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Biosafety evaluation of Janus Fe 3 O 4 -TiO 2 nanoparticles in Sprague Dawley rats after intravenous injection.
- Source :
-
International journal of nanomedicine [Int J Nanomedicine] 2018 Oct 31; Vol. 13, pp. 6987-7001. Date of Electronic Publication: 2018 Oct 31 (Print Publication: 2018). - Publication Year :
- 2018
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Abstract
- Introduction: Newly synthesized Janus-structured Fe <subscript>3</subscript> O <subscript>4</subscript> -TiO <subscript>2</subscript> nanoparticles (NPs) appear to be a promising candidate for the diagnosis and therapy of cancer. Although the toxicity of individual Fe <subscript>3</subscript> O <subscript>4</subscript> or TiO <subscript>2</subscript> NPs has been studied extensively, the toxicity of Janus Fe <subscript>3</subscript> O <subscript>4</subscript> -TiO <subscript>2</subscript> NPs is not clear.<br />Methods: In this study, the biosafety of both Janus Fe <subscript>3</subscript> O <subscript>4</subscript> -TiO <subscript>2</subscript> NPs (20-25 nm) and the maternal material TiO <subscript>2</subscript> NPs (7-10 nm) were evaluated in Sprague Dawley rats after one intravenous injection into the tail vein. Healthy rats were randomly divided into one control group and six experimental groups. Thirty days after treatment, rats were killed, then blood and tissue samples were collected for hematological, biochemical, element-content, histopathological, and Western blot analysis.<br />Results: The results show that only a slight Ti element accumulation in the heart, spleen, and liver could be found in the Janus Fe <subscript>3</subscript> O <subscript>4</subscript> -TiO <subscript>2</subscript> NP groups ( P >0.05 compared with control). However, significant Ti element accumulation in the spleen, lungs, and liver was found in the TiO <subscript>2</subscript> NP-treated rats. Both Fe <subscript>3</subscript> O <subscript>4</subscript> -TiO <subscript>2</subscript> NPs and TiO <subscript>2</subscript> NPs could induce certain histopathological abnormalities. Western blot analysis showed that both NPs could induce certain apoptotic or inflammatory-related molecular protein upregulation in rat livers. A certain degree of alterations in liver function and electrolyte and lipid parameters was also observed in rats treated with both materials. However, compared to Janus structure Fe <subscript>3</subscript> O <subscript>4</subscript> -TiO <subscript>2</subscript> NP-treated groups, TiO <subscript>2</subscript> NPs at 30 mg/kg showed more severe adverse effects.<br />Conclusion: Our results showed that under a low dose (5 mg/kg), both NP types had no significant toxicity in rats. Janus NPs certainly seem less toxic than TiO <subscript>2</subscript> NPs in rats at 30 mg/kg. To ensure safe use of these newly developed Janus NPs in cancer diagnosis and therapy, further animal studies are needed to evaluate long-term bioeffects.<br />Competing Interests: Disclosure The authors report no conflicts of interest in this work.
- Subjects :
- Animals
Body Weight
Injections, Intravenous
Liver drug effects
Liver pathology
Lung drug effects
Lung pathology
Male
Nanoparticles ultrastructure
Organ Size
Particle Size
Rats, Sprague-Dawley
Signal Transduction
Spleen drug effects
Spleen metabolism
Spleen pathology
Nanoparticles administration & dosage
Nanoparticles adverse effects
Titanium administration & dosage
Titanium adverse effects
Subjects
Details
- Language :
- English
- ISSN :
- 1178-2013
- Volume :
- 13
- Database :
- MEDLINE
- Journal :
- International journal of nanomedicine
- Publication Type :
- Academic Journal
- Accession number :
- 30464454
- Full Text :
- https://doi.org/10.2147/IJN.S167851