2015
DOI: 10.1088/1742-6596/617/1/012002
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Preparation, Characterization and Tests of Incorporation in Stem Cells of Superparamagnetic Iron Oxide

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Cited by 9 publications
(7 citation statements)
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“…Given that SPION toxicity mainly stems from oxidative stress, surface modification with an antioxidant (such as N-Acetylcysteine or Trolox) may be a new method to suppress oxidative damage and injury. The thiolated SPIONs with mercaptosuccinic acid (MSA) and cysteine (Cys) have no toxic effects for stem cells [118]. Long-term in vivo studies in murine models have shown that dimercaptosuccinic acid (DMSA)-coated MNPs accumulate in spleen, liver and lung tissues during extended periods of time (at least up to 3 months) without any significant signs of toxicity detected [119].…”
Section: Toxicity Assessmentmentioning
confidence: 99%
“…Given that SPION toxicity mainly stems from oxidative stress, surface modification with an antioxidant (such as N-Acetylcysteine or Trolox) may be a new method to suppress oxidative damage and injury. The thiolated SPIONs with mercaptosuccinic acid (MSA) and cysteine (Cys) have no toxic effects for stem cells [118]. Long-term in vivo studies in murine models have shown that dimercaptosuccinic acid (DMSA)-coated MNPs accumulate in spleen, liver and lung tissues during extended periods of time (at least up to 3 months) without any significant signs of toxicity detected [119].…”
Section: Toxicity Assessmentmentioning
confidence: 99%
“…Superparamagnetic iron oxide nanoparticles, such as Fe 3 O 4 (magnetite), have been employed in a variety of biomedical applications, including diagnostics and drug delivery. [1][2][3][4][5][6][7][8][9][10] Due to the superparamagnetic behavior of Fe 3 O 4 at room temperature, these NPs have a large constant magnetic moment and act as a giant paramagnetic atom, quickly responding to applied magnetic elds without residual magnetism and coercivity. This behavior makes Fe 3 O 4 NPs attractive in a number of biomedical applications.…”
Section: Introductionmentioning
confidence: 99%
“…[25] Studies show that DMSA-coated iron oxide nanoparticles can greatly enhance the rate of cellular acceptance, leading to nonspecific adsorption to the cell surface, followed by endocytosis. [8,26,27] Taking advantage of DMSA-SPIONs, in this study, we obtained Fe 3 O 4 nanoparticles by the co-precipitation method using ferrous and ferric chlorides in an aqueous solution.…”
Section: Introductionmentioning
confidence: 99%
“…In the last decades, the use of superparamagnetic iron oxide nanoparticles (SPIONs) in biomedicine and pharmaceutical sciences were carefully investigated, especially magnetite nanoparticles (Fe 3 O 4 ), once they have been successfully used in different biomedical applications such as drug delivery, contrast agents for imaging, controlled drug release, hyperthermia, among others[ 6 , 7 , 8 , 9 ] SPIONs present superparamagnetic behavior and act as a single magnetic domain [10] providing fast response under an external magnetic field and consequently can be guided to a specific target. [8] In addition, when the magnetic field is removed, no residual magnetization remains, avoiding agglomeration of the nanoparticles in vivo. [11] This feature permits the guided administration of these nanoparticles to the target tissue/organ with minimum side effects.…”
Section: Introductionmentioning
confidence: 99%