Chinese Journal of Tissue Engineering Research ›› 2012, Vol. 16 ›› Issue (16): 2884-2888.doi: 10.3969/j.issn.1673-8225.2012.16.008

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Target inhibitory effect of magnetic carbon nanotubes loaded with 5-fluorouracil on lymph node metastasis of colon cancer 

Jin Yan-zhao, Tan Min   

  1. Department of Minimal Invasive Surgery, First Affiliated Hospital of Sun Yat-Sen University, Guangzhou  510080, Guangdong Province, China
  • Received:2011-09-09 Revised:2011-10-03 Online:2012-04-15 Published:2012-04-15
  • Contact: author: Tan Min, Professor, Doctoral supervisor, Department of Minimal Invasive Surgery, First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, Guangdong Province, China tantommy@163.com
  • About author:Jin Yan-zhao☆, Studying for doctorate, Physician, Department of Minimal Invasive Surgery, First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, Guangdong Province, China jyz998152@126.com

Abstract:

BACKGROUND: Carbon nanotubes are prepared by magnetic targeting drug carrier in the magnetic field to better drug delivery to target organs or tissues in vivo.
OBJECTIVE: To evaluate the inhibitory effect of the magnetic carbon nanotubes as a new chemotherapy carrier on lymph node metastasis of colon cancer.
METHODS: The inhibitory effects of different concentrations of 5-fluorouracil (5-FU), magnetic multi-walled carbon nanotubes-5-fluorouracil (mMWNTs-5-FU) and magnetic multi-walled carbon nanotubes (mMWNTs) (0.000 3, 0.003, 0.03, 0.3,   3 g/L 5-FU) on the growth of SW480 cells in vitro were measured by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. 5-FU, mMWNTs-5-FU and mMWNTs were injected into subcutaneous footpad of Sprague-Dawley rats and lymph node metastasis of colon cancer nude mice.
RESULTS AND CONCLUSION: Treatment of the cancer cells with various concentrations (0.000 3, 0.003, 0.03, 0.3, 3 g/L 5-FU) of mMWNTs-5-FU caused a dose-dependent decrease in cell viability relative to the control culture, with the same 5-FU levels. The in vitro inhibition of SW480 cells had no significant difference, showing the main ingredient of mMWNTs-5-FU is 5-FU. High pressure liquid chromatography detection in vivo showed that mMWNTs-5-FU could effectively gather in the lymph nodes and prolong release. Lymph concentration was better than 5-FU (P < 0.05), and adverse reactions were less, visually easy to identify, cell-penetrating good; terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling method detected clear apoptosis of lymph node metastasis cells after the mMWNTs-5-FU chemotherapy. This shows colon cancer lymph node metastasis is significantly inhibited by mMWNTs-5-FU chemotherapy.

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