Gadolinium (III) oxide nanoparticles coated with folic acid-functionalized poly(β-cyclodextrin-co-pentetic acid) as a biocompatible targeted nano-contrast agent for cancer diagnostic: in vitro and in vivo studies

  • Tohid Mortezazadeh
  • Elham Gholibegloo
  • Nader Riyahi AlamEmail author
  • Sadegh Dehghani
  • Soheila Haghgoo
  • Hossein Ghanaati
  • Mehdi KhoobiEmail author
Research Article



In this study, a novel targeted MRI contrast agent was developed by coating gadolinium oxide nanoparticles (Gd2O3 NPs) with β-cyclodextrin (CD)-based polyester and targeted by folic acid (FA).

Materials and methods

The developed Gd2O3@PCD–FA MRI contrast agent was characterized and evaluated in relaxivity, in vitro cell targeting, cell toxicity, blood compatibility and in vivo tumor MR contrast enhancement.


In vitro cytotoxicity and hemolysis assays revealed that Gd2O3@PCD–FA NPs have no significant cytotoxicity after 24 and 48 h against normal human breast cell line (MCF-10A) at concentration of up to 50 µg Gd+3/mL and have high blood compatibility at concentration of up to 500 µg Gd+3/mL. In vitro MR imaging experiments showed that Gd2O3@PCD–FA NPs enable targeted contrast T1- and T2-weighted MR imaging of M109 as overexpressing folate receptor cells. Besides, the in vivo analysis indicated that the maximum contrast-to-noise ratio (CNR) of tumor in mice increased after injection of Gd2O3@PCD–FA up to 5.89 ± 1.3 within 1 h under T1-weighted imaging mode and reduced to 1.45 ± 0.44 after 12 h. While CNR increased up to maximum value of 1.98 ± 0.28 after injection of Gd2O3@PCD within 6 h and reduced to 1.12 ± 0.13 within 12 h.


The results indicate the potential of Gd2O3@PCD–FA to serve as a novel targeted nano-contrast agent in MRI.


Targeted nano-contrast agent Magnetic resonance imaging Longitudinal relaxivity Contrast enhancement 



This work was supported in part by the research chancellor of Tehran University of Medical Sciences (Grant no. 96-04-30-36739), Tehran, Iran.

Compliance with ethical standards

Conflict of interest

The authors do not have any conflict of interest.

Ethical approval

All in vivo protocols were performed based on the European Community guidelines and was approved by local ethical committee, Tehran University of Medical Sciences (TUMS), Tehran, Iran (Approval number: IR.TUMS.REC0.1394.1461).


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Copyright information

© European Society for Magnetic Resonance in Medicine and Biology (ESMRMB) 2019

Authors and Affiliations

  1. 1.Department of Medical Physic, School of MedicineTabriz University of Medical SciencesTabrizIran
  2. 2.Biomaterials Group, The Institute of Pharmaceutical Sciences (TIPS)Tehran University of Medical SciencesTehranIran
  3. 3.Department of Medical Physics and Biomedical EngineeringTehran University of Medical SciencesTehranIran
  4. 4.Department of Pharmaceutical Biomaterials, Faculty of PharmacyTehran University of Medical SciencesTehranIran
  5. 5.Pharmaceutical Department, Food and Drug Laboratory Research Center, Food and Drug Organization (FDO)Ministry of HealthTehranIran
  6. 6.Medical Imaging Center, Imam Hospital Complex, School of MedicineTehran University of Medical Sciences (TUMS)TehranIran

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