Acta Chimica Sinica ›› 2010, Vol. 68 ›› Issue (23): 2449-2456. Previous Articles     Next Articles

Full Papers

MePEG-b-PCL-b-PDMAEMA的可控合成及性能研究

朱亚明,张琰*,刘子路,郎美东*   

  1. (华东理工大学材料科学与工程学院 超细材料制备与应用教育部重点实验室 上海先进聚合物材料重点实验室
    上海 200237)
  • 投稿日期:2010-07-18 修回日期:2010-08-18 发布日期:2010-08-18
  • 通讯作者: 郎美东 E-mail:mdlang@ecust.edu.cn;mdlang@fudan.edu.cn

Controlled Synthesis and Properties of Triblock MePEG-b-PCL-b-PDMAEMA

ZHU Ya-Ming, ZHANG Yan, LIU Zi-Lu, LANG Mei-Dong   

  1. (Shanghai Key Laboratory of Advanced Polymeric Materials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237)
  • Received:2010-07-18 Revised:2010-08-18 Published:2010-08-18
  • Contact: Lang Meidong E-mail:mdlang@ecust.edu.cn;mdlang@fudan.edu.cn

A series of well-controlled triblock methoxy poly(ethylene glycol)-b-poly(ε-caprolactone)-b- poly[2-(dimethylamino) ethyl methacrylate] (MePEG-b-PCL-b-PDMAEMA) was obtained by ring open polymerization (ROP) and atom transfer radical polymerization (ATRP) methods. Their structures and composition were confirmed by 1H nuclear magnetic resonance (1H NMR), and the molecule weight and molecular weight distribution of the copolymers were obtained by 1H NMR and gel permeation chromatography (GPC). The thermal stability, crystallization property and hydrophiphilicity were evidenced by thermogravimetric analysis, X-ray diffraction (XRD) and static water contact angle measurements. The formation of the nanoparticles was studied by 1H NMR in D2O and fluorescence probe method. The transmission electron microscopy (TEM) displayed that the morphologies of the nanoparticles were spherical and the size was on nano scale. Dynamic light scattering (DLS) indicated that the nanoparticles were in the range of 40~70 nm, and in different pH solution, the nanoparticles showed good pH-sensitivity. Due to the hydrophobic core and the cationic hydrophilic shell, the nanoparticles has great potential application for the codelivery of hydrophobic drugs and negative drugs.

Key words: atom transfer radical polymerization (ATRP), self-assembly, amphiphilic, pH-responsive