Evidence map›Paper›PMID 26597417›Full record

ArticleAnnals of biomedical engineering2016

Siloxane Nanoprobes for Labeling and Dual Modality Functional Imaging of Neural Stem Cells.

Caroline P Addington, Alex Cusick, Rohini Vidya Shankar, Shubhangi Agarwal, Sarah E Stabenfeldt, Vikram D Kodibagkar

Open access · greenAbstract read
In one paragraph

Article in Annals of biomedical engineering, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Bypassing Heteronuclear MRI: Metal-Free Organosilicon Nanotracers for Background-Free HotspotAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Nanoparticle-Based Therapeutics for Brain Injury.Advanced healthcare materials · 2018
    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

6 authors at 1 institution in 1 country.

Caroline P AddingtonSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA.
Alex CusickSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA.
Rohini Vidya ShankarSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA.
Shubhangi AgarwalSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA.
Sarah E StabenfeldtSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA. Sarah.Stabenfeldt@asu.edu.
Vikram D KodibagkarSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, 85287, USA. Vikram.Kodibagkar@asu.edu.
Arizona State University · US

Funding

Detecting and Treating Traumatic Brain Injury Pathology Progression from the Inside-OutDP2HD084067 · NICHD · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI STABENFELDT, SARAH E · 2014 to 2018
$2.8M
NCCDPHP CDC HHS 1DP2HD084067NICHD NIH HHS DP2 HD084067
6 · The paper itself

Abstract

Cell therapy represents a promising therapeutic for a myriad of medical conditions, including cancer, traumatic brain injury, and cardiovascular disease among others. A thorough understanding of the efficacy and cellular dynamics of these therapies necessitates the ability to non-invasively track cells in vivo. Magnetic resonance imaging (MRI) provides a platform to track cells as a non-invasive modality with superior resolution and soft tissue contrast. We recently reported a new nanoprobe platform for cell labeling and imaging using fluorophore doped siloxane core nanoemulsions as dual modality ((1)H MRI/Fluorescence), dual-functional (oximetry/detection) nanoprobes. Here, we successfully demonstrate the labeling, dual-modality imaging, and oximetry of neural progenitor/stem cells (NPSCs) in vitro using this platform. Labeling at a concentration of 10 μL/10(4) cells with a 40%v/v polydimethylsiloxane core nanoemulsion, doped with rhodamine, had minimal effect on viability, no effect on migration, proliferation and differentiation of NPSCs and allowed for unambiguous visualization of labeled NPSCs by (1)H MR and fluorescence and local pO2 reporting by labeled NPSCs. This new approach for cell labeling with a positive contrast (1)H MR probe has the potential to improve mechanistic knowledge of current therapies, and guide the design of future cell therapies due to its clinical translatability.

Indexed as

Fluorescent DyesNeural Stem CellsSiloxanesAnimalsCell DifferentiationCell MovementCell ProliferationCell TrackingMiceMolecular ImagingNanoparticlesStaining and LabelingFluorescent DyesSiloxanesCell-labelingDual-modality imagingFluorescenceMR oximetryNanoemulsionsNeural progenitor/stem cellsPolydimethylsiloxaneRhodamine

Identifiers

PMID26597417
PMCPMC4792673
OpenAlexW2175108637

What OpenQuestion holds

Textmetadata
LicenceTDM
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.