Skip to content
2000
Volume 20, Issue 16
  • ISSN: 1871-5206
  • E-ISSN: 1875-5992

Abstract

Objective: Polydopamine coated iron oxide nanoparticles (FeO@PDA NPs) were synthesized, characterized, and their MR imaging contrast agents and photothermal potency were evaluated on melanoma (B16-F10 and A-375) cells and normal skin cells. To this end, MTT assay, Fe concentration, and MR imaging of both coated and uncoated NPs were assessed in C57BL/6 mice. Methods: Fe3O4 nanoparticles were synthesized using co-precipitation, and coated with polydopamine. The cytotoxicity of FeO and FeO@PDA NPs on melanoma cells, with different concentrations, were obtained using MTT assay. MR images and Fe concentrations of nanoprobe and nanoparticles were evaluated under in vivo conditions. Results: Findings indicated that uncoated FeO showed the highest toxicity in animal (B16-F10) cells at 450μg/ml after 72h, while the highest toxicity in human (A-375) cells were observed at 350μg/ml. These nanoparticles did not reveal any cytotoxicity to normal skin cells, despite having some toxicity features in A-375 cells. MR image signals in the tumor were low compared with other tissues. The iron concentration in the tumor was higher than that of other organs. Conclusion: It is concluded that the cytotoxicity of FeO@PDA was found to be significantly lower than uncoated nanoparticles (p <0.001), which allows some positive effects on reducing toxicity. The prepared nanoprobe may be used as a contrast agent in MR imaging.

Loading

Article metrics loading...

/content/journals/acamc/10.2174/1871520620666200513084616
2020-11-01
2025-04-04
Loading full text...

Full text loading...

/content/journals/acamc/10.2174/1871520620666200513084616
Loading

  • Article Type:
    Research Article
Keyword(s): A-375; B16-F10; cytotoxicity; Fe3O4; Fe3O4@PDA NPs; MR imaging
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test