Cited by 93Advanced MRI Techniques and ApplicationsTissue Engineering and Regenerative MedicineCollagen: Extraction and Characterization

Iron Oxide‐Labeled Collagen Scaffolds for Non‐Invasive MR Imaging in Tissue Engineering

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Mertens, Marianne E., Hermann, Alina, Bühren, Anne, Olde‐Damink, Leon, Möckel, Diana, Gremse, Felix, Ehling, Josef, Kiessling, Fabian +1 more·2014·Advanced Functional Materials

Abstract

Non‐invasive imaging holds significant potential for implementation in tissue engineering. It can be used to monitor the localization and function of tissue‐engineered implants, as well as their resorption and remodelling. Thus far, however, the vast majority of effort in this area of research have focused on the use of ultrasmall super‐paramagnetic iron oxide (USPIO) nanoparticle‐labeled cells, colonizing the scaffolds, to indirectly image the implant material. Reasoning that directly labeling scaffold materials might be more beneficial (enabling imaging also in the case of non‐cellularized implants), more informative (enabling the non‐invasive visualization and quantification of scaffold degradation), and easier to translate into the clinic (cell‐free materials are less complex from a regulatory point‐of‐view), three different types of USPIO nanoparticles are prepared and incorporated both passively and actively (via chemical conjugation; during collagen crosslinking) into collagen‐based scaffold materials. The amount of USPIO incorporated into the scaffolds is optimized, and correlated with MR signal intensity, showing that the labeled scaffolds are highly biocompatible, and that scaffold degradation can be visualized using MRI. This provides an initial proof‐of‐principle for the in vivo visualization of the scaffolds. Consequently, USPIO‐labeled scaffold materials seem to be highly suitable for image‐guided tissue engineering applications.

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  • Several clinical studies have been performed with SPION-loaded cells, including labeled neuronal stem cells for traumatic brain injury and labeled pancreatic islet cells for diabetes.

    “Several clinical studies have been performed with SPION-loaded cells, including e.g. labeled neuronal stem cells for traumatic brain injury and labeled pancreatic islet cells for diabetes [257, 258].”

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Authors
Mertens, M. E., Hermann, A., Bühren, A., Olde‐Damink, L., Möckel, D., Gremse, F., Ehling, J., Kiessling, F., & Lammers, T.
Affiliations
  • Universitätsklinikum Aachen (DE)
  • Matricel GmbH Kaiserstraße 100 52134 Herzogenrath Germany
Corresponding author
Lammers, Twan
Venue
Advanced Functional Materials
Publisher
Wiley
Published
2013-08-28
Volume
24
Issue
6
Pages
754-762
ISSN
  • 1616-301X (ISSN-L)
  • 1616-3028
OpenAlex
W1995415354
Cited by
93
References
2
Citations by year
2026: 2 · 2025: 3 · 2024: 3 · 2023: 8 · 2022: 12 · 2021: 11 · 2020: 7 · 2019: 13 · 2018: 9 · 2017: 8 · 2016: 6 · 2015: 4 · 2014: 7
FWCI
4.40
Type
journal article
Language
en
Open access
Locations
  • Advanced Functional Materials (publishedVersion)
  • PubMed (publishedVersion)
  • University of Twente Research Information (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • RWTH Publications (RWTH Aachen) (submittedVersion)
  • University of Twente Research Information (submittedVersion)
Funders
  • European Regional Development Fund (2007 – 2013)
  • FP7 Ideas: European Research Council (309495)
Topics
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
  • Physical Sciences › Materials Science › Biomaterials › Collagen: Extraction and Characterization
Keywords
superparamagnetic iron oxide nanoparticles, collagen scaffolds, magnetic resonance imaging, non-invasive imaging, tissue-engineered implants, scaffold degradation, chemical conjugation, collagen cross-linking, biocompatibility

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