

11 authors at 3 institutions in 2 countries.

Iida MartiskainenDepartment of Biotechnology, University of Turku, 20014, Turku, Finland.
Sheikh M TalhaDepartment of Biotechnology, University of Turku, 20014, Turku, Finland.
Karoliina VuorenpääDepartment of Biotechnology, University of Turku, 20014, Turku, Finland.
Teppo SalminenDepartment of Biotechnology, University of Turku, 20014, Turku, Finland.
Etvi JuntunenDepartment of Biotechnology, University of Turku, 20014, Turku, Finland.
Souvick ChattopadhyayTranslational Health Science and Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, India.
Dinesh KumarArrow weighing systems Pvt Ltd (unit Designinnova), New Delhi, 110028, India.
Tytti VuorinenDepartment of Virology and Clinical Microbiology, University of Turku, 20520, Turku, Finland.
Kim PetterssonDepartment of Biotechnology, University of Turku, 20014, Turku, Finland.
Navin KhannaInternational Centre for Genetic Engineering & Biotechnology, New Delhi, 110067, India.
Gaurav BatraTranslational Health Science and Technology Institute, NCR Biotech Science Cluster, Faridabad, 121001, India. gaurav.batra@thsti.res.in.ORCID http://orcid.org/0000-0003-1669-4310
University of Turku · FITranslational Health Science and Technology Institute · INInternational Centre for Genetic Engineering and Biotechnology · IN

Funding

Wellcome Trust 106295/A/14/ZWellcome Trust 106295/Z/14/Z
6 · The paper itself

Abstract

Detection of hepatitis B Virus surface antigen (HBsAg) is an established method for diagnosing both acute and chronic hepatitis B virus (HBV) infection. In addition to enzyme immunoassays (EIAs), rapid diagnostic tests (RDTs) are available for the detection of HBsAg in resource-poor settings. However, the available RDTs have inadequate sensitivity and therefore are not suitable for diagnosis of patients with low levels of HBsAg and for blood screening. To provide a high-sensitivity RDT, we developed a lateral flow immunoassay (LFIA) for HBsAg utilizing upconverting nanoparticle (UCNP) reporter. The UCNP-LFIA can use whole blood, serum, or plasma and the results can be read in 30 min using a reader device. When compared with a commercial conventional visually read LFIA, the developed UCNP-LFIA had a Limit of Detection (LoD) of 0.1 IU HBsAg/ml in spiked serum, whereas the LoD of the conventional LFIA was 3.2 IU HBsAg/ml. The developed UCNP-LFIA fulfills the WHO criterion for blood screening (LoD ≤ 0.13 IU HBsAg/ml) in terms of LoD. The UCNP-LFIA and conventional LFIA were evaluated with well-characterized sample panels. The UCNP-LFIA detected 20/24 HBsAg-positive samples within the HBsAg Performance Panel and 8/10 samples within the Mixed Titer Performance Panel, whereas the conventional LFIA detected 8/24 and 4/10 samples in these panels, respectively. The performance of the assays was further evaluated with HBsAg-positive (n = 108) and HBsAg-negative (n = 315) patient samples. In comparison with a central laboratory test, UCNP-LFIA showed 95.4% (95% CI: 89.5-98.5%) sensitivity whereas sensitivity of the conventional LFIA was 87.7% (95%CI: 79.9-93.3%).

Indexed as

Antibodies, ImmobilizedEquipment DesignHepatitis BHepatitis B Surface AntigensHepatitis B virusHumansImmunoassayLimit of DetectionLuminescent MeasurementsNanoparticlesAntibodies, ImmobilizedHepatitis B Surface AntigensHBsAgHBV diagnosticsLateral flowPoint-of-care testUpconverting nanophosphors

Identifiers

PMID33230700
PMCPMC7813740
OpenAlexW3110407840

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.