Chinese Journal of Tissue Engineering Research ›› 2017, Vol. 21 ›› Issue (18): 2821-2827.doi: 10.3969/j.issn.2095-4344.2017.18.006

Previous Articles     Next Articles

Fabrication of multifunctional bismuth-doped iron nanoparticle and its radiotherapy sensitization in glioblastoma

Niu Yuan-yuan1, Yu Ming1, Du Feng-yi2, Chen Si-yuan1, Zhao Tian3, Xu Yu-hao1, Zhou Qian-wen1, Xu Xiu-jian1
  

  1. 1Department of Neurology, 3Department of Imaging, Affiliated Hospital of Jiangsu University, Zhenjiang 212001, Jiangsu Province, China; 2Jiangsu University Medical School, Zhenjiang 212013, Jiangsu Province, China
  • Received:2017-01-13 Online:2017-06-28 Published:2017-07-07
  • Contact: Yu Ming, M.D., Master’s supervisor, Chief physician, Associate professor, Department of Neurology, Affiliated Hospital of Jiangsu University, Zhenjiang 212001, Jiangsu Province, China
  • About author:Niu Yuan-yuan, Studying for master’s degree, Department of Neurology, Affiliated Hospital of Jiangsu University, Zhenjiang 212001, Jiangsu Province, China
  • Supported by:

    the “333 Engineering” Scientific Research Project of Jiangsu Province, No. BRA2014173; the “Six Talent Peaks” Scientific Research Project of Jiangsu Province, No. WSN-038

Abstract:

BACKGROUND: Bismth-doped iron nanoparticles modified by hyaluronic acid (HA-BiIOPs) not only act as an effective MRI contrast agent, but also as a radiotherapy sensitizer.
OBJECTIVE: To fabricate the HA-BiIOPs and to observe its effect to enhance the radiosensitivity of glioblastoma cells U87MG under X-ray radiation.
METHODS: HA-BiIOPs were synthesized using hydrothermal polyol method. (1) Cytotoxicity: A cytotoxicity test was carried out on U87MG cells and rat vascular smooth muscle cells (VSMCs). Cell proliferation rate of two kinds of cells cultured with different concentrations of HA-BiIOPs (0, 12.5, 25, 50, 100, 200, 400 mg/L) at 24 hours after culture were determined by cell counting kit-8 assay. (2) Histological analysis: ICR mice were sacrificed after intravenous injection of HA-BiIOPs, and pathological changes of mouse visceral organs were observed under an optical microscope. (3) Cellular uptake: The HA-BiIOPs after entered into the cytoplasm were observed by Prussian blue staining. (4) Radiosensitization test: U87MG cells at Logarithmic growth stage were cultured in culture medium as control group, subjected to X-ray irradiation (0, 3, 6, 9 Gy) as radiotherapy group, cultured in HA-BiIOPs (0, 12.5, 25, 50, 100, 200 and 400 mg/L) as HA-BiIOPs group or subjected to HA-BiIOPs culture plus X-ray irradiation as combined therapy group. Then, the cell proliferation rate and cloning efficiency were measured at 24 hours after treatment.
RESULTS AND CONCLUSION: (1) The HA-BiIOPs at different concentrations were non-cytotoxic for VSMC and U87MG cells. (2) After intravenous injection of HA-BiIOPs, there was no obvious toxicity to the mouse susceptible organs. (3) After 6 hours of culture, the HA-BiIOPs could be internalized by U87MG cells. (4) The proliferation rate of U87cells was negatively correlated with the concentration of HA-BiIOPs (0-200 mg/L) and X-ray dose (0-9 Gy). Especially, the combination of 6 Gy X-ray irradiation with 200 mg/L HA-BiIOPs dramatically decreased the cell viability that was decreased to (41±7)%. In the combined therapy group with 6 Gy X-ray and 100 mg/L HA-BiIOPs, the cells proliferation rate was significantly lower than that in the control and radiotherapy groups (P < 0.05). These results indicate that HA-BiIOPs have a radiosensitizative effect on glioblastoma cells U87MG.

Key words: Hyaluronic Acid, Nanocomposites, Glioblastoma, Tissue Engineering

CLC Number: