Evidence map›Paper›PMID 30568445›Full record

ArticleInternational journal of nanomedicine2018

Chemiplasmonics for high-throughput biosensors.

Achyut J Raghavendra, Jingyi Zhu, Wren Gregory, Fengjiao Case, Pradyumna Mulpur, Shahzad Khan, Anurag Srivastava, Ramakrishna Podila

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Laboratory-on-a-Smartphone.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry
    Article
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

8 authors at 2 institutions in 2 countries.

Achyut J RaghavendraLaboratory of Nano-biophysics, Clemson University, Clemson, SC 29634, USA, rpodila@g.clemson.edu.
Jingyi ZhuLaboratory of Nano-biophysics, Clemson University, Clemson, SC 29634, USA, rpodila@g.clemson.edu.
Wren GregoryLaboratory of Nano-biophysics, Clemson University, Clemson, SC 29634, USA, rpodila@g.clemson.edu.
Fengjiao CaseLaboratory of Nano-biophysics, Clemson University, Clemson, SC 29634, USA, rpodila@g.clemson.edu.
Pradyumna MulpurClemson Nanomaterials Institute, Clemson University, Anderson, SC 29625, USA.
Shahzad KhanABV-Indian Institute of Information Technology and Management, Gwalior, MP, India.
Anurag SrivastavaABV-Indian Institute of Information Technology and Management, Gwalior, MP, India.
Ramakrishna PodilaLaboratory of Nano-biophysics, Clemson University, Clemson, SC 29634, USA, rpodila@g.clemson.edu.
Clemson University · USAtal Bihari Vajpayee Indian Institute of Information Technology and Management · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe sensitivity of ELISA for biomarker detection can be significantly increased by integrating fluorescence with plasmonics. In surface-plasmon-coupled emission, the fluorophore emission is generally enhanced through the so-called physical mechanism due to an increase in the local electric field. Despite its fairly high enhancement factors, the use of surface-plasmon-coupled emission for high-throughput and point-of-care applications is still hampered due to the need for expensive focusing optics and spectrometers.

methodsHere, we describe a new chemiplasmonic-sensing paradigm for enhanced emission through the molecular interactions between aromatic dyes and C

resultsA 20-fold enhancement in the emission from rhodamine B-labeled biomolecules can be readily elicited without quenching its red color emission. As a proof of concept, we demonstrate two model bioassays using: 1) the RhB-streptavidin and biotin complexes in which the dye was excited using an inexpensive laser pointer and the ensuing enhanced emission was recorded by a smartphone camera without the need for focusing optics and 2) high-throughput 96-well plate assay for a model antigen (rabbit immunoglobulin) that showed detection sensitivity as low as 6.6 pM.

conclusionOur results show clear evidence that chemiplasmonic sensors can be extended to detect biomarkers in a point-of-care setting through a smartphone in simple normal incidence geometry without the need for focusing optics. Furthermore, chemiplasmonic sensors also facilitate high-throughput screening of biomarkers in the conventional 96-well plate format with 10-20 times higher sensitivity.

Indexed as

AnimalsBiosensing TechniquesBiotinFluorescent DyesImmunoassayImmunoglobulin GRabbitsRhodaminesSpectrometry, FluorescenceStatic ElectricityStreptavidinSurface Plasmon ResonanceBiotinFluorescent DyesImmunoglobulin Grhodamine BRhodaminesStreptavidinbiosensorfluorescencefullerenesnanosilversurface plasmons

Identifiers

PMID30568445
PMCPMC6267718
OpenAlexW2902065994

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.