Hematotoxicity of magnetite nanoparticles coated with polyethylene glycol: in vitro and in vivo studies

被引:15
作者
Ruiz, A. [1 ,2 ]
Ali, Lamiaa M. A. [3 ,4 ]
Caceres-Velez, P. R. [5 ]
Cornudella, R. [6 ]
Gutierrez, M. [6 ]
Moreno, J. A. [6 ]
Pinol, R. [3 ,4 ]
Palacio, F. [3 ,4 ]
Fascineli, M. L. [5 ]
de Azevedo, R. B. [5 ]
Morales, M. P. [1 ]
Millan, A. [3 ,4 ]
机构
[1] CSIC, Inst Ciencia Mat Madrid, Dept Biomat & Mat Bioinspirados, Madrid 28049, Spain
[2] Ctr Estudios Avanzados Cuba, Havana, Cuba
[3] Univ Zaragoza, Inst Ciencia Mat Aragon, CSIC, E-50009 Zaragoza, Spain
[4] Univ Zaragoza, Fac Ciencias, Dept Fis Mat Condensada, E-50009 Zaragoza, Spain
[5] Univ Brasilia, Dept Genet & Morfol, BR-70910900 Brasilia, DF, Brazil
[6] Univ Zaragoza, Dept Med, Fac Med, E-50009 Zaragoza, Spain
关键词
DNA-DAMAGE; MICRONUCLEUS ASSAY; BONE-MARROW; COMET ASSAY; OXIDE; HEMOCOMPATIBILITY; GENOTOXICITY; PNIPAAM; CELLS; SIZE;
D O I
10.1039/c4tx00241e
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Hematotoxicity of magnetite nanoparticles coated with dimercaptosuccinic acid (DMSA) and polyethylene glycol (PEG) has been evaluated by determining their safety in vitro and in vivo in a rat model up to 30 days after administration of a single dose. The in vitro analysis consists of global plasma coagulation (PT, aPTT, and fibrinogen) and platelet aggregation tests while the hematotoxicity studies in vivo include a complete blood count and the possible genotoxic effect analysis in the bone marrow hematopoietic function. Prolonged aPTT values indicate a higher anticoagulant effect for NP-DMSA compared with PEG-coated nanoparticles as a consequence of the higher surface charge of the former. The in vivo tests showed that these bioferrofluids do not cause genotoxic effects, affect erythropoiesis or increase the number of immature erythrocytes in the bone marrow at the analyzed dose. However, nanoparticle administration showed a significant effect on the leukocyte counts in animals treated with DMSA coated nanoparticles 24 h after injection. This response is not observed in animals treated with PEG modified nanoparticles which justifies the use of this polymer in biomasking strategies.
引用
收藏
页码:1555 / 1564
页数:10
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