Label-free magnetic resonance imaging to locate live cells in three-dimensional porous scaffolds

Porous scaffolds are widely tested materials used for various purposes in tissue engineering. A critical feature of a porous scaffold is its ability to allow cell migration and growth on its inner surface. Up to now, there has not been a method to locate live cells deep inside a material, or in an e...

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Bibliographic Details
Published inJournal of the Royal Society interface Vol. 9; no. 74; pp. 2321 - 2331
Main Authors Abarrategi, A., Fernandez-Valle, M. E., Desmet, T., Castejón, D., Civantos, A., Moreno-Vicente, C., Ramos, V., Sanz-Casado, J. V., Martínez-Vázquez, F. J., Dubruel, P., Miranda, P., López-Lacomba, J. L.
Format Journal Article
LanguageEnglish
Published England The Royal Society 07.09.2012
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Summary:Porous scaffolds are widely tested materials used for various purposes in tissue engineering. A critical feature of a porous scaffold is its ability to allow cell migration and growth on its inner surface. Up to now, there has not been a method to locate live cells deep inside a material, or in an entire structure, using real-time imaging and a non-destructive technique. Herein, we seek to demonstrate the feasibility of the magnetic resonance imaging (MRI) technique as a method to detect and locate in vitro non-labelled live cells in an entire porous material. Our results show that the use of optimized MRI parameters (4.7 T; repetition time = 3000 ms; echo time = 20 ms; resolution 39 × 39 µm) makes it possible to obtain images of the scaffold structure and to locate live non-labelled cells in the entire material, with a signal intensity higher than that obtained in the culture medium. In the current study, cells are visualized and located in different kinds of porous scaffolds. Moreover, further development of this MRI method might be useful in several three-dimensional biomaterial tests such as cell distribution studies, routine qualitative testing methods and in situ monitoring of cells inside scaffolds.
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These authors contributed equally to the study.
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ISSN:1742-5689
1742-5662
DOI:10.1098/rsif.2012.0068