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Related Experiment Video

Updated: Jun 20, 2026

Labeling Stem Cells with Ferumoxytol, an FDA-Approved Iron Oxide Nanoparticle
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Labeling Stem Cells with Ferumoxytol, an FDA-Approved Iron Oxide Nanoparticle

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Accelerated stem cell labeling with ferucarbotran and protamine.

Daniel M Golovko1, Tobias Henning, Jan S Bauer

  • 1Department of Radiology & Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.

European Radiology
|September 17, 2009
PubMed
Summary
This summary is machine-generated.

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Protamine accelerates ferucarbotran uptake in mesenchymal stem cells (MSCs) for enhanced MRI visualization. This clinically applicable method significantly reduces labeling time without affecting cell viability.

Area of Science:

  • Biomedical Engineering
  • Cell Biology
  • Medical Imaging

Background:

  • Accurate stem cell tracking is crucial for regenerative medicine.
  • Clinical Magnetic Resonance Imaging (MRI) requires efficient and reliable cell labeling methods.
  • Ferucarbotran is an iron oxide contrast agent, but its uptake can be slow.

Purpose of the Study:

  • To develop a fast and clinically applicable method for labeling human mesenchymal stem cells (MSCs) with ferucarbotran for MRI.
  • To investigate the role of protamine in enhancing ferucarbotran uptake.
  • To characterize the physicochemical properties and MRI performance of labeled cells.

Main Methods:

  • Ferucarbotran and protamine physicochemical properties were analyzed.
  • MSCs were labeled with ferucarbotran and protamine at various concentrations and incubation times.

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Published on: April 2, 2008

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Last Updated: Jun 20, 2026

Labeling Stem Cells with Ferumoxytol, an FDA-Approved Iron Oxide Nanoparticle
05:05

Labeling Stem Cells with Ferumoxytol, an FDA-Approved Iron Oxide Nanoparticle

Published on: November 4, 2011

Labeling hESCs and hMSCs with Iron Oxide Nanoparticles for Non-Invasive in vivo Tracking with MR Imaging
09:06

Labeling hESCs and hMSCs with Iron Oxide Nanoparticles for Non-Invasive in vivo Tracking with MR Imaging

Published on: March 31, 2008

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07:42

Labeling Stem Cells with Fluorescent Dyes for non-invasive Detection with Optical Imaging

Published on: April 2, 2008

  • Cell viability was assessed using Trypan blue exclusion.
  • Labeled cells were imaged using 3 T MRI (T1, T2, T2*-weighted sequences).
  • Intracellular iron uptake was confirmed via electron microscopy.
  • Main Results:

    • Protamine significantly accelerated ferucarbotran labeling in MSCs from 24 hours to 1 hour.
    • Cell viability remained unaffected by the labeling process.
    • Increased R2 and R2* relaxation rates were observed, indicating effective labeling.
    • Electron microscopy confirmed intracellular iron oxide uptake in lysosomes.
    • Relaxation rates correlated with ICP-AES measurements.

    Conclusions:

    • Protamine acts as an effective uptake-enhancing agent for ferucarbotran in MSCs.
    • This accelerated labeling method is potentially clinically applicable for stem cell MRI.
    • The developed method offers a faster and efficient approach for stem cell tracking.