Chemical Research in Chinese Universities ›› 2010, Vol. 26 ›› Issue (5): 780-784.

• Articles • Previous Articles     Next Articles

Preparation, Release-control and Cell Apoptosis of C6 Glioma Cells in PEG-PLGA-Rg3 Nanoparticles

BIE Li1, YUAN Hong-yan2, WANG Xin3, ZHAO Gang1* and LIU Xing-ji1*   

  1. 1. Department of Neurosurgery, First Clinical Hospital,
    2. Department of Immunology, Norman Bethune College of Medicine, Jilin University, Changchun 130021, P. R. China;
    3. Center of Tumor Biotherapy, Second Clinical Hospital, Jilin University,  Changchun 130041, P. R. China
  • Received:2010-05-11 Revised:2010-07-06 Online:2010-09-25 Published:2010-11-26
  • Contact: LIU Xing-ji. E-mail: xjl9831@163.com; ZHAO Gang. E-mail: zhaogang20052000@yahoo.com.cn
  • Supported by:

    Supported by the National Natural Science Foundation of China(No.30471769).

Abstract: With biodegradable material poly(ethylene glycol)-poly(lactide-co-glycolide) (PEG-PLGA) as substrate, the size distribution of Rg3-NPs was approved by the scanning electron microscopy. MTT assay was used to detect the effects of Rg3-NPs on the growth rate of C6 cells at various concentrations and flow cytometry(FCM) was applied to assay the cell cycle and cell apoptosis of C6 glioma cells. Western blot analysis was used to measure the protein level of PCNA. The results show that Rg3-NPs are slick and uniformity, the average diameter of the nanoparticles is about 75―90 nm, entrapment efficiency is (89.7±1.7)%. MTT assay shows the growth of C6 Glioma Cells can be significantly inhibited by Rg3-NPs in a dose-dependence manner. FCM and Western blot analysis show Rg3 can be released from the conjugated nanoparticles to function in the cell nuclei so as to lead to the changes in the growth cycle of the cells, which results in the arrest of G0-G1 cell cycle and induces the apoptosis of C6 cells. Therefore, Rg3-NPs may be used for the auxiliary therapy of brain glioma.

Key words: Ginsenoside Rg3, Poly(D,L-lactide-co-glycolide), Characteristics of physical chemistry, C6 glioma cell, Apotosis