de Souza Gustavo Torres, Louzada Ruy Andrade, Rosado-de-Castro Paulo Henrique, Mendez-Otero Rosalia, Campos de Carvalho Antonio Carlos
NUMPEX-Bio, Federal University of Rio de Janeiro, Duque de Caxias, RJ.
Laboratory of Animal Reproduction, Embrapa Dairy Cattle, Juiz de Fora, MG; Laboratory of Genetics, Federal University of Juiz de Fora, Juiz de Fora, MG, Brazil.
Int J Nanomedicine. 2017 Jan 25;12:779-793. doi: 10.2147/IJN.S126530. eCollection 2017.
Superparamagnetic iron oxide nanoparticles (SPIONs) have been used for diagnoses in biomedical applications, due to their unique properties and their apparent safety for humans. In general, SPIONs do not seem to produce cell damage, although their long-term in vivo effects continue to be investigated. The possibility of efficiently labeling cells with these magnetic nanoparticles has stimulated their use to noninvasively track cells by magnetic resonance imaging after transplantation. SPIONs are attracting increasing attention and are one of the preferred methods for cell labeling and tracking in preclinical and clinical studies. For clinical protocol approval of magnetic-labeled cell tracking, it is essential to expand our knowledge of the time course of SPIONs after cell incorporation and transplantation. This review focuses on the recent advances in tracking SPION-labeled stem cells, analyzing the possibilities and limitations of their use, not only focusing on myocardial infarction but also discussing other models.
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