Evidence map›Paper›PMID 25145492›Full record

ArticleJournal of visualized experiments : JoVE2014

Hydrogel nanoparticle harvesting of plasma or urine for detecting low abundance proteins.

Ruben Magni, Benjamin H Espina, Lance A Liotta, Alessandra Luchini, Virginia Espina

Registry-linked trialAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03800342 (Recovery, Fatigability, and Proteomic Response to Aerobic Exercise Training in Healthy Individuals), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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.

NCT03800342 nacompletednot on this mapstarted 2019, after this paper: background citation

Recovery, Fatigability, and Proteomic Response to Aerobic Exercise Training in Healthy Individuals

TypeinterventionalSponsorGeorge Mason UniversityRan2019 to 2019Enrolled21ConditionsAdult, FatigueArmsAerobic Exercise Training
3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Proteomics for cancer drug design.Expert review of proteomics · 2019
    Article
  5. Review
  6. Article
  7. 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.

Ruben MagniCenter for Applied Proteomics and Molecular Medicine, George Mason University.
Benjamin H EspinaCeres Nanosciences.
Lance A LiottaCenter for Applied Proteomics and Molecular Medicine, George Mason University.
Alessandra LuchiniCenter for Applied Proteomics and Molecular Medicine, George Mason University.
Virginia EspinaCenter for Applied Proteomics and Molecular Medicine, George Mason University; vespina@gmu.edu.

Funding

Nanotrap technology for one step preservation and amplification of cancer biomarkR33CA173359 · NCI · GEORGE MASON UNIVERSITY · PI LIOTTA, LANCE ALLEN · 2012 to 2014
$1.1M
Nanotechnology for One Step Concentration and Preservation of Labile Biomarkers iR21CA137706 · NCI · GEORGE MASON UNIVERSITY · PI LIOTTA, LANCE ALLEN · 2009 to 2010
$530k
NCI NIH HHS 1R21CA137706-01NCI NIH HHS 1R33CA173359-01NCI NIH HHS R21 CA137706NCI NIH HHS R33 CA173359
6 · The paper itself

Abstract

Novel biomarker discovery plays a crucial role in providing more sensitive and specific disease detection. Unfortunately many low-abundance biomarkers that exist in biological fluids cannot be easily detected with mass spectrometry or immunoassays because they are present in very low concentration, are labile, and are often masked by high-abundance proteins such as albumin or immunoglobulin. Bait containing poly(N-isopropylacrylamide) (NIPAm) based nanoparticles are able to overcome these physiological barriers. In one step they are able to capture, concentrate and preserve biomarkers from body fluids. Low-molecular weight analytes enter the core of the nanoparticle and are captured by different organic chemical dyes, which act as high affinity protein baits. The nanoparticles are able to concentrate the proteins of interest by several orders of magnitude. This concentration factor is sufficient to increase the protein level such that the proteins are within the detection limit of current mass spectrometers, western blotting, and immunoassays. Nanoparticles can be incubated with a plethora of biological fluids and they are able to greatly enrich the concentration of low-molecular weight proteins and peptides while excluding albumin and other high-molecular weight proteins. Our data show that a 10,000 fold amplification in the concentration of a particular analyte can be achieved, enabling mass spectrometry and immunoassays to detect previously undetectable biomarkers.

Indexed as

Acrylic ResinsAdultBiomarkersBlood Chemical AnalysisBlood ProteinsFemaleHumansHydrogelsMaleNanoparticlesProteinsProteinuriaTumor Necrosis Factor-alphaUrinalysisAcrylic ResinsBiomarkersBlood ProteinsHydrogelspoly-N-isopropylacrylamideProteinsTumor Necrosis Factor-alpha

Identifiers

PMID25145492
PMCPMC5783330

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.