Evidence map›Paper›PMID 29732889›Full record

ArticleAnalytical chemistry2018

Nanoparticle Enhancement Cascade for Sensitive Multiplex Measurements of Biomarkers in Complex Fluids with Surface Plasmon Resonance Imaging.

Jan Hendriks, Ivan Stojanovic, Richard B M Schasfoort, Daniël B F Saris, Marcel Karperien

Open access · hybridAbstract read
In one paragraph

Article in Analytical chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Label-free optical biosensors in the pandemic era.Nanophotonics (Berlin, Germany) · 2022
    Review
  5. Review
  6. Review
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

5 authors at 2 institutions in 1 country.

Jan HendriksDepartment of Developmental BioEngineering, MIRA Institute for Biomedical Technology and Technical Medicine , University of Twente , Enschede , 7522 NB , The Netherlands.ORCID 0000-0002-3321-6866
Ivan StojanovicMedical Cell Biophysics, MIRA Institute for Biomedical Technology and Technical Medicine , University of Twente , Enschede , 7522 NB , The Netherlands.
Richard B M SchasfoortMedical Cell Biophysics, MIRA Institute for Biomedical Technology and Technical Medicine , University of Twente , Enschede , 7522 NB , The Netherlands.
Daniël B F SarisDepartment of Orthopedics , UMC Utrecht , Utrecht , 3584 CX , The Netherlands.
Marcel KarperienDepartment of Developmental BioEngineering, MIRA Institute for Biomedical Technology and Technical Medicine , University of Twente , Enschede , 7522 NB , The Netherlands.
University of Twente · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a large unmet need for reliable biomarker measurement systems for clinical application. Such systems should meet challenging requirements for large scale use, including a large dynamic detection range, multiplexing capacity, and both high specificity and sensitivity. More importantly, these requirements need to apply to complex biological samples, which require extensive quality control. In this paper, we present the development of an enhancement detection cascade for surface plasmon resonance imaging (SPRi). The cascade applies an antibody sandwich assay, followed by neutravidin and a gold nanoparticle enhancement for quantitative biomarker measurements in small volumes of complex fluids. We present a feasibility study both in simple buffers and in spiked equine synovial fluid with four cytokines, IL-1β, IL-6, IFN-γ, and TNF-α. Our enhancement cascade leads to an antibody dependent improvement in sensitivity up to 40 000 times, resulting in a limit of detection as low as 50 fg/mL and a dynamic detection range of more than 7 logs. Additionally, measurements at these low concentrations are highly reliable with intra- and interassay CVs between 2% and 20%. We subsequently showed this assay is suitable for multiplex measurements with good specificity and limited cross-reactivity. Moreover, we demonstrated robust detection of IL-6 and IL-1β in spiked undiluted equine synovial fluid with small variation compared to buffer controls. In addition, the availability of real time measurements provides extensive quality control opportunities, essential for clinical applications. Therefore, we consider this method is suitable for broad application in SPRi for multiplex biomarker detection in both research and clinical settings.

Indexed as

Surface Plasmon ResonanceAnimalsBiomarkersCytokinesHorsesHumansNanoparticlesSynovial FluidBiomarkersCytokines

Identifiers

PMID29732889
PMCPMC5990928
OpenAlexW2801301490

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.