Tracking stem cells with superparamagnetic iron oxide nanoparticles: perspectives and considerations

被引:57
作者
Jasmin [1 ]
de Souza, Gustavo Torres [2 ,3 ]
Louzada, Ruy Andrade [4 ]
Rosado-de-Castro, Paulo Henrique [5 ]
Mendez-Otero, Rosalia [6 ]
Campos de Carvalho, Antonio Carlos [6 ]
机构
[1] Univ Fed Rio de Janeiro, NUMPEX Bio, Duque De Caxias, RJ, Brazil
[2] Embrapa Dairy Cattle, Lab Anim Reprod, Juiz De Fora, MG, Brazil
[3] Univ Fed Juiz de Fora, Lab Genet, Juiz De Fora, MG, Brazil
[4] Paris Sud Univ, Inst Gustave Roussy Oncol, Villejuif, France
[5] Univ Fed Rio de Janeiro, Inst Biomed Sci, Rio De Janeiro, RJ, Brazil
[6] Univ Fed Rio de Janeiro, Inst Carlos Chagas Filho Biophys, Rio De Janeiro, RJ, Brazil
关键词
nanoparticles; superparamagnetic iron oxide nanoparticles; stem cells; cell tracking; in vivo imaging; myocardial infarction;
D O I
10.2147/IJN.S126530
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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.
引用
收藏
页码:779 / 793
页数:15
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